Herbicidal pyrimidine compounds

The present invention relates to pyrimidine compounds of the general formula (I) defined below and to their use as herbicides. Moreover, the invention relates to compositions for crop protection and to a method for controlling unwanted vegetation.

Compounds having a 5-phenyl pyrimidine moiety are known in the art. WO 2000/073278 describes such compounds being antagonists of the Neurokinin 1 receptor and thus having pharmaceutical properties.

In agriculture, there is a constant demand to develop novel active ingredients, which complement or outperform present methods of treatment regarding activity, selectivity and environmental safety.

These and further objects are achieved by pyrimidine compounds of formula (I), defined below, and by their agriculturally suitable salts.

Accordingly, the present invention provides the use of pyrimidine compounds of formula (I)

including agriculturally acceptable salts or derivatives of the pyrimidine compounds of formula

(I) having an acidic functionality, as herbicides,

wherein in formula (I) the variables have the following meanings:

R ¹ d-Ce-alkyl, C C ₆ -haloalkyl, HO-C C ₆ -alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -haloalkenyl, C ₂ -C ₆ -al- kynyl, C3-C6-haloalkynyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxy, C3-C6-alkenyloxy, C3-C6- haloalkenyloxy, C3-C6-alkynyloxy, C3-C6-haloalkynyloxy, Ci-C6-haloalkoxy, C3-C6-cycloal- koxy, C3-C6-halocycloalkoxy, C3-C6-cycloalkenyloxy, C3-C6-halocycloalkenyloxy, C1-C6- alkylthio, Ci-C6-haloalkylthio, (Ci-C6-alkyl)amino, di(Ci-C6-alkyl)amino, Ci-C6-alkylsulfinyl, Ci-C6-alkylsulfonyl, C3-C6-cycloalkyl, C3-C6-cycloalkenyl, C3-C6-halocycloalkyl, C3-C6-halo- cycloalkenyl, [1-(Ci-C ₆ -alkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -alkenyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C ₂ - C ₆ -alkynyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(Ci-C ₆ -haloalkyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(C ₂ -C ₆ -haloal- kenyl)]-C3-C6-cycloalkyl, [1 -(C3-C6-haloalkynyl)]-C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C6- alkyl, C3-C6-cycloalkyl-Ci-C6-haloalkyl, C3-C6-cycloalkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl-Ci- C6-haloalkoxy, phenyl, 5-, 6- or 9-membered heteroaryl, or 3- to 6-membered heterocyclyl; wherein the cyclic groups of R ¹ are unsubstituted or substituted by R ^a ;

R ² is Ci-C6-alkyl, Ci-C6-haloalkyl, C ₂ -C6-alkenyl, C ₂ -C6-haloalkenyl, Ci-C6-alkoxy-C ₂ -C6-alke- nyl, Ci-C6-alkoxy-C ₂ -C6-haloalkenyl, Ci-C6-haloalkoxy-C ₂ -C6-alkenyl, Ci-C6-haloalkoxy-C ₂ - C6-haloalkenyl, C ₂ -C6-alkynyl, C ₂ -C6-haloalkynyl, Ci-C6-alkoxy-C ₂ -C6-alkynyl, Ci-C6-alk- oxy-C ₃ -C6-haloalkynyl, CrC ₆ -haloalkoxy-C ₂ -C6-alkynyl, CrC ₆ -haloalkoxy-C ₃ -C6-haloalky- nyl, C ₃ -C6-cycloalkyl, C ₃ -C6-halocycloalkyl, C ₃ -C6-cycloalkenyl, C ₃ -C6-halocycloalkenyl, C ₃ - C6-cycloalkyl- Ci-C6-alkyl, C3-C6-cycloalkyl-Ci-C6-haloalkyl, C3-C6-halocycloalkyl-Ci-C6- alkyl, C3-C6- alocycloalkyl-Ci-C6- aloalkyl, C3-C6-cycloalkenyl-Ci-C6-alkyl, C3-C6-cycloal- kenyl-Ci-C6- aloalkyl, C3-C6-halocycloalkenyl-Ci-C6-alkyl, C3-C6- alocycloalkenyl-Ci-C6- haloalkyl, C3-C6-cycloalkyl- C2-C6-alkenyl, C3-C6-cycloalkyl-C2-C6- aloalkenyl, C3-C6- alo- cycloalkyl-C2-C6-alkenyl, C3-C6- alocycloalkyl-C2-C6- aloalkenyl, C3-C6-cycloalkenyl-C2- C6-alkenyl, C3-C6-cycloalkenyl-C2-C6- aloalkenyl, C3-C6- alocycloalkenyl-C2-C6-alkenyl, C3-C6- alocycloalkenyl-C2-C6-haloalkenyl, C3-C6-cycloalkyl-C2-C6-alkynyl, C3-C6-cycloal- kyl-C3-C6- aloalkynyl, C3-C6- alocycloalkyl-C2-C6-alkynyl, C3-C6- alocycloalkyl-C3-C6-ha- loalkynyl, C3-C6-cycloalkenyl-C2-C6-alkynyl, C3-C6-cycloalkenyl-C3-C6- aloalkynyl, C3-C6- halocycloalkenyl-C2-C6-alkynyl, C3-C6- alocycloalkenyl-C3-C6-haloalkynyl, C3-C6-cycloal- kyl-Ci-C6-alkylidenyl, C3-C6-cycloalkyl-C2-C6- aloalkylidenyl, C3-C6- alocycloalkyl-Ci-C6- alkylidenyl, C3-C6- alocycloalkyl-C2-C6- aloalkylidenyl, C3-C6-cycloalkenyl-Ci-C6-alkyli- denyl, C3-C6-cycloalkenyl-C2-C6- aloalkylidenyl, C3-C6- alocycloalkenyl-Ci-C6-alkylidenyl, C3-C6- alocycloalkenyl-C2-C6-haloalkylidenyl, heterocyclyl-Ci-C6-alkylidenyl, heterocyclyl- C2-C6- aloalkylidenyl, C3-C6- ydroxycycloalkyl-Ci-C6-alkyl, C3-C6- ydroxycycloalkyl-Ci-C6 haloalkyi, C3-C6-hydroxycycloalkenyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkenyl-Ci-C6-haloal kyl, CrC ₆ -hydroxyalkyl, C2-C6-hydroxyhaloalkyl, C3-C6-hydroxyalkenyl, C3-C6-hydroxy- haloalkenyl, C3-C6-hydroxyalkynyl, C4-C6-hydroxyhaloalkynyl, C3-C6-hydroxycycloalkyl, C3 C6-hydroxyhalocycloalkyl, C3-C6-hydroxycycloalkenyl, C3-C6-hydroxyhalocycloalkenyl, C3- C6-cycloalkyl-Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl-C2-C6-hydroxyhaloalkyl, C3-C6-halocy- cloalkyl-Ci-C6-hydroxyalkyl, C3-C6-halocycloalkyl-C2-C6-hydroxyhaloalkyl, C3-C6-cycloal- kenyl-Ci-C6-hydroxyalkyl, C3-C6-cycloalkenyl-C2-C6-hydroxyhaloalkyl, C3-C6-halocycloal- kenyl-Ci-C6-hydroxyalkyl, C3-C6-halocycloalkenyl-C2-C6-hydroxyhaloalkyl, C3-C6-cycloal- kyl-C3-C6-hydroxyalkenyl, C3-C6-cycloalkyl-C3-C6-hydroxyhaloalkenyl, C3-C6-halocycloal- kyl-C3-C6-hydroxyalkenyl, C3-C6-halocycloalkyl-C3-C6-hydroxyhaloalkenyl, C3-C6-cycloal- kenyl-C3-C6-hydroxyalkenyl, C3-C6-cycloalkenyl-C3-C6-hydroxyhaloalkenyl, C3-C6-halocy- cloalkenyl-C3-C6-hydroxyalkenyl, C3-C6-halocycloalkenyl-C3-C6-hydroxyhaloalkenyl, C3-C6 cycloalkyl-C3-C6-hydroxyalkynyl, C3-C6-halocycloalkyl-C3-C6-hydroxyalkynyl, C3-C6-cyclo- alkenyl-C3-C6-hydroxyalkynyl, C3-C6-halocycloalkenyl-C3-C6-hydroxyalkynyl, C3-C6-cyclo- alkyl-C2-C6-hydroxyalkylidenyl, C3-C6-halocycloalkyl-C2-C6-hydroxyalkylidenyl, C3-C6-cy- cloalkenyl-C2-C6-hydroxyalkylidenyl, C3-C6-halocycloalkyl-C2-C6-hydroxyalkylidenyl, heter- ocyclyl-C2-C6-hydroxyalkylidenyl, hydroxycarbonyl-Ci-C6-hydroxyalkyl, hydroxycarbonyl- Ci-C6-alkyl, hydroxycarbonyl-Ci-C6-haloalkyl, Ci-C6-alkoxycarbonyl-CrC ₆ -hydroxyalkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6-hydroxyalkyl, Ci-C6-alkoxycarbonyl-Ci-C6-haloalkyl, Ci- C6-haloalkoxycarbonyl-Ci-C6-haloalkyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, Ci-C6-haloal- koxycarbonyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C3-C6-hydroxycy- cloalkenyl-Ci-C6-hydroxyalkyl, C3-C6-hydroxycycloalkyl-C3-C6-hydroxyalkenyl, C3-C6-hy- droxycycloalkenyl-C3-C6-hydroxyalkenyl, C3-C6-hydroxycycloalkyl-C3-C6-hydroxyalkynyl, C3-C6-hydroxycycloalkenyl-C3-C6-hydroxyalkenyl, C2-C6-dihydroxyalkyl, C3-C6-dihydroxy- haloalkyl, C4-C6-dihydroxyalkenyl, C4-C6-dihydroxyhaloalkenyl, C4-C6-dihydroxyalkynyl, C5-C6-dihydroxyhaloalkynyl, C4-C6-dihydroxycycloalkyl, C4-C6-dihydroxyhalocycloalkyl, C4 C6-dihydroxycycloalkenyl, C4-C6-dihydroxyhalocycloalkenyl, C3-C6-cycloalkyl-C2-C6-dihy- droxyalkyl, C3-C6-halocycloalkyl-C2-C6-dihydroxyalkyl, C3-C6-cycloalkenyl-C2-C6-dihydrox- yalkyl, C3-C6-halocycloalkenyl-C2-C6-dihydroxyalkyl, C3-C6-cycloalkyl-C3-C6-dihydroxyal- kenyl, C3-C6-halocycloalkyl-C3-C6-dihydroxyalkenyl, C3-C6-cycloalkenyl-C3-C6-dihydroxy- alkenyl, C3-C6-halocycloalkenyl-C3-C6-dihydroxyalkenyl, C3-C6-cycloalkyl-C4-C6-dihydroxy- alkynyl, C3-C6-halocycloalkyl-C4-C6-dihydroxyalkynyl, C3-C6-cycloalkenyl-C4-C6-dihydroxy- alkynyl, C3-C6-halocycloalkyl-C4-C6-dihydroxyalkynyl, C3-C6-cycloalkyl-C3-C6-dihydroxyal- kylidenyl, C3-C6-halocycloalkyl-C3-C6-dihydroxyalkylidenyl, heterocyclyl-C3-C6-dihydroxy- alkylidenyl, hydroxycarbonyl-C2-C6-dihydroxyalkyl, hydroxycarbonyl-C3-C6-dihydroxyhalo- alkyl, Ci-C6-alkoxycarbonyl-C2-C6-dihydroxyalkyl, Ci-C6-haloalkoxycarbonyl-C2-C6-dihy- droxyalkyl, CrC ₆ -haloalkoxycarbonyl-C3-C6-dihydroxyhaloalkyl, C3-C6-dihydroxycycloalkyl Ci-C6-alkyl, C3-C6-dihydroxycycloalkyl- Ci-C6-haloalkylC ₃ -C6-dihydroxycycloalkyl- C ₂ -C6- alkenyl, C3-C6-dihydroxycycloalkyl- C2-C6-haloalkenyl, C3-C6-dihydroxycycloalkyl- C2-C6- alkynyl, C3-C6-dihydroxycycloalkyl- C3-C6-haloalkynyl, Ci-C6-alkylcarbonyl-Ci-C6-alkyl, Ci- C6-haloalkylcarbonyl-Ci-C6-alkyl, Ci-C6-alkylcarbonyl-Ci-C6-haloalkyl, Ci-C6-haloalkylcar- bonyl-Ci-C6-haloalkyl, hydroxycarbonyl-C2-C6-alkenyl, hydroxycarbonyl-C2-C6-haloalke- nyl, Ci-C6-alkoxycarbonyl-C2-C6-alkenyl, Ci-C6-haloalkoxycarbonyl-C2-C6-alkenyl, C1-C6- alkoxycarbonyl-C2-C6-haloalkenyl, Ci-C6-haloalkoxycarbonyl-C2-C6-haloalkenyl, hydroxy- carbonyl-C2-C6-alkynyl, hydroxycarbonyl-C3-C6-haloalkynyl, CrC6-alkoxycarbonyl-C2-C6- alkynyl, CrC ₆ -haloalkoxycarbonyl-C ₂ -C6-alkynyl, CrC ₆ -alkoxycarbonyl-C3-C6-haloalkynyl, Ci-C6-haloalkoxycarbonyl-C3-C6-haloalkynyl, Ci-C6-cyanoalkyl, C2-C6-cyanohaloalkyl, Ci- C6-dicyanoalkyl, C2-C6-dicyanohaloalkyl, di(hydroxycarbonyl)-Ci-C6-alkyl, di(hydroxycar- bonyl)-Ci-C6-haloalkyl, di(Ci-C6-alkoxycarbonyl)-Ci-C6-alkyl, di(Ci-C6-haloalkoxycarbo- nyl)-Ci-C6-alkyl, di(Ci-C6-alkoxycarbonyl)-Ci-C6-haloalkyl, di(Ci-C6-haloalkoxycarbonyl)- Ci-C6-haloalkyl, di(Ci-C6-alkoxyl)phosphoryl-Ci-C6-alkyl, di(Ci-C6-haloalkoxyl)phosphoryl- Ci-C6-alkyl, di(CrC ₆ -alkoxyl)phosphoryl-Ci-C6-haloalkyl, di(Ci-C6-haloalkoxyl)phosphoryl- CrC ₆ -haloalkyl, phosphoryl-Ci-C6-alkyl , phosphoryl-CrC ₆ -haloalkyl , di[di(Ci-C6-alk- oxyl)phosphoryl-)]Ci-C6-alkyl, di[di(Ci-C6-haloalkoxyl)phosphoryl-)]Ci-C6-alkyl, di[di(Ci-C6 alkoxyl)phosphoryl-)]Ci-C6-haloalkyl, di[di(Ci-C6-haloalkoxyl)phosphoryl-)]Ci-C6-haloalkyl, diphosphoryl-Ci-C6-alkyl , diphosphoryl-Ci-C6-haloalkyl, Ci-C6-alkylthio-Ci-C6-alkyl, C1-C6 haloalkylthio-Ci-C ₆ -alkyl, Ci-C ₆ -alkylthio-Ci-C ₆ -haloalkyl, Ci-C ₆ -haloalkylthio-Ci-C ₆ -haloal- kyl, Ci-C6-alkylsulfinly-Ci-C6-alkyl, Ci-C6-haloalkylsulfinly-Ci-C6-alkyl, Ci-C6-alkylsulfinly- Ci-C6-haloalkyl, Ci-C6-haloalkylsulfinly-Ci-C6-haloalkyl, Ci-C6-alkylsulfonyl-Ci-C6-alkyl, Ci-C6-haloalkylsulfonyl-CrC ₆ -alkyl, Ci-C6-haloalkylsulfonyl-CrC ₆ -haloalkyl, phenyl, 5-, 6- or 9 membered heteroaryl, 3- to 6-membered heterocyclyl, (Ci-C6-alkyl)carbonylaminocar bonyl, (C3-C6-alkenyl)carbonylaminocarbonyl, (C3-C6-alkynyl)carbonylaminocarbonyl, (Ci- C6-haloalkyl)carbonylaminocarbonyl, alkynylphenylcarbonylaminocarbonyl, (C3-C6-cycloal kyl)carbonylaminocarbonyl, [di(Ci-C6-alkyl)amino]carbonylaminocarbonyl, heterocyclylcar bonylaminocarbonyl, heteroarylcarbonylaminocarbonyl, [(Ci-C6-alkyl)carbonyl](Ci-C6-al- kyl)aminocarbonyl, [(Ci-C6-haloalkyl)carbonyl](Ci-C6-alkyl)aminocarbonyl, [(C3-C6-cycloal- kyl)carbonyl](Ci-C6-alkyl)aminocarbonyl, (phenylcarbonyl)(Ci-C6-alkyl)aminocarbonyl, (he terocyclylcarbonyl)(Ci-C6-alkyl)aminocarbonyl, (heteroarylcarbonyl)(Ci-C6-alkyl)aminocar- bonyl, [(Ci-C6-alkyl)carbonyl](Ci-C6-alkoxy)aminocarbonyl, [(Ci-C6-haloalkyl)carbonyl](Cr C6-alkoxy)aminocarbonyl, [(C3-C6-cycloalkyl)carbonyl](Ci-C6-alkyloxy)aminocarbonyl, (phenylcarbonyl)(Ci-C6-alkoxy)aminocarbonyl, (heterocyclylcarbonyl)(Ci-C6-alkoxy)ami- nocarbonyl, (heteroarylcarbonyl)(Ci-C6-alkoxy)aminocarbonyl, [(Ci-C6-alkyl)carbonyl](C3- C6-alkenyl)aminocarbonyl, [(Ci-C6-haloalkyl)carbonyl](C2-C6- alkenyl)aminocarbonyl, [(C3- C6-cycloalkyl)carbonyl](C3-C6-alkenyl)aminocarbonyl, (phenylcarbonyl)(C ₃ -C6-alkenyl)ami- nocarbonyl, (heterocyclylcarbonyl)(C3-C6-alkenyl)aminocarbonyl, (heteroarylcarbonyl)(C3- C6-alkenyl)aminocarbonyl, [(Ci-C6-alkyl)carbonyl](C3-C6-alkynyl)aminocarbonyl, [(C1-C6- haloalkyl)carbonyl](C3-C6-alkynyl)aminocarbonyl, [(C3-C6-cycloalkyl)carbonyl](C3-C6-al- kynyl)aminocarbonyl, (phenylcarbonyl)(C3-C6-alkynyl)aminocarbonyl, (heterocyclylcar- bonyl)(C3-C6-alkynyl)aminocarbonyl, (heteroarylcarbonyl)(C3-C6-alkynyl)aminocarbonyl, [(C2-C6-alkenyl)carbonyl]aminocarbonyl, [(C2-C6-alkenyl)carbonyl](Ci-C6-alkyl)aminocar- bonyl, [(C ₂ -C6-alkenyl)carbonyl](Ci-C6-alkoxy)aminocarbonyl, [(C ₃ -C6-alkynyl)carbo- nyl]aminocarbonyl, [(C3-C6-alkynyl)carbonyl](Ci-C6-alkyl)aminocarbonyl, [(C3-C6-alky- nyl)carbonyl](Ci-C6-alkoxy)aminocarbonyl, [di(Ci-C6-alkyl)amino]carbonylaminocarbonyl, [di(Ci-C6-alkyl)aminocarbonyl](Ci-C6-alkyl)aminocarbonyl, [di(Ci-C6-alkyl)aminocarbo- nyl](Ci-C6-alkoxy)aminocarbonyl;

wherein OH groups of R ² are unsubstituted or substituted by R ^b ;

cyclic groups of R ² are unsubstituted or substituted by R ^c ; and

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

R ^b is d-Ce-alkyl, C C ₆ -haloalkyl, C ₃ -C ₆ -alkenyl, C ₃ -C ₆ -haloalkenyl, C ₃ -C ₆ -alkynyl, C ₃ -C ₆ - haloalkynyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C4-C6-cycloalkenyl, C3-C6-halocy- cloalkenyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6-alkyl, Ci- C6-alkoxycarbonyl-Ci-C6-haloalkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6-haloalkyl, C1-C6- alkylcarbonyl, Ci-C6-haloalkylcarbonyl, hydroxycarbonyl-Ci-C6-alkyl, hydroxycarbonyl- Ci-C6-haloalkyl, Ci-C6-alkyloxycarbonyl, Ci-C6-haloalkyloxycarbonyl, Ci-C6-alkylthio- carbonyl, Ci-C6-haloalkylthiocarbonyl, Ci-C6-alkylaminocarbonyl, Ci-C6-haloalkylamino- carbonyl, Ci-C6-dialkylaminocarbonyl, Ci-C6-dihaloalkylaminocarbonyl, Ci-C6-alkylsul- fonyl, Ci-C6-haloalkylsulfonyl, CrC ₆ -alkoxy-Ci-C6-alkyl, Ci-C6-haloalkoxy-CrC ₆ -alkyl, Ci-C6-alkoxy-Ci-C6-haloalkyl, Ci-C6-haloalkoxy-Ci-C6-haloalkyl, phenyl-Ci-C6-alkyl, or phenyl-Ci-C6-haloalkyl;

R ^c is halogen, CN, N0 ₂ , Ci-Ce-alkyl, Ci-C ₆ -haloalkyl, OH, Ci-C ₆ -alkoxy, Ci-C ₆ -haloalkoxy,

Ci-C6-alkylthio, Ci-C6-alkylsulfinyl, or Ci-C6-alkylsulfonyl;

R ^d is phenyl, 5- or 6- membered heteroaryl, or 3- to 6-membered heterocyclyl;

wherein the substituent R ^d is unsubstituted or substituted by R ^e ;

R ^e is halogen, CN, N0 ₂ , Ci-C ₆ -alkyl, CrC ₆ -haloalkyl, OH, CrC ₆ -alkoxy, CrC ₆ -haloalkoxy,

Ci-C6-alkylsulfonyl;

R ³ halogen, CN, N0 ₂ , Ci-Ce-alkyl, Ci-C ₆ -haloalkyl, Ci-Ce-alkylcarbonyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ - haloalkenyl, C2-C6-alkynyl, C2-C6-haloalkynyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, C3-C6-alke- nyloxy, C3-C6-haloalkenyloxy, C3-C6-alkynyloxy, C3-C6-haloalkynyloxy, Ci-C6-alkoxy-Ci- C6-alkoxy, hydroxycarbonyl, Ci-C6-alkoxycarbonyl, Ci-C6-alkylthio, Ci-C6-haloalkylthio, NH2, (Ci-C6-alkyl)amino, di(Ci-C6-alkyl)amino, (Ci-C6-alkyl)sulfinyl, (Ci-C6-alkyl)sulfonyl, C3-C6-cycloalkyl, (C3-C6-cycloalkyl)oxy or phenyl;

wherein the cyclic groups of R ³ are unsubstituted or substituted by substituents R ^a ;

R ⁴ , R ⁵ , R ⁶ and R ⁷ independently of one another are H, halogen, CN, NO ₂ , Ci-C6-alkyl, Ci-C6-ha- loalkyl, Ci-C6-alkylcarbonyl, C2-C6-alkenyl, C2-C6-haloalkenyl, C2-C6-alkynyl, C2-C6-haloal- kynyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, C3-C6-alkenyloxy, C3-C6-haloalkenyloxy, C3-C6-al- kynyloxy, C3-C6-haloalkynyloxy, Ci-C6-alkoxy-Ci-C6-alkoxy, hydroxycarbonyl, C1-C6- alkoxycarbonyl, CrC6-alkylthio, Ci-C6-haloalkylthio, NH ₂ , (CrC6-alkyl)amino, di(Ci-C6-al- kyl)amino, (Ci-C6-alkyl)sulfinyl, (Ci-C6-alkyl)sulfonyl, C3-C6-cycloalkyl, (Cs-Grcycloal- kyl)oxy or phenyl;

wherein the cyclic groups of R ⁴ , R ⁵ , R ⁶ and R ⁷ are unsubstituted or substituted by R ^a ; R ^a is halogen, CN, NO2, Ci-Ce-alkyl, d-Ce-haloalkyl, d-Ce-alkoxy, or d-Ce-haloalkoxy.

The present invention also provides pyrimidine compounds of formula (I) as described herein including agriculturally acceptable salts or derivatives of the pyrimidine compounds of formula (I) having an acidic functionality, with the exception of

5-(2-bromophenyl)-2-cyclopropyl-4-methyl-pyrimidine;

5-(2-bromophenyl)-2-ethyl-4-methyl-pyrimidine; and

5-(2-bromophenyl)-2-methoxy-4-methyl-pyrimidine.

The present invention also provides pyrimidine compounds of formula (l)wherein the variables R ² , R ³ , R ⁴ , R ⁵ , R ⁶ and R ⁷ are as defined herein, and wherein

R ¹ is Ci-Ce-alkyl, Ci-Ce-haloalkyl, HO-d-Ce-alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -haloalkenyl, C ₂ -C ₆ - alkynyl, C3-C6-haloalkynyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxy, C3-C6-alkenyloxy, C3- C6-haloalkenyloxy, d-dralkynyloxy, C3-C6-haloalkynyloxy, Ci-C6-haloalkoxy, d-Ce-cyclo- alkoxy, Cs-drhalocycloalkoxy, C3-C6-cycloalkenyloxy, C3-C6-halocycloalkenyloxy, d-dr alkylthio, Ci-C6-haloalkylthio, (Ci-C6-alkyl)amino, di(Ci-C6-alkyl)amino, Ci-C6-alkylsulfinyl, Ci-C6-alkylsulfonyl, Cs-d-cycloalkyl, C3-C6-cycloalkenyl, C3-C6-halocycloalkyl, d-d-halo- cycloalkenyl, [1-(Ci-C ₆ -alkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -alkenyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C ₂ - C ₆ -alkynyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(Ci-C ₆ -haloalkyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(C ₂ -C ₆ -haloal- kenyl)]-C3-C6-cycloalkyl, [1 -(C3-C6-haloalkynyl)]-C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C6- alkyl, C3-C6-cycloalkyl-Ci-C6-haloalkyl, C3-C6-cycloalkyl-Ci-C6-alkoxy, d-Ce-cycloalkyl-d- C6-haloalkoxy, 5-membered heteroaryl, or 3- to 6-membered heterocyclyl;

wherein the cyclic groups of R ¹ are unsubstituted or substituted by R ^a ;

R ^a is halogen, CN, N0 ₂ , Ci-Ce-alkyl, Ci-Ce-haloalkyl, Ci-Ce-alkoxy, or Ci-Ce-haloalkoxy; including agriculturally acceptable salts or derivatives of the pyrimidine compounds of formula (I) having an acidic functionality, with the exception of

5-(2-bromophenyl)-2-cyclopropyl-4-methyl-pyrimidine;

5-(2-bromophenyl)-2-ethyl-4-methyl-pyrimidine; and

5-(2-bromophenyl)-2-methoxy-4-methyl-pyrimidine.

The pyrimidine compounds of formula (I) according to the invention can be prepared by standard processes of organic chemistry, e.g. by the following processes:

Process A:

The pyrimidines of formula (II) can be obtained by reacting respective pyrimidines of formula (I) (prepared analogous to known procedures like e.g. in WO 2013186229) with base and an electrophile, e.g. a carbonyl compound (III):

wherein R independent of each other are hydrogen, alkyl, cycloalkyl, halocycloalkyl, haloalkyl, cycloalkenyl, halocycloalkenyl, alkenyl, haloalkenyl, alkynyl, phenyl, heterocyclyl, heteroaryl or both R together form a carbocycle or a heterocycle, The reaction of the pyrimidine (I) with the electrophile (III), is usually carried out at temperatures of from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 20°C, particularly from -80°C to -20°C, in an inert organic solvent in the presence of a base.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether (TBME), dioxane, anisole and tet- rahydrofuran (THF), and also dimethyl sulfoxide (DMSO), dimethylformamide (DMF) and N,N- dimethylacetamide (DMAC), particularly diethyl ether, dioxane and THF. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as lithium hydride (LiH), sodium hydride (NaH), potassium hydride (KH) and calcium hydride (CaH), alkali metal amides, such as lithium hexamethyidisilazide (LHMDS) and lithium diisopropylamide (LDA), organometallic compounds, in particular alkali metal alkyls, such as methyllithium (MeLi), butyllithium (BuLi) and phenyllithium (PhLi), and also alkali metal and alkaline earth metal alkoxides, such as sodium methoxide (NaOCH ₃ ), sodium ethoxide (NaOC2H ₅ ), potassium ethoxide (KOC2H5), potassium tert-butoxide ( BuOK), potassium tert- pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as tri- methylamine (TMA), triethylamine (TEA), diisopropylethylamine (DIPEA) and N-methylpiperi- dine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, LHMDS and lithium diisopropylamide (LDA).

The bases are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile, based on the pyrimidine compounds

(I)-

The elimination of the alcohol of the pyrimidine (II) is usually carried out at temperatures from -100° C to the boiling point of the reaction mixture, preferably from 0°C to 120°C, particularly from 20°C to 100°C, in an inert solvent optionally in the presence of an acid.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, 0-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole, and THF, and also DMSO, DMF and DMAC, particularly toluene and o-xylene. It is also possible to use mixtures of the solvents mentioned.

Suitable acids are inorganic acids, such as HCI, HBr, sulfuric acid; organic acids, p-toluenesul- fonic acid, benzene sulfonic acid, pyridinium p-toluol sulfonic acid, methansulfonic acid, acetic acid; preferably p-toluenesulfonic acid and HCI. The acids are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The oxidation of the olefin (IV) to the diol (V) is usually carried out at temperatures of from -100° C to the boiling point of the reaction mixture, preferably from 0° C to 120° C, particularly from 20° C to 100° C, in an inert solvent.

The reaction may in principle be carried out in substance. However, preference is given to reacting the pyrimidines (IV) with the oxidant in an organic solvent with or without water as co-solvent.

Suitable solvents are those are capable of dissolving the pyrimidines (IV) and the oxidant at least partly and preferably fully under reaction conditions.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF, and also DMSO, DMF and DMAC, particularly tert-butyl methyl ether, THF. It is also possible to use mixtures of the solvents mentioned.

Suitable oxidants are e.g. potassium permanganate, potassium perruthenate, osmium tetrox- ide and other osmium salts, like potassium osmate. The oxidant can be used in equimolar amounts or in catalytic amounts together with a reoxidant like N-methylmorpholine-N-oxide or potassium hexacyanoferrate in stochiometric amounts or in excess.

Process B:

The halopyrimidines VI are known or can be prepared by known procedures (X=CI, Br, I). The boronic acids or esters required for the preparation of pyrimidine compounds of formula (VII) are commercially available, known from literature or can easily be prepared analogously to published procedure - 4247).

The pyrimidine compounds of formula (VII) can be obtained by reacting phenyl boronic acids or esters with halides of formula (VI) in which X is CI, Br, or I in presence of a base and a catalyst in analogy to WO 2014202493.

The reaction may in principle be carried out in substance. However, preference is given to reacting the pyrimidines (VI) with the boronic acid or ester in an organic solvent with or without water as co-solvent.

Suitable solvents are those capable of dissolving the pyrimidines (VI) and the boronic acid or ester at least partly and preferably fully under reaction conditions. Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, 1 ,3-dimethyl-2-imidazolidinone (DMI), Ν,Ν'-dimethylpropylene urea (DMPU), DMSO and 1-me- thyl-2 pyrrolidinone (NMP).

Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO, and NMP.

More preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF. It is also possible to use mixtures of the solvents mentioned.

Examples of suitable metal-containing bases are inorganic compounds including metal-containing bases such as alkali metal and alkaline earth metal hydroxides, and other metal hydroxides, such as LiOH, NaOH, KOH, Mg(OH) ₂ , Ca(OH) ₂ and AI(OH) ₃ ; alkali metal and alkaline earth metal oxide, and other metal oxides, such as U2O , Na20 , K2O, MgO , and CaO, Fe203, Ag20; alkali metal and alkaline earth metal carbonates such as U2CO3, Na2C03, K2CO3,

CS2CO3, MgC03, and CaC03, as well as alkali metal hydrogen carbonates (bicarbonates) such as UHCO3, NaHC03, KHCO3; alkali metal and alkaline earth metal phosphates such as potassium phosphate (K3PO4), calcium phosphate (Ca3(P0 ₄ )2); alkali metal and alkaline earth metal acetates such as sodium acetate or potassium acetate.

Preferred bases are inorganic compounds such as alkali metal and alkaline earth metal hydroxides, and other metal hydroxides, such as LiOH, NaOH, KOH, MgOH, CaOH and AIOH and alkali metal or alkaline earth metal carbonates such as L12CO3, Na2C03, K2CO3, CS2CO3,

MgC03, and CaC03 and alkaline earth metal phosphates such as K ₃ P0 ₄ ; alkali metal and alkaline earth metal acetates such as sodium acetate. Especially preferred bases are inorganic compounds such as alkali metal and alkaline earth metal hydroxides, and other metal hydroxides, such as LiOH, NaOH, KOH, Mg(OH) ₂ , Ca(OH) ₂ and AI(OH) ₃ and alkaline earth metal phosphates such as K3PO4.

The term base as used herein also includes mixtures of two or more, preferably two of the above compounds. Particular preference is given to the use of one base.

The bases are used preferably at from 1 to 10 equivalents based on the pyrimidine (VI), more preferably at from 1 .0 to 5.0 equivalents based on the pyrimidine (VI), most preferably from 1 .2 to 2.5 equivalents based on the pyrimidine (VI).

It may be advantageous to add the base offset over a period of time.

The reaction of the pyrimidines (VI) with the phenyl boronic acid or ester is carried out in the presence of a catalyst. Examples of suitable catalysts include e.g., palladium based catalysts like, e.g., Palladium(ll)acetate, tetrakis(triphenylphosphine)palladium(0), bis(triphenylphosphi- ne)palladium(ll)chloride, or (1 ,1 ,-bis(diphenylphosphino)ferrocene)-dichloropalladium(ll), and optionally suitable additives such as, e.g., phosphines like, e.g., P(o-tolyl)3, triphenylphosphine, or BINAP (2,2'-Bis(diphenylphospino)-1 ,1 -binaphthyl).

The amount of catalyst is usually 0.01 to 10 mol% (0.0001 to 0.1 equivalents) based on the pyrimidine (VI).

The pyrimidine compounds of formula (VIII) can be obtained by reacting respective pyrimidines of formula (VII) with base and an electrophile, e.g. a carbonyl compound (III):

The reaction of the pyrimidine (VII) with the electrophile (III), with R independent of each other equals hydrogen, alkyl, cycloalkyl, halocycloalkyl, haloalkyl, cycloalkenyl, halocycloalkenyl, alkenyl, haloalkenyl, alkynyl, phenyl, heterocyclyl, heteroaryl or both R form together a carbocy- cle or a heterocycle, is usually carried out at temperatures from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 20°C, particularly from -80°C to -20°C, in an inert organic solvent in the presence of a base.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and THF, and also DMSO, DMF and DMAC, particularly diethyl ether, dioxane and THF.

It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LDA, LHMDS, lithium 2,2,6,6-tetramethylpiperidide (LTMP), organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkox- ides, such as NaOCH3, NaOC2H5, KOC2H5, tBuOK, potassium tert-pentoxide and dimethox- ymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N- methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethyla- minpyridine, and also bicyclic amines. Particular preference is given to NaH, LTMP and LDA. The bases are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile, based on the pyrimidine (VII).

Process C:

The pyrimidine compounds of formula (IX,) can be obtained by reacting respective amino- ketones of formula (X) with base and amidine (XI):

The reaction of the aminoketones (X) with amidines (XI) is usually carried out at temperatures of from -100°C to the boiling point of the reaction mixture, preferably from 20°C to the boiling point, particularly from 40°C to 120°C, in an inert organic solvent in the presence of a base.

The reaction may in principle be carried out in substance. However, preference is given to reacting the aminoketones (X) with the amidine (XI) in an organic solvent.

Suitable solvents are those capable of dissolving the aminoketones (X) with the amidine (XI) at least partly and preferably fully under reaction conditions. Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2- dichloroethane, chloroform, carbon tetrachloride (CCU) and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF, esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and propionitrile, alcohols such as methanol, etha- nol, n-propanol, isopropanol, n-butanol and tert.-butanol, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP. Preferred solvents are alcohols such as methanol and ethanol. It is also possible to use mixtures of the solvents mentioned. Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS or

LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaOCH ₃ , NaOC2H ₅ , KOC2H5, tBuOK and potassium tert-pentoxide. The bases are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advanta- geous to employ an excess of base and/or the amidine (XI), based on the aminoketone (X).

Amidines (XI) are known from literature or commercially available. In cases in which R ² resem- Ibes a carbo- oder a heterocycle further, literature known, manipulations are possible: For example oxazoles can selectively be halogenated following published procedures (e.g. Bioorganic & Medicinal Chemistry, 2010, 18, 4821 ).

Preparation of compound (X):

The aminoketones (X) are prepared from the corresponding ketones (XII) with N,N-Dimethyl- formamide dimethyl acetal (CAS 4637-24-5; DMFDMA). The reaction is usually carried out at temperatures from -100° C to the boiling point of the reaction mixture, preferably from 20°C to 160°C, particularly from 50°C to 130°C. The reaction can optionally be catalyzed by an acid.

The reaction may be carried out in substance or in an organic solvent. Suitable solvents are those capable of dissolving the ketones (XII) and DMFDMA (CAS 4637-24-5) at least partly, preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2- dichloroethane, chloroform, carbon tetrachloride and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF, esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP; preferably DMFDMA is used as solvent. It is also possible to use mixtures of the solvents mentioned.

Suitable acids are inorganic acids, such as HCI, HBr, sulfuric acid (H2SO4); organic acids p- toluenesulfonic acid, benzene sulfonic acid, pyridinium p-toluol sulfonic acid, methanesulfonic acid, acetic acid; preferably p-toluenesulfonic acid and HCI. Most preferred is no use of acid.

The acids are generally employed in equimolar amounts; however, they can also be employed in catalytic amount

The ketones (XII) are prepared by reacting Grignard-reagent (XI II) with a carbonyl-electrophile (XIV) (e.g. an acid halide (Z = F, CI or Br) or a Weinreb-Amide (Z = N(Me)OMe)). The reaction is carried out at temperatures of from -100° C to the boiling point of the reaction mixture, preferably from -80° C to 60° C, particularly from -80° C to 20° C, in an inert solvent.

Suitable solvents are those capable of dissolving the Grignard-reagent (XIII) and the carbonyl- electrophile (XIV) at least partly and preferably fully under reaction conditions. Examples of suitable solvents are aliphatic aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, an- isole and THF, esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP. Preferred solvents are ethers such as tert-butyl methyl ether or THF. It is also possible to use mixtures of the solvents mentioned.

The Grignard-reagents (XIII) are either commercially available or can be prepared from the corresponding halides by known methods.

The carbonyl electrophiles (XIV) are either commercially available or can be prepared from the corresponding carbo

Ketones (XII) can as well be prepared from morpholinonitriles (XV) as described in the literature (European Journal of Organic Chemistry 2013, 36, 8083)

The morpholinonitriles (XV) are prepared from morpholinonitriles (XVI) and benzylhalides (XVII) in the presence of a base. The reaction is usually carried out at temperatures of from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 60°C, particularly from -50°C to 20°C, in an inert organic solvent in the presence of a base. Suitable solvents are those capable of dissolving the morpholinonitriles (XVI) and the benzyl- halides (XVII) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, halogenated hydrocarbons such as dichloromethane, 1 ,2- dichloroethane, chloroform, carbon tetrachloride and chlorobenzene, ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF, esters such as ethyl acetate and butyl acetate; nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP. Preferred solvents are dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO, and NMP. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS and LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, LHMDS and LDA.

The bases are generally employed in equimolar amounts; however, they can also be em- ployed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the halide (XVII), based on the morpholinonitrile (XVI). Benzylhalides (XVII) a

Morpholinonitriles (XVI) are prepared from the corresponding aldehydes (XVIII) as described in the literature (WO 2009/013462). Aldehydes (XVIII) are commercially available.

Process D:

Pyrimidine compounds (XIX), with R equals alkyl, haloalkyl, alkoxy, haloalkoxy, X is a leaving group and L is halogen, alkyl, haloalkyl, alkenyl and alkynyl, can be obtained by reacting respective pyrimidine compounds of formula (XX) with base and an electrophile (XXI).

Electrophile (XXI) can be an alkyl-, alkenyl- or alkynyl-halide, e.g. methyl iodide, allyl bromide or propargyl bromide, or a halogenating agent, e.g. C , Br2, I2, NCS (N-Chlorosuccinimide), NBS (N-Bromosuccinimide), NIS (N-lodosuccinimide), NFSI (N-Fluorobenzenesulfonimide), Se- lectfluor (1 -Chloromethyl-4-fluoro-1 ,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)).

The reaction of the pyrimidine (XX) with the electrophile is usually carried out at temperatures of from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 80°C, particularly from -80°C to 30°C, in an inert organic solvent in the presence of a base. Suitable solvents are those capable of dissolving the pyrimidine (XX) and the electrophile (XXI) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI , DMPU, DMSO and NMP. Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI , DMPU, DMSO and NMP. More preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS and LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DI PEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, lithium hexamethyldisilazide and LDA.

The bases are generally employed in equimolar amounts; however, they can also be em- ployed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile (XXI), based on the pyrimidine (XX).

The pyrimidine compounds of formula (XX) can be obtained by reacting respective pyrimidines of formula (I) (prepared analogous to known procedures e.g. in WO 2013186229) with base and an electrophile (XXII), e.g. a dialkylcarbonate (X = R = alkoxy), an alkyl chloroformiate (X = halogene, R = alkoxy) or an acid halide (X = halogene, R = alkyl or haloalkyl):

The reaction of the pyrimidine (I) with the electrophile (XXII) is usually carried out at temperatures of from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 80°C, particularly from -80°C to 30°C, in an inert organic solvent in the presence of a base.

Suitable solvents are those capable of dissolving the pyrimidine (I) and the electrophile (XXII) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP.

Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI , DMPU, DMSO and NMP. More preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, diox- ane, anisole and THF. It is also possible to use mixtures of the solvents mentioned. Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS and LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, lithium hexamethyldisilazide and LDA.

The bases are generally employed in equimolar amounts; however, they can also be em- ployed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile (XXII), based on the pyrimidine (I).

Process E:

The pyrimidine compounds of formula (XXIII), wherein R is alkyl, haloalkyl, alkenyl, alkynyl, cy- doalkyi, phenyl, heterocyclyl, heteroaryl or dialkylamino, can be obtained by reacting respective pyrimidines of formula (XXIV) with base and an electrophile, e.g. an acid halide or an acid anhydride (XXV), wherein X stands for F, CI, Br or OC(0)R:

(XXIII)

The reaction of the pyrimidine (XXIV) with the electrophile (XXV) is usually carried out at tem- peratures of from -100°C to the boiling point of the reaction mixture, preferably from -80°C to 80°C, particularly from -30°C to 60°C, in an inert organic solvent in the presence of a base.

Suitable solvents are those capable of dissolving the pyrimidine (XX) and the electrophile (XXI) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP.

Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP. More preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS and LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, lithium hexamethyldisilazide and LDA. The bases are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile (XXV), based on the pyrimidine (XXIV).

The pyrimidines of formula (XXIV) can be obtained from the acid of formula (XXVI) by known methods (analogo J. Med. Chem. 2010, 53, 2601-261 1 ).

Pyrimidine compounds (XXVI) can be easily obtained from a corresponding methyl ester (XXVII) by m skilled in the art.

The pyrimidines of formula (XXVII) can be obtained by reacting respective pyrimidines of formula (XXVIII) with boronic acids/esters of formula (XXIX):

(XXVII)

The reaction of pyrimidines (XXVIII) with boronic acids/esters (XXIX) is usually carried out at from 0 °C to the boiling point of the reaction mixture, preferably at from 15 °C to 1 10 °C, particularly at from 40 °C to 100 °C, in an inert organic solvent in the presence of a base and a catalyst.

The reaction may in principle be carried out in substance. However, preference is given to reacting the pyrimidines (XXVIII) with the boronic acids/esters (XXIX) in an organic solvent with or without water as co-solvent.

Suitable solvents are those capable of dissolving the pyrimidines (XXVIII) and the boronic acids (XXIX) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP.

Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and MP). More preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF. It is also possible to use mixtures of the solvents mentioned. Examples of suitable metal-containing bases are inorganic compounds including metal-containing bases such as alkali metal and alkaline earth metal hydroxides, and other metal hydroxides, such as LiOH, NaOH, KOH, Mg(OH) ₂ , Ca(OH) ₂ and AI(OH) ₃ ; alkali metal and alkaline earth metal oxide, and other metal oxides, such as L12O, Na20, K2O, MgO, and CaO, Fe2C>3, Ag2<D; alkali metal and alkaline earth metal carbonates such as U2CO3, Na2CC>3, K2CO3,

CS2CO3, MgCC>3, and CaCC , as well as alkali metal bicarbonates such as LiHCC>3, NaHCC , KHCO3; alkali metal and alkaline earth metal phosphates such as K3PO4, Ca3(P0 ₄ )2; alkali metal and alkaline earth metal acetates such as sodium acetate or potassium acetate.

Preferred bases are inorganic compounds such as alkali metal and alkaline earth metal hy- droxides, and other metal hydroxides, such as LiOH, NaOH, KOH, Mg(OH) ₂ , Ca(OH) ₂ and AI(OH)3 and alkali metal or alkaline earth metal carbonates such as U2CO3, Na2C03, K2CO3, CS2CO3, MgC03, and CaC03 and alkaline earth metal phosphates such as K3PO4; alkali metal and alkaline earth metal acetates such as sodium acetate. Especially preferred bases are inorganic compounds such as alkali metal and alkaline earth metal hydroxides, and other metal hy- droxides, such as LiOH, NaOH, KOH, Mg(OH) ₂ , Ca(OH) ₂ and AI(OH) ₃ and alkaline earth metal phosphates such as K ₃ P0 ₄ .

The term base as used herein also includes mixtures of two or more, preferably two of the above compounds. Particular preference is given to the use of one base.

The bases are used preferably at from 1 to 10 equivalents based on the pyrimidine (XXVIII), more preferably at from 1.0 to 5.0 equivalents based on the pyrimidine (XXVIII), most preferably from 1.2 to 2.5 equivalents based on the pyrimidine (XXVIII).

It may be advantageous to add the base offset over a period of time.

The reaction of the pyridines (XXVIII) with the boronic acids/esters (XXIX) is carried out in the presence of a catalyst. Examples of suitable catalysts include e.g., palladium based catalysts like, e.g., palladium(ll)acetate, tetrakis(triphenylphosphine)- palladium(O), bis(triphenylphos- phine)palladium(ll)chloride or (1 ,1 ,-bis(diphenylphosphino)- ferrocene)-dichloropalladium(ll), and optionally suitable additives such as, e.g., phosphines like, e.g., P(o-tolyl)3, triphenylphos- phine or BINAP (2,2'-Bis(diphenylphospino)-1 ,1 -binaphthyl).

The amount of catalyst is usually 0.01 to 20 mol % (0.0001 to 0.2 equivalents) based on the pyrimidine (II).

The halopyrimidines XXVIII are known from the literature (e.g. WO 201 1 154327), are commercially available or can be prepared by known procedures.

The boronic acids/esters XXIX required for the preparation of pyrimidines of formula (XVII) are commercially available, known from literature or can easily be prepared analogously to pub- lished procedures (e.g. Kamei et al. Tetrahedron Lett. 2014, 55, 4245 - 4247).

Process F:

The pyrimidines of formula (XXX) can be obtained by reacting respective pyrimidines of formula (XXVII) with a reducing agent such as LAH or DIBAIH.

The reduction of pyrimidines (XXVII) is usually carried out from - 80 °C to the boiling point of the reaction mixture, preferably at from -20 °C to 60 °C, particularly at from 0 °C °C to 25 °C, in an inert organic solvent.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mix- tures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and THF, and also DMSO, DMF and DMAC, particularly diethyl ether, dioxane and THF. It is also possible to use mixtures of the solvents mentioned.

Examples of reducing agents for pyridines (XXVII) include LAH, DIBALH, LiBH ₄ or lithium tri- ethylborohydride. Preferred agents include LAH and DIBALH.

The hydride-source is used preferably from 1 to 10 equivalents based on the pyrimidine (XXVII), more preferably at from 1.0 to 5.0 equivalents based on the pyrimidine (XXVII), most preferably from 1 .2 to 2.5 equivalents based on the pyrimidine (XXVII).

Process G:

The pyrimidines of formula (XXXI) can be obtained by reacting respective pyrimidines of formula (XXVII) with a metal organic species like a Grignard reagent (R'MgX, X = CI, Br, I; R' = al- kyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, phenyl, heterocyclyl, or heteroaryl).

The reaction of pyrimidines (XXVII) with a metal organic species is usually carried out from - 80 °C to the boiling point of the reaction mixture, preferably at from -20 °C to 60 °C, particularly at from -20 °C to 25 °C, in an inert organic solvent.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Cs-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and THF, and also DMSO, DMF and DMAC, particularly diethyl ether, dioxane and THF. It is also possible to use mixtures of the solvents mentioned.

Examples of metal organic species for the synthesis of pyridines (XXXI) Grignard reagents like R'MgCI, R'MgBr or R'Mgl, lithium organic species, aluminum organic species like R 3AI, R'2AIX and and R'AIX2, titanium organic species like R' ₄ Ti, R'sTiX, R'2TiX2 and RT1X3,

Preferred agents include Grignard reagents and lithium organic species.

The metal organic species is used preferably from 2 to 10 equivalents based on the pyrimidine (XXVII), more preferably at from 2.0 to 5.0 equivalents based on the pyrimidine (XXVII), most preferably from 2.0 to 3.0 equivalents based on the pyrimidine (XXVII).

Process H:

The pyrimidines of formula (XXXII) can be obtained by reacting respective pyrimidines of formula (XXIII) with a metal organic species like a Grignard reagent (R'MgX, X = CI, Br, I; R' = al- kyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, phenyl, heterocyclyl or heteroaryl). (XXXII)

The reaction of pyrimidines (XXXIII) with a metal organic species is usually carried out from - 80 °C to the boiling point of the reaction mixture, preferably at from -20 °C to 60 °C, particularly at from -20 °C to 25 °C, in an inert organic solvent.

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and mixtures of Cs-Ce-alkanes, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and THF, and also DMSO, DMF and DMAC, particularly diethyl ether, dioxane and THF.

It is also possible to use mixtures of the solvents mentioned.

Examples of metal organic species for the synthesis of pyridines (XXXII) Grignard reagents like R'MgCI, R'MgBr or R'Mgl, lithium organic species, aluminum organic species like R'sAI, R' ₂ AIX and R'AIX ₂ , titanium organic species like R' ₄ Ti, R' ₃ TiX, R' ₂ TiX ₂ and RTiX ₃ .

Preferred agents include Grignard reagents and lithium organic species.

The metal organic species is used preferably from 2 to 10 equivalents based on the pyrimidine (XXXIII), more preferably at from 2.0 to 5.0 equivalents based on the pyrimidine (XXXIII), most preferably from 2.0 to 3.0 equivalents based on the pyrimidine (XXXIII).

Process I:

The pyrimidines of formula (XXXIII) can be obtained by oxidizing respective pyrimidines of formula (XXX).

(XXXIII)

The oxidation of pyrimidines (XXX) is usually carried out from - 80 °C to the boiling point of the reaction mixture, preferably at from -20 °C to 100 °C, particularly at from 0 °C to 75 °C, in an inert organic solvent.

The reaction may in principle be carried out in substance. However, preference is given to re- acting the pyrimidines (XXX) in an organic solvent.

Suitable solvents are those capable of dissolving the pyrimidines (XXX) at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, o-, m- and p-xylene, halogenated hydrocarbons such as CH ₂ CI ₂ , CHC , CCH ₂ CICH ₂ CI or CCI ₄ , ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP.

Preferred solvents are halogenated hydrocarbons such as CH ₂ CI ₂ , CHC , CCH ₂ CICH ₂ CI or CCI ₄ , and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, N,N'-dimethyhpropyl- ene urea (DMPU), DMSO and NMP. More preferred solvents halogenated hydrocarbons such as CH2CI2, CHCI3, CCH2CICH2CI or CCI4. It is also possible to use mixtures of the solvents mentioned.

Examples of oxidizing agents for the synthesis of pyridines (XXXIII) are metal oxides such as Μηθ2, ΚΜηθ4, OO3 or PCC, and non-metal oxides such as NaCIO, Nal0 ₄ or pyridine/SC>3- complex. In addition methods like the Swern oxidation or the TEMPO oxidation known to a person skilled in the art can be used to obtain pyridines of formula (XXXIII).

Preferred agents include Μηθ2, KMn0 ₄ and PCC, more preferred MnC>2.

The oxidizing agent is used preferably from 1 to 50 equivalents based on the pyrimidine (XXX), more preferably at from 1 .0 to 20.0 equivalents based on the pyrimidine (XXX), most preferably from 1 .0 to 10.0 equivalents based on the pyrimidine (XXX).

Process J:

The pyrimidines of formula (XXXIV; Z = cycloalkyl, halocycloalkyl, alkyl, haloalkyl, alkenyl, al- kynyl, phenyl, heteroaryl, heterocyclyl, alkylidenyl or halo alkylidenyl and R' = alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, alkoxycarbonylalkyl) can be obtained reacting respec- tive pyrimidines of formula (XXXV) with base and an electrophile.

(XXXIV)

Electrophiles can be an alkyl-, alkenyl- or alkynyl-halide, e.g. methyl iodide, allyl bromide pro- pargyl bromide, ethyl iodide, propyl bromide, or ethyl 2-bromoacetate.

The reaction of the pyrimidine (XXXV) with the electrophile is usually carried out at tempera- tures of from -100°C to the boiling point of the reaction mixture, preferably from -20°C to 100°C, particularly from -0 °C to 30°C, in an inert organic solvent in the presence of a base.

Suitable solvents are those capable of dissolving the pyrimidine (XXXV) and the electrophile at least partly and preferably fully under reaction conditions.

Examples of suitable solvents are aromatic hydrocarbons such as benzene, chlorobenzene, toluene, cresols, 0-, m- and p-xylene, ethers such as diethyl ether, diisopropyl ether, TBME, di- oxane, anisole and THF, nitriles such as acetonitrile and propionitrile, as well as dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP.

Preferred solvents are ethers such as diethyl ether, diisopropyl ether, TBME, dioxane, anisole and THF and dipolar aprotic solvents such as sulfolane, DMF, DMAC, DMI, DMPU, DMSO and NMP. More preferred solvents are dipolar aprotic solvents such as DMF, and NMP. It is also possible to use mixtures of the solvents mentioned.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal anhydrides, such as LiH, NaH, KH and CaH, alkali metal amides, such as LHMDS and LDA, organometallic compounds, in particular alkali metal alkyls, such as MeLi, BuLi and PhLi, and also alkali metal and alkaline earth metal alkoxides, such as NaOCH3, NaOC2Hs, KOC2H5, tBuOK, potassium tert-pentoxide and dimethoxymagnesium, moreover organic bases, e.g. tertiary amines, such as TMA, TEA, DIPEA and N-methylpiperidine, pyridine, substituted pyridines, such as collidine, lutidine and 4-dimethylaminpyridine, and also bicyclic amines. Particular preference is given to NaH, lithium hexamethyldisilazide and LDA. The bases are generally employed in equimolar amounts; however, they can also be employed in catalytic amounts, in excess or, if appropriate, as solvents.

The starting materials are reacted with one another in equimolar amounts. It may be advantageous to employ an excess of base and/or the electrophile, based on the pyrimidine (XXXV). The end of the reaction can easily be determined by the skilled worker by means of routine methods.

The reaction mixtures are worked up in a customary manner, e.g. by mixing with water, separation of the phases and, if appropriate, chromatographic purification of the crude product.

Some of the intermediates and end products are obtained in the form of viscous oils, which can be purified or freed from volatile components under reduced pressure and at moderately elevated temperature.

If the intermediates and the end products are obtained as solid, purification can also be carried out by recrystallization or digestion.

The present invention also provides agrochemical compositions comprising at least one pyrimidine compounds of formula (I) and auxiliaries customary for formulating crop protection agents.

The present invention furthermore provides a method for controlling unwanted vegetation where a herbicidal effective amount of at least one pyrimidine compounds of formula (I) is allowed to act on plants, their seeds and/or their habitat. Application can be done before, during and/or after, preferably during and/or after, the emergence of the undesirable plants.

Further embodiments of the present invention are evident from the claims, the description and the examples. It is to be understood that the features mentioned above and still to be illustrated below of the subject matter of the invention can be applied not only in the combination given in each particular case but also in other combinations, without leaving the scope of the invention. As used herein, the terms "controlling" and "combating" are synonyms.

As used herein, the terms "undesirable vegetation" and "harmful plants" are synonyms.

If the pyrimidine compounds of formula (I) as described herein are capable of forming geomet- rical isomers, e.g. E/Z isomers, it is possible to use both, the pure isomers and mixtures thereof, in the compositions according to the invention.

If the pyrimidine compounds of formula (I) as described herein have one or more centres of chirality and, as a consequence, are present as enantiomers or diastereomers, it is possible to use both, the pure enantiomers and diastereomers and their mixtures, in the compositions ac- cording to the invention.

If the pyrimidine compounds of formula (I) as described herein have ionisable functional groups, they can also be employed in the form of their agriculturally acceptable salts. Suitable are, in general, the salts of those cations and the acid addition salts of those acids whose cations and anions, respectively, have no adverse effect on the activity of the active compounds. Preferred cations are the ions of the alkali metals, preferably of lithium, sodium and potassium, of the alkaline earth metals, preferably of calcium and magnesium, and of the transition metals, preferably of manganese, copper, zinc and iron, further ammonium and substituted ammonium in which one to four H atoms are replaced by Ci-C4-alkyl, HO-Ci-C4-alkyl, Ci-C4-alkoxy-Ci-C4- alkyl, HO-Ci-C4-alkoxy-Ci-C4-alkyl, phenyl or benzyl, preferably ammonium, methyl-ammonium, isopropylammonium, dimethylammonium, diethylammonium, diisopropylammonium, trimethyl- ammonium, triethylammonium, tris(isopropyl)ammonium, heptylammonium, dodecylammonium, tetradecylammonium, tetramethylammonium, tetraethylammonium, tetrabutylammonium, 2-hy- droxyethylammonium (olamine salt), 2-(2-hydroxyeth-1 -oxy)eth-1 -ylammonium (diglycolamine salt), di(2-hydroxyeth-1-yl)ammonium (diolamine salt), tris(2-HO-ethyl)ammonium (trolamine salt), tris(2-hydroxypropyl)ammonium, benzyltrimethylammonium, benzyltriethylammonium, Ν,Ν,Ν-trimethylethanolammonium (choline salt), furthermore phosphonium ions, sulfonium ions, preferably tri(Ci-C4-alkyl)sulfonium, such as trimethylsulfonium, and sulfoxonium ions, preferably tri(Ci-C4-alkyl)sulfoxonium, and finally the salts of polybasic amines such as N,N-bis-(3-ami- nopropyl)methylamine and diethylenetriamine.

Anions of useful acid addition salts are primarily chloride, bromide, fluoride, iodide, hydrogen- sulfate, methylsulfate, sulfate, dihydrogenphosphate, hydrogenphosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and also the anions of Ci-C4-al- kanoic acids, preferably formate, acetate, propionate and butyrate.

Pyrimidine compounds of formula (I) as described herein having an acidic functionality can be employed, if applicable, in the form of the acid, in the form of an agriculturally suitable salt as mentioned above or else in the form of an agriculturally acceptable derivative, e.g. as amides, such as mono- and di-Ci-C6-alkylamides or arylamides, as esters, e.g. as allyl esters, propargyl esters, Ci-Cio-alkyl esters, alkoxyalkyl esters, tefuryl ((tetrahydrofuran-2-yl)methyl) esters and also as thioesters, e.g. as Ci-Cio-alkylthio esters. Preferred mono- and di-Ci-C6-alkylamides are the CH3 and the dimethylamides. Preferred arylamides are, e.g., the anilides and the 2-chloro- anilides. Preferred alkyl esters are, e.g., the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pen- tyl, mexyl (1-methylhexyl), meptyl (1-methylheptyl), heptyl, octyl or isooctyl (2-ethylhexyl) esters. Preferred Ci-C4-alkoxy-Ci-C4-alkyl esters are the straight-chain or branched Ci-C4-alkoxy ethyl esters, e.g. the 2-methoxyethyl, 2-ethoxyethyl, 2-butoxyethyl (butotyl), 2-butoxypropyl or 3-but- oxypropyl ester. An example of a straight-chain or branched Ci-Cio-alkylthio ester is the ethyl- thio ester.

The organic moieties mentioned in the definition of the variables R ¹ , R ² , A, Z, R ³ , R ^3A , and R ⁴ are - like the term halogen - collective terms for individual enumerations of the individual group members. The term halogen denotes in each case F, CI, Br, or I. All hydrocarbon chains, e.g. all alkyl, alkenyl, alkynyl, alkoxy chains can be straight-chain or branched, the prefix C _n -C _m denoting in each case the possible number of carbon atoms in the group.

Examples of such meanings are:

- Ci-C ₄ -alkyl: e.g. CH ₃ , C2H5, n-propyl, CH(CH ₃ ) ₂ , n-butyl, CH(CH ₃ )-C ₂ H ₅ , CH ₂ -CH(CH ₃ ) ₂ , and C(CH ₃ ) ₃ ;

- Ci-C6-alkyl: Ci-C4-alkyl as mentioned above, and also, e.g., n-pentyl, 1 -methylbutyl, 2- methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1 -ethylpropyl, n-hexyl, 1 ,1 -dimethylpropyl, 1 ,2- dimethylpropyl, 1 -methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 ,1-dimethyl- butyl, 1 ,2-dimethylbutyl, 1 ,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethyl- butyl, 1-ethylbutyl, 2-ethylbutyl, 1 ,1 ,2-tri methyl propyl, 1 ,2,2-trimethylpropyl, 1 -ethyl-1 -methylpro- pyl or 1 -ethyl-2-methylpropyl, preferably methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1 ,1-di- methylethyl, n-pentyl, or n-hexyl;

- Ci-C4-haloalkyl: Ci-C4-alkyl as mentioned above which is partially or fully substituted by fluo- rine, chlorine, bromine and/or iodine, e.g., chloromethyl, dichloromethyl, trichloromethyl, fluoro- methyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoro- methyl, bromomethyl, iodomethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl, 2,2- difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro- 2-fluoroethyl, 2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl, 3-fluoropropyl, 2,2-difluoro- propyl, 2,3-difluoropropyl, 2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl, 3- bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl, 2,2,3,3,3-pentafluoropropyl, heptaflu- oro-propyl, 1 -(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl, l -(bromomethyl)-

2- bromo-ethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl, nonafluorobutyl, 1 ,1 ,2,2,-tetrafluoro- ethyl, and 1 -trifluoromethyl-1 ,2,2,2-tetrafluoroethyl;

- Ci-C6-haloalkyl: Ci-C4-haloalkyl as mentioned above, and also, e.g., 5-fluoropentyl, 5-chloro- pentyl, 5-bromopentyl, 5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromo- hexyl, 6-iodohexyl, and dodecafluorohexyl;

- C3-C6-cycloalkyl: monocyclic saturated hydrocarbons having 3 to 6 ring members, such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl;

- C3-C6-alkenyl: e.g. 1 -propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl,

1- methyl-1-propenyl, 2-methyl-1 -propenyl, 1 -methyl-2-propenyl, 2-methyl-2-propenyl, 1-pente- nyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1 -butenyl, 3-methyl-1 -bu- tenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1 -methyl-3-butenyl, 2-methyl-

3- butenyl, 3-methyl-3-butenyl, 1 ,1-dimethyl-2-propenyl, 1 ,2-dimethyl-1 -propenyl, 1 ,2-dimethyl-2- propenyl, 1-ethyl-1 -propenyl, 1 -ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5- hexenyl, 1-methyl-1-pentenyl, 2-methyl-1 -pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1 - methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3- pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl,

2- methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1 ,1 -dimethyl-2-butenyl, 1 ,1 -di- methyl-3-butenyl, 1 ,2-dimethyl-1-butenyl, 1 ,2-dimethyl-2-butenyl, 1 ,2-dimethyl-3-butenyl, 1 ,3- dimethyl-1 -butenyl, 1 ,3-dimethyl-2-butenyl, 1 ,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3- dimethyl-1 -butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3- dimethyl-2-butenyl, 1-ethyl-1 -butenyl, 1 -ethyl-2-butenyl, 1 -ethyl-3-butenyl, 2-ethyl-1 -butenyl, 2- ethyl-2-butenyl, 2-ethyl-3-butenyl, 1 ,1 ,2-trimethyl-2-propenyl, 1 -ethyl-1 -methyl-2-propenyl, 1 - ethyl-2-methyl-1-propenyl, and 1-ethyl-2-methyl-2-propenyl;

- C3-C6-haloalkenyl: a C3-C6-alkenyl substituent as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, e.g. 2-chloroprop-2-en-1 -yl, 3-chloro- prop-2-en-1 -yl, 2,3-dichloroprop-2-en-1 -yl, 3,3-dichloroprop-2-en-1-yl, 2,3,3-trichloro-2-en-1-yl, 2,3-dichlorobut-2-en-1-yl, 2-bromoprop-2-en-1-yl, 3-bromoprop-2-en-1-yl, 2,3-dibromoprop-2- en-1-yl, 3,3-dibromoprop-2-en-1 -yl, 2,3,3-tribromo-2-en-1-yl, or 2,3-dibromobut-2-en-1 -yl;

- C3-C6-alkynyl: e.g. 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1 -methyl-2-pro- pynyl, 1 -pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1 -methyl-3-butynyl, 2- methyl-3-butynyl, 3-methyl-1 -butynyl, 1 ,1-dimethyl-2-propynyl, 1 -ethyl-2-propynyl, 1 -hexynyl, 2- hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1 -methyl-4- pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1 -pentynyl, 3-methyl-4-pentynyl, 4- methyl-1 -pentynyl, 4-methyl-2-pentynyl, 1 ,1-dimethyl-2-butynyl, 1 ,1 -dimethyl-3-butynyl, 1 ,2-di- methyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1 -ethyl-2-butynyl , 1-ethyl-3-bu- tynyl, 2-ethyl-3-butynyl, and 1-ethyl-1 -methyl-2-propynyl; - C2-C6-alkynyl: C3-C6-alkynyl as mentioned above and also ethynyl;

- C3-C6-haloalkynyl: a C3-C6-alkynyl radical as mentioned above which is partially or fully substituted by F, CI, Br and/or I, e.g. 1 ,1 -difluoroprop-2-yn-1-yl, 3-chloroprop-2-yn-1-yl, 3-bromo- prop-2-yn-1-yl, 3-iodoprop-2-yn-1-yl, 4-fluorobut-2-yn-1-yl, 4-chlorobut-2-yn-1 -yl, 1 ,1 -difluorobut- 2-yn-1-yl, 4-iodobut-3-yn-1-yl, 5-fluoropent-3-yn-1 -yl, 5-iodopent-4-yn-1 -yl, 6-fluorohex-4-yn-1 -yl, or 6-iodohex-5-yn-1-yl;

- Ci-C4-alkoxy: e.g. methoxy, ethoxy, propoxy, 1 -methylethoxy butoxy, 1-methylpropoxy, 2- methylpropoxy, and 1 ,1-dimethylethoxy;

- Ci-C6-alkoxy: Ci-C4-alkoxy as mentioned above, and also, e.g., pentoxy, 1-methylbutoxy, 2- methylbutoxy, 3-methoxylbutoxy, 1 ,1-dimethylpropoxy, 1 ,2-dimethylpropoxy, 2,2-dimethylprop- oxy, 1 -ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methyl- pentoxy, 1 ,1-dimethylbutoxy, 1 ,2-dimethylbutoxy, 1 ,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3- dimethylbutoxy, 3,3-dimethylbutoxy, 1 -ethylbutoxy, 2-ethylbutoxy, 1 ,1 ,2-trimethylpropoxy, 1 ,2,2- trimethylpropoxy, 1 -ethyl-1 -methylpropoxy, and 1 -ethyl-2-methylpropoxy.

- Ci-C4-haloalkoxy: a Ci-C4-alkoxy radical as mentioned above which is partially or fully substituted by fluorine, chlorine, bromine and/or iodine, i.e., e.g., fluoromethoxy, difluoromethoxy, tri- fluoromethoxy, chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2- bromomethoxy, 2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy, pentafluoroeth- oxy, 2-fluoropropoxy, 3-fluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2-bromopropoxy, 3- bromopropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 2,3-dichloropropoxy, 3,3,3-trifluoro- propoxy, 3,3,3-trichloropropoxy, 2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy, 1-(fluorome- thyl)-2-fluoroethoxy, 1 -(chloromethyl)-2-chloroethoxy, 1 -(bromomethyl)-2-bromoethoxy, 4-fluoro- butoxy, 4-chlorobutoxy, 4-bromobutoxy, and nonafluorobutoxy;

- Ci-C6-haloalkoxy: a Ci-C4-haloalkoxy as mentioned above, and also, e.g., 5-fluoropentoxy, 5- chloropentoxy, 5-bromopentoxy, 5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy, 6-chloro- hexoxy, 6-bromohexoxy, 6-iodohexoxy and dodecafluorohexoxy;

- Ci-C4-alkylthio: e.g. methylthio, ethylthio, propylthio, 1 -methylethylthio, butylthio, 1 -methyl- propylthio, 2-methylpropylthio, and 1 ,1 -dimethylethylthio;

- Ci-C6-alkylthio: Ci-C4-alkylthio as mentioned above, and also, e.g., pentylthio, 1-methyl- butylthio, 2-methylbutylthio, 3-methylbutylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hex- ylthio, 1 ,1 -dimethylpropylthio, 1 ,2-dimethylpropylthio, 1 -methylpentylthio, 2-methylpentylthio, 3- methylpentylthio, 4-methylpentylthio, 1 ,1-dimethylbutylthio, 1 ,2-dimethylbutylthio, 1 ,3-dimethyl- butylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1 -ethylbutylthio, 2- ethylbutylthio, 1 , 1 ,2-trimethylpropylthio, 1 ,2,2-trimethylpropylthio, 1 -ethyl-1 -methylpropylthio, and 1- ethyl-2-methylpropylthio;

- (Ci-C4-alkyl)amino: e.g. methylamino, ethylamino, propylamino, 1-methylethylamino, butyla- mino, 1 -methylpropylamino, 2-methylpropylamino, or 1 ,1 -dimethylethylamino;

- (Ci-C6-alkyl)amino: (Ci-C4-alkylamino) as mentioned above, and also, e.g., pentyl-amino, 1- methylbutylamino, 2-methylbutylamino, 3-methylbutylamino, 2,2-dimethylpropylamino, 1 -ethyl- propylamino, hexylamino, 1 ,1-dimethylpropylamino, 1 ,2-dimethylpropylamino, 1 -methylpentyla- mino, 2-methylpentylamino, 3-methylpentylamino, 4-methylpentylamino, 1 ,1-dimethylbutyla- mino, 1 ,2-dimethylbutylamino, 1 ,3-dimethylbutylamino, 2,2-dimethylbutylamino, 2,3-dimethylbu- tyl-amino 3,3-dimethylbutylamino, 1-ethylbutylamino, 2-ethylbutylamino, 1 ,1 ,2-trimethylpropyla- mino, 1 ,2,2-trimethyl-propylamino, 1-ethyl-1-methylpropylamino, or 1-ethyl-2-methylpropylami- no;

- di(Ci-C4-alkyl)amino: e.g. N,N-dimethylamino, Ν,Ν-diethylamino, N,N-di(1-methyl-ethyl)ami- no, N,N-dipropylamino, Ν,Ν-dibutylamino, N,N-di(1-methylpropyl)amino, N,N-di(2-methyl-pro- pyl)amino, N,N-di(1 ,1-dimethylethyl)amino, N-ethyl-N-methylamino, N-methyl-N-propyl-amino, N-methyl-N-(1-methylethyl)amino, N-butyl-N-methylamino, N-methyl-N-(1 -methylpropyl)amino, N-methyl-N-(2-methylpropyl)amino, N-(1 ,1-dimethylethyl)-N-methylamino, N-ethyl-N-propyla- mino, N-ethyl-N-(1 -methylethyl)amino, N-butyl-N-ethylamino, N-ethyl-N-(1 -methylpropyl)-amino, N-ethyl-N-(2-methylpropyl)amino, N-ethyl-N-(1 ,1-dimethylethyl)amino, N-(1 -methylethyl)-N-prop- ylamino, N-butyl-N-propylamino, N-(1 -methylpropyl)-N-propylamino, N-(2-methylpropyl)-N-prop- ylamino, N-(1 ,1-dimethylethyl)-N-propylamino, N-butyl-N-(1-methylethyl)amino, N-(1-methyl- ethyl)-N-(1 -methyl-propyl)amino, N-(1 -methylethyl)-N-(2-methylpropyl)amino, N-(1 ,1 -dime- thylethyl)-N-(1-methylethyl)amino, N-butyl-N-(1-methylpropyl)amino, N-butyl-N-(2-methylpro- pyl)amino, N-butyl-N-(1 ,1-dimethylethyl)amino, N-(1 -methylpropyl)-N-(2-methylpropyl)amino, N- (1 ,1-dimethyl-ethyl)-N-(1-methylpropyl)amino, or N-(1 ,1-dimethylethyl)-N-(2-methylpropyl)amino;

- di(Ci-C6-alkyl)amino: di(Ci-C4-alkyl)amino as mentioned above, and also, e.g., N-methyl-N- pentylamino, N-methyl-N-(1 -methylbutyl)amino, N-methyl-N-(2-methylbutyl)amino, N-methyl-N- (3-methylbutyl)amino, N-methyl-N-(2,2-dimethylpropyl)amino, N-methyl-N-(1 -ethylpropyl)amino, N-methyl-N-hexylamino, N-methyl-N-(1 ,1 -dimethylpropyl)amino, N-methyl-N-(1 ,2-dimethylpro- pyl)amino, N-methyl-N-(1-methylpentyl)amino, N-methyl-N-(2-methylpentyl)amino, N-methyl-N- (3-methylpentyl)amino, N-methyl-N-(4-methylpentyl)amino, N-methyl-N-(1 ,1-dimethylbutyl)ami- no, N-methyl-N-(1 ,2-dimethylbutyl)amino, N-methyl-N-(1 ,3-dimethylbutyl)amino, N-methyl-N- (2,2-dimethylbutyl)amino, N-methyl-N-(2,3-dimethylbutyl)amino, N-methyl-N-(3,3-dimethylbu- tyl)amino, N-methyl-N- (l-ethylbutyl)amino, N-methyl-N-(2-ethylbutyl)amino, N-methyl-N-(1 ,1 ,2- trimethylpropyl)amino, N-methyl-N- (1 ,2,2-trimethylpropyl)amino, N-methyl-N-(1 -ethyl-1 -methyl- propyl)amino, N-methyl-N- (1-ethyl-2-methylpropyl)amino, N-ethyl-N-pentylamino, N-ethyl-N-(1 - methylbutyl)amino, N-ethyl-N-(2-methylbutyl)amino, N-ethyl-N-(3-methylbutyl)amino, N-ethyl-N- (2,2-dimethylpropyl)amino, N-ethyl-N-(1 -ethylpropyl)amino, N-ethyl-N-hexylamino, N-ethyl-N-

(1 ,1-dimethylpropyl)amino, N-ethyl-N-(1 ,2-dimethylpropyl)amino, N-ethyl-N-(1-methylpentyl)ami- no, N-ethyl-N-(2-methylpentyl)amino, N-ethyl-N-(3-methylpentyl)amino, N-ethyl-N-(4-methylpen- tyl)amino, N-ethyl-N-(1 ,1 -dimethylbutyl)amino, N-ethyl-N-(1 ,2-dimethylbutyl)amino, N-ethyl-N- (1 ,3-dimethylbutyl)amino, N-ethyl-N-(2,2-dimethylbutyl)amino, N-ethyl-N-(2,3-dimethylbutyl)ami- no, N-ethyl-N-(3,3-dimethylbutyl)amino, N-ethyl-N-(1 -ethylbutyl)amino, N-ethyl-N-(2-ethylbu- tyl)amino, N-ethyl-N-(1 ,1 ,2-trimethylpropyl)amino, N-ethyl-N-(1 ,2,2-trimethylpropyl)amino, N- ethyl-N-(1 -ethyl-1-methylpropyl)amino, N-ethyl-N-(1 -ethyl-2-methylpropyl)amino, N-propyl-N- pentylamino, N-butyl-N-pentylamino, Ν,Ν-dipentylamino, N-propyl-N-hexylamino, N-butyl-N-hex- ylamino, N-pentyl-N-hexylamino, or N,N-dihexylamino;

- Ci-C6-alkylsulfinyl (Ci-C6-Alkyl-S(=0)-): e.g. methylsulfinyl, ethylsulfinyl, propylsulfinyl, 1-me- thylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl, 2-methylpropylsulfinyl, 1 ,1 -dimethylethyl- sulfinyl, pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl, 2,2-di- methylpropylsulfinyl, 1 -ethylpropylsulfinyl, 1 ,1 -dimethylpropylsulfinyl, 1 ,2-dimethylpropyl-sulfinyl, hexylsulfinyl, 1 -methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl, 4-methylpen- tyl-sulfinyl, 1 ,1 -dimethylbutylsulfinyl, 1 ,2-dimethylbutylsulfinyl, 1 ,3-dimethylbutyl-sulfinyl, 2,2-di- methylbutylsulfinyl, 2,3-dimethylbutylsulfinyl, 3,3-dimethylbutyl-sulfinyl, 1 -ethylbutylsulfinyl, 2- ethylbutylsulfinyl, 1 ,1 ,2-trimethylpropylsulfinyl, 1 ,2,2-trimethylpropylsulfinyl, 1-ethyl-1-methylpro- pyl-sulfinyl, and l-ethyl-2-methylpropylsulfinyl;

- Ci-C6-alkylsulfonyl (Ci-C6-alkyl-S(0)2-) : e.g. methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1- methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methyl-propylsulfonyl, 1 ,1-dimethyl- ethylsulfonyl, pentylsulfonyl, 1 -methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 1 ,1-dimethylpropylsulfonyl, 1 ,2-dimethylpropylsulfonyl, 2,2-dimethylpropyl-sulfonyl, 1 -ethylpro- pylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfo- nyl, 4-methylpentylsulfonyl, 1 ,1-dimethylbutylsulfonyl, 1 ,2-dimethylbutylsulfonyl, 1 ,3-dimethyl- butylsulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl, 3,3-dimethylbutyl-sulfonyl, 1- ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1 ,1 ,2-trimethyl-propylsulfonyl, 1 ,2,2-trimethyl-propyl- sulfonyl, 1 -ethyl-1-methylpropylsulfonyl, and 1 -ethyl-2-methyl propylsulfonyl;

- C3-C6-cycloalkyl: a monocyclic saturated hydrocarbon having 3 to 6 ring members, such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl;

- C3-C6-cycloalkenyl: 1 -cyclopropenyl, 2-cyclopropenyl, 1 -cyclobutenyl, 2-cyclobutenyl, 1 -cy- clopentenyl, 2-cyclopentenyl, 1 ,3-cyclopentadienyl, 1 ,4-cyclopentadienyl, 2,4-cyclopentadienyl,

1- cyclohexenyl, 2-cyclohexenyl, 3-cyclohexenyl, 1 ,3-cyclohexadienyl, 1 ,4-cyclohexadienyl, or 2,5-cyclohexadienyl;

- heterocyclyl: a 3- to 6-membered heterocyclyl: a saturated or partial unsaturated cycle having three to six ring members which comprises apart from carbon atoms one to four nitrogen atoms, or one or two oxygen atoms, or one or two sulfur atoms, or one to three nitrogen atoms and an oxygen atom, or one to three nitrogen atoms and a sulfur atom, or one sulfur and one oxygen atom, e.g. 3- or 4-membered heterocycles like 2-oxiranyl, 2-aziridinyl, 2-thiiranyl, 2-ox- etanyl, 3-oxetanyl, 2-thietanyl, 3-thietanyl, 1 -azetidinyl, 2-azetidinyl, 1 -azetinyl, or 2-azetinyl;

5-membered saturated heterocycles like2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahy- drothienyl, 3-tetrahydrothienyl, 1-pyrrolidinyl,2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isox azolidinyl, 5-isoxazolidinyl, 2-isothiazolidinyl, 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazoli- dinyl, 1 -pyrazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl, 2-oxazolidinyl, 4-oxazoli- dinyl, 5-oxazolidinyl, 2-thiazolidinyl, 4-thiazolidinyl, 5-thiazolidinyl, 1 -imidazolidinyl, 2-imidazoli- dinyl, 4-imidazolidinyl, 3-oxazolidinyl, 1 ,2,4-oxadiazolidin-3-yl, 1 ,2,4-oxadiazolidin-5-yl, 3-thiazol idinyl, 1 ,2,4-thiadiazolidin-3-yl, 1 ,2,4-thiadiazolidin-5-yl, 1 ,2,4-triazolidin-3-yl, 1 ,2,4-oxadiazolidin

2- yl, 1 ,2,4-oxadiazolidin-4-yl, 1 ,3,4-oxadiazolidin-2-yl, 1 ,2,4-thiadiazolidin-2-yl, 1 ,2,4-thiadiazoli- din-4-yl, 1 ,3,4-thiadiazolidin-2-yl, 1 ,2,4-triazolidin-1-yl, or 1 ,3,4-triazolidin-2-yl;

5-membered partial unsaturated heterocycles like 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,4- dihydrofur-2-yl, 2,4-dihydrofur-3-yl, dioxolan-2-yl, 1 ,3-dioxol-2-yl, 2,3-dihydrothien-2-yl, 2,3-dihy- drothien-3-yl, 2,4-dihydrothien-2-yl, 2,4-dihydrothien-3-yl, 4,5-dihydropyrrol-1 -yl, 4,5-dihydropyr- rol-2-yl, 4,5-dihydropyrrol-3-yl, 2,5-dihydropyrrol-1 -yl, 2,5-dihydropyrrol-2-yl, 2,5-dihydropyrrol-3 yl, 2,3-dihydroisoxazol-1-yl, 2,3-dihydroisoxazol-3-yl, 2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxa- zol-5-yl, 2,5-dihydroisoxazol-3-yl, 2,5-dihydroisoxazol-4-yl, 2,5-dihydroisoxazol-5-yl, 4,5-dihydro isoxazol-2-yl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl, 2,3- dihydroisothiazol-1 -yl, 2,3-dihydroisothiazol-3-yl, 2,3-dihydroisothiazol-4-yl, 2,3-dihydroisothia- zol-5-yl, 2,5-dihydroisothiazol-3-yl, 2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl, 4,5-di- hydroisothiazol-1 -yl, 4,5-dihydroisothiazol-3-yl, 4,5-dihydroisothiazol-4-yl, 4,5-dihydroisothiazol- 5-yl, 2,3-dihydropyrazol-1 -yl, 2,3-dihydropyrazol-2-yl, 2,3-dihydropyrazol-3-yl, 2,3-dihydropyra- zol-4-yl, 2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl, 3,4-dihydropyrazol-3-yl, 3,4-dihydropy- razol-4-yl, 3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1 -yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydro- pyrazol-4-yl, 4,5-dihydropyrazol-5-yl, 2,3-dihydroimidazol-1 -yl, 2,3-dihydroimidazol-2-yl, 2,3-di- hydroimidazol-3-yl ,2,3-dihydroimidazol-4-yl, 2,3-dihydroimidazol-5-yl, 4,5-dihydroimidazol-1 -yl, 4,5-dihydroimidazol-2-yl, 4,5-dihydroimidazol-4-yl, 4,5-dihydroimidazol-5-yl, 2,5-dihydroimidazol-

1- yl, 2,5-dihydroimidazol-2-yl, 2,5-dihydroimidazol-4-yl, 2,5-dihydroimidazol-5-yl, 2,3-dihydroox- azol-2-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxa- zol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl, 2,3-dihydrothia- zol-2-yl, 2,3-dihydrothiazol-3-yl, 2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 3,4-dihydrothia- zol-2-yl, 3,4-dihydrothiazol-3-yl, 3,4-dihydrothiazol-4-yl, 3,4-dihydrothiazol-5-yl, 3,4-dihydrothia- zol-2-yl, 3,4-dihydrothiazol-3-yl, or 3,4-dihydrothiazol-4-yl;

6-membered saturated heterocycles like 1 -piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-piperidinyl, 1 ,3-dioxan-5-yl, 1 ,4-dioxanyl, 1 , 3-d ith ia n-5-y 1 , 1 ,3-dithianyl, 1 ,3-oxathian-5-yl, 1 ,4-oxathianyl, 2-tetrahydropyranyl, 3-tetrahydopyranyl, 4-tetrahydropyranyl, 2-tetrahydrothiopyranyl, 3-tetra- hydrothiopyranyl,4-tetrahydrothiopyranyl, 1 -hexahydropyridazinyl, 3-hexahydropyridazinyl, 4- hexahydropyridazinyl, 1 -hexahydropyrimidinyl, 2-hexahydropyrimidinyl, 4-hexahydropyrimidinyl, 5-hexahydropyrimidinyl, 1-piperazinyl, 2-piperazinyl, 1 ,3,5-hexahydrotriazin-1-yl, 1 ,3,5-hexahy- drotriazin-2-yl, 1 ,2,4-hexahydrotriazin-1 -yl, 1 ,2,4-hexahydrotriazin-3-yl, tetrahydro-1 ,3-oxazin-1- yl, tetrahydro-1 ,3-oxazin-2-yl, tetrahydro-1 ,3-oxazin-6-yl, 1 -morpholinyl, or 2-morpholinyl, 3-mor- pholinyl;

6-membered partial unsaturated heterocycles like 2H-pyran-2-yl, 2H-pyran-3-yl, 2H-pyran-4-yl, 2H-pyran-5-yl, 2H-pyran-6-yl, 2H-thiopyran-2-yl, 2H-thiopyran-3-yl, 2H-thiopyran-4-yl, 2H-thiopy- ran-5-yl, 2H-thiopyran-6-yl, or 5,6-dihydro-4H-1 ,3-oxazin-2-yl.

- heteroaryl: a 5-, 6- or 9-membered heteroaryl: monocyclic or bicyclic aromatic heteroaryl having 5, 6 or 9 ring members which, in addition to carbon atoms and independent of their position in the ring, contains 1 to 4 nitrogen atoms, or 1 to 3 nitrogen atoms and an oxygen or sulfur atom, or an oxygen or a sulfur atom, e.g. 5-membered aromatic rings like furyl (e.g. 2-furyl, 3- furyl), thienyl (e.g. 2-thienyl, 3-thienyl), pyrrolyl (e.g. pyrrol-2-yl, pyrrol-3-yl), pyrazolyl (e.g. pyra- zol-3-yl, pyrazol-4-yl), isoxazolyl (e.g. isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl), isothiazolyl (e.g. isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl), imidazolyl (e.g. imidazole-2-yl, imidazole-4- yl), oxazolyl (e.g. oxazol-2-yl, oxazol-4-yl, oxazol-5-yl), thiazolyl (e.g. thiazol-2-yl, thiazol-4-yl, thiazol-5-yl), oxadiazolyl (e.g. 1 ,2,3-oxadiazol-4-yl, 1 ,2,3-oxadiazol-5-yl, 1 ,2,4-oxadiazol-3-yl, 1 ,2,4-oxadiazol-5-yl, 1 ,3,4-oxadiazol-2-yl), thiadiazolyl (e.g. 1 ,2,3-thiadiazol-4-yl, 1 ,2,3-thiadia- zol-5-yl, 1 ,2,4-thiadiazol-3-yl, 1 ,2,4-thiadiazol-5-yl, 1 ,3,4-thiadiazolyl-2-yl), triazolyl (e.g. 1 ,2,3- triazol-4-yl, 1 ,2,4-triazol-3-yl); 1 -tetrazolyl; 6-membered aromatic rings like pyridyl (e.g. pyridine-

2- yl, pyridine-3-yl, pyridine-4-yl), pyrazinyl (e.g. pyridazin-3-yl, pyridazin-4-yl), pyrimidinyl (e.g. pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl), pyrazin-2-yl, triazinyl (e.g. 1 ,3,5-triazin-2-yl, or

1 ,2,4— triazin-3-yl, 1 ,2,4-triazin-5-yl, 1 ,2,4-triazin-6-yl); 9-membered bicyclic aromatic rings like benzothiophene, indole, benzofuran;

The term "substituted" if not specified otherwise refers to substituted by 1 , 2 or maximum possible number of substituents. If substituents as defined in compounds of formula I are more than one then they are independently from each other are same or different if not mentioned otherwise. The term "acidic functionality" if not specified otherwise refers to a functionality capable of donating a hydrogen (proton or hydrogen ion H ⁺ ), such as a caboxylic group or a sulphonic group, or, alternatively, capable of forming a covalent bond with an electron pair.

The terms "compounds of formula (I)", "Pyrimidine compounds of formula (I)", "Compounds I" and "compounds of invention" are synonyms.

The preferred embodiments of the invention mentioned herein below have to be understood as being preferred either independently from each other or in combination with one another.

In general, pyrimidine compounds of formula (I) are suitable as herbicides.

According to a preferred embodiment of the invention preference is given pyrimidine com- pounds of formula (I), and their use as herbicides, wherein the variables, either independently of one another or in combination with one another, have the following meanings:

Preferred R ¹ is Ci-C ₆ -alkyl, d-Ce-haloalkyl, HO-d-Ce-alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -haloalkenyl, C2-C6-alkynyl, C3-C6-haloalkynyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxy, C3-C6-alkenyloxy, d- C6-haloalkenyloxy, C3-C6-alkynyloxy, C3-C6-haloalkynyloxy, Ci-C6-haloalkoxy, d-C6-cycloalk- oxy, C3-C6-halocycloalkoxy, C3-C6-cycloalkenyloxy, C3-C6-halocycloalkenyloxy, Ci-C6-alkylthio, Ci-C6-haloalkylthio, (Ci-C6-alkyl)amino, di(Ci-C6-alkyl)amino, Ci-C6-alkylsulfinyl, Ci-C6-alkyl- sulfonyl, C ₃ -C6-cycloalkyl, C ₃ -C6-cycloalkenyl, C ₃ -C6-halocycloalkyl, C ₃ -C6-halocycloalkenyl, [1 - (Ci-C ₆ -alkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -alkenyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(C ₂ -C ₆ -alkynyl)]-d-C ₆ - cycloalkyl, [1-(Ci-C ₆ -haloalkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -haloalkenyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C ₃ - C6-haloalkynyl)]-C3-C6-cycloalkyl, C3-C6-cycloalkyl-Ci-C6-alkyl, C3-C6-cycloalkyl-Ci-C6-haloalkyl, C3-C6-cycloalkyl-Ci-C6-alkoxy, C3-C6-cycloalkyl-Ci-C6-haloalkoxy, 5-membered heteroaryl, or 3- to 6-membered heterocyclyl;

wherein the cyclic groups of R ¹ are unsubstituted or substituted by R ^a ;

also preferred R ¹ is Ci-C6-alkyl, Ci-C6-haloalkyl, HO- Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-haloal- kenyl, C2-C6-alkynyl, C3-C6-haloalkynyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxy, d-C6-alkenyl- oxy, C3-C6-haloalkenyloxy, C3-C6-alkynyloxy, C3-C6-haloalkynyloxy, Ci-C6-haloalkoxy, C3-C6-cy- cloalkoxy, C3-C6-halocycloalkoxy, C3-C6-cycloalkenyloxy, C3-C6-halocycloalkenyloxy, Ci-C6-al- kylthio, Ci-C6-haloalkylthio, (Ci-C6-alkyl)amino, di(Ci-C6-alkyl)amino, Ci-C6-alkylsulfinyl, C1-C6- alkylsulfonyl, C3-C6-cycloalkyl, C3-C6-cycloalkenyl, C3-C6-halocycloalkyl, C3-C6-halocycloalkenyl, [1-(Ci-C ₆ -alkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -alkenyl)]-C ₃ -C ₆ -cycloalkyl, [1 -(C ₂ -C ₆ -alkynyl)]-d-C ₆ - cycloalkyl, [1-(Ci-C ₆ -haloalkyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C2-C ₆ -haloalkenyl)]-C ₃ -C ₆ -cycloalkyl, [1-(C ₃ - C6-haloalkynyl)]-C ₃ -C6-cycloalkyl, C ₃ -C6-cycloalkyl-Ci-C6-alkyl, C ₃ -C6-cycloalkyl-Ci-C6-haloalkyl, C3-C6-cycloalkyl-Ci-C6-alkoxy, or C3-C6-cycloalkyl-Ci-C6-haloalkoxy,

wherein the cyclic groups of R ¹ are unsubstituted or substituted by R ^a ;

also preferred R ¹ is Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-haloalkoxy, C3-C6-alkenyloxy, d-C6-halo- alkenyloxy, C3-C6-alkynyloxy, C4-C6-haloalkynyloxy, Ci-C6-alkylthio, C3-C6-cycloalkyl, wherein the cycloalkyl substituent is unsubstituted;

particularly preferred R ¹ is Ci-C6-alkyl, Ci-C6-alkoxy, or C3-C6-cycloalkyl, wherein the cycloalkyl substituent is unsubstituted;

especially preferred R ¹ is C ₃ -C6-cycloalkyl, wherein the cycloalkyl substituent is unsubstituted; also especially preferred R ¹ is C2H5, 1-C3H7, 1-C4H9, OCH3, C-C3H5, or C-C4H7;

more preferred R ¹ is C2H5, OCH3, or C-C3H5; most preferred R ¹ is C-C3H5.

Preferred R ² is C2-C6-alkenyl, C2-C6-haloalkenyl, Ci-C6-alkoxy-C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkenyl, C3-C6-cycloalkenyl-Ci-C6-alkyl, C3-C6-cycloalkyl-Ci-C6-alkylidenyl, C3-C6- halocycloalkyl-CrC ₆ -alkylidenyl, C3-C6-cycloalkenyl-Ci-C6-alkylidenyl, C3-C6-hydroxycycloalkyl- Ci-C6-alkyl, C3-C6-hydroxycycloalkenyl-Ci-C6-alkyl, Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl-C2-C6- hydroxyalkylidenyl, hydroxycarbonyl-Ci-C6-alkyl, hydroxycarbonyl-Ci-C6-haloalkyl, Ci-C6-alk- oxycarbonyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C2-C6-dihydroxyalkyl, C3- C6-cycloalkyl-C3-C6-dihydroxyalkylidenyl, hydroxycarbonyl-C2-C6-dihydroxyalkyl, Ci-C6-alkoxy- carbonyl-C2-C6-dihydroxyalkyl, Ci-C6-dicyanoalkyl, 5- or 6-membered heteroaryl, or (Ci-C6-al- kyl)carbonylaminocarbonyl; wherein OH groups of R ² are unsubstituted or substituted by R ^b , cyclic groups of R ² are unsubstituted or substituted by R ^c , and acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

Particularly preferred R ² is C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkenyl, C3-C6-cycloalkyl- Ci-C6-alkylidenyl, C3-C6-halocycloalkyl-Ci-C6-alkylidenyl, C3-C6-hydroxycycloalkyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C2-C6-dihydroxyalkyl, phenyl or 5- or 6-membered heteroaryl; wherein OH groups of R ² are unsubstituted or substituted by R ^b , cyclic groups of R ² are unsubstituted or substituted by R ^c , and acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

Also particularly preferred R ² is C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkenyl-Ci-C6-alkyl, C3-C6-cycloalkyl-Ci-C6-alkylidenyl, CrC ₆ -hydroxyalkyl, Ci-C6-alkoxycarbonyl-CrC ₆ -alkyl, C2-C6- dihydroxyalkyl, Ci-C6-dicyanoalkyl, 5- or 6-membered heteroaryl, or (Ci-C6-alkyl)carbonylamino- carbonyl; wherein OH groups of R ² are unsubstituted or substituted by R ^b , cyclic groups of R ² are unsubstituted or substituted by R ^c , and acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

Especially preferred R ² is C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl-Ci-C6-alkylidenyl, C3- C6-hydroxycycloalkyl-Ci-C6-alkyl, and 5- or 6-membered heteroaryl;

also especially preferred R ² is C2-C6-alkenyl, Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl-Ci-C6-alkyli- denyl, C2-C6-dihydroxyalkyl, Ci-C6-dicyanoalkyl and 5- or 6-membered heteroaryl;

also especially preferred R ² is C2-C6-alkenyl, C3-C6-cycloalkyl-Ci-C6-alkylidenyl, Ci-C6-hydrox- yalkyl, C2-C6-dihydroxyalkyl, or 5- or 6-membered heteroaryl;

wherein OH groups of R ² are unsubstituted or substituted by R ^b ,

cyclic groups of R ² are unsubstituted or substituted by R ^c , and

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

More preferred R ² is C2-C6-alkenyl, C3-C6-cycloalkyl-CrC ₆ -alkylidenyl, or 5- or 6-membered heteroaryl;

also more preferred R ² is Ci-C6-hydroxyalkyl, C2-C6-dihydroxyalkyl, C3-C6-cycloalkyl-Ci-C6-al- kylidenyl, or 5- or 6-membered heteroaryl;

wherein OH groups of R ² are unsubstituted or substituted by R ^b ,

cyclic groups of R ² are unsubstituted or substituted by R ^c , and

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d ;

most preferred R ² is C2-C6-alkenyl;

also most preferred R ² is C3-C6-cycloalkyl-CrC ₆ -alkylidenyl;

also most preferred R ² is 5- or 6-membered heteroaryl;

also most preferred R ² is 5-membered heteroaryl;

also most preferred R ² is Ci-C6-hydroxyalkyl

also most preferred R ² is C2-C6-dihydroxyalkyl;

wherein OH groups of R ² are unsubstituted or substituted by R ^b , cyclic groups of R ² are unsubstituted or substituted by R ^c , and

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d .

also more preferred R ² is CH=CH-CH ₃ , CH=C(CH ₂ ) ₃ , or CH=C(CH ₂ ) ₄ ;

also more preferred R ² is 2-furyl, 3-furyl, 2-methyl-3-furyl, or 3-methyl-2-furyl;

also most preferred R ² is CH=CH-CH ₃ , CH=C(CH ₂ )3, 2-furyl, or 3-furyl;

also most preferred R ² is CHOH-CHOH-C ₆ H ₅ , CHOH-CHOH-2-furyl, CHOH-CHOH-2-furyl, or 4-methyloxazol-5-yl;

also most preferred R ² is CHOH-CHOH-C ₆ H ₅ , CHOH-CHOH-2-furyl, CHOH-CHOH-CH ₃ , or 4- methyloxazol-5-yl;

also most preferred R ² is selected from R ² -1 to R ² -16 as shown below,

wherein # denotes attachment to the pyrimidine ring, X and Y denotes R ^c which independently of each other are identical or different;

preferred R ² is R ² -1 , R ² -2, R ² -3, R ² -4, R ² -5, R ² -6, R ² -7, or R ² -8;

also preferred R ² is R ² -9, R ² -10, R ² -1 1 , R ² -13, R ² -14, or R ² -15;

more preferred R ² is R ² -9, R ² -10, or R ² -15;

most preferred R ² is R ² -9;

preferred X is H, halogen, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, OH, Ci-C6-alkoxy, Ci-C6-haloal- koxy, or Ci-C6-alkylthio;

particularrly preferred X is H, halogen, CN, Ci-C6-alkyl, OH, Ci-C6-alkoxy, or Ci-C6-alkylthio; also particularrly preferred X is H, halogen, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, or Ci-C6-haloalkoxy;

especially preferred X is H, halogen, CN, Ci-C ₄ -alkyl, OH, Ci-C ₄ -alkoxy, or Ci-C ₄ -alkylthio; more preferred X is H, CH3, C2H5, n-propyl, iso-propyl, iso-butyl, n-butyl, OH, OCH3, SCH3, F, CI, Br, or I;

most preferred X is H, CH ₃ , C2H5, OH, or OCH ₃ ;

also most preferred X is H, CH3, C2H5, or SCH3;

also most preferred X is H, CH3, C2H5, F, CI, Br, or I.

Preferred Y is H, halogen, CN, Ci-C ₆ -alkyl, Ci-Ce-haloalkyI, OH, Ci-Ce-alkoxy, Ci-C ₆ -haloal- koxy, or Ci-C6-alkylthio;

particularrly preferred Y is H, halogen, CN, Ci-C6-alkyl, OH, Ci-C6-alkoxy, or Ci-C6-alkylthio; also particularrly preferred Y is H, halogen, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy, or Ci-C6-haloalkoxy;

especially preferred Y is H, halogen, CN, Ci-C4-alkyl, Ci-C2-fluoroalkyl, OH, Ci-C4-alkoxy, or Ci-C ₄ -alkylthio;

more preferred Y is H, CH3, C2H5, n- propyl, iso-propyl, iso-butyl, n-butyl, 2-butyl, t-butyl, OH, OCH3, SCHs, F, CI, Br, or I;

most preferred Y is H, CH3, C2H5, n- propyl, iso-propyl, iso-butyl, n-butyl, 2-butyl, OH, or OCH3; also most preferred Y is H, CH ₃ , C2H5, n-propyl, iso-propyl, OH, OCH ₃ , or SCH ₃ ;

also most preferred Y is H, CH ₃ , C2H5, n-propyl, iso-propyl, F, CI, Br, or I .

X and Y preferably are selected from H, halogen, Ci-C6-alkyl, Ci-C6-alkoxy, and Ci-C ₄ -al- kylthio; more preferably from H, CH3, C2H5, n-propyl, iso-propyl, t-butyl, OCH3, SCH3, and CI;

Particulalrly preferred R ² is 4-methyl-5-oxazolyl, 4-ethyl-5-oxazolyl, 2,4-dimethyl-5-oxazolyl, 2- ethyl-4-methyl-5-oxazolyl, 2-methyl-4-ethyl-5-oxazolyl, or 2,4-diethyl-5-oxazolyl.

Examples of particularly preferred R ² are provided in Table R ² -9, Table R ² -10, and Table R ² - 15.

Table R ² -9: examples of particularly preferred R ² are R ² -9.1 to R ² -9.676 wherein R ² is R ² -9 and combinitions of variables X and Y are as defined in each row of table R2, numbering of each compound e.g. R ² -9.1 means R ² is R ² -9 wherein X and Y are as defined in row 1 of table R2;

Table R ² -10: examples of particularly preferred R ² are R ² -10.1 to R ² -10.676 wherein R ² is R ² - 10 and combinitions of variables X and Y are as defined in each row of table R2, numbering of each compound e.g. R ² -10.1 means R ² is R ² -10 wherein X and Y are as defined in row 1 of table R2;

Table R ² -15: examples of particularly preferred R ² are R ² -15.1 to R ² -15.676 wherein R ² is R ² - 15 and combinitions of variables X and Y are as defined in each row of table R2, numbering of each compound e.g. R ² -15.1 means R ² is R ² -15 wherein X and Y are as defined in row 1 of table R2.

Table R2:

Preferred R ³ is halogen, CN, N0 ₂ , Ci-C ₆ -alkyl, CrC ₆ -haloalkyl, Ci-C ₆ -alkoxy, or C ₃ -C ₆ -cycloal- kyl;

also preferred R ³ is halogen, CN, Ci-Ce-alkyI, d-Ce-haloalkyl, or Ci-C6-alkoxy;

particularly preferred halogen, CN, Ci-Ce-alkyl, or Ci-Ce-alkoxy;

especially preferred R ³ is halogen or CH3;

also especially preferred R ³ is halogen;

more preferred R ³ is CI, Br, or I;

most preferred R ³ is Br or I.

also most preferred R ³ is Br or CI.

Also preferred are compounds of formula (I), and their use as herbicide, wherein

R ⁴ ' R ⁵ , R ⁶ and R ⁷ independently of one another are H, halogen, CN, N0 ₂ , Ci-Ce-alkyI, Ci-C ₆ - haloalkyl, Ci-Ce-alkylcarbonyl, C ₂ -C ₆ -alkenyl, Ci-Ce-alkoxy, Ci-Ce-haloalkoxy, Ci-C ₆ -alkoxy-Ci- Ce-alkoxy, hydroxycarbonyl, Ci-Ce-alkoxycarbonyl, Ci-C ₆ -alkylthio, Ci-C ₆ -haloalkylthio, NH ₂ , (Ci-C ₆ -alkyl)amino, di(Ci-C ₆ -alkyl)amino, (Ci-C ₆ -alkyl)sulfinyl, (Ci-C ₆ -alkyl)sulfonyl, C ₃ -C ₆ -cyclo- alkyl, (C3-C6-cycloalkyl)oxy, or phenyl;

wherein the cyclic groups are unsubstituted or substituted by R ^a .

Preferred R ⁴ is H, halogen, CN, Ci-C ₆ -alkyl, CrC ₆ -haloalkyl, or Ci-C ₆ -alkoxy;

particularly preferred R ⁴ is H, halogen, or Ci-C6-alkyl,

especially preferred R ⁴ is H or halogen;

more preferred R ⁴ is H or F;

most preferred R ⁴ is H;

also most preferred R ⁴ is F.

Preferred R ⁵ is H, halogen, CN, Ci-C ₆ -alkyl, CrC ₆ -haloalkyl, or Ci-C ₆ -alkoxy;

particularly preferred R ⁵ is H, halogen, CrC ₆ -alkyl CrC ₆ -haloalkyl, or Ci-Ce-alkoxy;

especially preferred R ⁵ is H, halogen, Ci-Ce-alkyl, or d-Ce-haloalkoyl;

more preferred R ⁵ is H, F, CI, CH3, or CF3;

also more preferred R ⁵ is H or halogen;

most preferred R ⁵ is H or F;

also most preferred R ⁵ is H;

also most preferred R ⁵ is F.

Preferred R ⁶ is H, halogen, CrC ₆ -alkyl, or Ci-C ₆ -haloalkyl;

particularly preferred R ⁶ is H, halogen, or CrC ₆ -haloalkyl;

especially preferred R ⁶ is H, halogen, or CF3;

more preferred R ⁶ is H or CF3;

also more preferred R ⁶ is halogen or CF3;

also more preferred R ⁶ is H or halogen;

most preferred R ⁶ is H, F or CF3;

also most preferred R ⁶ is H or CF3;

also most preferred R ⁶ is F or CF ₃ ;

also most preferred R ⁶ is H or F;

also most preferred R ⁶ is H;

also most preferred R ⁶ is F;

also most preferred R ⁶ is CF3.

Preferred R ⁷ is H, halogen, CN, Ci-Ce-alkyl, or Ci-Ce-alkoxy; particularly preferred R ⁷ is H , halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

especially preferred R ⁷ is H , halogen, or Ci-C6-haloalkyl;

more preferred R ⁷ is H , F, CI, or CF3

most preferred R ⁷ is H , F, or CI;

also most preferred R ⁷ is CF3;

also most preferred R ⁷ is H .

Also preferred are compounds of formula (I), and their use as herbicide, wherein

R ¹ is Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-alkylthio, or C3-C6-cycloalkyl wherein cycloalkyl is un- substituted;

R ² Ci-C6-alkyl, Ci-C6-hydroxyalkyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxycarbonyl-Ci-C6-al- kyl, Ci-C6-alkoxycarbonyl-C2-C6-alkenyl, Ci-C6-alkoxy-C2-C6-alkenyl, Ci-C6-dicyanoalkyl, C2-C6-alkynyl, Ci-C6-alkoxy-C2-C6-alkynyl, Ci-C6-haloalkyl, C2-C6-alkenyl, hydroxycarbo- nyl-Ci-C6-hydroxyalkyl, hydroxycarbonyl-C2-C6-alkenyl, hydroxycarbonyl-Ci-C6-alkyl, Ci- C6-alkylcarbonyl-Ci-C6-alkyl, C2-C6-dihydroxyalkyl, Ci-C6-alkoxycarbonyl-Ci-C6-haloalkyl, C2-C6-hydroxyhaloalkyl, C3-C6-hydroxyalkenyl, hydroxycarbonyl-C2-C6-dihydroxyalkyl, Ci- C6-alkoxycarbonyl-CrC ₆ -hydroxyalkyl, C4-C6-dihydroxyalkenyl, C ₃ -C6-cycloalkenyl, Cs-Ce- cycloalkenyl- C2-C6-alkenyl, C3-C6-cycloalkenyl-CrC6-alkylidenyl, C3-C6-cycloalkyl-Ci-C6- alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl-Ci-C6-hydroxyalkyl, di(Ci-C6-alkoxyl)phosphoryl-Ci-C6-alkyl, diphospho- ryl-Ci-C6-alkyl, phosphoryl-Ci-C6-alkyl, di[di(Ci-C6-alkoxyl)phosphoryl-)]Ci-C6-alkyl, heter- ocyclyl-Ci-C6-alkylidenyl, phenyl, 5-, 6- or 9 membered heteroaryl, 3- to 6-membered het- erocyclyl,

wherein OH groups of R ² are unsubstituted or substituted by R ^b ;

R ^b is d-Ce-alkyl, C C ₆ -haloalkyl, C ₃ -C ₆ -alkenyl, C ₃ -C ₆ -haloalkenyl, C ₃ -C ₆ -alkynyl, C ₃ - C6-haloalkynyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C4-C6-cycloalkenyl, C3-C6-hal- ocycloalkenyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6- alkyl, Ci-C6-alkoxycarbonyl-Ci-C6-haloalkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6-haloal- kyl, Ci-C6-alkylcarbonyl, Ci-C6-haloalkylcarbonyl, hydroxycarbonyl-Ci-C6-alkyl, hy- droxycarbonyl-Ci-C6-haloalkyl, Ci-C6-alkyloxycarbonyl, Ci-C6-haloalkyloxycarbonyl, Ci-C6-alkylthiocarbonyl, Ci-C6-haloalkylthiocarbonyl, Ci-C6-alkylaminocarbonyl, Ci- C6-haloalkylaminocarbonyl, CrC ₆ -dialkylaminocarbonyl, CrC ₆ -dihaloalkylaminocar- bonyl, CrC ₆ -alkylsulfonyl, Ci-C6-haloalkylsulfonyl, Ci-C6-alkoxy-CrC ₆ -alkyl, C1-C6- haloalkoxy-Ci-C6-alkyl, Ci-C6-alkoxy-Ci-C6-haloalkyl, Ci-C6-haloalkoxy-Ci-C6-halo- alkyl, phenyl-Ci-C6-alkyl, or phenyl-Ci-C6-haloalkyl;

cyclic groups of R ² are unsubstituted or substituted by R ^c ; and

R ^c is halogen, CN , N0 ₂ , Ci-Ce-alkyl, Ci-C ₆ -haloalkyl, OH , Ci-C ₆ -alkoxy, Ci-C ₆ -haloal- koxy, Ci-C6-alkylthio, Ci-C6-alkylsulfinyl, or Ci-C6-alkylsulfonyl;

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d ;

R ^d is phenyl, 5- or 6-membered heteroaryl, or 3- to 6-membered heterocyclyl; wherein R ^d is unsubstituted or substituted by R ^e ;

R ^e is halogen, CN , N0 ₂ , Ci-Ce-alkyl, Ci-C ₆ -haloalkyl, OH , Ci-C ₆ -alkoxy or Ci-C ₆ - haloalkoxy, Ci-C6-alkylsulfonyl;

R ³ is halogen, CN , NO2, Ci-Ce-alkyl, d-Ce-haloalkyl, d-Ce-alkoxy, or Cs-Ce-cycloalkyl; R ⁴ is H , halogen, CN , Ci-Ce-alkyl, Ci-Ce-haloalkyl, or Ci-Ce-alkoxy; R ⁵ is H, halogen, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁶ is H, halogen, Ci-C6-alkyl, or Ci-C6-haloalkyl; and

R ⁷ is H, halogen, CN, Ci-Ce-alkyl, or Ci-Ce-alkoxy.

Also preferred are compounds of formula (I), and their use as herbicide, wherein

¹ is Ci-C6-alkyl, Ci-C6-alkoxy, Ci-C6-alkylthio, or C3-C6-cycloalkyl wherein cycloalkyl is un- substituted;

² Ci-C6-alkyl, Ci-C6-hydroxyalkyl, Ci-C6-alkoxy-Ci-C6-alkyl, Ci-C6-alkoxycarbonyl-Ci-C6-al- kyl, CrC ₆ -alkoxycarbonyl-C2-C6-alkenyl, CrC ₆ -alkoxy-C2-C6-alkenyl, Ci-C6-dicyanoalkyl, C2-C6-alkynyl, CrC ₆ -alkoxy-C2-C6-alkynyl, Ci-C6-haloalkyl, C2-C6-alkenyl, hydroxycarbo- nyl-Ci-C6-hydroxyalkyl, hydroxycarbonyl-C2-C6-alkenyl, hydroxycarbonyl-Ci-C6-alkyl, Ci- C6-alkylcarbonyl-Ci-C6-alkyl, C2-C6-dihydroxyalkyl, Ci-C6-alkoxycarbonyl-Ci-C6-haloalkyl, C2-C6-hydroxyhaloalkyl, C3-C6-hydroxyalkenyl, hydroxycarbonyl-C2-C6-dihydroxyalkyl, Ci- C6-alkoxycarbonyl-Ci-C6-hydroxyalkyl, C4-C6-dihydroxyalkenyl, C3-C6-cycloalkenyl, Cs-Ce- cycloalkenyl- C2-C6-alkenyl, C3-C6-cycloalkenyl-Ci-C6-alkylidenyl, C3-C6-cycloalkyl-Ci-C6- alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C ₃ -C6-cycloalkyl-Ci-C6-hydroxyalkyl, di(Ci-C6-alkoxyl)phosphoryl-Ci-C6-alkyl, diphos- phoryl-Ci-C6-alkyl, phosphoryl-Ci-C6-alkyl, di[di(Ci-C6-alkoxyl)phosphoryl-)]Ci-C6-alkyl, heterocyclyl-Ci-C6-alkylidenyl, phenyl, 5-, 6- or 9 membered heteroaryl, 3- to 6-membered heterocyclyl,

wherein OH groups of R ² are unsubstituted or substituted by R ^b ;

R ^b is Ci-C6-alkyl, C3-C6-alkynyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, Ci-C6-alkylcarbonyl, hydroxycarbonyl-Ci-C6-alkyl, or phenyl-Ci-C6-alkyl;

cyclic groups of R ² are unsubstituted or substituted by R ^c ;

R ^c is halogen, CN, CrC ₆ -alkyl, CrC ₆ -haloalkyl, OH, Ci-C ₆ -alkoxy, CrC ₆ -alkylthio, or

Ci-C6-alkylsulfonyl; and

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d ;

R ^d is phenyl, 5- or 6-membered heteroaryl, or 3- to 6-membered heterocyclyl; wherein

R ^d is unsubstituted or substituted by R ^e ; and

R ^e is halogen or hydroxy;

³ is halogen, CN, NO2, Ci-Ce-alkyl, or Ci-Ce-haloalkyl;

⁴ is H;

R ⁵ is H, halogen, or Ci-C6-haloalkyl;

R ⁶ is H, halogen, or Ci-C6-haloalkyl; and

R ⁷ is H, halogen, or Ci-C6-alkoxy.

Also preferred are compounds of formula (I), and their use as herbicide, wherein is C2-C6-alkenyl, C2-C6-haloalkenyl, Ci-C6-alkoxy-C2-C6-alkenyl, C2-C6-alkynyl, Cs-Ce-cycloalkenyl, C3-C6-cycloalkenyl-Ci-C6-alkyl, C3-C6-cycloalkyl-Ci-C6-alkylidenyl, C3-C6-halo- cycloalkyl-Ci-C6-alkylidenyl, C ₃ -C6-cycloalkenyl-CrC ₆ -alkylidenyl, C ₃ -C6-hydroxycycloal- kyl-Ci-C6-alkyl, C ₃ -C6-hydroxycycloalkenyl-Ci-C6-alkyl, Ci-C6-hydroxyalkyl, C ₃ -C6-cycloal- kyl-C2-C6-hydroxyalkylidenyl, hydroxycarbonyl-Ci-C6-alkyl, hydroxycarbonyl-Ci-C6-haloal- kyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, C3-C6-hydroxycycloalkyl-Ci-C6-hydroxyalkyl, C2-C6- dihydroxyalkyl, C3-C6-cycloalkyl-C3-C6-dihydroxyalkylidenyl, hydroxycarbonyl-C2-C6-dihy- droxyalkyl, Ci-C6-alkoxycarbonyl-C2-C6-dihydroxyalkyl, Ci-C6-dicyanoalkyl, 5- or 6-membered heteroaryl, or (Ci-C6-alkyl)carbonylaminocarbonyl;

wherein OH groups of R ² are unsubstituted or substituted by R ^b ,

R ^b is Ci-Ce-alkyl, d-Ce-haloalkyl, C ₃ -C ₆ -alkenyl, C ₃ -C ₆ -haloalkenyl, C ₃ -C ₆ -alkynyl, C ₃ -

C6-haloalkynyl, C ₃ -C6-cycloalkyl, C ₃ -C6-halocycloalkyl, C4-C6-cycloalkenyl, C ₃ -C6-hal- ocycloalkenyl, Ci-C6-alkoxycarbonyl-Ci-C6-alkyl, Ci-C6-haloalkoxycarbonyl-Ci-C6- alkyl, Ci-C6-alkoxycarbonyl-CrC ₆ -haloalkyl, Ci-C6-haloalkoxycarbonyl-CrC ₆ -haloal- kyl, CrC ₆ -alkylcarbonyl, CrC ₆ -haloalkylcarbonyl, hydroxycarbonyl-Ci-C6-alkyl, hy- droxycarbonyl-Ci-C6-haloalkyl, Ci-C6-alkyloxycarbonyl, Ci-C6-haloalkyloxycarbonyl,

Ci-C6-alkylthiocarbonyl, Ci-C6-haloalkylthiocarbonyl, Ci-C6-alkylaminocarbonyl, Ci- C6-haloalkylaminocarbonyl, Ci-C6-dialkylaminocarbonyl, Ci-C6-dihaloalkylaminocar- bonyl, Ci-C6-alkylsulfonyl, Ci-C6-haloalkylsulfonyl, Ci-C6-alkoxy-Ci-C6-alkyl, C1-C6- haloalkoxy-Ci-C6-alkyl, Ci-C6-alkoxy-Ci-C6-haloalkyl, Ci-C6-haloalkoxy-Ci-C6-halo- alkyl, phenyl-Ci-C6-alkyl, or phenyl-Ci-C6-haloalkyl;

cyclic groups of R ² are unsubstituted or substituted by R ^c ,

R ^c is halogen, CN, N0 ₂ , Ci-Ce-alkyl, C C ₆ -haloalkyl, OH, C C ₆ -alkoxy, d-C ₆ -haloal- koxy, Ci-C6-alkylthio, Ci-C6-alkylsulfinyl, or Ci-C6-alkylsulfonyl;

acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d ;

R ^d is phenyl, 5- or 6-membered heteroaryl, or 3- to 6-membered heterocyclyl; wherein

R ^d is unsubstituted or substituted by R ^e ;

R ^e is halogen, CN, N0 ₂ , Ci-Ce-alkyl, Ci-Ce-haloalkyl, OH, Ci-C ₆ -alkoxy, Ci-C ₆ - haloalkoxy, Ci-C6-alkylsulfonyl;

R ³ is CI, Br, I, CH ₃ , CF ₃ , or CF ₂ H;

R ⁴ is H;

R ⁵ is H or F;

R ⁶ is H, F, CF ₃ , CI, or Br; and

R ⁷ is H or F.

Also preferred are compounds of formula (I), and their use as herbicide, wherein

R ¹ is Ci-C6-alkyl, Ci-C6-alkoxy, or C ₃ -C6-cycloalkyl wherein cycloalkyl is unsubstituted;

R ² is preferably C2-C6-alkenyl, C ₃ -C6-cycloalkyl-Ci-C6-alkylidenyl, 5- or 6-membered heteroaryl, Ci-C6-hydroxyalkyl, or C2-C6-dihydroxyalkyl;

particularly preferred R ² is C2-C6-alkenyl, 5- or 6-membered heteroaryl, or Ci-C6-hydroxyalkyl; also particularly preferred R ² is C ₃ -C6-cycloalkyl-Ci-C6-alkylidenyl, C2-C6-dihydroxyalkyl or 5- or 6-membered heteroaryl;

more preferred R ² is CH=CH-CH ₃ , CH=C(CH ₂ ) ₃ , or CH=C(CH ₂ ) ₄ ;

also more preferred R ² is 2-furyl, 3-furyl, 2-methyl-3-furyl, or 3-methyl-2-furyl;

most preferred R ² is CH=CH-CH ₃ , CH=C(CH ₂ ) ₃ , 2-furyl, 3-furyl, CHOH-CHOH-C ₆ H ₅ , CHOH- CHOH-2-furyl, or 4-methyloxazol-5-yl, wherein acyclic aliphatic groups of R ² are unsubstituted or substituted by R ^d ;

R ³ is preferably halogen, CN, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

particularly preferred halogen or CH _3;

R ⁴ is preferably H;

R ⁵ is preferably H or halogen; R ⁶ is preferably H or halogen;

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy.

Also preferred are compounds of formula (I) wherein R ⁴ is H, which correspond to formula (1.1 ), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ² is CH=CH-CH ₃ , CH=C(CH ₂ ) ₃ , 2-furyl, 3-furyl, CHOH-CHOH-C ₆ H ₅ , CHOH-CHOH-2-furyl, or 4-methyloxazol-5-yl;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy.

Also preferred are compounds of formula (I) wherein R ² is CH=CH-CH3, R ⁴ is H, which correspond to formula (I.A), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy.

Also preferred are compounds of formula (I) wherein R ² is CH=C(CH ₂ )3, R ⁴ is H, which corresponds to formula (I.B), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy.

Also preferred are compounds of formula (I) wherein R ² is CH=C(CH2)4, R ⁴ is H which corre- spond to formula (I.C), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is 2-furyl, R ⁴ is H, which correspond to formula (I.D), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is 3-furyl, R ⁴ is H, whichcorrespond to formula (I.E), and their use as herbici

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is 3-methyl-2-furyl, R ⁴ is H, which correspond to formula (I.F), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy; R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is 2-methyl-3-furyl, R ⁴ is H, which correspond to formula (I.G), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is CHOH-CHOH-C6H5, R ⁴ is H, which correspond to formula (I.H), and th

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is CHOH-CHOH-2-furyl, R ⁴ is H, which correspond to formula (I.I),

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ² is 4-methyloxazol-5-yl, R ⁴ is H, which correspond to formula (I.J), and their use as herbicide,

wherein R ¹ is C3-C6-cycloalkyl, Ci-C6-alkyl, or Ci-C6-alkoxy;

R ³ is halogen, Ci-C6-alkyl, Ci-C6-haloalkyl, or Ci-C6-alkoxy;

R ⁵ is H or halogen;

R ⁶ is H, halogen, or haloalkyl; preferably H or halogen; and

R ⁷ is H, halogen, Ci-C6-alkyl, or Ci-C6-alkoxy;

Also preferred are compounds of formula (I) wherein R ⁴ is H, which correspond to formula (I.K), and their use as herbicide,

wherein

X and Y independently are selected from H, CH ₃ , C2H5, n-propyl, iso-propyl, iso-butyl, n-butyl, 2-butyl, t-butyl, OH, OCH ₃ , SCH ₃ , S(0)CH ₃ , S(0) ₂ CH ₃ , CN, F, CI, Br, I, CH2CF3, CF2CF3, CF2CH3, CF ₃ , CF ₂ H, OCF2H, and OCF ₃ ;

R ³ is CI, Br, I, CH ₃ , CF ₃ , or CF ₂ H;

R ⁵ is H or F;

R ⁶ is H, F, CF ₃ , CI, or Br;

R ⁷ is H or F.

Particularly preferred are compounds of formula 1.1 , wherein

R ¹ is C2H5, c-CsHs, C-C4H7, or OCH ₃ ;

R ² is selected from CH=CH-CH ₃ , CH=C(CH ₂ ) ₃ , CH=C(CH ₂ ) ₄ , 2-furyl, 3-furyl, 2-CH ₃ -3-furyl, CHOH-CHOH-C ₆ H ₅ , CHOH-CHOH-2-furyl, CHOH-CHOH-2-furyl, 4-CH ₃ -oxazol-5-yl, R ² -9.1 to R2-9.676 from Table R ² -9, R ² -10.1 to R ² -10.676 from Table R ² -10, and R ² -15.1 to R ² -15.676 from Table R ² -15; preferably R ² -9.1 to R ² -9.676 from Table R ² -9, R ² -10.1 to R ² -10.676 from Ta- ble R ² -10, and R ² -15.1 to R ² -15.676 from Table R ² -15; more preferably R ² -9.1 to R ² -9.676 from Table R ² -9, R ² -10.1 to R ² -10.676 from Table R ² -10; most preferably R ² -9.1 to R ² -9.676 from Table R ² -9;

R ³ is F, CI, Br, I, CH ₃ , OCH ₃ , CF ₃ , or CF ₂ H;

R ⁵ is H or F;

R ⁶ is H or F;

R ⁷ is H, CI, Br, CH ₃ , OCH ₃ or F.

According to a particularly preferred embodiment of the compounds of formula I and their use as herbicide, compounds of the invention are the compounds of the formulae I that are compiled in the Tables 1 to 10, wherein the meaning for the combination of variables R ¹ , R ³ , R ⁵ , R ⁶ and R ⁷ for each individual compound of tables 1 to 10 corresponds to each line of Table A. Each of the groups mentioned for a substituent in the tables is furthermore per se, independently of the combination in which it is mentioned, a particularly preferred aspect of the substituent in ques- tion. The term "formula" used in below tables 1 to 10 denotes "compounds of formula".

Table 1. Compounds of formula 1.1 , wherein R2 is CH=CH-CH ₃ (=formula 1 .1 ).

Table 2. Compounds of formula 1.1 , wherein R2 is CH=C(CH ₂ ) ₃ (=formula 1.2).

Table 3. Compounds of formula 1.1 , wherein R2 is CH=C(CH ₂ ) ₄ (=formula 1.3).

Table 4. Compounds of formula 1.1 , wherein R2 is 2-furyl (=formula 1.4).

Table 5. Compounds of formula 1.1 , wherein R2 is 3-furyl (=formula 1 .5).

Table 6. Compounds of formula 1.1 , wherein R2 is 3-CH ₃ -2-furyl (=formula 1.6).

Table 7. Compounds of formula 1.1 , wherein R2 is 2-CH ₃ -3-furyl (=formula 1.7).

Table 8. Compounds of formula 1.1 , wherein R2 is CHOH-CHOH-C ₆ H ₅ (=formula 1.8).

Table 9. Compounds of formula 1.1 , wherein R2 is CHOH-CHOH-2-furyl (=formula 1.9)

Table 10. Compounds of formula 1.1 , wherein R ² is 4-CH ₃ -oxazol-5-yl (=formula 1 .10).

According to a particularly preferred embodiment of the compounds of formula I and their use as herbicide, compounds of the invention are the compounds of formulae I that are compiled in tables 1 1 to 2038, wherein the meaning for the combination of variables R ¹ , R ³ , R ⁵ , R ⁶ and R ⁷ for each individual compound tables 1 1 to 2038 corresponds to each line of Table A. Each of the groups mentioned for a substituent in the tables is furthermore per se, independently of the combination in which it is mentioned, a particularly preferred aspect of the substituent in ques- tion. The term "formula" used in below tables 1 1 to 2038 denotes "compounds of formula".

Tab e 1 1 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.1 (= formula 1 .1 1 ).

Tab e 12. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.2(= formula 1 .12).

Tab e 13. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.3(= formula 1 .13).

Tab e 14. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.4(= formula 1 .14).

Tab e 15. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.5(= formula 1 .15).

Tab e 16. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.6(= formula 1 .16).

Tab e 17. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.7(= formula 1 .17).

Tab e 18. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.8(= formula 1 .18).

Tab e 19. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.9(= formula 1 .19).

Tab e 20. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.10 ^formula 1.20)

Tab e 21 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.1 1 ^formula 1.21 )

Tab e 22. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.12 ^formula 1.22)

Tab e 23. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.13 ^formula 1.23)

Tab e 24. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.14 ^formula 1.24)

Tab e 25. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.15 ^formula 1.25)

Tab e 26. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.16 ^formula 1.26)

Tab e 27. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.17 ^formula 1.27)

Tab e 28. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.18 ^formula 1.28)

Tab e 29. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.19 ^formula 1.29)

Tab e 30. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.20 =formula 1.30)

Tab e 31 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.21 ^formula 1.31 )

Tab e 32. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.22 ^formula 1.32)

Tab e 33. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.23 =formula 1.33)

Tab e 34. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9.24 ^formula 1.34) Tab e 35. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 25( =formu a ' 1.35

Tab e 36. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 26( =formu a ' 1.36

Tab e 37. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 27( =formu a ' 1.37

Tab e 38. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 28( =formu a ' 1.38

Tab e 39. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 29( =formu a ' 1.39

Tab e 40. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 30( =formu a ' 1.40

Tab e 41 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 31 ( =formu a ' 1.41

Tab e 42. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 32( =formu a ' 1.42

Tab e 43. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 33( =formu a ' 1.43

Tab e 44. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 34( =formu a ' 1.44

Tab e 45. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 35( =formu a ' 1.45

Tab e 46. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 36( =formu a ' 1.46

Tab e 47. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 37( =formu a ' 1.47

Tab e 48. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 38( =formu a ' 1.48

Tab e 49. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 39( =formu a ' 1.49

Tab e 50. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 40( =formu a ' 1.50

Tab e 51 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 41 ( =formu a ' 1.51

Tab e 52. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 42( =formu a ' 1.52

Tab e 53. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 43( =formu a ' 1.53

Tab e 54. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 44( =formu a ' 1.54

Tab e 55. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 45( =formu a ' 1.55

Tab e 56. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 46( =formu a ' 1.56

Tab e 57. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 47( =formu a ' 1.57

Tab e 58. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 48( =formu a ' 1.58

Tab e 59. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 49( =formu a ' 1.59

Tab e 60. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 50( =formu a ' 1.60

Tab e 61 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 51 ( =formu a ' 1.61

Tab e 62. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 52( =formu a ' 1.62

Tab e 63. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 53( =formu a ' 1.63

Tab e 64. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 54( =formu a ' 1.64

Tab e 65. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 55( =formu a ' 1.65

Tab e 66. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 56( =formu a ' 1.66

Tab e 67. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 57( =formu a ' 1.67

Tab e 68. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 58( =formu a ' 1.68

Tab e 69. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 59( =formu a ' 1.69

Tab e 70. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 60( =formu a ' 1.70

Tab e 71 . Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 61 ( =formu a ' 1.71

Tab e 72. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 62( =formu a ' 1.72

Tab e 73. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 63( =formu a ' 1.73

Tab e 74. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 64( =formu a ' 1.74

Tab e 75. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 65( =formu a ' 1.75

Tab e 76. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 66( =formu a ' 1.76

Tab e 77. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 67( =formu a ' 1.77

Tab e 78. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 68( =formu a ' 1.78 Table 79. Compounds of formula 1.1 , wherein R2 is R2-9.69( =formula ' .79)

Table 80. Compounds of formula 1. 1 , wherein R2 is R2-9.70( =formula ' .80)

Table 81. Compounds of formula 1. 1 , wherein R2 is R2-9.71( =formula ' .81)

Table 82. Compounds of formula 1. 1 , wherein R2 is R2-9.72( =formula ' .82)

Table 83. Compounds of formula 1. 1 , wherein R2 is R2-9.73( =formula ' .83)

Table 84. Compounds of formula 1. 1 , wherein R2 is R2-9.74( =formula ' .84)

Table 85. Compounds of formula 1. 1 , wherein R2 is R2-9.75( =formula ' .85)

Table 86. Compounds of formula 1. 1 , wherein R2 is R2-9.76( =formula ' .86)

Table 87. Compounds of formula 1. 1 , wherein R2 is R2-9.77( =formula ' .87)

Table 88. Compounds of formula 1. 1 , wherein R2 is R2-9.78( =formula ^' .88)

Table 89. Compounds of formula 1. 1 , wherein R2 is R2-9.79( =formula ^' .89)

Table 90. Compounds of formula 1. 1 , wherein R2 is R2-9.80( =formula ^' 1.90)

Table 91. Compounds of formula 1. 1 , wherein R2 is R2-9.8K =formula ^' 1.91)

Table 92. Compounds of formula 1. 1 , wherein R2 is R2-9.82( =formula ^' 1.92)

Table 93. Compounds of formula 1. 1 , wherein R2 is R2-9.83( =formula ^' 1.93)

Table 94. Compounds of formula 1. 1 , wherein R2 is R2-9.84( =formula ^' 1.94)

Table 95. Compounds of formula 1. 1 , wherein R2 is R2-9.85( =formula ^' 1.95)

Table 96. Compounds of formula 1. 1 , wherein R2 is R2-9.86( =formula ^' 1.96)

Table 97. Compounds ol formula 1. 1 , wherein R2 is R2-9.87 ^formula 1.97)

Table 98. Compounds ol formula 1. 1 , wherein R2 is R2-9.88 ^formula 1.98)

Table 99. Compounds ol formula 1. 1 , wherein R2 is R2-9.89 ^formula 1.99)

Table 100. Compounds of formula I. 1, wherein R2 is R2-9 90(=formula 1. 100).

Table 101. Compounds of formula I. 1, wherein R2 is R2-9 91(=formula 1. 101).

Table 102. Compounds of formula I. 1, wherein R2 is R2-9 92(=formula 1. 102).

Table 103. Compounds of formula I. 1, wherein R2 is R2-9 93(=formula 1. 103).

Table 104. Compounds of formula I. 1, wherein R2 is R2-9 94(=formula 1. 104).

Table 105. Compounds of formula I. 1, wherein R2 is R2-9 95(=formula 1. 105).

Table 106. Compounds of formula I. 1, wherein R2 is R2-9 96(=formula 1. 106).

Table 107. Compounds of formula I. 1, wherein R2 is R2-9 97(=formula 1. 107).

Table 108. Compounds of formula I. 1, wherein R2 is R2-9 98(=formula 1. 108).

Table 109. Compounds of formula I. 1, wherein R2 is R2-9 99(=formula 1. 109).

Table 110. Compounds of formula I. 1, wherein R2 is R2-9 100(=formula 1 .110)

Table 111. Compounds of formula I. 1, wherein R2 is R2-9 101(=formula 1 .111)

Table 112. Compounds of formula I. 1, wherein R2 is R2-9 102(=formula 1 .112)

Table 113. Compounds of formula I. 1, wherein R2 is R2-9 103(=formula 1 .113)

Table 114. Compounds of formula I. 1, wherein R2 is R2-9 104(=formula 1 .114)

Table 115. Compounds of formula I. 1, wherein R2 is R2-9 105(=formula 1 .115)

Table 116. Compounds of formula I. 1, wherein R2 is R2-9 106(=formula 1 .116)

Table 117. Compounds of formula I. , wherein R2 is R2-9 107(=formula ¹ .117)

Table 118. Compounds of formula I. 1, wherein R2 is R2-9 108(=formula ' .118)

Table 119. Compounds of formula I. 1, wherein R2 is R2-9 109(=formula ' .119)

Table 120. Compounds of formula I. 1, wherein R2 is R2-9 110(=formula ' .120)

Table 121. Compounds of formula I. 1, wherein R2 is R2-9 111(=formula ' .121)

Table 122. Compounds of formula I. 1, wherein R2 is R2-9 112(=formula ' .122) Tab e 123. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 1 13< =formu a 1.123)

Tab e 124. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 14( =formu a 1 .124)

Tab e 125. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 15( =formu a 1 .125)

Tab e 126. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 16< =formu a 1 .126)

Tab e 127. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 17( =formu a 1 .127)

Tab e 128. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 18< =formu a 1 .128)

Tab e 129. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 1 19< =formu a 1 .129)

Tab e 130. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 120( =formu a 1 .130)

Tab e 131. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 121 ( =formu a 1 .131 )

Tab e 132. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 122( =formu a 1 .132)

Tab e 133. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 123( =formu a 1 .133)

Tab e 134. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 124( =formu a 1 .134)

Tab e 135. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 125( =formu a 1 .135)

Tab e 136. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 126( =formu a 1 .136)

Tab e 137. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 127( =formu a 1 .137)

Tab e 138. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 128( =formu a 1 .138)

Tab e 139. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 129( =formu a 1 .139)

Tab e 140. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 130( =formu a 1 .140)

Tab e 141. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 131 < =formu a 1 .141 )

Tab e 142. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 132( =formu a 1 .142)

Tab e 143. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 133( =formu a 1 .143)

Tab e 144. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 134( =formu a 1 .144)

Tab e 145. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 135( =formu a 1 .145)

Tab e 146. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 136( =formu a 1 .146)

Tab e 147. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 137( =formu a 1 .147)

Tab e 148. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 138( =formu a 1 .148)

Tab e 149. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 139( =formu a 1 .149)

Tab e 150. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 140( =formu a 1 .150)

Tab e 151. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 141 ( =formu a 1 .151 )

Tab e 152. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 142( =formu a 1 .152)

Tab e 153. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 143( =formu a 1 .153)

Tab e 154. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 144( =formu a 1 .154)

Tab e 155. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 145( =formu a 1 .155)

Tab e 156. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 146( =formu a 1 .156)

Tab e 157. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 147( =formu a 1 .157)

Tab e 158. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 148( =formu a 1 .158)

Tab e 159. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 149( =formu a 1 .159)

Tab e 160. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 150( =formu a 1 .160)

Tab e 161. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 151 ( =formu a 1 .161 )

Tab e 162. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 152( =formu a 1 .162)

Tab e 163. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 153( =formu a 1 .163)

Tab e 164. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 154( =formu a 1 .164)

Tab e 165. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 155( =formu a 1 .165)

Tab e 166. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 156( =formu a 1 .166) Table 167. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 157( =formu a ' .167)

Table 168. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 158( =formu a ' .168)

Table 169. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 159( =formu a ' .169)

Table 170. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 160( =formu a ' .170)

Table 171. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 161 ( =formu a ' .171 )

Table 172. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 162( =formu a ' .172)

Table 173. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 163( =formu a ' .173)

Table 174. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 164( =formu a ' .174)

Table 175. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 165( =formu a ' .175)

Table 176. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 166( =formu a ' .176)

Table 177. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 167( =formu a ' .177)

Table 178. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 168( =formu a ' .178)

Table 179. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 169( =formu a ' .179)

Table 180. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 170( =formu a ' .180)

Table 181. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 171 ( =formu a ' .181 )

Table 182. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 172( =formu a ' .182)

Table 183. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 173( =formu a ' .183)

Table 184. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 174( =formu a ' .184)

Table 185. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 175( =formu a ' .185)

Table 186. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 176( =formu a ' .186)

Table 187. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 177( =formu a ' .187)

Table 188. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 178( =formu a ' .188)

Table 189. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 179( =formu a ' .189)

Table 190. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 180( =formu a ' .190)

Table 191. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 181 ( =formu a ' .191 )

Table 192. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 182( =formu a ' .192)

Table 193. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 183( =formu a ' .193)

Table 194. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 184( =formu a ' .194)

Table 195. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 185( =formu a ' .195)

Table 196. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 186( =formu a ' .196)

Table 197. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 187( =formu a ' .197)

Table 198. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 188( =formu a ' .198)

Table 199. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 189( =formu a ' .199)

Table 200. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 190( =formu a ' .200)

Table 201. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 191 ( =formu a ' .201 )

Table 202. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 192( =formu a ' .202)

Table 203. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 193( =formu a ' .203)

Table 204. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 194( =formu a ' .204)

Table 205. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 195( =formu a ' .205)

Table 206. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 196( =formu a ' .206)

Table 207. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 197( =formu a ' .207)

Table 208. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 198( =formu a ' .208)

Table 209. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 199( =formu a ' .209)

Table 210. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 200( =formu a ' .210) Tab e 21 1. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 201 ( =formula ' .21 1 ).

Tab e 212. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 202( =formula ' .212).

Tab e 213. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 203( =formula ' .213).

Tab e 214. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 204( =formula ' .214).

Tab e 215. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 205( =formula ' .215).

Tab e 216. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 206( =formula ' .216).

Tab e 217. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 207( =formula ' .217).

Tab e 218. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 208( =formula ' .218).

Tab e 219. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 209( =formula ' .219).

Tab e 220. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 210( =formula ' .220).

Tab e 221. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 21 1 ( =formula ' .221 ).

Tab e 222. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 212( =formula ' .222).

Tab e 223. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 213( =formula ' .223).

Tab e 224. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 214( =formula ' .224).

Tab e 225. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 215( =formula ' .225).

Tab e 226. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 216( =formula ' .226).

Tab e 227. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 217( =formula ' .227).

Tab e 228. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 218( =formula ' .228).

Tab e 229. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 219( =formula ' .229).

Tab e 230. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 220( =formula ' .230).

Tab e 231. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 221 ( =formula ' .231 ).

Tab e 232. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 222( =formula ' .232).

Tab e 233. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 223( =formula ' .233).

Tab e 234. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 224( =formula ' .234).

Tab e 235. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 225( =formula ' .235).

Tab e 236. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 226( =formula ' .236).

Tab e 237. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 227( =formula ' .237).

Tab e 238. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 228( =formula ' .238).

Tab e 239. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 229( =formula ' .239).

Tab e 240. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 230( =formula ' .240).

Tab e 241. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 231 ( =formula ' .241 ).

Tab e 242. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 232( =formula ' .242).

Tab e 243. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 233( =formula ' .243).

Tab e 244. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 234( =formula ' .244).

Tab e 245. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 235( =formula ' .245).

Tab e 246. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 236( =formula ' .246).

Tab e 247. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 237( =formula ' .247).

Tab e 248. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 238( =formula ' .248).

Tab e 249. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 239( =formula ' .249).

Tab e 250. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 240( =formula ' .250).

Tab e 251. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 241 ( =formula ' .251 ).

Tab e 252. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 242( =formula ' .252).

Tab e 253. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 243 (=formula 1 .253)

Tab e 254. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 244( =formula ' .254). Tab e255. Compounds of formu a I.1, wherein R2 is R2- ^■ 9245( =formula ' .255).

Tab e256. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 246( =formula ' .256).

Tab e257. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 247( =formula ' .257).

Tab e258. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 248( =formula ' .258).

Tab e259. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 249( =formula ' .259).

Tab e260. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 250( =formula ' .260).

Tab e261. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 251( =formula ' .261).

Tab e262. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 252( =formula ' .262).

Tab e263. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 253( =formula ' .263).

Tab e264. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 254( =formula ' .264).

Tab e265. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 255( =formula ' .265).

Tab e266. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 256( =formula ' .266).

Tab e267. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 257( =formula ' .267).

Tab e268. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 258( =formula ' .268).

Tab e269. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 259( =formula ' .269).

Tab e270. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 260( =formula ' .270).

Tab e271. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 261( =formula ' .271).

Tab e272. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 262( =formula ' .272).

Tab e273. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 263( =formula ' .273).

Tab e274. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 264( =formula ' .274).

Tab e275. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 265 (=formula 1.275)

Tab e276. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 266 (=formula 1.276)

Tab e277. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 267( =formula ' .277).

Tab e278. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 268( =formula ' .278).

Tab e279. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 269( =formula ' .279).

Tab e280. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 270 (=formula 1.280)

Tab e281. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 271( =formula ' .281).

Tab e282. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 272( =formula ' .282).

Tab e283. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 273 (=formula 1.283)

Tab e284. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 274 (=formula 1.284)

Tab e285. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 275 (=formula 1.285)

Tab e286. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 276 (=formula 1.286)

Tab e287. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 277( =formula ' .287).

Tab e288. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 278( =formula ' .288).

Tab e289. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 279( =formula ' .289).

Tab e290. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 280( =formula ' .290).

Tab e291. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 281( =formula ' .291).

Tab e292. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 282( =formula ' .292).

Tab e293. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 283( =formula ' .293).

Tab e294. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 284( =formula ' .294).

Tab e295. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 285( =formula ' .295).

Tab e296. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 286( =formula ' .296).

Tab e297. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 287( =formula ' .297).

Tab e298. Compounds of formu a I. 1, wherein R2 is R2- ^■ 9 288( =formula ' .298). Tab e 299. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 289( =formu a ' .299).

Tab e 300. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 290( =formu a ' .300).

Tab e 301. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 291 ( =formu a ' .301 ).

Tab e 302. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 292( =formu a ' .302).

Tab e 303. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 293( =formu a ' .303).

Tab e 304. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 294( =formu a ' .304).

Tab e 305. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 295( =formu a ' .305).

Tab e 306. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 296( =formu a ' .306).

Tab e 307. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 297( =formu a ' .307).

Tab e 308. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 298( =formu a ' .308).

Tab e 309. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 299( =formu a ' .309).

Tab e 310. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 300 (=formula 1 .310)

Tab e 31 1. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 301 ( =formu a ' .31 1 ).

Tab e 312. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 302( =formu a ' .312).

Tab e 313. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 303( =formu a ' .313).

Tab e 314. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 304( =formu a ' .314).

Tab e 315. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 305( =formu a ' .315).

Tab e 316. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 306( =formu a ' .316).

Tab e 317. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 307( =formu a ' .317).

Tab e 318. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 308( =formu a ' .318).

Tab e 319. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 309( =formu a ' .319).

Tab e 320. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 310( =formu a ' .320).

Tab e 321. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 31 1 < =formu a ' .321 ).

Tab e 322. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 312( =formu a ' .322).

Tab e 323. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 313( =formu a ' .323).

Tab e 324. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 314( =formu a ' .324).

Tab e 325. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 315( =formu a ' .325).

Tab e 326. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 316( =formu a ' .326).

Tab e 327. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 317( =formu a ' .327).

Tab e 328. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 318( =formu a ' .328).

Tab e 329. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 319( =formu a ' .329).

Tab e 330. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 320( =formu a ' .330).

Tab e 331. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 321 ( =formu a ' .331 ).

Tab e 332. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 322( =formu a ' .332).

Tab e 333. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 323( =formu a ' .333).

Tab e 334. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 324( =formu a ' .334).

Tab e 335. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 325( =formu a ' .335).

Tab e 336. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 326( =formu a ' .336).

Tab e 337. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 327( =formu a ' .337).

Tab e 338. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 328( =formu a ' .338).

Tab e 339. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 329( =formu a ' .339).

Tab e 340. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 330( =formu a ' .340).

Tab e 341. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 331 ( =formu a ' .341 ).

Tab e 342. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 332( =formu a ' .342). Tab e 343. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 333(=formula 1.343).

Tab e 344. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 334(=formula 1.344).

Tab e 345. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 335(=formula 1.345).

Tab e 346. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 336(=formula 1.346).

Tab e 347. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 334(=formula 1.347).

Tab e 348. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 338(=formula 1.348).

Tab e 349. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 339(=formula 1.349).

Tab e 350. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 340(=formula 1.350).

Tab e 351. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 341 (=formula 1.351 ).

Tab e 352. Compounds of formula I. 1 , wherein R ² is R ² -9.342(=formula 1 .352)

Tab e 353. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 343(=formula 1.353).

Tab e 354. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 344(=formula 1.354).

Tab e 355. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 345(=formula 1.355).

Tab e 356. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 346(=formula 1.356).

Tab e 357. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 347(=formula 1.357).

Tab e 358. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 348(=formula 1.358).

Tab e 359. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 349(=formula 1.359).

Tab e 360. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 350(=formula 1.360).

Tab e 361. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 351 (=formula 1.361 ).

Tab e 362. Compounds of formula I. 1 , wherein R ² is R ² -9 .352(=formula 1 .362)

Tab e 363. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 353(=formula 1.363).

Tab e 364. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 354(=formula 1.364).

Tab e 365. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 355(=formula 1.365).

Tab e 366. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 356(=formula 1.366).

Tab e 367. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 357(=formula 1.367).

Tab e 368. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 358(=formula 1.368).

Tab e 369. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 359(=formula 1.369).

Tab e 370. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 360(=formula 1.370).

Tab e 371. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 361 (=formula 1.371 ).

Tab e 372. Compounds of formula I. 1 , wherein R ² is R ² -9 .362(=formula 1 .372)

Tab e 373. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 363(=formula 1.373).

Tab e 374. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 364(=formula 1.374).

Tab e 375. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 365(=formula 1.375).

Tab e 376. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 366(=formula 1.376).

Tab e 377. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 367(=formula 1.377).

Tab e 378. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 368(=formula 1.378).

Tab e 379. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 369(=formula 1.379).

Tab e 380. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 370(=formula 1.380).

Tab e 381. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 371 (=formula 1.381 ).

Tab e 382. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 372(=formula 1.382).

Tab e 383. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 373(=formula 1.383).

Tab e 384. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 374(=formula 1.384).

Tab e 385. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 375(=formula 1.385).

Tab e 386. Compounds of formula I. I , wherein R ² is R ² - ^■ 9 376(=formula 1.386). Tab e 387. Compounds of formu a I wherein R2 is R2- ^■ 9 377( =formu a 1.387).

Tab e 388. Compounds of formu a I wherein R2 is R2- ^■ 9 378( =formu a 1.388).

Tab e 389. Compounds of formu a I wherein R2 is R2- ^■ 9 379( =formu a 1.389).

Tab e 390. Compounds of formu a I wherein R2 is R2- ^■ 9 380( =formu a 1.390).

Tab e 391. Compounds of formu a I wherein R2 is R2- ^■ 9 381 ( =formu a 1.391 ).

Tab e 392. Compounds of formu a I wherein R2 is R2- ^■ 9 382( =formu a 1.392).

Tab e 393. Compounds of formu a I wherein R2 is R2- ^■ 9 383( =formu a 1.393).

Tab e 394. Compounds of formu a I wherein R2 is R2- ^■ 9 384( =formu a 1.394).

Tab e 395. Compounds of formu a I wherein R2 is R2- ^■ 9 385( =formu a 1.395).

Tab e 396. Compounds of formu a I wherein R2 is R2- ^■ 9 386( =formu a 1.396).

Tab e 397. Compounds of formu a I wherein R2 is R2- ^■ 9 387( =formu a 1.397).

Tab e 398. Compounds of formu a I wherein R2 is R2- ^■ 9 388( =formu a 1.398).

Tab e 399. Compounds of formu a I wherein R2 is R2- ^■ 9 389( =formu a 1.399).

Tab e 400. Compounds of formu a I wherein R2 is R2- ^■ 9 390( =formu a 1.400).

Tab e 401. Compounds of formu a I wherein R2 is R2- ^■ 9 391 ( =formu a 1.401 ).

Tab e 402. Compounds of formula , wherein R ² is R2-9.392(=formula 1 .402)

Tab e 403. Compounds of formu a I wherein R2 is R2- ^■ 9 393( =formu a 1.403).

Tab e 404. Compounds of formu a I wherein R2 is R2- ^■ 9 394( =formu a 1.404).

Tab e 405. Compounds of formu a I wherein R2 is R2- ^■ 9 395( =formu a 1.405).

Tab e 406. Compounds of formu a I wherein R2 is R2- ^■ 9 396( =formu a 1.406).

Tab e 407. Compounds of formu a I wherein R2 is R2- ^■ 9 397( =formu a 1.407).

Tab e 408. Compounds of formu a I wherein R2 is R2- ^■ 9 398( =formu a 1.408).

Tab e 409. Compounds of formu a I wherein R2 is R2- ^■ 9 399( =formu a 1.409).

Tab e 410. Compounds of formu a I wherein R2 is R2- ^■ 9 400( =formu a 1.410).

Tab e 41 1. Compounds of formu a I wherein R2 is R2- ^■ 9 401 ( =formu a 1.41 1 ).

Tab e 412. Compounds of formu a I wherein R2 is R2- ^■ 9 402( =formu a 1.412).

Tab e 413. Compounds of formu a I wherein R2 is R2- ^■ 9 403( =formu a 1.413).

Tab e 414. Compounds of formu a I wherein R2 is R2- ^■ 9 404( =formu a 1.414).

Tab e 415. Compounds of formu a I wherein R2 is R2- ^■ 9 405( =formu a 1.415).

Tab e 416. Compounds of formu a I wherein R2 is R2- ^■ 9 406( =formu a 1.416).

Tab e 417. Compounds of formu a I wherein R2 is R2- ^■ 9 407( =formu a 1.417).

Tab e 418. Compounds of formu a I wherein R2 is R2- ^■ 9 408( =formu a 1.418).

Tab e 419. Compounds of formu a I wherein R2 is R2- ^■ 9 409( =formu a 1.419).

Tab e 420. Compounds of formu a I wherein R2 is R2- ^■ 9 410( =formu a 1.420).

Tab e 421. Compounds of formu a I wherein R2 is R2- ^■ 9 41 1 ( =formu a 1.421 ).

Tab e 422. Compounds of formu a I wherein R2 is R2- ^■ 9 412( =formu a 1.422).

Tab e 423. Compounds of formu a I wherein R2 is R2- ^■ 9 413( =formu a 1.423).

Tab e 424. Compounds of formu a I wherein R2 is R2- ^■ 9 414( =formu a 1.424).

Tab e 425. Compounds of formu a I wherein R2 is R2- ^■ 9 415( =formu a 1.425).

Tab e 426. Compounds of formu a I wherein R2 is R2- ^■ 9 416( =formu a 1.426).

Tab e 427. Compounds of formu a I wherein R2 is R2- ^■ 9 417( =formu a 1.427).

Tab e 428. Compounds of formu a I wherein R2 is R2- ^■ 9 418( =formu a 1.428).

Tab e 429. Compounds of formu a I wherein R2 is R2- ^■ 9 419( =formu a 1.429).

Tab e 430. Compounds of formu a I wherein R2 is R2- ^■ 9 420( =formu a 1.430). Table 431. Compounds of formula I.1 , wherein R ² is R ² -9.421 ( formula 1.431 ). Table 432. Compounds of formula I .1 , wherein R ² is R ² -9.422( =formula 1 .432). Table 433. Compounds of formula wherein R ² R ² - ^■ 9. .423 =formu .433). Table 434. Compounds of formula wherein R ² R ² - ^■ 9. .424 =formu .434). Table 435. Compounds of formula wherein R ² R ² - ^■ 9. .425 =formu .435). Table 436. Compounds of formula wherein R ² R ² - ^■ 9. .426 =formu .436). Table 437. Compounds of formula wherein R ² R ² - ^■ 9. .427 =formu .437). Table 438. Compounds of formula wherein R ² R ² - ^■ 9. .428 =formu .438). Table 439. Compounds of formula wherein R ² R ² - ^■ 9. .429 =formu .439). Table 440. Compounds of formula wherein R ² R ² - ^■ 9. .430 =formu .440). Table 441. Compounds of formula wherein R ² R ² - ^■ 9. .431 =formu .441 ). Table 442. Compounds of formula wherein R ² R ² - ^■ 9. .432 =formu .442). Table 443. Compounds of formula wherein R ² R ² - ^■ 9. .433 =formu .443). Table 444. Compounds of formula wherein R ² R ² - ^■ 9. .434 =formu .444). Table 445. Compounds of formula wherein R ² R ² - ^■ 9. .435 =formu .445). Table 446. Compounds of formula wherein R ² R ² - ^■ 9. .436 =formu .446). Table 447. Compounds of formula wherein R ² R ² - ^■ 9. .437 =formu .447). Table 448. Compounds of formula wherein R ² R ² - ^■ 9. .438 =formu .448). Table 449. Compounds of formula wherein R ² R ² - ^■ 9. .439 =formu .449). Table 450. Compounds of formula wherein R ² R ² - ^■ 9. .440 =formu .450). Table 451. Compounds of formula wherein R ² R ² - ^■ 9. .441 =formu .451 ). Table 452. Compounds of formula wherein R ² R ² - ^■ 9. .442 =formu .452). Table 453. Compounds of formula wherein R ² R ² - ^■ 9. .443 =formu .453). Table 454. Compounds of formula wherein R ² R ² - ^■ 9. .444 =formu .454). Table 455. Compounds of formula wherein R ² R ² - ^■ 9. .445 =formu .455). Table 456. Compounds of formula wherein R ² R ² - ^■ 9. .446 =formu .456). Table 457. Compounds of formula wherein R ² R ² - ^■ 9. .447 =formu .457). Table 458. Compounds of formula wherein R ² R ² - ^■ 9. .448 =formu .458). Table 459. Compounds of formula wherein R ² R ² - ^■ 9. .449 =formu .459). Table 460. Compounds of formula wherein R ² R ² - ^■ 9. .450 =formu .460). Table 461. Compounds of formula wherein R ² R ² - ^■ 9. .451 =formu .461 ). Table 462. Compounds of formula wherein R ² R ² - ^■ 9. .452 =formu .462). Table 463. Compounds of formula wherein R ² R ² - ^■ 9. .453 =formu .463). Table 464. Compounds of formula wherein R ² R ² - ^■ 9. .454 =formu .464). Table 465. Compounds of formula wherein R ² R ² - ^■ 9. .455 =formu .465). Table 466. Compounds of formula wherein R ² R ² - ^■ 9. .456 =formu .466). Table 467. Compounds of formula wherein R ² R ² - ^■ 9. .457 =formu .467). Table 468. Compounds of formula wherein R ² R ² - ^■ 9. .458 =formu .468). Table 469. Compounds of formula wherein R ² R ² - ^■ 9. .459 =formu .469). Table 470. Compounds of formula wherein R ² R ² - ^■ 9. .460 =formu .470). Table 471. Compounds of formula wherein R ² R ² - ^■ 9. .461 =formu .471 ). Table 472. Compounds of formula wherein R ² R ² - ^■ 9. .462 =formu .472). Table 473. Compounds of formula wherein R ² R ² - ^■ 9. .463 =formu .473). Table 474. Compounds of formula wherein R ² R ² - ^■ 9. .464 =formu .474). Tab e 475. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 465( =formu a ' .475).

Tab e 476. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 466( =formu a ' .476).

Tab e 477. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 467( =formu a ' .477).

Tab e 478. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 468( =formu a ' .478).

Tab e 479. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 469( =formu a ' .479).

Tab e 480. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 470( =formu a ' .480).

Tab e 481. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 471 ( =formu a ' .481 ).

Tab e 482. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 472( =formu a ' .482).

Tab e 483. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 473( =formu a ' .483).

Tab e 484. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 474( =formu a ' .484).

Tab e 485. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 475( =formu a ' .485).

Tab e 486. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 476( =formu a ' .486).

Tab e 487. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 477( =formu a ' .487).

Tab e 488. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 478( =formu a ' .488).

Tab e 489. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 479( =formu a ' .489).

Tab e 490. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 480( =formu a ' .490).

Tab e 491. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 481 ( =formu a ' .491 ).

Tab e 492. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 482( =formu a ' .492).

Tab e 493. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 483( =formu a ' .493).

Tab e 494. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 484( =formu a ' .494).

Tab e 495. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 485( =formu a ' .495).

Tab e 496. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 486( =formu a ' .496).

Tab e 497. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 487( =formu a ' .497).

Tab e 498. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 488( =formu a ' .498).

Tab e 499. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 489( =formu a ' .499).

Tab e 500. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 490( =formu a ' .500).

Tab e 501. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 491 ( =formu a ' .501 ).

Tab e 502. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 492 (=formula 1 .502)

Tab e 503. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 493( =formu a ' .503).

Tab e 504. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 494( =formu a ' .504).

Tab e 505. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 495( =formu a ' .505).

Tab e 506. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 496( =formu a ' .506).

Tab e 507. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 497( =formu a ' .507).

Tab e 508. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 498( =formu a ' .508).

Tab e 509. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 499( =formu a ' .509).

Tab e 510. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 500( =formu a ' .510).

Tab e 51 1. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 501 ( =formu a ' .51 1 ).

Tab e 512. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 502( =formu a ' .512).

Tab e 513. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 503( =formu a ' .513).

Tab e 514. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 504( =formu a ' .514).

Tab e 515. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 505( =formu a ' .515).

Tab e 516. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 506( =formu a ' .516).

Tab e 517. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 507( =formu a ' .517).

Tab e 518. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 508( =formu a ' .518). Tab e 519. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 509( =formula 1 .519).

Tab e 520. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 510( =formula 1 .520).

Tab e 521. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 51 1 ( =formula 1 .521 ).

Tab e 522. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 512 (=formula 1 .522)

Tab e 523. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 513 (=formula 1 .523)

Tab e 524. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 514( =formula 1 .524).

Tab e 525. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 515( =formula 1 .525).

Tab e 526. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 516( =formula 1 .526).

Tab e 527. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 517( =formula 1 .527).

Tab e 528. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 518( =formula 1 .528).

Tab e 529. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 519( =formula 1 .529).

Tab e 530. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 520( =formula 1 .530).

Tab e 531. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 521 ( =formula 1 .531 ).

Tab e 532. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 522( =formula 1 .532).

Tab e 533. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 523( =formula 1 .533).

Tab e 534. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 524( =formula 1 .534).

Tab e 535. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 525( =formula 1 .535).

Tab e 536. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 526( =formula 1 .536).

Tab e 537. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 527( =formula 1 .537).

Tab e 538. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 528( =formula 1 .538).

Tab e 539. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 529( =formula 1 .539).

Tab e 540. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 530( =formula 1 .540).

Tab e 541. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 531 ( =formula 1 .541 ).

Tab e 542. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 532( =formula 1 .542).

Tab e 543. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 533( =formula 1 .543).

Tab e 544. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 534( =formula 1 .544).

Tab e 545. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 535( =formula 1 .545).

Tab e 546. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 536( =formula 1 .546).

Tab e 547. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 537( =formula 1 .547).

Tab e 548. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 538( =formula 1 .548).

Tab e 549. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 539( =formula 1 .549).

Tab e 550. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 540( =formula 1 .550).

Tab e 551. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 541 ( =formula 1 .551 ).

Tab e 552. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 542( =formula 1 .552).

Tab e 553. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 543( =formula 1 .553).

Tab e 554. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 544( =formula 1 .554).

Tab e 555. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 545( =formula 1 .555).

Tab e 556. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 546( =formula 1 .556).

Tab e 557. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 547( =formula 1 .557).

Tab e 558. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 548( =formula 1 .558).

Tab e 559. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 549( =formula 1 .559).

Tab e 560. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 550( =formula 1 .560).

Tab e 561. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 551 ( =formula 1 .561 ).

Tab e 562. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 552( =formula 1 .562). Table 563. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 553( =formu a 1.563).

Table 564. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 554( =formu a 1.564).

Table 565. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 555( =formu a 1.565).

Table 566. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 556( =formu a 1.566).

Table 567. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 557( =formu a 1.567).

Table 568. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 558( =formu a 1.568).

Table 569. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 559( =formu a 1.569).

Table 570. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 560 (=formula 1 .570)

Table 571. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 561 ( =formu a 1.571 ).

Table 572. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 562( =formu a 1.572).

Table 573. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 563( =formu a 1.573).

Table 574. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 564( =formu a 1.574).

Table 575. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 565( =formu a 1.575).

Table 576. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 566( =formu a 1.576).

Table 577. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 567( =formu a 1.577).

Table 578. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 568( =formu a 1.578).

Table 579. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 569( =formu a 1.579).

Table 580. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 570( =formu a 1.580).

Table 581. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 571 ( =formu a 1.581 ).

Table 582. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 572( =formu a 1.582).

Table 583. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 573( =formu a 1.583).

Table 584. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 574( =formu a 1.584).

Table 585. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 575( =formu a 1.585).

Table 586. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 576( =formu a 1.586).

Table 587. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 577( =formu a 1.587).

Table 588. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 578( =formu a 1.588).

Table 589. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 579( =formu a 1.589).

Table 590. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 580( =formu a 1.590).

Table 591. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 581 ( =formu a 1.591 ).

Table 592. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 582( =formu a 1.592).

Table 593. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 583( =formu a 1.593).

Table 594. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 584( =formu a 1.594).

Table 595. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 585( =formu a 1.595).

Table 596. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 586( =formu a 1.596).

Table 597. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 587( =formu a 1.597).

Table 598. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 588( =formu a 1.598).

Table 599. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 589( =formu a 1.599).

Table 600. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 590( =formu a 1.600).

Table 601. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 591 ( =formu a 1.601 ).

Table 602. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 592( =formu a 1.602).

Table 603. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 593( =formu a 1.603).

Table 604. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 594( =formu a 1.604).

Table 605. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 595( =formu a 1.605).

Table 606. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 596( =formu a 1.606). Tab e 607. Compounds of formu a I.1 , wherein R2 is R2- ^■ 9 597( =formu a ' 1.607)

Tab e 608. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 598( =formu a ' 1.608)

Tab e 609. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 599( =formu a ' 1.609)

Tab e 610. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 600( =formu a ' 1.610)

Tab e 61 1. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 601 ( =formu a ' 1.61 1 )

Tab e 612. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 602( =formu a ' 1.612)

Tab e 613. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 603( =formu a ' 1.613)

Tab e 614. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 604( =formu a ' 1.614)

Tab e 615. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 605( =formu a ' 1.615)

Tab e 616. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 606( =formu a ' 1.616)

Tab e 617. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 607( =formu a ' 1.617)

Tab e 618. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 608( =formu a ' 1.618)

Tab e 619. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 609( =formu a ' 1.619)

Tab e 620. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 610( =formu a ' 1.620)

Tab e 621. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 61 1 < =formu a ' 1.621 )

Tab e 622. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 612( =formu a ' 1.622)

Tab e 623. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 613( =formu a ' 1.623)

Tab e 624. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 614( =formu a ' 1.624)

Tab e 625. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 615( =formu a ' 1.625)

Tab e 626. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 616( =formu a ' 1.626)

Tab e 627. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 617( =formu a ' 1.627)

Tab e 628. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 618( =formu a ' 1.628)

Tab e 629. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 619( =formu a ' 1.629)

Tab e 630. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 620( =formu a ' 1.630)

Tab e 631. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 621 ( =formu a ' 1.631 )

Tab e 632. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 622( =formu a ' 1.632)

Tab e 633. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 623( =formu a ' 1.633)

Tab e 634. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 624( =formu a ' 1.634)

Tab e 635. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 625( =formu a ' 1.635)

Tab e 636. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 626( =formu a ' 1.636)

Tab e 637. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 627( =formu a ' 1.637)

Tab e 638. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 628( =formu a ' 1.638)

Tab e 639. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 629( =formu a ' 1.639)

Tab e 640. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 630( =formu a ' 1.640)

Tab e 641. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 631 ( =formu a ' 1.641 )

Tab e 642. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 632( =formu a ' 1.642)

Tab e 643. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 633( =formu a ' 1.643)

Tab e 644. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 634( =formu a ' 1.644)

Tab e 645. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 635( =formu a ' 1.645)

Tab e 646. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 636( =formu a ' 1.646)

Tab e 647. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 637( =formu a ' 1.647)

Tab e 648. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 638( =formu a ' 1.648)

Tab e 649. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 639( =formu a ' 1.649)

Tab e 650. Compounds of formu a I. 1 , wherein R2 is R2- ^■ 9 640( =formu a ' 1.650) Table 651. Compounds of formu a I.1 , wherein R2 is R2- 9.641 =formula 1.651 )

Table 652. Compounds of formu a I. 1 , wherein R2 is R2- 9.642 =formula 1.652)

Table 653. Compounds of formu a I. 1 , wherein R2 is R2- 9.643 =formula 1.653)

Table 654. Compounds of formu a I. 1 , wherein R2 is R2- 9.644 ^formula 1.654)

Table 655. Compounds of formu a I. 1 , wherein R2 is R2- 9.645 =formula 1.655)

Table 656. Compounds of formu a I. 1 , wherein R2 is R2- 9.646 =formula 1.656)

Table 657. Compounds of formu a I. 1 , wherein R2 is R2- 9.647 =formula 1.657)

Table 658. Compounds of formu a I. 1 , wherein R2 is R2- 9.648 =formula 1.658)

Table 659. Compounds of formu a I. 1 , wherein R2 is R2- 9.649 =formula 1.659)

Table 660. Compounds of formu a I. 1 , wherein R2 is R2- 9.650 =formula 1.660)

Table 661. Compounds of formu a I. 1 , wherein R2 is R2- 9.651 =formula 1.661 )

Table 662. Compounds of formu a I. 1 , wherein R2 is R2- 9.652 =formula 1.662)

Table 663. Compounds of formu a I. 1 , wherein R2 is R2- 9.653 =formula 1.663)

Table 664. Compounds of formu a I. 1 , wherein R2 is R2- 9.654 =formula 1.664)

Table 665. Compounds of formu a I. 1 , wherein R2 is R2- 9.655 =formula 1.665)

Table 666. Compounds of formu a I. 1 , wherein R2 is R2- 9.656 =formula 1.666)

Table 667. Compounds of formu a I. 1 , wherein R2 is R2- 9.657 ^formula 1.667)

Table 668. Compounds of formu a I. 1 , wherein R2 is R2- 9.658 =formula 1.668)

Table 669. Compounds of formu a I. 1 , wherein R2 is R2- 9.659 =formula 1.669)

Table 670. Compounds of formu a I. 1 , wherein R2 is R2- 9.660 ^formula 1.670)

Table 671. Compounds of formu a I. 1 , wherein R2 is R2- 9.661 =formula 1.671 )

Table 672. Compounds of formu a I. 1 , wherein R2 is R2- 9.662 =formula 1.672)

Table 673. Compounds of formu a I. 1 , wherein R2 is R2- 9.663 =formula 1.673)

Table 674. Compounds of formu a I. 1 , wherein R2 is R2- 9.664 ^formula 1.674)

Table 675. Compounds of formu a I. 1 , wherein R2 is R2- 9.665 =formula 1.675)

Table 676. Compounds of formu a I. 1 , wherein R2 is R2- 9.666 ^formula 1.676)

Table 677. Compounds of formu a I. 1 , wherein R2 is R2- 9.667 ^formula 1.677)

Table 678. Compounds of formu a I. 1 , wherein R2 is R2- 9.668 ^formula 1.678)

Table 679. Compounds of formu a I. 1 , wherein R2 is R2- 9.669 ^formula 1.679)

Table 680. Compounds of formu a I. 1 , wherein R2 is R2- 9.670 =formula 1.680)

Table 681. Compounds of formu a I. 1 , wherein R2 is R2- 9.671 =formula 1.681 )

Table 682. Compounds of formu a I. 1 , wherein R2 is R2- 9.672 =formula 1.682)

Table 683. Compounds of formu a I. 1 , wherein R2 is R2- 9.673 =formula 1.683)

Table 684. Compounds of formu a I. 1 , wherein R2 is R2- 9.674 =formula 1.684)

Table 685. Compounds of formu a I. 1 , wherein R2 is R2- 9.675 =formula 1.685)

Table 686. Compounds of formu a I. 1 , wherein R2 is R2- 9.676 =formula 1.686)

Table 687. Compounds of formu a I. 1 , wherein R2 is R2- 10.1 (= formula 1 .687).

Table 688. Compounds of formu a I. 1 , wherein R2 is R2- 10.2(= formula 1 .688).

Table 689. Compounds of formu a I. 1 , wherein R2 is R2- 10.3(= formula 1 .689).

Table 690. Compounds of formu a I. 1 , wherein R2 is R2- 10.4(= formula 1 .690).

Table 691. Compounds of formu a I. 1 , wherein R2 is R2- 10.5(= formula 1 .691 ).

Table 692. Compounds of formu a I. 1 , wherein R2 is R2- 10.6(= formula 1 .692).

Table 693. Compounds of formu a I. 1 , wherein R2 is R2- 10.7(= formula 1 .693).

Table 694. Compounds of formu a I. 1 , wherein R2 is R2- 10.8(= formula 1 .694). Tab e 695. Compounds of formu a I.1, wherein R2 is R2-- I09(=formula 1.695).

Tab e 696. Compounds of formu a I. 1, wherein R2 is R2-- I0 10( =formu a ' 1.696)

Tab e 697. Compounds of formu a I. 1, wherein R2 is R2-- I0 11( =formu a ' 1.697)

Tab e 698. Compounds of formu a I. 1, wherein R2 is R2-- I0 12( =formu a ' 1.698)

Tab e 699. Compounds of formu a I. 1, wherein R2 is R2-- I0 13( =formu a ' 1.699)

Tab e 700. Compounds of formu a I. 1, wherein R2 is R2-- I0 14( =formu a ' 1.700)

Tab e 701. Compounds of formu a I. 1, wherein R2 is R2-- I0 15( =formu a ' 1.701)

Tab e 702. Compounds of formu a I. 1, wherein R2 is R2-- I0 16( =formu a ' 1.702)

Tab e 703. Compounds of formu a I. 1, wherein R2 is R2-- I0 17( =formu a ' 1.703)

Tab e 704. Compounds of formu a I. 1, wherein R2 is R2-- I0 18( =formu a ' 1.704)

Tab e 705. Compounds of formu a I. 1, wherein R2 is R2-- I0 19( =formu a ' 1.705)

Tab e 706. Compounds of formu a I. 1, wherein R2 is R2-- I0 20( =formu a ' 1.706)

Tab e 707. Compounds of formu a I. 1, wherein R2 is R2-- I0 21( =formu a ' 1.707)

Tab e 708. Compounds of formu a I. 1, wherein R2 is R2-- I0 22( =formu a ' 1.708)

Tab e 709. Compounds of formu a I. 1, wherein R2 is R2-- I0 23( =formu a ' 1.709)

Tab e 710. Compounds of formu a I. 1, wherein R2 is R2-- I0 24( =formu a ' 1.710)

Tab e 711. Compounds of formu a I. 1, wherein R2 is R2-- I0 25( =formu a ' 1.711)

Tab e 712. Compounds of formu a I. 1, wherein R2 is R2-- I0 26( =formu a ' 1.712)

Tab e 713. Compounds of formu a I. 1, wherein R2 is R2-- I0 27( =formu a ' 1.713)

Tab e 714. Compounds of formu a I. 1, wherein R2 is R2-- I0 28( =formu a ' 1.714)

Tab e 715. Compounds of formu a I. 1, wherein R2 is R2-- I0 29( =formu a ' 1.715)

Tab e 716. Compounds of formu a I. 1, wherein R2 is R2-- I0 30( =formu a ' 1.716)

Tab e 717. Compounds of formu a I. 1, wherein R2 is R2-- I0 31( =formu a ' 1.717)

Tab e 718. Compounds of formu a I. 1, wherein R2 is R2-- I0 32( =formu a ' 1.718)

Tab e 719. Compounds of formu a I. 1, wherein R2 is R2-- I0 33( =formu a ' 1.719)

Tab e 720. Compounds of formu a I. 1, wherein R2 is R2-- I0 34( =formu a ' 1.720)

Tab e 721. Compounds of formu a I. 1, wherein R2 is R2-- I0 35( =formu a ' 1.721)

Tab e 722. Compounds of formu a I. 1, wherein R2 is R2-- I0 36( =formu a ' 1.722)

Tab e 723. Compounds of formu a I. 1, wherein R2 is R2-- I0 37( =formu a ' 1.723)

Tab e 724. Compounds of formu a I. 1, wherein R2 is R2-- I0 38( =formu a ' 1.724)

Tab e 725. Compounds of formu a I. 1, wherein R2 is R2-- I0 39( =formu a ' 1.725)

Tab e 726. Compounds of formu a I. 1, wherein R2 is R2-- I0 40( =formu a ' 1.726)

Tab e 727. Compounds of formu a I. 1, wherein R2 is R2-- I0 41( =formu a ' 1.727)

Tab e 728. Compounds of formu a I. 1, wherein R2 is R2-- I0 42( =formu a ' 1.728)

Tab e 729. Compounds of formu a I. 1, wherein R2 is R2-- I0 43( =formu a ' 1.729)

Tab e 730. Compounds of formu a I. 1, wherein R2 is R2-- I0 44( =formu a ' 1.730)

Tab e 731. Compounds of formu a I. 1, wherein R2 is R2-- I0 45( =formu a ' 1.731)

Tab e 732. Compounds of formu a I. 1, wherein R2 is R2-- I0 46( =formu a ' 1.732)

Tab e 733. Compounds of formu a I. 1, wherein R2 is R2-- I0 47( =formu a ' 1.733)

Tab e 734. Compounds of formu a I. 1, wherein R2 is R2-- I0 48( =formu a ' 1.734)

Tab e 735. Compounds of formu a I. 1, wherein R2 is R2-- I0 49( =formu a ' 1.735)

Tab e 736. Compounds of formu a I. 1, wherein R2 is R2-- I0 50( =formu a ' 1.736)

Tab e 737. Compounds of formu a I. 1, wherein R2 is R2-- I0 51( =formu a ' 1.737)

Tab e 738. Compounds of formu a I. 1, wherein R2 is R2-- I0 52( =formu a ' 1.738) Table 739. Compounds of formu a I.1, wherein R2 is R2-- I053( =formu a ' 1.739)

Table 740. Compounds of formu a I. 1, wherein R2 is R2-- I0 54( =formu a ' 1.740)

Table 741. Compounds of formu a I. 1, wherein R2 is R2-- I0 55( =formu a ' 1.741)

Table 742. Compounds of formu a I. 1, wherein R2 is R2-- I0 56( =formu a ' 1.742)

Table 743. Compounds of formu a I. 1, wherein R2 is R2-- I0 57( =formu a ' 1.743)

Table 744. Compounds of formu a I. 1, wherein R2 is R2-- I0 58( =formu a ' 1.744)

Table 745. Compounds of formu a I. 1, wherein R2 is R2-- I0 59( =formu a ' 1.745)

Table 746. Compounds of formu a I. 1, wherein R2 is R2-- I0 60( =formu a ' 1.746)

Table 747. Compounds of formu a I. 1, wherein R2 is R2-- I0 61( =formu a ' 1.747)

Table 748. Compounds of formu a I. 1, wherein R2 is R2-- I0 62( =formu a ' 1.748)

Table 749. Compounds of formu a I. 1, wherein R2 is R2-- I0 63( =formu a ' 1.749)

Table 750. Compounds of formu a I. 1, wherein R2 is R2-- I0 64( =formu a ' 1.750)

Table 751. Compounds of formu a I. 1, wherein R2 is R2-- I0 65( =formu a ' 1.751)

Table 752. Compounds of formu a I. 1, wherein R2 is R2-- I0 66( =formu a ' 1.752)

Table 753. Compounds of formu a I. 1, wherein R2 is R2-- I0 67( =formu a ' 1.753)

Table 754. Compounds of formu a I. 1, wherein R2 is R2-- I0 68( =formu a ' 1.754)

Table 755. Compounds of formu a I. 1, wherein R2 is R2-- I0 69( =formu a ' 1.755)

Table 756. Compounds of formu a I. 1, wherein R2 is R2-- I0 70( =formu a ' 1.756)

Table 757. Compounds of formu a I. 1, wherein R2 is R2-- I0 71( =formu a ' 1.757)

Table 758. Compounds of formu a I. 1, wherein R2 is R2-- I0 72( =formu a ' 1.758)

Table 759. Compounds of formu a I. 1, wherein R2 is R2-- I0 73( =formu a ' 1.759)

Table 760. Compounds of formu a I. 1, wherein R2 is R2-- I0 74( =formu a ' 1.760)

Table 761. Compounds of formu a I. 1, wherein R2 is R2-- I0 75( =formu a ' 1.761)

Table 762. Compounds of formu a I. 1, wherein R2 is R2-- I0 76( =formu a ' 1.762)

Table 763. Compounds of formu a I. 1, wherein R2 is R2-- I0 77( =formu a ' 1.763)

Table 764. Compounds of formu a I. 1, wherein R2 is R2-- I0 78( =formu a ' 1.764)

Table 765. Compounds of formu a I. 1, wherein R2 is R2-- I0 79( =formu a ' 1.765)

Table 766. Compounds of formu a I. 1, wherein R2 is R2-- I0 80( =formu a ' 1.766)

Table 767. Compounds of formu a I. 1, wherein R2 is R2-- I0 81( =formu a ' 1.767)

Table 768. Compounds of formu a I. 1, wherein R2 is R2-- I0 82( =formu a ' 1.768)

Table 769. Compounds of formu a I. 1, wherein R2 is R2-- I0 83( =formu a ' 1.769)

Table 770. Compounds of formu a I. 1, wherein R2 is R2-- I0 84( =formu a ' 1.770)

Table 771. Compounds of formu a I. 1, wherein R2 is R2-- I0 85( =formu a ' 1.771)

Table 772. Compounds of formu a I. 1, wherein R2 is R2-- I0 86( =formu a ' 1.772)

Table 773. Compounds of formu a I. 1, wherein R2 is R2-- I0 87( =formu a ' 1.773)

Table 774. Compounds of formu a I. 1, wherein R2 is R2-- I0 88( =formu a ' 1.774)

Table 775. Compounds of formu a I. 1, wherein R2 is R2-- I0 89( =formu a ' 1.775)

Table 776. Compounds of formu a I. 1, wherein R2 is R2-- I0 90( =formu a ' 1.776)

Table 777. Compounds of formu a I. 1, wherein R2 is R2-- I0 91( =formu a ' 1.777)

Table 778. Compounds of formu a I. 1, wherein R2 is R2-- I0 92( =formu a ' 1.778)

Table 779. Compounds of formu a I. 1, wherein R2 is R2-- I0 93( =formu a ' 1.779)

Table 780. Compounds of formu a I. 1, wherein R2 is R2-- I0 94( =formu a ' 1.780)

Table 781. Compounds of formu a I. 1, wherein R2 is R2-- I0 95( =formu a ' 1.781)

Table 782. Compounds of formu a I. 1, wherein R2 is R2-- I0 96( =formu a ' 1.782) Table 783. Compounds of formula I.1, wherein R2 is R2-- I0.97(=formula 1.783).

Table 784. Compounds of formula I. 1, wherein R2 is R2-- I0.98(=formula 1.784).

Table 785. Compounds of formula I. 1, wherein R2 is R2-- I0.99(=formula 1.785).

Table 786. Compounds of formula I. 1, wherein R2 is R2-- I0.100( =formula 1.786

Table 787. Compounds of formula I. 1, wherein R2 is R2-- I0.10K =formula 1.787

Table 788. Compounds of formula I. 1, wherein R2 is R2-- I0.102( =formula 1.788

Table 789. Compounds of formula I. 1, wherein R2 is R2-- I0.103( =formula 1.789

Table 790. Compounds of formula I. 1, wherein R2 is R2-- I0.104( =formula 1.790

Table 791. Compounds of formula I. 1, wherein R2 is R2-- I0.105( =formula 1.791

Table 792. Compounds of formula I. 1, wherein R2 is R2-- I0.106( =formula 1.792

Table 793. Compounds of formula I. 1, wherein R2 is R2-- I0.107( =formula 1.793

Table 794. Compounds of formula I. 1, wherein R2 is R2-- I0.108( =formula 1.794

Table 795. Compounds of formula I. 1, wherein R2 is R2-- I0.109( =formula 1.795

Table 796. Compounds of formula I. 1, wherein R2 is R2-- 10.110< =formula 1.796

Table 797. Compounds of formula I. 1, wherein R2 is R2-- 10.111 ( =formula 1.797

Table 798. Compounds of formula I. 1, wherein R2 is R2-- 10.112< =formula 1.798

Table 799. Compounds of formula I. 1, wherein R2 is R2-- 10.113< =formula 1.799

Table 800. Compounds of formula I. 1, wherein R2 is R2-- 10.114< =formula 1.800

Table 801. Compounds of formula I. 1, wherein R2 is R2-- 10.115< =formula 1.801

Table 802. Compounds of formula I. 1, wherein R2 is R2-- 10.116< =formula 1.802

Table 803. Compounds of formula I. 1, wherein R2 is R2-- 10.117< =formula 1.803

Table 804. Compounds of formula I. 1, wherein R2 is R2-- 10.118< =formula 1.804

Table 805. Compounds of formula I. 1, wherein R2 is R2-- 10.119< =formula 1.805

Table 806. Compounds of formula I. 1, wherein R2 is R2-- 10.120( =formula 1.806

Table 807. Compounds of formula I. 1, wherein R2 is R2-- 10.121( =formula 1.807

Table 808. Compounds of formula I. 1, wherein R2 is R2-- 10.122( =formula 1.808

Table 809. Compounds of formula I. 1, wherein R2 is R2-- 10.123( =formula 1.809

Table 810. Compounds of formula I. 1, wherein R2 is R2-- 10.124( =formula 1.810

Table 811. Compounds of formula I. 1, wherein R2 is R2-- 10.125( =formula 1.811

Table 812. Compounds of formula I. 1, wherein R2 is R2-- 10.126( =formula 1.812

Table 813. Compounds of formula I. 1, wherein R2 is R2-- 10.127( =formula 1.813

Table 814. Compounds of formula I. 1, wherein R2 is R2-- 10.128( =formula 1.814

Table 815. Compounds of formula I. 1, wherein R2 is R2-- 10.129( =formula 1.815

Table 816. Compounds of formula I. 1, wherein R2 is R2-- 10.130( =formula 1.816

Table 817. Compounds of formula I. 1, wherein R2 is R2-- 10.13K =formula 1.817

Table 818. Compounds of formula I. 1, wherein R2 is R2-- 10.132( =formula 1.818

Table 819. Compounds of formula I. 1, wherein R2 is R2-- 10.133( =formula 1.819

Table 820. Compounds of formula I. 1, wherein R2 is R2-- 10.134( =formula 1.820

Table 821. Compounds of formula I. 1, wherein R2 is R2-- 10.135( =formula 1.821

Table 822. Compounds of formula I. 1, wherein R2 is R2-- 10.136( =formula 1.822

Table 823. Compounds of formula I. 1, wherein R2 is R2-- 10.137( =formula 1.823

Table 824. Compounds of formula I. 1, wherein R2 is R2-- 10.138( =formula 1.824

Table 825. Compounds of formula I. 1, wherein R2 is R2-- 10.139( =formula 1.825

Table 826. Compounds of formula I. 1, wherein R2 is R2-- 10.140( =formula 1.826 Tab e827. Compounds of formu a I.1, wherein R2 is R2-- I0141 ( =formu a ' .827)

Tab e828. Compounds of formu a I. 1, wherein R2 is R2-- I0 142( =formu a ' .828)

Tab e829. Compounds of formu a I. 1, wherein R2 is R2-- I0 143( =formu a ' .829)

Tab e830. Compounds of formu a I. 1, wherein R2 is R2-- I0 144( =formu a ' .830)

Tab e831. Compounds of formu a I. 1, wherein R2 is R2-- I0 145( =formu a ' .831)

Tab e832. Compounds of formu a I. 1, wherein R2 is R2-- I0 146( =formu a ' .832)

Tab e833. Compounds of formu a I. 1, wherein R2 is R2-- I0 147( =formu a ' .833)

Tab e834. Compounds of formu a I. 1, wherein R2 is R2-- I0 148( =formu a ' .834)

Tab e835. Compounds of formu a I. 1, wherein R2 is R2-- I0 149( =formu a ' .835)

Tab e836. Compounds of formu a I. 1, wherein R2 is R2-- I0 150( =formu a ' .836)

Tab e837. Compounds of formu a I. 1, wherein R2 is R2-- I0 151 ( =formu a ' .837)

Tab e838. Compounds of formu a I. 1, wherein R2 is R2-- I0 152( =formu a ' .838)

Tab e839. Compounds of formu a I. 1, wherein R2 is R2-- I0 153( =formu a ' .839)

Tab e840. Compounds of formu a I. 1, wherein R2 is R2-- I0 154( =formu a ' .840)

Tab e841. Compounds of formu a I. 1, wherein R2 is R2-- I0 155( =formu a ' .841)

Tab e842. Compounds of formu a I. 1, wherein R2 is R2-- I0 156( =formu a ' .842)

Tab e843. Compounds of formu a I. 1, wherein R2 is R2-- I0 157( =formu a ' .843)

Tab e844. Compounds of formu a I. 1, wherein R2 is R2-- I0 158( =formu a ' .844)

Tab e845. Compounds of formu a I. 1, wherein R2 is R2-- I0 159( =formu a ' .845)

Tab e846. Compounds of formu a I. 1, wherein R2 is R2-- I0 160( =formu a ' .846)

Tab e847. Compounds of formu a I. 1, wherein R2 is R2-- I0 161 < =formu a ' .847)

Tab e848. Compounds of formu a I. 1, wherein R2 is R2-- I0 162( =formu a ' .848)

Tab e849. Compounds of formu a I. 1, wherein R2 is R2-- I0 163( =formu a ' .849)

Tab e850. Compounds of formu a I. 1, wherein R2 is R2-- I0 164( =formu a ' .850)

Tab e851. Compounds of formu a I. 1, wherein R2 is R2-- I0 165( =formu a ' .851)

Tab e852. Compounds of formu a I. 1, wherein R2 is R2-- I0 166( =formu a ' .852)

Tab e853. Compounds of formu a I. 1, wherein R2 is R2-- I0 167( =formu a ' .853)

Tab e854. Compounds of formu a I. 1, wherein R2 is R2-- I0 168( =formu a ' .854)

Tab e855. Compounds of formu a I. 1, wherein R2 is R2-- I0 169( =formu a ' .855)

Tab e856. Compounds of formu a I. 1, wherein R2 is R2-- I0 170( =formu a ' .856)

Tab e857. Compounds of formu a I. 1, wherein R2 is R2-- I0 1 1 ( =formu a ' .857)

Tab e858. Compounds of formu a I. 1, wherein R2 is R2-- I0 172( =formu a ' .858)

Tab e859. Compounds of formu a I. 1, wherein R2 is R2-- I0 173( =formu a ' .859)

Tab e860. Compounds of formu a I. 1, wherein R2 is R2-- I0 174( =formu a ' .860)

Tab e861. Compounds of formu a I. 1, wherein R2 is R2-- I0 175( =formu a ' .861)

Tab e862. Compounds of formu a I. 1, wherein R2 is R2-- I0 176( =formu a ' .862)

Tab e863. Compounds of formu a I. 1, wherein R2 is R2-- I0 177( =formu a ' .863)

Tab e864. Compounds of formu a I. 1, wherein R2 is R2-- I0 178( =formu a ' .864)

Tab e865. Compounds of formu a I. 1, wherein R2 is R2-- I0 179( =formu a ' .865)

Tab e866. Compounds of formu a I. 1, wherein R2 is R2-- I0 180( =formu a ' .866)

Tab e867. Compounds of formu a I. 1, wherein R2 is R2-- I0 181 < =formu a ' .867)

Tab e868. Compounds of formu a I. 1, wherein R2 is R2-- I0 182( =formu a ' .868)

Tab e869. Compounds of formu a I. 1, wherein R2 is R2-- I0 183( =formu a ' .869)

Tab e870. Compounds of formu a I. 1, wherein R2 is R2-- I0 184( =formu a ' .870) Tab e 871. Compounds of formu a I.1, wherein R2 is R2-- I0185( =formu a ' .871)

Tab e 872. Compounds of formu a I. 1, wherein R2 is R2-- I0 186( =formu a ' .872)

Tab e 873. Compounds of formu a I. 1, wherein R2 is R2-- I0 187( =formu a ' .873)

Tab e 874. Compounds of formu a I. 1, wherein R2 is R2-- I0 188( =formu a ' .874)

Tab e 875. Compounds of formu a I. 1, wherein R2 is R2-- I0 189( =formu a ' .875)

Tab e 876. Compounds of formu a I. 1, wherein R2 is R2-- I0 190( =formu a ' .876)

Tab e 877. Compounds of formu a I. 1, wherein R2 is R2-- I0 191 < =formu a ' .877)

Tab e 878. Compounds of formu a I. 1, wherein R2 is R2-- I0 192( =formu a ' .878)

Tab e 879. Compounds of formu a I. 1, wherein R2 is R2-- I0 193( =formu a ' .879)

Tab e 880. Compounds of formu a I. 1, wherein R2 is R2-- I0 194( =formu a ' .880)

Tab e 881. Compounds of formu a I. 1, wherein R2 is R2-- I0 195( =formu a ' .881)

Tab e 882. Compounds of formu a I. 1, wherein R2 is R2-- I0 196( =formu a ' .882)

Tab e 883. Compounds of formu a I. 1, wherein R2 is R2-- I0 197( =formu a ' .883)

Tab e 884. Compounds of formu a I. 1, wherein R2 is R2-- I0 198( =formu a ' .884)

Tab e 885. Compounds of formu a I. 1, wherein R2 is R2-- I0 199( =formu a ' .885)

Tab e 886. Compounds of formu a I. 1, wherein R2 is R2-- I0 200( =formu a ' .886)

Tab e 887. Compounds of formu a I. 1, wherein R2 is R2-- I0 201 ( =formu a ' .887)

Tab e 888. Compounds of formu a I. 1, wherein R2 is R2-- I0 202( =formu a ' .888)

Tab e 889. Compounds of formu a I. 1, wherein R2 is R2-- I0 203( =formu a ' .889)

Tab e 890. Compounds of formu a I. 1, wherein R2 is R2-- I0 204( =formu a ' .890)

Tab e 891. Compounds of formu a I. 1, wherein R2 is R2-- I0 205( =formu a ' .891)

Tab e 892. Compounds of formu a I. 1, wherein R2 is R2-- I0 206( =formu a ' .892)

Tab e 893. Compounds of formu a I. 1, wherein R2 is R2-- I0 207( =formu a ' .893)

Tab e 894. Compounds of formu a I. 1, wherein R2 is R2-- I0 208( =formu a ' .894)

Tab e 895. Compounds of formu a I. 1, wherein R2 is R2-- I0 209( =formu a ' .895)

Tab e 896. Compounds of formu a I. 1, wherein R2 is R2-- I0 210( =formu a ' .896)

Tab e 897. Compounds of formu a I. 1, wherein R2 is R2-- I0 211 ( =formu a ' .897)

Tab e 898. Compounds of formu a I. 1, wherein R2 is R2-- I0 212( =formu a ' .898)

Tab e 899. Compounds of formu a I. 1, wherein R2 is R2-- I0 213( =formu a ' .899)

Tab e 900. Compounds of formu a I. 1, wherein R2 is R2-- I0 214( =formu a ' .900)

Tab e 901. Compounds of formu a I. 1, wherein R2 is R2-- I0 215( =formu a ' .901)

Tab e 902. Compounds of formu a I. 1, wherein R2 is R2-- I0 216( =formu a ' .902)

Tab e 903. Compounds of formu a I. 1, wherein R2 is R2-- I0 217( =formu a ' .903)

Tab e 904. Compounds of formu a I. 1, wherein R2 is R2-- I0 218( =formu a ' .904)

Tab e 905. Compounds of formu a I. 1, wherein R2 is R2-- I0 219( =formu a ' .905)

Tab e 906. Compounds of formu a I. 1, wherein R2 is R2-- I0 220( =formu a ' .906)

Tab e 907. Compounds of formu a I. 1, wherein R2 is R2-- I0 221 ( =formu a ' .907)

Tab e 908. Compounds of formu a I. 1, wherein R2 is R2-- I0 222( =formu a ' .908)

Tab e 909. Compounds of formu a I. 1, wherein R2 is R2-- I0 223( =formu a ' .909)

Tab e 910. Compounds of formu a I. 1, wherein R2 is R2-- I0 224( =formu a ' .910)

Tab e 911. Compounds of formu a I. 1, wherein R2 is R2-- I0 225( =formu a ' .911)

Tab e 912. Compounds of formu a I. 1, wherein R2 is R2-- I0 226( =formu a ' .912)

Tab e 913. Compounds of formu a I. 1, wherein R2 is R2-- I0 227( =formu a ' .913)

Tab e 914. Compounds of formu a I. 1, wherein R2 is R2-- I0 228( =formu a ' .914) Tab e 915. Compounds of formu a I.1, wherein R2 is R2-- I0229( =formu a ' .915)

Tab e 916. Compounds of formu a I. 1, wherein R2 is R2-- I0 230( =formu a ' .916)

Tab e 917. Compounds of formu a I. 1, wherein R2 is R2-- I0 231 ( =formu a ' .917)

Tab e 918. Compounds of formu a I. 1, wherein R2 is R2-- I0 232( =formu a ' .918)

Tab e 919. Compounds of formu a I. 1, wherein R2 is R2-- I0 233( =formu a ' .919)

Tab e 920. Compounds of formu a I. 1, wherein R2 is R2-- I0 234( =formu a ' .920)

Tab e 921. Compounds of formu a I. 1, wherein R2 is R2-- I0 235( =formu a ' .921)

Tab e 922. Compounds of formu a I. 1, wherein R2 is R2-- I0 236( =formu a ' .922)

Tab e 923. Compounds of formu a I. 1, wherein R2 is R2-- I0 237( =formu a ' .923)

Tab e 924. Compounds of formu a I. 1, wherein R2 is R2-- I0 238( =formu a ' .924)

Tab e 925. Compounds of formu a I. 1, wherein R2 is R2-- I0 239( =formu a ' .925)

Tab e 926. Compounds of formu a I. 1, wherein R2 is R2-- I0 240( =formu a ' .926)

Tab e 927. Compounds of formu a I. 1, wherein R2 is R2-- I0 241 ( =formu a ' .927)

Tab e 928. Compounds of formu a I. 1, wherein R2 is R2-- I0 242( =formu a ' .928)

Tab e 929. Compounds of formu a I. 1, wherein R2 is R2-- I0 243( =formu a ' .929)

Tab e 930. Compounds of formu a I. 1, wherein R2 is R2-- I0 244( =formu a ' .930)

Tab e 931. Compounds of formu a I. 1, wherein R2 is R2-- I0 245( =formu a ' .931)

Tab e 932. Compounds of formu a I. 1, wherein R2 is R2-- I0 246( =formu a ' .932)

Tab e 933. Compounds of formu a I. 1, wherein R2 is R2-- I0 247( =formu a ' .933)

Tab e 934. Compounds of formu a I. 1, wherein R2 is R2-- I0 248( =formu a ' .934)

Tab e 935. Compounds of formu a I. 1, wherein R2 is R2-- I0 249( =formu a ' .935)

Tab e 936. Compounds of formu a I. 1, wherein R2 is R2-- I0 250( =formu a ' .936)

Tab e 937. Compounds of formu a I. 1, wherein R2 is R2-- I0 251 ( =formu a ' .937)

Tab e 938. Compounds of formu a I. 1, wherein R2 is R2-- I0 252( =formu a ' .938)

Tab e 939. Compounds of formu a I. 1, wherein R2 is R2-- I0 253( =formu a ' .939)

Tab e 940. Compounds of formu a I. 1, wherein R2 is R2-- I0 254( =formu a ' .940)

Tab e 941. Compounds of formu a I. 1, wherein R2 is R2-- I0 255( =formu a ' .941)

Tab e 942. Compounds of formu a I. 1, wherein R2 is R2-- I0 256( =formu a ' .942)

Tab e 943. Compounds of formu a I. 1, wherein R2 is R2-- I0 257( =formu a ' .943)

Tab e 944. Compounds of formu a I. 1, wherein R2 is R2-- I0 258( =formu a ' .944)

Tab e 945. Compounds of formu a I. 1, wherein R2 is R2-- I0 259( =formu a ' .945)

Tab e 946. Compounds of formu a I. 1, wherein R2 is R2-- I0 260( =formu a ' .946)

Tab e 947. Compounds of formu a I. 1, wherein R2 is R2-- I0 261 ( =formu a ' .947)

Tab e 948. Compounds of formu a I. 1, wherein R2 is R2-- I0 262( =formu a ' .948)

Tab e 949. Compounds of formu a I. 1, wherein R2 is R2-- I0 263( =formu a ' .949)

Tab e 950. Compounds of formu a I. 1, wherein R2 is R2-- I0 264( =formu a ' .950)

Tab e 951. Compounds of formu a I. 1, wherein R2 is R2-- I0 265( =formu a ' .951)

Tab e 952. Compounds of formu a I. 1, wherein R2 is R2-- I0 266( =formu a ' .952)

Tab e 953. Compounds of formu a I. 1, wherein R2 is R2-- I0 267( =formu a ' .953)

Tab e 954. Compounds of formu a I. 1, wherein R2 is R2-- I0 268( =formu a ' .954)

Tab e 955. Compounds of formu a I. 1, wherein R2 is R2-- I0 269( =formu a ' .955)

Tab e 956. Compounds of formu a I. 1, wherein R2 is R2-- I0 270( =formu a ' .956)

Tab e 957. Compounds of formu a I. 1, wherein R2 is R2-- I0 271 ( =formu a ' .957)

Tab e 958. Compounds of formu a I. 1, wherein R2 is R2-- I0 272( =formu a ' .958) Tab e 959. Compounds of formu a I.1, wherein R ² is R ² -- I0273( =formu a ' .959).

Tab e 960. Compounds of formu a I. 1, wherein R ² is R ² -- I0 274( =formu a ' .960).

Tab e 961. Compounds of formu a I. 1, wherein R ² is R ² -- I0 275( =formu a ' .961).

Tab e 962. Compounds of formu a I. 1, wherein R ² is R ² -- I0 276( =formu a ' .962).

Tab e 963. Compounds of formu a I. 1, wherein R ² is R ² -- I0 277( =formu a ' .963).

Tab e 964. Compounds of formu a I. 1, wherein R ² is R ² -- I0 278( =formu a ' .964).

Tab e 965. Compounds of formu a I. 1, wherein R ² is R ² -- I0 279( =formu a ' .965).

Tab e 966. Compounds of formu a I. 1, wherein R ² is R ² -- I0 280( =formu a ' .966).

Tab e 967. Compounds of formu a I. 1, wherein R ² is R ² -- I0 281 ( =formu a ' .967).

Tab e 968. Compounds of formu a I. 1, wherein R ² is R ² -- I0 282( =formu a ' .968).

Tab e 969. Compounds of formu a I. 1, wherein R ² is R ² -- I0 283( =formu a ' .969).

Tab e 970. Compounds of formu a I. 1, wherein R ² is R ² -- I0 284( =formu a ' .970).

Tab e 971. Compounds of formu a I. 1, wherein R ² is R ² -- I0 285( =formu a ' .971).

Tab e 972. Compounds of formu a I. 1, wherein R ² is R ² -- I0 286( =formu a ' .972).

Tab e 973. Compounds of formu a I. 1, wherein R ² is R ² -- I0 287( =formu a ' .973).

Tab e 974. Compounds of formu a I. 1, wherein R ² is R ² -- I0 288( =formu a ' .974).

Tab e 975. Compounds of formu a I. 1, wherein R ² is R ² -- I0 289( =formu a ' .975).

Tab e 976. Compounds of formu a I. 1, wherein R ² is R ² -- I0 290( =formu a ' .976).

Tab e 977. Compounds of formu a I. 1, wherein R ² is R ² -- I0 291 ( =formu a ' .977).

Tab e 978. Compounds of formu a I. 1, wherein R ² is R ² -- I0 292( =formu a ' .978).

Tab e 979. Compounds of formu a I. 1, wherein R ² is R ² -- I0 293( =formu a ' .979).

Tab e 980. Compounds of formu a I. 1, wherein R ² is R ² -- I0 294( =formu a ' .980).

Tab e 981. Compounds of formu a I. 1, wherein R ² is R ² -- I0 295( =formu a ' .981).

Tab e 982. Compounds of formu a I. 1, wherein R ² is R ² -- I0 296( =formu a ' .982).

Tab e 983. Compounds of formu a I. 1, wherein R ² is R ² -- I0 297( =formu a ' .983).

Tab e 984. Compounds of formu a I. 1, wherein R ² is R ² -- I0 298( =formu a ' .984).

Tab e 985. Compounds of formu a I. 1, wherein R ² is R ² -- I0 299( =formu a ' .985).

Tab e 986. Compounds of formu a I. 1, wherein R ² is R ² -- I0 300( =formu a ' .986).

Tab e 987. Compounds of formu a I. 1, wherein R ² is R ² -- I0 301 ( =formu a ' .987).

Tab e 988. Compounds of formu a I. 1, wherein R ² is R ² -- I0 302( =formu a ' .988).

Tab e 989. Compounds of formu a I. 1, wherein R ² is R ² -- I0 303( =formu a ' .989).

Tab e 990. Compounds of formu a I. 1, wherein R ² is R ² -- I0 304( =formu a ' .990).

Tab e 991. Compounds of formu a I. 1, wherein R ² is R ² -- I0 305( =formu a ' .991).

Tab e 992. Compounds of formu a I. 1, wherein R ² is R ² -- I0 306( =formu a ' .992).

Tab e 993. Compounds of formu a I. 1, wherein R ² is R ² -- I0 307( =formu a ' .993).

Tab e 994. Compounds of formu a I. 1, wherein R ² is R ² -- I0 308( =formu a ' .994).

Tab e 995. Compounds of formu a I. 1, wherein R ² is R ² -- I0 309( =formu a ' .995).

Tab e 996. Compounds of formu a I. 1, wherein R ² is R ² -- I0 310( =formu a ' .996).

Tab e 997. Compounds of formu a I. 1, wherein R ² is R ² -- I0 311 < =formu a ' .997).

Tab e 998. Compounds of formu a I. 1, wherein R ² is R ² -- I0 312( =formu a ' .998).

Tab e 999. Compounds of formu a I. 1, wherein R ² is R ² -- I0 313( =formu a ' .999).

Tab e 1000. Compounds o f formula 1.1, wherein R ² is R ² -10.314(=formula 1.1000

Tab e 1001 . Compounds o f formula 1.1, wherein R ² is R ² -10.315(=formula 1.1001

Tab e 1002. Compounds o f formula 1.1, wherein R ² is R ² -10.316(=formula 1.1002 Tab e 1003. Compounds of formu a I.1 , wherein R2 is R2-- I 0 317( =formu a 1.1003)

Tab e 1004. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 318( =formu a 1 .1004)

Tab e 1005. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 319( =formu a 1 .1005)

Tab e 1006. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 320( =formu a 1 .1006)

Tab e 1007. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 321 ( =formu a 1 .1007)

Tab e 1008. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 322( =formu a 1 .1008)

Tab e 1009. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 323( =formu a 1 .1009)

Tab e 1010. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 324( =formu a 1 .1010)

Tab e 101 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 325( =formu a 1 .101 1 )

Tab e 1012. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 326( =formu a 1 .1012)

Tab e 1013. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 327( =formu a 1 .1013)

Tab e 1014. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 328( =formu a 1 .1014)

Tab e 1015. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 329( =formu a 1 .1015)

Tab e 1016. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 330( =formu a 1 .1016)

Tab e 1017. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 331 ( =formu a 1 .1017)

Tab e 1018. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 332( =formu a 1 .1018)

Tab e 1019. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 333( =formu a 1 .1019)

Tab e 1020. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 334( =formu a 1 .1020)

Tab e 1021 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 335( =formu a 1 .1021 )

Tab e 1022. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 336( =formu a 1 .1022)

Tab e 1023. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 334( =formu a 1 .1023)

Tab e 1024. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 338( =formu a 1 .1024)

Tab e 1025. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 339( =formu a 1 .1025)

Tab e 1026. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 340( =formu a 1 .1026)

Tab e 1027. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 341 ( =formu a 1 .1027)

Tab e 1028. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 342( =formu a 1 .1028)

Tab e 1029. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 343( =formu a 1 .1029)

Tab e 1030. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 344( =formu a 1 .1030)

Tab e 1031 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 345( =formu a 1 .1031 )

Tab e 1032. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 346( =formu a 1 .1032)

Tab e 1033. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 347( =formu a 1 .1033)

Tab e 1034. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 348( =formu a 1 .1034)

Tab e 1035. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 349( =formu a 1 .1035)

Tab e 1036. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 350( =formu a 1 .1036)

Tab e 1037. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 351 ( =formu a 1 .1037)

Tab e 1038. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 352( =formu a 1 .1038)

Tab e 1039. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 353( =formu a 1 .1039)

Tab e 1040. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 354( =formu a 1 .1040)

Tab e 1041 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 355( =formu a 1 .1041 )

Tab e 1042. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 356( =formu a 1 .1042)

Tab e 1043. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 357( =formu a 1 .1043)

Tab e 1044. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 358( =formu a 1 .1044)

Tab e 1045. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 359( =formu a 1 .1045)

Tab e 1046. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 360( =formu a 1 .1046) Tab e 1047. Compounds of formu a I.1 , wherein R2 is R2-- I 0 361 ( =formu a 1 .1047)

Tab e 1048. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 362( =formu a 1 .1048)

Tab e 1049. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 363( =formu a 1 .1049)

Tab e 1050. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 364( =formu a 1 .1050)

Tab e 1051 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 365( =formu a 1 .1051 )

Tab e 1052. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 366( =formu a 1 .1052)

Tab e 1053. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 367( =formu a 1 .1053)

Tab e 1054. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 368( =formu a 1 .1054)

Tab e 1055. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 369( =formu a 1 .1055)

Tab e 1056. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 370( =formu a 1 .1056)

Tab e 1057. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 371 ( =formu a 1 .1057)

Tab e 1058. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 372( =formu a 1 .1058)

Tab e 1059. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 373( =formu a 1 .1059)

Tab e 1060. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 374( =formu a 1 .1060)

Tab e 1061 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 375( =formu a 1 .1061 )

Tab e 1062. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 376( =formu a 1 .1062)

Tab e 1063. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 377( =formu a 1 .1063)

Tab e 1064. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 378( =formu a 1 .1064)

Tab e 1065. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 379( =formu a 1 .1065)

Tab e 1066. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 380( =formu a 1 .1066)

Tab e 1067. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 381 ( =formu a 1 .1067)

Tab e 1068. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 382( =formu a 1 .1068)

Tab e 1069. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 383( =formu a 1 .1069)

Tab e 1070. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 384( =formu a 1 .1070)

Tab e 1071 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 385( =formu a 1 .1071 )

Tab e 1072. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 386( =formu a 1 .1072)

Tab e 1073. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 387( =formu a 1 .1073)

Tab e 1074. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 388( =formu a 1 .1074)

Tab e 1075. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 389( =formu a 1 .1075)

Tab e 1076. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 390( =formu a 1 .7076)

Tab e 1077. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 391 ( =formu a 1 .1077)

Tab e 1078. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 392( =formu a 1 .1078)

Tab e 1079. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 393( =formu a 1 .1079)

Tab e 1080. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 394( =formu a 1 .1080)

Tab e 1081 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 395( =formu a 1 .1081 )

Tab e 1082. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 396( =formu a 1 .1082)

Tab e 1083. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 397( =formu a 1 .1083)

Tab e 1084. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 398( =formu a 1 .1084)

Tab e 1085. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 399( =formu a 1 .1085)

Tab e 1086. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 400( =formu a 1 .1086)

Tab e 1087. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 401 ( =formu a 1 .1087)

Tab e 1088. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 402( =formu a 1 .1088)

Tab e 1089. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 403( =formu a 1 .1089)

Tab e 1090. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 404( =formu a 1 .1090) Table 091 . Compounds o formu wherein R ² s R ² - 10.405 =formu .1091

Table 092. Compounds o formu wherein R ² s R ² - 10.406 =formu .1092

Table 093. Compounds o formu wherein R ² s R ² - 10.407 =formu .1093

Table 094. Compounds o formu wherein R ² s R ² - 10.408 =formu .1094

Table 095. Compounds o formu wherein R ² s R ² - 10.409 =formu .1095

Table 096. Compounds o formu wherein R ² s R ² - 10.410 =formu .1096

Table 097. Compounds o formu wherein R ² s R ² - 10.41 1 =formu .1097

Table 098. Compounds o formu wherein R ² s R ² - 10.412 =formu .1098

Table 099. Compounds o formu wherein R ² s R ² - 10.413 =formu .1099

Table 100. Compounds o formu wherein R ² s R ² - 10.414 =formu .1 100

Table 101 . Compounds o formu wherein R ² s R ² - 10.415 =formu .1 101

Table 102. Compounds o formu wherein R ² s R ² - 10.416 =formu .1 102

Table 103. Compounds o formu wherein R ² s R ² - 10.417 =formu .1 103

Table 104. Compounds o formu wherein R ² s R ² - 10.418 =formu .1 104

Table 105. Compounds o formu wherein R ² s R ² - 10.419 =formu .1 105

Table 106. Compounds o formu wherein R ² s R ² - 10.420 =formu .1 106

Table 107. Compounds o formu wherein R ² s R ² - 10.421 =formu .1 107

Table 108. Compounds o formu wherein R ² s R ² - 10.422 =formu .1 108

Table 109. Compounds o formu wherein R ² s R ² - 10.423 =formu .1 109

Table 1 10. Compounds o formu wherein R ² s R ² - 10.424 =formu .1 1 10

Table 1 1 1 . Compounds o formu wherein R ² s R ² - 10.425 =formu .1 1 1 1

Table 1 12. Compounds o formu wherein R ² s R ² - 10.426 =formu .1 1 12

Table 1 13. Compounds o formu wherein R ² s R ² - 10.427 =formu .1 1 13

Table 1 14. Compounds o formu wherein R ² s R ² - 10.428 =formu .1 1 14

Table 1 15. Compounds o formu wherein R ² s R ² - 10.429 =formu .1 1 15

Table 1 16. Compounds o formu wherein R ² s R ² - 10.430 =formu .1 1 16

Table 1 17. Compounds o formu wherein R ² s R ² - 10.431 =formu .1 1 17

Table 1 18. Compounds o formu wherein R ² s R ² - 10.432 =formu .1 1 18

Table 1 19. Compounds o formu wherein R ² s R ² - 10.433 =formu .1 1 19

Table 120. Compounds o formu wherein R ² s R ² - 10.434 =formu .1 120

Table 121 . Compounds o formu wherein R ² s R ² - 10.435 =formu .1 121

Table 122. Compounds o formu wherein R ² s R ² - 10.436 =formu .1 122

Table 123. Compounds o formu wherein R ² s R ² - 10.437 =formu .1 123

Table 124. Compounds o formu wherein R ² s R ² - 10.438 =formu .1 124

Table 125. Compounds o formu wherein R ² s R ² - 10.439 =formu .1 125

Table 126. Compounds o formu wherein R ² s R ² - 10.440 =formu .1 126

Table 127. Compounds o formu wherein R ² s R ² - 10.441 =formu .1 127

Table 128. Compounds o formu wherein R ² s R ² - 10.442 =formu .1 128

Table 129. Compounds o formu wherein R ² s R ² - 10.443 =formu .1 129

Table 130. Compounds o formu wherein R ² s R ² - 10.444 =formu .1 130

Table 131 . Compounds o formu wherein R ² s R ² - 10.445 =formu .1 131

Table 132. Compounds o formu wherein R ² s R ² - 10.446 =formu .1 132

Table 133. Compounds o formu wherein R ² s R ² - 10.447 =formu .1 133

Table 134. Compounds o formu wherein R ² s R ² - 10.448 =formu .1 134 Tab 135. Compounds o formu wherein R ² s R ² - 10.449 =formu 135 Tab 136. Compounds o formu wherein R ² s R ² - 10.450 =formu 136 Tab 137. Compounds o formu wherein R ² s R ² - 10.451 =formu 137 Tab 138. Compounds o formu wherein R ² s R ² - 10.452 =formu 138 Tab 139. Compounds o formu wherein R ² s R ² - 10.453 =formu 139 Tab 140. Compounds o formu wherein R ² s R ² - 10.454 =formu 140 Tab 141 . Compounds o formu wherein R ² s R ² - 10.455 =formu 141 Tab 142. Compounds o formu wherein R ² s R ² - 10.456 =formu 142 Tab 143. Compounds o formu wherein R ² s R ² - 10.457 =formu 143 Tab 144. Compounds o formu wherein R ² s R ² - 10.458 =formu 144 Tab 145. Compounds o formu wherein R ² s R ² - 10.459 =formu 145 Tab 146. Compounds o formu wherein R ² s R ² - 10.460 =formu 146 Tab 147. Compounds o formu wherein R ² s R ² - 10.461 =formu 147 Tab 148. Compounds o formu wherein R ² s R ² - 10.462 =formu 148 Tab 149. Compounds o formu wherein R ² s R ² - 10.463 =formu 149 Tab 150. Compounds o formu wherein R ² s R ² - 10.464 =formu 150 Tab 151 . Compounds o formu wherein R ² s R ² - 10.465 =formu 151 Tab 152. Compounds o formu wherein R ² s R ² - 10.466 =formu 152 Tab 153. Compounds o formu wherein R ² s R ² - 10.467 =formu 153 Tab 154. Compounds o formu wherein R ² s R ² - 10.468 =formu 154 Tab 155. Compounds o formu wherein R ² s R ² - 10.469 =formu 154 Tab 156. Compounds o formu wherein R ² s R ² - 10.470 =formu 156 Tab 157. Compounds o formu wherein R ² s R ² - 10.471 =formu 157 Tab 158. Compounds o formu wherein R ² s R ² - 10.472 =formu 158 Tab 159. Compounds o formu wherein R ² s R ² - 10.473 =formu 159 Tab 160. Compounds o formu wherein R ² s R ² - 10.474 =formu 160 Tab 161 . Compounds o formu wherein R ² s R ² - 10.475 =formu 161 Tab 162. Compounds o formu wherein R ² s R ² - 10.476 =formu 162 Tab 163. Compounds o formu wherein R ² s R ² - 10.477 =formu 163 Tab 164. Compounds o formu wherein R ² s R ² - 10.478 =formu 164 Tab 165. Compounds o formu wherein R ² s R ² - 10.479 =formu 165 Tab 166. Compounds o formu wherein R ² s R ² - 10.480 =formu 166 Tab 167. Compounds o formu wherein R ² s R ² - 10.481 =formu 167 Tab 168. Compounds o formu wherein R ² s R ² - 10.482 =formu 168 Tab 169. Compounds o formu wherein R ² s R ² - 10.483 =formu 169 Tab 170. Compounds o formu wherein R ² s R ² - 10.484 =formu 170 Tab 171 . Compounds o formu wherein R ² s R ² - 10.485 =formu 171 Tab 172. Compounds o formu wherein R ² s R ² - 10.486 =formu 172 Tab 173. Compounds o formu wherein R ² s R ² - 10.487 =formu 173 Tab 174. Compounds o formu wherein R ² s R ² - 10.488 =formu 174 Tab 175. Compounds o formu wherein R ² s R ² - 10.489 =formu 175 Tab 176. Compounds o formu wherein R ² s R ² - 10.490 =formu 176 Tab 177. Compounds o formu wherein R ² s R ² - 10.491 =formu 177 Tab 178. Compounds o formu wherein R ² s R ² - 10.492 =formu 178 Tab e 1179. Compounds of formu a I.1 , wherein R2 is R2-- I0493( =formu a 1.1179)

Tab e 1180. Compounds of formu a I. 1 , wherein R2 is R2-- I0 494( =formu a 1 .1180)

Tab e 1181. Compounds of formu a I. 1 , wherein R2 is R2-- I0 495( =formu a 1 .1181)

Tab e 1182. Compounds of formu a I. 1 , wherein R2 is R2-- I0 496( =formu a 1 .1182)

Tab e 1183. Compounds of formu a I. 1 , wherein R2 is R2-- I0 497( =formu a 1 .1183)

Tab e 1184. Compounds of formu a I. 1 , wherein R2 is R2-- I0 498( =formu a 1 .1184)

Tab e 1185. Compounds of formu a I. 1 , wherein R2 is R2-- I0 499( =formu a 1 .1185)

Tab e 1186. Compounds of formu a I. 1 , wherein R2 is R2-- I0 500( =formu a 1 .1186)

Tab e 1187. Compounds of formu a I. 1 , wherein R2 is R2-- I0 501( =formu a 1 .1187)

Tab e 1188. Compounds of formu a I. 1 , wherein R2 is R2-- I0 502( =formu a 1 .1188)

Tab e 1189. Compounds of formu a I. 1 , wherein R2 is R2-- I0 503( =formu a 1 .1189)

Tab e 1190. Compounds of formu a I. 1 , wherein R2 is R2-- I0 504( =formu a 1 .1190)

Tab e 1191. Compounds of formu a I. 1 , wherein R2 is R2-- I0 505( =formu a 1 .1191)

Tab e 1192. Compounds of formu a I. 1 , wherein R2 is R2-- I0 506( =formu a 1 .1192)

Tab e 1193. Compounds of formu a I. 1 , wherein R2 is R2-- I0 507( =formu a 1 .1193)

Tab e 1194. Compounds of formu a I. 1 , wherein R2 is R2-- I0 508( =formu a 1 .1194)

Tab e 1195. Compounds of formu a I. 1 , wherein R2 is R2-- I0 509( =formu a 1 .1195)

Tab e 1196. Compounds of formu a I. 1 , wherein R2 is R2-- I0 510( =formu a 1 .1196)

Tab e 1197. Compounds of formu a I. 1 , wherein R2 is R2-- I0 511( =formu a 1 .1197)

Tab e 1198. Compounds of formu a I. 1 , wherein R2 is R2-- I0 512( =formu a 1 .1198)

Tab e 1199. Compounds of formu a I. 1 , wherein R2 is R2-- I0 513( =formu a 1 .1199)

Tab e 1200. Compounds of formu a I. 1 , wherein R2 is R2-- I0 514( =formu a 1 .1200)

Tab e 1201. Compounds of formu a I. 1 , wherein R2 is R2-- I0 515( =formu a 1 .1201)

Tab e 1202. Compounds of formu a I. 1 , wherein R2 is R2-- I0 516( =formu a 1 .1202)

Tab e 1203. Compounds of formu a I. 1 , wherein R2 is R2-- I0 517( =formu a 1 .1203)

Tab e 1204. Compounds of formu a I. 1 , wherein R2 is R2-- I0 518( =formu a 1 .1204)

Tab e 1205. Compounds of formu a I. 1 , wherein R2 is R2-- I0 519( =formu a 1 .1205)

Tab e 1206. Compounds of formu a I. 1 , wherein R2 is R2-- I0 520( =formu a 1 .1206)

Tab e 1207. Compounds of formu a I. 1 , wherein R2 is R2-- I0 521 ( =formu a 1 .1207)

Tab e 1208. Compounds of formu a I. 1 , wherein R2 is R2-- I0 522( =formu a 1 .1208)

Tab e 1209. Compounds of formu a I. 1 , wherein R2 is R2-- I0 523( =formu a 1 .1209)

Tab e 1210. Compounds of formu a I. 1 , wherein R2 is R2-- I0 524( =formu a 1 .1210)

Tab e 1211. Compounds of formu a I. 1 , wherein R2 is R2-- I0 525( =formu a 1 .1211)

Tab e 1212. Compounds of formu a I. 1 , wherein R2 is R2-- I0 526( =formu a 1 .1212)

Tab e 1213. Compounds of formu a I. 1 , wherein R2 is R2-- I0 527( =formu a 1 .1213)

Tab e 1214. Compounds of formu a I. 1 , wherein R2 is R2-- I0 528( =formu a 1 .1212)

Tab e 1215. Compounds of formu a I. 1 , wherein R2 is R2-- I0 529( =formu a 1 .1215)

Tab e 1216. Compounds of formu a I. 1 , wherein R2 is R2-- I0 530( =formu a 1 .1216)

Tab e 1217. Compounds of formu a I. 1 , wherein R2 is R2-- I0 531( =formu a 1 .1217)

Tab e 1218. Compounds of formu a I. 1 , wherein R2 is R2-- I0 532( =formu a 1 .1218)

Tab e 1219. Compounds of formu a I. 1 , wherein R2 is R2-- I0 533( =formu a 1 .1219)

Tab e 1220. Compounds of formu a I. 1 , wherein R2 is R2-- I0 534( =formu a 1 .1220)

Tab e 1221. Compounds of formu a I. 1 , wherein R2 is R2-- I0 535( =formu a 1 .1221)

Tab e 1222. Compounds of formu a I. 1 , wherein R2 is R2-- I0 536( =formu a 1 .1222) Tab e 1223. Compounds of formu a I.1 , wherein R2 is R2-- I 0 537( =formu a 1.1223)

Tab e 1224. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 538( =formu a 1 .1224)

Tab e 1225. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 539( =formu a 1 .1225)

Tab e 1226. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 540( =formu a 1 .1226)

Tab e 1227. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 541 ( =formu a 1 .1227)

Tab e 1228. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 542( =formu a 1 .1228)

Tab e 1229. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 543( =formu a 1 .1229)

Tab e 1230. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 544( =formu a 1 .1230)

Tab e 1231 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 545( =formu a 1 .1231 )

Tab e 1232. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 546( =formu a 1 .1232)

Tab e 1233. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 547( =formu a 1 .1233)

Tab e 1234. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 548( =formu a 1 .1234)

Tab e 1235. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 549( =formu a 1 .1235)

Tab e 1236. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 550( =formu a 1 .1236)

Tab e 1237. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 551 ( =formu a 1 .1237)

Tab e 1238. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 552( =formu a 1 .1238)

Tab e 1239. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 553( =formu a 1 .1239)

Tab e 1240. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 554( =formu a 1 .1240)

Tab e 1241 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 555( =formu a 1 .1241 )

Tab e 1242. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 556( =formu a 1 .1242)

Tab e 1243. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 557( =formu a 1 .1243)

Tab e 1244. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 558( =formu a 1 .1244)

Tab e 1245. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 559( =formu a 1 .1245)

Tab e 1246. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 560( =formu a 1 .1246)

Tab e 1247. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 561 ( =formu a 1 .1247)

Tab e 1248. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 562( =formu a 1 .1248)

Tab e 1249. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 563( =formu a 1 .1249)

Tab e 1250. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 564( =formu a 1 .1350)

Tab e 1251 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 565( =formu a 1 .1251 )

Tab e 1252. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 566( =formu a 1 .1252)

Tab e 1253. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 567( =formu a 1 .1253)

Tab e 1254. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 568( =formu a 1 .1254)

Tab e 1255. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 569( =formu a 1 .1255)

Tab e 1256. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 570( =formu a 1 .1256)

Tab e 1257. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 571 ( =formu a 1 .1257)

Tab e 1258. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 572( =formu a 1 .1258)

Tab e 1259. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 573( =formu a 1 .1259)

Tab e 1260. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 574( =formu a 1 .1260)

Tab e 1261 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 575( =formu a 1 .1261 )

Tab e 1262. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 576( =formu a 1 .1262)

Tab e 1263. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 577( =formu a 1 .1263)

Tab e 1264. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 578( =formu a 1 .1264)

Tab e 1265. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 579( =formu a 1 .1265)

Tab e 1266. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 580( =formu a 1 .1266) Tab e 1267. Compounds of formu a I.1 , wherein R2 is R2-- I 0 581 ( =formu a 1.1267)

Tab e 1268. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 582( =formu a 1 .1268)

Tab e 1269. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 583( =formu a 1 .1269)

Tab e 1270. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 584( =formu a 1 .1270)

Tab e 1271 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 585( =formu a 1 .1271 )

Tab e 1272. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 586( =formu a 1 .1272)

Tab e 1273. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 587( =formu a 1 .1273)

Tab e 1274. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 588( =formu a 1 .1274)

Tab e 1275. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 589( =formu a 1 .1275)

Tab e 1276. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 590( =formu a 1 .1276)

Tab e 1277. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 591 ( =formu a 1 .1277)

Tab e 1278. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 592( =formu a 1 .1278)

Tab e 1279. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 593( =formu a 1 .1279)

Tab e 1280. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 594( =formu a 1 .1280)

Tab e 1281 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 595( =formu a 1 .1281 )

Tab e 1282. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 596( =formu a 1 .1282)

Tab e 1283. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 597( =formu a 1 .1283)

Tab e 1284. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 598( =formu a 1 .1284)

Tab e 1285. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 599( =formu a 1 .1285)

Tab e 1286. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 600( =formu a 1 .1286)

Tab e 1287. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 601 ( =formu a 1 .1287)

Tab e 1288. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 602( =formu a 1 .1288)

Tab e 1289. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 603( =formu a 1 .1289)

Tab e 1290. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 604( =formu a 1 .1290)

Tab e 1291 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 605( =formu a 1 .1291 )

Tab e 1292. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 606( =formu a 1 .1292)

Tab e 1293. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 607( =formu a 1 .1293)

Tab e 1294. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 608( =formu a 1 .1294)

Tab e 1295. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 609( =formu a 1 .1295)

Tab e 1296. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 610( =formu a 1 .1296)

Tab e 1297. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 61 1 < =formu a 1 .1297)

Tab e 1298. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 612( =formu a 1 .1298)

Tab e 1299. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 613( =formu a 1 .1299)

Tab e 1300. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 614( =formu a 1 .1300)

Tab e 1301 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 615( =formu a 1 .1301 )

Tab e 1302. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 616( =formu a 1 .1302)

Tab e 1303. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 617( =formu a 1 .1303)

Tab e 1304. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 618( =formu a 1 .1304)

Tab e 1305. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 619( =formu a 1 .1305)

Tab e 1306. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 620( =formu a 1 .1306)

Tab e 1307. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 621 ( =formu a 1 .1307)

Tab e 1308. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 622( =formu a 1 .1308)

Tab e 1309. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 623( =formu a 1 .1309)

Tab e 1310. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 624( =formu a 1 .1310) Tab e 131 1 . Compounds of formu a I.1 , wherein R2 is R2-- I 0 625( =formu a 1.131 1 )

Tab e 1312. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 626( =formu a 1 .1312)

Tab e 1313. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 627( =formu a 1 .1313)

Tab e 1314. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 628( =formu a 1 .1314)

Tab e 1315. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 629( =formu a 1 .1315)

Tab e 1316. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 630( =formu a 1 .1316)

Tab e 1317. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 631 ( =formu a 1 .1317)

Tab e 1318. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 632( =formu a 1 .1318)

Tab e 1319. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 633( =formu a 1 .1319)

Tab e 1320. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 634( =formu a 1 .1320)

Tab e 1321 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 635( =formu a 1 .1321 )

Tab e 1322. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 636( =formu a 1 .1322)

Tab e 1323. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 637( =formu a 1 .1323)

Tab e 1324. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 638( =formu a 1 .1324)

Tab e 1325. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 639( =formu a 1 .1325)

Tab e 1326. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 640( =formu a 1 .1326)

Tab e 1327. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 641 ( =formu a 1 .1327)

Tab e 1328. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 642( =formu a 1 .1328)

Tab e 1329. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 643( =formu a 1 .1329)

Tab e 1330. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 644( =formu a 1 .1330)

Tab e 1331 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 645( =formu a 1 .1331 )

Tab e 1332. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 646( =formu a 1 .1332)

Tab e 1333. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 647( =formu a 1 .1333)

Tab e 1334. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 648( =formu a 1 .1334)

Tab e 1335. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 649( =formu a 1 .1335)

Tab e 1336. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 650( =formu a 1 .1336)

Tab e 1337. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 651 ( =formu a 1 .1337)

Tab e 1338. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 652( =formu a 1 .1338)

Tab e 1339. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 653( =formu a 1 .1339)

Tab e 1340. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 654( =formu a 1 .1340)

Tab e 1341 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 655( =formu a 1 .1341 )

Tab e 1342. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 656( =formu a 1 .1342)

Tab e 1343. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 657( =formu a 1 .1343)

Tab e 1344. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 658( =formu a 1 .1344)

Tab e 1345. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 659( =formu a 1 .1345)

Tab e 1346. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 660( =formu a 1 .1346)

Tab e 1347. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 661 ( =formu a 1 .1347)

Tab e 1348. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 662( =formu a 1 .1348)

Tab e 1349. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 663( =formu a 1 .1349)

Tab e 1350. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 664( =formu a 1 .1350)

Tab e 1351 . Compounds of formu a I. 1 , wherein R2 is R2-- I 0 665( =formu a 1 .1351 )

Tab e 1352. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 666( =formu a 1 .1352)

Tab e 1353. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 667( =formu a 1 .1353)

Tab e 1354. Compounds of formu a I. 1 , wherein R2 is R2-- I 0 668( =formu a 1 .1354) Tab e 1355. Compounds of formu a I.1 , wherein R2 is R2-- I0669(=formula 1.1355)

Tab e 1356. Compounds of formu a I. 1 , wherein R2 is R2-- I0 670(=formula 1.1356)

Tab e 1357. Compounds of formu a I. 1 , wherein R2 is R2-- I0 671(=formula 1.1357)

Tab e 1358. Compounds of formu a I. 1 , wherein R2 is R2-- I0 672(=formula 1.1358)

Tab e 1359. Compounds of formu a I. 1 , wherein R2 is R2-- I0 673(=formula 1.1359)

Tab e 1360. Compounds of formu a I. 1 , wherein R2 is R2-- I0 674(=formula 1.1360)

Tab e 1361. Compounds of formu a I. 1 , wherein R2 is R2-- I0 675(=formula 1.1361)

Tab e 1362. Compounds of formu a I. 1 , wherein R2 is R2-- I0 676(=formula 1.1362)

Tab e 1363. Compounds of formu a I. 1 , wherein R2 is R2-- I5 1(=formula 1 1363).

Tab e 1364. Compounds of formu a I. 1 , wherein R2 is R2-- I5 2(=formula 1 1364).

Tab e 1365. Compounds of formu a I. 1 , wherein R2 is R2-- I5 3(=formula 1 1365).

Tab e 1366. Compounds of formu a I. 1 , wherein R2 is R2-- I5 4(=formula 1 1366).

Tab e 1367. Compounds of formu a I. 1 , wherein R2 is R2-- I5 5(=formula 1 1367).

Tab e 1368. Compounds of formu a I. 1 , wherein R2 is R2-- I5 6(=formula 1 1368).

Tab e 1369. Compounds of formu a I. 1 , wherein R2 is R2-- I5 7(=formula 1 1369).

Tab e 1370. Compounds of formu a I. 1 , wherein R2 is R2-- I5 8(=formula 1 1370).

Tab e 1371. Compounds of formu a I. 1 , wherein R2 is R2-- I5 9(=formula 1 1371).

Tab e 1372. Compounds of formu a I. 1 , wherein R2 is R2-- I5 10(=formula 1.1372).

Tab e 1373. Compounds of formu a I. 1 , wherein R2 is R2-- I5 11(=formula 1.1373).

Tab e 1374. Compounds of formu a I. 1 , wherein R2 is R2-- I5 12(=formula 1.1374).

Tab e 1375. Compounds of formu a I. 1 , wherein R2 is R2-- I5 13(=formula 1.1375).

Tab e 1376. Compounds of formu a I. 1 , wherein R2 is R2-- I5 14(=formula 1.1376).

Tab e 1377. Compounds of formu a I. 1 , wherein R2 is R2-- I5 15(=formula 1.1377).

Tab e 1378. Compounds of formu a I. 1 , wherein R2 is R2-- I5 16(=formula 1.1378).

Tab e 1379. Compounds of formu a I. 1 , wherein R2 is R2-- I5 17(=formula 1.1379).

Tab e 1380. Compounds of formu a I. 1 , wherein R2 is R2-- I5 18(=formula 1.1380).

Tab e 1381. Compounds of formu a I. 1 , wherein R2 is R2-- I5 19(=formula 1.1381).

Tab e 1382. Compounds of formu a I. 1 , wherein R2 is R2-- I5 20(=formula 1.1382).

Tab e 1383. Compounds of formu a I. 1 , wherein R2 is R2-- I5 21(=formula 1.1383).

Tab e 1384. Compounds of formu a I. 1 , wherein R2 is R2-- I5 22(=formula 1.1384).

Tab e 1385. Compounds of formu a I. 1 , wherein R2 is R2-- I5 23(=formula 1.1385).

Tab e 1386. Compounds of formu a I. 1 , wherein R2 is R2-- I5 24(=formula 1.1386).

Tab e 1387. Compounds of formu a I. 1 , wherein R2 is R2-- I5 25(=formula 1.1387).

Tab e 1388. Compounds of formu a I. 1 , wherein R2 is R2-- I5 26(=formula 1.1388).

Tab e 1389. Compounds of formu a I. 1 , wherein R2 is R2-- I5 27(=formula 1.1389).

Tab e 1390. Compounds of formu a I. 1 , wherein R2 is R2-- I5 28(=formula 1.1390).

Tab e 1391. Compounds of formu a I. 1 , wherein R2 is R2-- I5 29(=formula 1.1391).

Tab e 1392. Compounds of formu a I. 1 , wherein R2 is R2-- I5 30(=formula 1.1392).

Tab e 1393. Compounds of formu a I. 1 , wherein R2 is R2-- I5 31(=formula 1.1393).

Tab e 1394. Compounds of formu a I. 1 , wherein R2 is R2-- I5 32(=formula 1.1394).

Tab e 1395. Compounds of formu a I. 1 , wherein R2 is R2-- I5 33(=formula 1.1395).

Tab e 1396. Compounds of formu a I. 1 , wherein R2 is R2-- I5 34(=formula 1.1396).

Tab e 1397. Compounds of formu a I. 1 , wherein R2 is R2-- I5 35(=formula 1.1397).

Tab e 1398. Compounds of formu a I. 1 , wherein R2 is R2-- I5 36(=formula 1.1398). Tab e 1399. Compounds of formu a I.1 , wherein R2 is R2-- I 5 37( =formu a 1 .1399).

Tab e 1400. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 38( =formu a 1 .1400).

Tab e 1401 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 39( =formu a 1 .1401 ).

Tab e 1402. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 40( =formu a 1 . 1402)

Tab e 1403. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 41 ( =formu a 1 . 1403)

Tab e 1404. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 42( =formu a 1 . 1404)

Tab e 1405. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 43( =formu a 1 . 1405)

Tab e 1406. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 44( =formu a 1 . 1406)

Tab e 1407. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 45( =formu a 1 . 1407)

Tab e 1408. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 46( =formu a 1 .1408).

Tab e 1409. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 47( =formu a 1 .1409).

Tab e 1410. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 48( =formu a 1 .1410).

Tab e 141 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 49( =formu a 1 .141 1 ).

Tab e 1412. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 50( =formu a 1 .1412).

Tab e 1413. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 51 ( =formu a 1 .1413).

Tab e 1414. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 52( =formu a 1 .1414).

Tab e 1415. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 53( =formu a 1 .1415).

Tab e 1416. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 54( =formu a 1 .1416).

Tab e 1417. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 55( =formu a 1 .1417).

Tab e 1418. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 56( =formu a 1 .1418).

Tab e 1419. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 57( =formu a 1 .1419).

Tab e 1420. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 58( =formu a 1 .1420).

Tab e 1421 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 59( =formu a 1 .1421 ).

Tab e 1422. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 60( =formu a 1 .1422).

Tab e 1423. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 61 ( =formu a 1 .1423).

Tab e 1424. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 62( =formu a 1 .1424).

Tab e 1425. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 63( =formu a 1 .1425).

Tab e 1426. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 64( =formu a 1 .1426).

Tab e 1427. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 65( =formu a 1 .1427).

Tab e 1428. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 66( =formu a 1 .1428).

Tab e 1429. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 67( =formu a 1 .1429).

Tab e 1430. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 68( =formu a 1 .1430).

Tab e 1431 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 69( =formu a 1 .1431 ).

Tab e 1432. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 70( =formu a 1 .1432).

Tab e 1433. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 71 ( =formu a 1 .1433).

Tab e 1434. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 72( =formu a 1 .1434).

Tab e 1435. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 73( =formu a 1 .1435).

Tab e 1436. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 74( =formu a 1 .1436).

Tab e 1437. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 75( =formu a 1 .1437).

Tab e 1438. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 76( =formu a 1 .1438).

Tab e 1439. Compounds of formu a I . 1 , wherein R2 is R2-- I 5 77( =formu a 1 .1439).

Tab e 1440. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 78( =formu a 1 .1440).

Tab e 1441 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 79( =formu a 1 .1441 ).

Tab e 1442. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 80( =formu a 1 .1442). Tab e 1443. Compounds of formu a I.1 , wherein R2 is R2 5.81 (= formula 1 .1443).

Tab e 1444. Compounds of formu a I. 1 , wherein R2 is R2 5.82(= formula 1 . 1444).

Tab e 1445. Compounds of formu a I. 1 , wherein R2 is R2 5.83(= formula 1 . 1445).

Tab e 1446. Compounds of formu a I. 1 , wherein R2 is R2 5.84(= formula 1 . 1446).

Tab e 1447. Compounds of formu a I. 1 , wherein R2 is R2 5.85(= formula 1 . 1447).

Tab e 1448. Compounds of formu a I. 1 , wherein R2 is R2 5.86(= formula 1 . 1448).

Tab e 1449. Compounds of formu a I. 1 , wherein R2 is R2 5.87(= formula 1 . 1449).

Tab e 1450. Compounds of formu a I. 1 , wherein R2 is R2 5.88(= formula 1 . 1450).

Tab e 1451 . Compounds of formu a I. 1 , wherein R2 is R2 5.89(= formula 1 . 1451 ).

Tab e 1452. Compounds of formu a I. 1 , wherein R2 is R2 5.90(= formula 1 . 1452).

Tab e 1453. Compounds of formu a I. 1 , wherein R2 is R2 5.91 (= formula 1 . 1453).

Tab e 1454. Compounds of formu a I. 1 , wherein R2 is R2 5.92(= formula 1 . 1454).

Tab e 1455. Compounds of formu a I. 1 , wherein R2 is R2 5.93(= formula 1 . 1455).

Tab e 1456. Compounds of formu a I. 1 , wherein R2 is R2 5.94(= formula 1 . 1456).

Tab e 1457. Compounds of formu a I. 1 , wherein R2 is R2 5.95(= formula 1 . 1457).

Tab e 1458. Compounds of formu a I. 1 , wherein R2 is R2 5.96(= formula 1 . 1458).

Tab e 1459. Compounds of formu a I. 1 , wherein R2 is R2 5.97(= formula 1 . 1459).

Tab e 1460. Compounds of formu a I. 1 , wherein R2 is R2 5.98(= formula 1 . 1460).

Tab e 1461 . Compounds of formu a I. 1 , wherein R2 is R2 5.99(= formula 1 . 1461 ).

Tab e 1462. Compounds of formu a I. 1 , wherein R2 is R2 5.100 ^formula ' 1.1462)

Tab e 1463. Compounds of formu a I. 1 , wherein R2 is R2 5.101 ^formula ' 1.1463)

Tab e 1464. Compounds of formu a I. 1 , wherein R2 is R2 5.102 ^formula ' 1.1464)

Tab e 1465. Compounds of formu a I. 1 , wherein R2 is R2 5.103 ^formula ' 1.1465)

Tab e 1466. Compounds of formu a I. 1 , wherein R2 is R2 5.104 ^formula ' 1.1466)

Tab e 1467. Compounds of formu a I. 1 , wherein R2 is R2 5.105 ^formula ' 1.1467)

Tab e 1468. Compounds of formu a I. 1 , wherein R2 is R2 5.106 ^formula ' 1.1468)

Tab e 1469. Compounds of formu a I. 1 , wherein R2 is R2 5.107 ^formula ' 1.1469)

Tab e 1470. Compounds of formu a I. 1 , wherein R2 is R2 5.108 ^formula ' 1.1470)

Tab e 1471 . Compounds of formu a I. 1 , wherein R2 is R2 5.109 ^formula ' 1.1471 )

Tab e 1472. Compounds of formu a I. 1 , wherein R2 is R2 5.1 10 ^formula ' 1.1472)

Tab e 1473. Compounds of formu a I. 1 , wherein R2 is R2 5.1 1 1 ^formula ' 1.1473)

Tab e 1474. Compounds of formu a I. 1 , wherein R2 is R2 5.1 12 ^formula ' 1.1475)

Tab e 1475. Compounds of formu a I. 1 , wherein R2 is R2 5.1 13 ^formula ' 1.1475)

Tab e 1476. Compounds of formu a I. 1 , wherein R2 is R2 5.1 14 ^formula ' 1.1476)

Tab e 1477. Compounds of formu a I. 1 , wherein R2 is R2 5.1 15 ^formula ' 1.1477)

Tab e 1478. Compounds of formu a I. 1 , wherein R2 is R2 5.1 16 ^formula ' 1.1478)

Tab e 1479. Compounds of formu a I. 1 , wherein R2 is R2 5.1 17 ^formula ' 1.1479)

Tab e 1480. Compounds of formu a I. 1 , wherein R2 is R2 5.1 18 ^formula ' 1.1480)

Tab e 1481 . Compounds of formu a I. 1 , wherein R2 is R2 5.1 19 ^formula ' 1.1481 )

Tab e 1482. Compounds of formu a I. 1 , wherein R2 is R2 5.120 ^formula ' 1.1482)

Tab e 1483. Compounds of formu a I. 1 , wherein R2 is R2 5.121 ^formula ' 1.1483)

Tab e 1484. Compounds of formu a I. 1 , wherein R2 is R2 5.122 ^formula ' 1.1484)

Tab e 1485. Compounds of formu a I. 1 , wherein R2 is R2 5.123 ^formula ' 1.1485)

Tab e 1486. Compounds of formu a I. 1 , wherein R2 is R2 5.124 ^formula ' 1.1486) Table 1487. Compounds o ormu a I.1 , wherein R2 is R2-- I 5 125( =formu a 1.1487

Table 1488. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 126( =formu a 1 .1488

Table 1489. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 127( =formu a 1 .1489

Table 1490. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 128( =formu a 1 .1490

Table 1491 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 129( =formu a 1 .1491

Table 1492. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 130( =formu a 1 .1492

Table 1493. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 131 ( =formu a 1 .1493

Table 1494. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 132( =formu a 1 .1494

Table 1495. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 133( =formu a 1 .1495

Table 1496. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 134( =formu a 1 .1496

Table 1497. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 135( =formu a 1 .1497

Table 1498. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 136( =formu a 1 .1498

Table 1499. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 137( =formu a 1 .1499

Table 1500. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 138( =formu a 1 .1500

Table 1501 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 139( =formu a 1 .1501

Table 1502. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 140( =formu a 1 .1502

Table 1503. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 141 ( =formu a 1 .1503

Table 1504. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 142( =formu a 1 .1504

Table 1505. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 143( =formu a 1 .1505

Table 1506. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 144( =formu a 1 .1506

Table 1507. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 145( =formu a 1 .1507

Table 1508. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 146( =formu a 1 .1508

Table 1509. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 147( =formu a 1 .1509

Table 1510. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 148( =formu a 1 .1510

Table 151 1 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 149( =formu a 1 .151 1

Table 1512. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 150( =formu a 1 .1512

Table 1513. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 151 ( =formu a 1 .1513

Table 1514. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 152( =formu a 1 .1514

Table 1515. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 153( =formu a 1 .1515

Table 1516. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 154( =formu a 1 .1516

Table 1517. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 155( =formu a 1 .1517

Table 1518. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 156( =formu a 1 .1518

Table 1519. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 157( =formu a 1 .1519

Table 1520. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 158( =formu a 1 .1520

Table 1521 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 159( =formu a 1 .1521

Table 1522. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 160( =formu a 1 .1522

Table 1523. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 161 ( =formu a 1 .1523

Table 1524. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 162( =formu a 1 .1524

Table 1525. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 163( =formu a 1 .1525

Table 1526. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 164( =formu a 1 .1526

Table 1527. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 165( =formu a 1 .1527

Table 1528. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 166( =formu a 1 .1528

Table 1529. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 167( =formu a 1 .1529

Table 1530. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5 168( =formu a 1 .1530 Table 1531 . Compounds o ormu a I.1 , wherein R2 is R2-- I 5.169( =formu a 1.1531

Table 1532. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.170( =formu a 1 .1532

Table 1533. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.171 ( =formu a 1 .1533

Table 1534. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.172( =formu a 1 .1534

Table 1535. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.173( =formu a 1 .1535

Table 1536. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.174( =formu a 1 .1536

Table 1537. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.175( =formu a 1 .1537

Table 1538. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.176( =formu a 1 .1538

Table 1539. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.177( =formu a 1 .1539

Table 1540. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.178( =formu a 1 .1540

Table 1541 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.179( =formu a 1 .1541

Table 1542. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.180( =formu a 1 .1542

Table 1543. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.18K =formu a 1 .1543

Table 1544. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.182( =formu a 1 .1544

Table 1545. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.183( =formu a 1 .1545

Table 1546. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.184( =formu a 1 .1546

Table 1547. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.185( =formu a 1 .1547

Table 1548. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.186( =formu a 1 .1548

Table 1549. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.187( =formu a 1 .1549

Table 1550. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.188( =formu a 1 .1550

Table 1551 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.189( =formu a 1 .1551

Table 1552. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.190( =formu a 1 .1552

Table 1553. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.19K =formu a 1 .1553

Table 1554. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.192( =formu a 1 .1554

Table 1555. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.193( =formu a 1 .1555

Table 1556. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.194( =formu a 1 .1556

Table 1557. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.195( =formu a 1 .1557

Table 1558. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.196( =formu a 1 .1558

Table 1559. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.197( =formu a 1 .1559

Table 1560. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.198( =formu a 1 .1560

Table 1561 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.199( =formu a 1 .1561

Table 1562. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.200( =formu a 1 .1562

Table 1563. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.20K =formu a 1 .1563

Table 1564. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.202( =formu a 1 .1564

Table 1565. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.203( =formu a 1 .1565

Table 1566. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.204( =formu a 1 .1566

Table 1567. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.205( =formu a 1 .1567

Table 1568. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.206( =formu a 1 .1568

Table 1569. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.207( =formu a 1 .1569

Table 1570. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.208( =formu a 1 .1570

Table 1571 . Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.209( =formu a 1 .1571

Table 1572. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.210( =formu a 1 .1572

Table 1573. Compounds o ormu a I. 1 , wherein R2 is R2-- 15.21 1 ( =formu a 1 .1573

Table 1574. Compounds o ormu a I. 1 , wherein R2 is R2-- I 5.212( =formu a 1 .1574 Table 1575. Compounds o ormu a I.1 , wherein R2 is R2- 15.213( =formu a 1.1575

Table 1576. Compounds o ormu a I. 1 , wherein R2 is R2- 15.214( =formu a 1 .1576

Table 1577. Compounds o ormu a I. 1 , wherein R2 is R2- 15.215( =formu a 1 .1577

Table 1578. Compounds o ormu a I. 1 , wherein R2 is R2- 15.216( =formu a 1 .1578

Table 1579. Compounds o ormu a I. 1 , wherein R2 is R2- 15.217( =formu a 1 .1579

Table 1580. Compounds o ormu a I. 1 , wherein R2 is R2- 15.218( =formu a 1 .1580

Table 1581 . Compounds o ormu a I. 1 , wherein R2 is R2- 15.219( =formu a 1 .1581

Table 1582. Compounds o ormu a I. 1 , wherein R2 is R2- 15.220( =formu a 1 .1582

Table 1583. Compounds o ormu a I. 1 , wherein R2 is R2- 15.221 ( =formu a 1 .1583

Table 1584. Compounds o ormu a I. 1 , wherein R2 is R2- 15.222( =formu a 1 .1584

Table 1585. Compounds o ormu a I. 1 , wherein R2 is R2- 15.223( =formu a 1 .1585

Table 1586. Compounds o ormu a I. 1 , wherein R2 is R2- 15.224( =formu a 1 .1586

Table 1587. Compounds o ormu a I. 1 , wherein R2 is R2- 15.225( =formu a 1 .1587

Table 1588. Compounds o ormu a I. 1 , wherein R2 is R2- 15.226( =formu a 1 .1588

Table 1589. Compounds o ormu a I. 1 , wherein R2 is R2- 15.227( =formu a 1 .1589

Table 1590. Compounds o ormu a I. 1 , wherein R2 is R2- 15.228( =formu a 1 .1590

Table 1591 . Compounds o ormu a I. 1 , wherein R2 is R2- 15.229( =formu a 1 .1591

Table 1592. Compounds o ormu a I. 1 , wherein R2 is R2- 15.230( =formu a 1 .1592

Table 1593. Compounds o ormu a I. 1 , wherein R2 is R2- 15.23K =formu a 1 .1593

Table 1594. Compounds o ormu a I. 1 , wherein R2 is R2- 15.232( =formu a 1 .1594

Table 1595. Compounds o ormu a I. 1 , wherein R2 is R2- 15.233( =formu a 1 .1595

Table 1596. Compounds o ormu a I. 1 , wherein R2 is R2- 15.234( =formu a 1 .1596

Table 1597. Compounds o ormu a I. 1 , wherein R2 is R2- 15.235( =formu a 1 .1597

Table 1598. Compounds o ormu a I. 1 , wherein R2 is R2- 15.236( =formu a 1 .1598

Table 1599. Compounds o ormu a I. 1 , wherein R2 is R2- 15.237( =formu a 1 .1599

Table 1600. Compounds o ormu a I. 1 , wherein R2 is R2- 15.238( =formu a 1 .1600

Table 1601 . Compounds o ormu a I. 1 , wherein R2 is R2- 15.239( =formu a 1 .1601

Table 1602. Compounds o ormu a I. 1 , wherein R2 is R2- 15.240( =formu a 1 .1602

Table 1603. Compounds o ormu a I. 1 , wherein R2 is R2- 15.241 ( =formu a 1 .1603

Table 1604. Compounds o ormu a I. 1 , wherein R2 is R2- 15.242( =formu a 1 .1604

Table 1605. Compounds o ormu a I. 1 , wherein R2 is R2- 15.243( =formu a 1 .1605

Table 1606. Compounds o ormu a I. 1 , wherein R2 is R2- 15.244( =formu a 1 .1606

Table 1607. Compounds o ormu a I. 1 , wherein R2 is R2- 15.245( =formu a 1 .1607

Table 1608. Compounds o ormu a I. 1 , wherein R2 is R2- 15.246( =formu a 1 .1608

Table 1609. Compounds o ormu a I. 1 , wherein R2 is R2- 15.247( =formu a 1 .1609

Table 1610. Compounds o ormu a I. 1 , wherein R2 is R2- 15.248( =formu a 1 .1610

Table 161 1 . Compounds o ormu a I. 1 , wherein R2 is R2- 15.249( =formu a 1 .161 1

Table 1612. Compounds o ormu a I. 1 , wherein R2 is R2- 15.250( =formu a 1 .1612

Table 1613. Compounds o ormu a I. 1 , wherein R2 is R2- 15.25K =formu a 1 .1613

Table 1614. Compounds o ormu a I. 1 , wherein R2 is R2- 15.252( =formu a 1 .1614

Table 1615. Compounds o ormu a I. 1 , wherein R2 is R2- 15.253( =formu a 1 .1615

Table 1616. Compounds o ormu a I. 1 , wherein R2 is R2- 15.254( =formu a 1 .1616

Table 1617. Compounds o ormu a I. 1 , wherein R2 is R2- 15.255( =formu a 1 .1617

Table 1618. Compounds o ormu a I. 1 , wherein R2 is R2- 15.256( =formu a 1 .1618 Tab e 1619. Compounds of formu a I.1 , wherein R2 is R2-- I 5 257( =formu a 1.1619)

Tab e 1620. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 258( =formu a 1 .1620)

Tab e 1621 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 259( =formu a 1 .1621 )

Tab e 1622. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 260( =formu a 1 .1622)

Tab e 1623. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 261 ( =formu a 1 .1623)

Tab e 1624. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 262( =formu a 1 .1624)

Tab e 1625. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 263( =formu a 1 .1625)

Tab e 1626. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 264( =formu a 1 .1626)

Tab e 1627. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 265( =formu a 1 .1627)

Tab e 1628. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 266( =formu a 1 .1628)

Tab e 1629. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 267( =formu a 1 .1629)

Tab e 1630. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 268( =formu a 1 .1630)

Tab e 1631 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 269( =formu a 1 .1631 )

Tab e 1632. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 270( =formu a 1 .1632)

Tab e 1633. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 271 ( =formu a 1 .1633)

Tab e 1634. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 272( =formu a 1 .1634)

Tab e 1635. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 273( =formu a 1 .1635)

Tab e 1636. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 274( =formu a 1 .1636)

Tab e 1637. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 275( =formu a 1 .1637)

Tab e 1638. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 276( =formu a 1 .1638)

Tab e 1639. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 277( =formu a 1 .1639)

Tab e 1640. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 278( =formu a 1 .1640)

Tab e 1641 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 279( =formu a 1 .1641 )

Tab e 1642. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 280( =formu a 1 .1642)

Tab e 1643. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 281 ( =formu a 1 .1643)

Tab e 1644. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 282( =formu a 1 .1644)

Tab e 1645. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 283( =formu a 1 .1645)

Tab e 1646. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 284( =formu a 1 .1646)

Tab e 1647. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 285( =formu a 1 .1647)

Tab e 1648. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 286( =formu a 1 .1648)

Tab e 1649. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 287( =formu a 1 .1649)

Tab e 1650. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 288( =formu a 1 .1650)

Tab e 1651 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 289( =formu a 1 .1651 )

Tab e 1652. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 290( =formu a 1 .1652)

Tab e 1653. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 291 ( =formu a 1 .1653)

Tab e 1654. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 292( =formu a 1 .1654)

Tab e 1655. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 293( =formu a 1 .1655)

Tab e 1656. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 294( =formu a 1 .1656)

Tab e 1657. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 295( =formu a 1 .1657)

Tab e 1658. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 296( =formu a 1 .1658)

Tab e 1659. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 297( =formu a 1 .1659)

Tab e 1660. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 298( =formu a 1 .1660)

Tab e 1661 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 299( =formu a 1 .1661 )

Tab e 1662. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 300( =formu a 1 .1662) Tab e 1663. Compounds of formu a I.1 , wherein R2 is R2-- I 5 301 ( =formu a 1.1663)

Tab e 1664. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 302( =formu a 1 .1664)

Tab e 1665. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 303( =formu a 1 .1665)

Tab e 1666. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 304( =formu a 1 .1666)

Tab e 1667. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 305( =formu a 1 .1667)

Tab e 1668. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 306( =formu a 1 .1668)

Tab e 1669. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 307( =formu a 1 .1669)

Tab e 1670. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 308( =formu a 1 .1670)

Tab e 1671 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 309( =formu a 1 .1671 )

Tab e 1672. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 310( =formu a 1 .1672)

Tab e 1673. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 31 1 < =formu a 1 .1673)

Tab e 1674. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 312( =formu a 1 .1674)

Tab e 1675. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 313( =formu a 1 .1675)

Tab e 1676. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 314( =formu a 1 .1676)

Tab e 1677. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 315( =formu a 1 .1676)

Tab e 1678. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 316( =formu a 1 .1678)

Tab e 1679. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 317( =formu a 1 .1679)

Tab e 1680. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 318( =formu a 1 .1680)

Tab e 1681 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 319( =formu a 1 .1681 )

Tab e 1682. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 320( =formu a 1 .1682)

Tab e 1683. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 321 ( =formu a 1 .1683)

Tab e 1684. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 322( =formu a 1 .1684)

Tab e 1685. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 323( =formu a 1 .1685)

Tab e 1686. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 324( =formu a 1 .1686)

Tab e 1687. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 325( =formu a 1 .1687)

Tab e 1688. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 326( =formu a 1 .1688)

Tab e 1689. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 327( =formu a 1 .1689)

Tab e 1690. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 328( =formu a 1 .1690)

Tab e 1691 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 329( =formu a 1 .1691 )

Tab e 1692. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 330( =formu a 1 .1692)

Tab e 1693. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 331 ( =formu a 1 .1693)

Tab e 1694. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 332( =formu a 1 .1694)

Tab e 1695. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 333( =formu a 1 .1695)

Tab e 1696. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 334( =formu a 1 .1696)

Tab e 1697. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 335( =formu a 1 .1697)

Tab e 1698. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 336( =formu a 1 .1698)

Tab e 1699. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 334( =formu a 1 .1699)

Tab e 1700. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 338( =formu a 1 .1700)

Tab e 1701 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 339( =formu a 1 .1701 )

Tab e 1702. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 340( =formu a 1 .1702)

Tab e 1703. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 341 ( =formu a 1 .1703)

Tab e 1704. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 342( =formu a 1 .1704)

Tab e 1705. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 343( =formu a 1 .1705)

Tab e 1706. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 344( =formu a 1 .1706) Tab e 1707. Compounds of formu a I.1 , wherein R2 is R2-- I 5 345( =formu a 1.1707)

Tab e 1708. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 346( =formu a 1 .1708)

Tab e 1709. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 347( =formu a 1 .1709)

Tab e 1710. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 348( =formu a 1 .1710)

Tab e 171 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 349( =formu a 1 .171 1 )

Tab e 1712. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 350( =formu a 1 .1712)

Tab e 1713. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 351 ( =formu a 1 .1713)

Tab e 1714. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 352( =formu a 1 .1714)

Tab e 1715. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 353( =formu a 1 .1715)

Tab e 1716. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 354( =formu a 1 .1716)

Tab e 1717. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 355( =formu a 1 .1717)

Tab e 1718. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 356( =formu a 1 .1718)

Tab e 1719. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 357( =formu a 1 .1719)

Tab e 1720. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 358( =formu a 1 .1720)

Tab e 1721 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 359( =formu a 1 .1721 )

Tab e 1722. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 360( =formu a 1 .1722)

Tab e 1723. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 361 ( =formu a 1 .1723)

Tab e 1724. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 362( =formu a 1 .1724)

Tab e 1725. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 363( =formu a 1 .1725)

Tab e 1726. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 364( =formu a 1 .1726)

Tab e 1727. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 365( =formu a 1 .1727)

Tab e 1728. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 366( =formu a 1 .1728)

Tab e 1729. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 367( =formu a 1 .1729)

Tab e 1730. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 368( =formu a 1 .1730)

Tab e 1731 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 369( =formu a 1 .1731 )

Tab e 1732. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 370( =formu a 1 .1732)

Tab e 1733. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 371 ( =formu a 1 .1733)

Tab e 1734. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 372( =formu a 1 .1734)

Tab e 1735. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 373( =formu a 1 .1735)

Tab e 1736. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 374( =formu a 1 .1736)

Tab e 1737. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 375( =formu a 1 .1737)

Tab e 1738. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 376( =formu a 1 .1738)

Tab e 1739. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 377( =formu a 1 .1739)

Tab e 1740. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 378( =formu a 1 .1740)

Tab e 1741 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 379( =formu a 1 .1741 )

Tab e 1742. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 380( =formu a 1 .1742)

Tab e 1743. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 381 ( =formu a 1 .1743)

Tab e 1744. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 382( =formu a 1 .1744)

Tab e 1745. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 383( =formu a 1 .1745)

Tab e 1746. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 384( =formu a 1 .1746)

Tab e 1747. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 385( =formu a 1 .1747)

Tab e 1748. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 386( =formu a 1 .1748)

Tab e 1749. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 387( =formu a 1 .1749)

Tab e 1750. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 388( =formu a 1 .1750) Tab e 1751 . Compounds of formu a I.1 , wherein R2 is R2-- I 5 389( =formu a 1.1751 )

Tab e 1752. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 390( =formu a 1 .1752)

Tab e 1753. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 391 ( =formu a 1 .1753)

Tab e 1754. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 392( =formu a 1 .1754)

Tab e 1755. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 393( =formu a 1 .1755)

Tab e 1756. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 394( =formu a 1 .1756)

Tab e 1757. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 395( =formu a 1 .1757)

Tab e 1758. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 396( =formu a 1 .1758)

Tab e 1759. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 397( =formu a 1 .1759)

Tab e 1760. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 398( =formu a 1 .1760)

Tab e 1761 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 399( =formu a 1 .1761 )

Tab e 1762. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 400( =formu a 1 .1762)

Tab e 1763. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 401 ( =formu a 1 .1763)

Tab e 1764. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 402( =formu a 1 .1764)

Tab e 1765. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 403( =formu a 1 .1765)

Tab e 1766. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 404( =formu a 1 .1766)

Tab e 1767. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 405( =formu a 1 .1767)

Tab e 1768. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 406( =formu a 1 .1768)

Tab e 1769. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 407( =formu a 1 .1769)

Tab e 1770. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 408( =formu a 1 .1770)

Tab e 1771 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 409( =formu a 1 .1771 )

Tab e 1772. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 410( =formu a 1 .1772)

Tab e 1773. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 41 1 ( =formu a 1 .1773)

Tab e 1774. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 412( =formu a 1 .1774)

Tab e 1775. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 413( =formu a 1 .1775)

Tab e 1776. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 414( =formu a 1 .1776)

Tab e 1777. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 415( =formu a 1 .1777)

Tab e 1778. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 416( =formu a 1 .1778)

Tab e 1779. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 417( =formu a 1 .1779)

Tab e 1780. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 418( =formu a 1 .1780)

Tab e 1781 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 419( =formu a 1 .1781 )

Tab e 1782. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 420( =formu a 1 .1782)

Tab e 1783. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 421 ( =formu a 1 .1783)

Tab e 1784. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 422( =formu a 1 .1784)

Tab e 1785. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 423( =formu a 1 .1785)

Tab e 1786. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 424( =formu a 1 .1786)

Tab e 1787. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 425( =formu a 1 .1787)

Tab e 1788. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 426( =formu a 1 .1788)

Tab e 1789. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 427( =formu a 1 .1789)

Tab e 1790. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 428( =formu a 1 .1790)

Tab e 1791 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 429( =formu a 1 .1791 )

Tab e 1792. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 430( =formu a 1 .1792)

Tab e 1793. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 431 ( =formu a 1 .1793)

Tab e 1794. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 432( =formu a 1 .1794) Tab e 1795. Compounds of formu a I.1 , wherein R2 is R2-- I 5 433( =formu a 1.1795)

Tab e 1796. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 434( =formu a 1 .1796)

Tab e 1797. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 435( =formu a 1 .1797)

Tab e 1798. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 436( =formu a 1 .1798)

Tab e 1799. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 437( =formu a 1 .1799)

Tab e 1800. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 438( =formu a 1 .1800)

Tab e 1801 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 439( =formu a 1 .1801 )

Tab e 1802. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 440( =formu a 1 .1802)

Tab e 1803. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 441 ( =formu a 1 .1803)

Tab e 1804. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 442( =formu a 1 .1804)

Tab e 1805. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 443( =formu a 1 .1805)

Tab e 1806. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 444( =formu a 1 .1806)

Tab e 1807. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 445( =formu a 1 .1807)

Tab e 1808. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 446( =formu a 1 .1808)

Tab e 1809. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 447( =formu a 1 .1809)

Tab e 1810. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 448( =formu a 1 .1810)

Tab e 181 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 449( =formu a 1 .181 1 )

Tab e 1812. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 450( =formu a 1 .1812)

Tab e 1813. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 451 ( =formu a 1 .1813)

Tab e 1814. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 452( =formu a 1 .1814)

Tab e 1815. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 453( =formu a 1 .1815)

Tab e 1816. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 454( =formu a 1 .1816)

Tab e 1817. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 455( =formu a 1 .1817)

Tab e 1818. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 456( =formu a 1 .1818)

Tab e 1819. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 457( =formu a 1 .1819)

Tab e 1820. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 458( =formu a 1 .1820)

Tab e 1821 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 459( =formu a 1 .1821 )

Tab e 1822. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 460( =formu a 1 .1822)

Tab e 1823. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 461 ( =formu a 1 .1823)

Tab e 1824. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 462( =formu a 1 .1824)

Tab e 1825. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 463( =formu a 1 .1825)

Tab e 1826. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 464( =formu a 1 .1826)

Tab e 1827. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 465( =formu a 1 .1827)

Tab e 1828. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 466( =formu a 1 .1828)

Tab e 1829. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 467( =formu a 1 .1829)

Tab e 1830. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 468( =formu a 1 .1830)

Tab e 1831 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 469( =formu a 1 .1831 )

Tab e 1832. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 470( =formu a 1 .1832)

Tab e 1833. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 471 ( =formu a 1 .1833)

Tab e 1834. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 472( =formu a 1 .1834)

Tab e 1835. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 473( =formu a 1 .1835)

Tab e 1836. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 474( =formu a 1 .1836)

Tab e 1837. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 475( =formu a 1 .1837)

Tab e 1838. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 476( =formu a 1 .1838) Tab e 1839. Compounds of formu a I.1 , wherein R2 is R2-- I 5 477( =formu a 1.1839)

Tab e 1840. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 478( =formu a 1 .1840)

Tab e 1841 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 479( =formu a 1 .1841 )

Tab e 1842. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 480( =formu a 1 .1842)

Tab e 1843. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 481 ( =formu a 1 .1843)

Tab e 1844. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 482( =formu a 1 .1844)

Tab e 1845. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 483( =formu a 1 .1845)

Tab e 1846. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 484( =formu a 1 .1846)

Tab e 1847. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 485( =formu a 1 .1847)

Tab e 1848. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 486( =formu a 1 .1848)

Tab e 1849. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 487( =formu a 1 .1849)

Tab e 1850. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 488( =formu a 1 .1850)

Tab e 1851 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 489( =formu a 1 .1851 )

Tab e 1852. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 490( =formu a 1 .1852)

Tab e 1853. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 491 ( =formu a 1 .1853)

Tab e 1854. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 492( =formu a 1 .1854)

Tab e 1855. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 493( =formu a 1 .1855)

Tab e 1856. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 494( =formu a 1 .1856)

Tab e 1857. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 495( =formu a 1 .1857)

Tab e 1858. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 496( =formu a 1 .1858)

Tab e 1859. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 497( =formu a 1 .1859)

Tab e 1860. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 498( =formu a 1 .1860)

Tab e 1861 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 499( =formu a 1 .1861 )

Tab e 1862. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 500( =formu a 1 .1862)

Tab e 1863. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 501 ( =formu a 1 .1863)

Tab e 1864. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 502( =formu a 1 .1864)

Tab e 1865. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 503( =formu a 1 .1865)

Tab e 1866. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 504( =formu a 1 .1866)

Tab e 1867. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 505( =formu a 1 .1867)

Tab e 1868. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 506( =formu a 1 .1868)

Tab e 1869. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 507( =formu a 1 .1869)

Tab e 1870. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 508( =formu a 1 .1870)

Tab e 1871 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 509( =formu a 1 .1871 )

Tab e 1872. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 510( =formu a 1 .1872)

Tab e 1873. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 51 1 ( =formu a 1 .1873)

Tab e 1874. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 512( =formu a 1 .1874)

Tab e 1875. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 513( =formu a 1 .1875)

Tab e 1876. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 514( =formu a 1 .1876)

Tab e 1877. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 515( =formu a 1 .1877)

Tab e 1878. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 516( =formu a 1 .1878)

Tab e 1879. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 517( =formu a 1 .1879)

Tab e 1880. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 518( =formu a 1 .1880)

Tab e 1881 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 519( =formu a 1 .1881 )

Tab e 1882. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 520( =formu a 1 .1882) Tab e 1883. Compounds of formu a I.1 , wherein R2 is R2-- I 5 521 ( =formu a 1.1883)

Tab e 1884. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 522( =formu a 1 .1884)

Tab e 1885. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 523( =formu a 1 .1885)

Tab e 1886. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 524( =formu a 1 .1886)

Tab e 1887. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 525( =formu a 1 .1887)

Tab e 1888. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 526( =formu a 1 .1888)

Tab e 1889. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 527( =formu a 1 .1889)

Tab e 1890. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 528( =formu a 1 .1890)

Tab e 1891 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 529( =formu a 1 .1891 )

Tab e 1892. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 530( =formu a 1 .1892)

Tab e 1893. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 531 ( =formu a 1 .1893)

Tab e 1894. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 532( =formu a 1 .1894)

Tab e 1895. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 533( =formu a 1 .1895)

Tab e 1896. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 534( =formu a 1 .1896)

Tab e 1897. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 535( =formu a 1 .1897)

Tab e 1898. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 536( =formu a 1 .1898)

Tab e 1899. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 537( =formu a 1 .1899)

Tab e 1900. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 538( =formu a 1 .1900)

Tab e 1901 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 539( =formu a 1 .1901 )

Tab e 1902. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 540( =formu a 1 .1902)

Tab e 1903. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 541 ( =formu a 1 .1903)

Tab e 1904. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 542( =formu a 1 .1904)

Tab e 1905. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 543( =formu a 1 .1905)

Tab e 1906. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 544( =formu a 1 .1906)

Tab e 1907. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 545( =formu a 1 .1907)

Tab e 1908. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 546( =formu a 1 .1908)

Tab e 1909. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 547( =formu a 1 .1909)

Tab e 1910. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 548( =formu a 1 .1910)

Tab e 191 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 549( =formu a 1 .191 1 )

Tab e 1912. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 550( =formu a 1 .1912)

Tab e 1913. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 551 ( =formu a 1 .1913)

Tab e 1914. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 552( =formu a 1 .1914)

Tab e 1915. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 553( =formu a 1 .1915)

Tab e 1916. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 554( =formu a 1 .1916)

Tab e 1917. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 555( =formu a 1 .1917)

Tab e 1918. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 556( =formu a 1 .1918)

Tab e 1919. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 557( =formu a 1 .1919)

Tab e 1920. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 558( =formu a 1 .1920)

Tab e 1921 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 559( =formu a 1 .1921 )

Tab e 1922. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 560( =formu a 1 .1922)

Tab e 1923. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 561 ( =formu a 1 .1923)

Tab e 1924. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 562( =formu a 1 .1924)

Tab e 1925. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 563( =formu a 1 .1925)

Tab e 1926. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 564( =formu a 1 .1926) Tab e 1927. Compounds of formu a I.1 , wherein R2 is R2-- I 5 565( =formu a 1.1927)

Tab e 1928. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 566( =formu a 1 .1928)

Tab e 1929. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 567( =formu a 1 .1929)

Tab e 1930. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 568( =formu a 1 .1930)

Tab e 1931 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 569( =formu a 1 .1931 )

Tab e 1932. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 570( =formu a 1 .1932)

Tab e 1933. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 571 ( =formu a 1 .1933)

Tab e 1934. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 572( =formu a 1 .1934)

Tab e 1935. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 573( =formu a 1 .1935)

Tab e 1936. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 574( =formu a 1 .1936)

Tab e 1937. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 575( =formu a 1 .1937)

Tab e 1938. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 576( =formu a 1 .1938)

Tab e 1939. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 577( =formu a 1 .1939)

Tab e 1940. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 578( =formu a 1 .1940)

Tab e 1941 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 579( =formu a 1 .1941 )

Tab e 1942. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 580( =formu a 1 .1942)

Tab e 1943. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 581 ( =formu a 1 .1943)

Tab e 1944. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 582( =formu a 1 .1944)

Tab e 1945. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 583( =formu a 1 .1945)

Tab e 1946. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 584( =formu a 1 .1946)

Tab e 1947. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 585( =formu a 1 .1947)

Tab e 1948. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 586( =formu a 1 .1948)

Tab e 1949. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 587( =formu a 1 .1949)

Tab e 1950. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 588( =formu a 1 .1950)

Tab e 1951 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 589( =formu a 1 .1951 )

Tab e 1952. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 590( =formu a 1 .1952)

Tab e 1953. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 591 ( =formu a 1 .1953)

Tab e 1954. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 592( =formu a 1 .1954)

Tab e 1955. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 593( =formu a 1 .1955)

Tab e 1956. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 594( =formu a 1 .1956)

Tab e 1957. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 595( =formu a 1 .1957)

Tab e 1958. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 596( =formu a 1 .1958)

Tab e 1959. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 597( =formu a 1 .1959)

Tab e 1960. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 598( =formu a 1 .1960)

Tab e 1961 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 599( =formu a 1 .1961 )

Tab e 1962. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 600( =formu a 1 .1962)

Tab e 1963. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 601 ( =formu a 1 .1963)

Tab e 1964. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 602( =formu a 1 .1964)

Tab e 1965. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 603( =formu a 1 .1965)

Tab e 1966. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 604( =formu a 1 .1966)

Tab e 1967. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 605( =formu a 1 .1967)

Tab e 1968. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 606( =formu a 1 .1968)

Tab e 1969. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 607( =formu a 1 .1969)

Tab e 1970. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 608( =formu a 1 .1970) Tab e 1971 . Compounds of formu a I.1 , wherein R2 is R2-- I 5 609( =formu a ' .1971 )

Tab e 1972. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 610( =formu a ' .1972)

Tab e 1973. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 61 1 < =formu a ' .1973)

Tab e 1974. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 612( =formu a ' .1974)

Tab e 1975. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 613( =formu a ' .1975)

Tab e 1976. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 614( =formu a ' .1976)

Tab e 1977. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 615( =formu a ' .1977)

Tab e 1978. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 616( =formu a ' .1978)

Tab e 1979. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 617( =formu a ' .1979)

Tab e 1980. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 618( =formu a ' .1980)

Tab e 1981 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 619( =formu a ' .1981 )

Tab e 1982. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 620( =formu a ' .1982)

Tab e 1983. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 621 ( =formu a ' .1983)

Tab e 1984. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 622( =formu a ' .1984)

Tab e 1985. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 623( =formu a ' .1985)

Tab e 1986. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 624( =formu a ' .1986)

Tab e 1987. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 625( =formu a ' .1987)

Tab e 1988. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 626( =formu a ' .1988)

Tab e 1989. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 627( =formu a ' .1989)

Tab e 1990. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 628( =formu a ' .1990)

Tab e 1991 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 629( =formu a ' .1991 )

Tab e 1992. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 630( =formu a ' .1992)

Tab e 1993. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 631 ( =formu a ' .1993)

Tab e 1994. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 632( =formu a ' .1994)

Tab e 1995. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 633( =formu a ' .1995)

Tab e 1996. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 634( =formu a ' .1996)

Tab e 1997. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 635( =formu a ' .1997)

Tab e 1998. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 636( =formu a ' .1998)

Tab e 1999. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 637( =formu a ' .1999)

Tab e 2000. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 638( =formu a ' .2000)

Tab e 2001 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 639( =formu a ' .2001 )

Tab e 2002. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 640( =formu a ' .2002)

Tab e 2003. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 641 ( =formu a ' .2003)

Tab e 2004. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 642( =formu a ' .2004)

Tab e 2005. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 643( =formu a ' .2005)

Tab e 2006. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 644( =formu a ' .2006)

Tab e 2007. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 645( =formu a ' .2007)

Tab e 2008. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 646( =formu a ' .2008)

Tab e 2009. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 647( =formu a ' .2009)

Tab e 2010. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 648( =formu a ' .2010)

Tab e 201 1 . Compounds of formu a I. 1 , wherein R2 is R2-- I 5 649( =formu a ' .201 1 )

Tab e 2012. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 650( =formu a ' .2012)

Tab e 2013. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 651 ( =formu a ' .2013)

Tab e 2014. Compounds of formu a I. 1 , wherein R2 is R2-- I 5 652( =formu a ' .2014) Table 2015. Compounds o ormu a I.1 , wherein R ² is R ² - 15 653( =formu a ' 1.2015) Table 2016. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 654( =formu a ' 1.2016)

Table 2017. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 655( =formu a ' 1.2017)

Table 2018. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 656( =formu a ' 1.2018)

Table 2019. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 657( =formu a ' 1.2019)

Table 2020. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 658( =formu a ' 1.2020)

Table 2021 . Compounds o ormu a I. 1 , wherein R ² is R ² - 15 659( =formu a ' 1.2021 )

Table 2022. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 660( =formu a ' 1.2022)

Table 2023. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 661 ( =formu a ' 1.2023)

Table 2024. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 662( =formu a ' 1.2024)

Table 2025. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 663( =formu a ' 1.2025)

Table 2026. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 664( =formu a ' 1.2026)

Table 2027. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 665( =formu a ' 1.2027)

Table 2028. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 666( =formu a ' 1.2028)

Table 2029. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 667( =formu a ' 1.2029)

Table 2030. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 668( =formu a ' 1.2030)

Table 2031 . Compounds o ormu a I. 1 , wherein R ² is R ² - 15 669( =formu a ' 1.2031 )

Table 2032. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 670( =formu a ' 1.2032)

Table 2033. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 671 ( =formu a ' 1.2033)

Table 2034. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 672( =formu a ' 1.2034)

Table 2035. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 673( =formu a ' 1.2035)

Table 2036. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 674( =formu a ' 1.2036)

Table 2037. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 675( =formu a ' 1.2037)

Table 2038. Compounds o ormu a I. 1 , wherein R ² is R ² - 15 676( =formu a ' 1.2038)

Table A:

No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R ¹ R ³ R ⁵ R ⁶ R ⁷

1-1 C-C3H5 F H H H 1-18 C-C3H5 F F H OCH3

I-2 C-C3H5 F H H F 1-19 C-C3H5 F F F H

I-3 C-C3H5 F H H CI I-20 C-C3H5 F F F F

I-4 C-C3H5 F H H Br 1-21 C-C3H5 F F F CI

I-5 C-C3H5 F H H CHs I-22 C-C3H5 F F F Br

I-6 C-C3H5 F H H OCH3 I-23 C-C3H5 F F F CH ₃

I-7 C-C3H5 F H F H I-24 C-C3H5 F F F OCH3

I-8 C-C3H5 F H F F I-25 C-C3H5 CI H H H

I-9 C-C3H5 F H F CI I-26 C-C3H5 CI H H F

1-10 C-C3H5 F H F Br I-27 C-C3H5 CI H H CI

1-1 1 C-C3H5 F H F CHs I-28 C-C3H5 CI H H Br

1-12 C-C3H5 F H F OCHs I-29 C-C3H5 CI H H CH ₃

1-13 C-C3H5 F F H H I-30 C-C3H5 CI H H OCH3

1-14 c-CsHs F F H F 1-31 c-C ₃ H ₅ CI H F H

1-15 c-CsHs F F H CI I-32 c-C ₃ H ₅ CI H F F

1-16 C-CsHs F F H Br I-33 c-C ₃ H ₅ CI H F CI

1-17 C-CsHs F F H CH ₃ I-34 c-C ₃ H ₅ CI H F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-35 c-CsHs CI H F CH ₃ I-77 C-CsHs I H H CHs

1-36 c-CsHs CI H F OCH3 I-78 C-CsHs I H H OCHs

1-37 C-C3H5 CI F H H I-79 C-C3H5 I H F H

1-38 C-C3H5 CI F H F I-80 C-C3H5 I H F F

1-39 C-C3H5 CI F H CI 1-81 C-C3H5 I H F CI

1-40 C-C3H5 CI F H Br I-82 C-C3H5 I H F Br

1-41 C-C3H5 CI F H CH ₃ I-83 C-C3H5 I H F CHs

I-42 C-C3H5 CI F H OCH3 I-84 C-C3H5 I H F OCHs

I-43 C-C3H5 CI F F H I-85 C-C3H5 I F H H

I-44 C-C3H5 CI F F F I-86 C-C3H5 I F H F

I-45 C-C3H5 CI F F CI I-87 C-C3H5 I F H CI

I-46 C-C3H5 CI F F Br I-88 C-C3H5 I F H Br

I-47 C-C3H5 CI F F CH ₃ I-89 C-C3H5 I F H CHs

I-48 C-C3H5 CI F F OCH3 I-90 C-C3H5 I F H OCHs

I-49 C-C3H5 Br H H H 1-91 C-C3H5 I F F H

I-50 C-C3H5 Br H H F I-92 C-C3H5 I F F F

1-51 C-C3H5 Br H H CI I-93 C-C3H5 I F F CI

I-52 C-C3H5 Br H H Br I-94 C-C3H5 I F F Br

I-53 C-C3H5 Br H H CH ₃ I-95 C-C3H5 I F F CHs

I-54 C-CsHs Br H H OCH3 I-96 C-CsHs I F F OCHs

I-55 C-CsHs Br H F H I-97 C-CsHs CHs H H H

I-56 C-CsHs Br H F F I-98 C-CsHs CHs H H F

I-57 C-CsHs Br H F CI I-99 C-CsHs CHs H H CI

I-58 C-CsHs Br H F Br 1-100 C-CsHs CHs H H Br

I-59 C-CsHs Br H F CH ₃ 1-101 C-CsHs CHs H H CHs

I-60 C-C3H5 Br H F OCH3 1-102 C-C3H5 CHs H H OCHs

1-61 C-C3H5 Br F H H 1-103 C-C3H5 CHs H F H

I-62 C-C3H5 Br F H F 1-104 C-C3H5 CHs H F F

I-63 C-C3H5 Br F H CI 1-105 C-C3H5 CHs H F CI

I-64 C-C3H5 Br F H Br 1-106 C-C3H5 CHs H F Br

I-65 C-C3H5 Br F H CH ₃ 1-107 C-C3H5 CHs H F CHs

I-66 C-C3H5 Br F H OCH3 1-108 C-C3H5 CHs H F OCHs

I-67 C-C3H5 Br F F H 1-109 C-C3H5 CHs F H H

I-68 C-C3H5 Br F F F 1-1 10 C-C3H5 CHs F H F

I-69 C-C3H5 Br F F CI 1-1 1 1 C-C3H5 CHs F H CI

I-70 C-C3H5 Br F F Br 1-1 12 C-C3H5 CHs F H Br

1-71 C-C3H5 Br F F CH ₃ 1-1 13 C-C3H5 CHs F H CHs

I-72 C-C3H5 Br F F OCH3 1-1 14 C-C3H5 CHs F H OCHs

I-73 C-C3H5 I H H H 1-1 15 C-C3H5 CHs F F H

I-74 C-C3H5 I H H F 1-1 16 C-C3H5 CHs F F F

I-75 C-C3H5 I H H CI 1-1 17 C-C3H5 CHs F F CI

I-76 C-C3H5 I H H Br 1-1 18 C-C3H5 CHs F F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷ -1 19 c-CsHs CH ₃ F F CH ₃ 1-161 C-CsHs CF ₃ F H CH ₃ -120 c-CsHs CH ₃ F F OCH3 1-162 C-CsHs CF ₃ F H OCH3-121 C-C3H5 OCH3 H H H 1-163 C-C3H5 CF ₃ F F H-122 C-C3H5 OCH3 H H F 1-164 C-C3H5 CF ₃ F F F-123 C-C3H5 OCH3 H H CI 1-165 C-C3H5 CF ₃ F F CI-124 C-C3H5 OCH3 H H Br 1-166 C-C3H5 CF ₃ F F Br-125 C-C3H5 OCH3 H H CH ₃ 1-167 C-C3H5 CF ₃ F F CH ₃ -126 C-C3H5 OCH3 H H OCH3 1-168 C-C3H5 CF ₃ F F OCH3-127 C-C3H5 OCH3 H F H 1-169 C-C4H7 F H H H-128 C-C3H5 OCH3 H F F 1-170 C-C4H7 F H H F-129 C-C3H5 OCH3 H F CI 1-171 C-C4H7 F H H CI-130 C-C3H5 OCH3 H F Br 1-172 C-C4H7 F H H Br-131 C-C3H5 OCH3 H F CH ₃ 1-173 C-C4H7 F H H CH ₃ -132 C-C3H5 OCH3 H F OCH3 1-174 C-C4H7 F H H OCH3-133 C-C3H5 OCH3 F H H 1-175 C-C4H7 F H F H-134 C-C3H5 OCH3 F H F 1-176 C-C4H7 F H F F-135 C-C3H5 OCH3 F H CI 1-177 C-C4H7 F H F CI-136 C-C3H5 OCH3 F H Br 1-178 C-C4H7 F H F Br-137 C-C3H5 OCH3 F H CH ₃ 1-179 C-C4H7 F H F CH ₃ -138 C-CsHs OCH3 F H OCH3 1-180 C-C4H7 F H F OCH3-139 C-CsHs OCH3 F F H 1-181 C-C4H7 F F H H-140 C-CsHs OCH3 F F F 1-182 C-C4H7 F F H F-141 C-CsHs OCH3 F F CI 1-183 C-C4H7 F F H CI-142 C-CsHs OCH3 F F Br 1-184 C-C4H7 F F H Br-143 C-CsHs OCH3 F F CH ₃ 1-185 C-C4H7 F F H CH ₃ -144 C-C3H5 OCH3 F F OCH3 1-186 C-C4H7 F F H OCH3-145 C-C3H5 CF ₃ H H H 1-187 C-C4H7 F F F H-146 C-C3H5 CF ₃ H H F 1-188 C-C4H7 F F F F-147 C-C3H5 CF ₃ H H CI 1-189 C-C4H7 F F F CI-148 C-C3H5 CF ₃ H H Br 1-190 C-C4H7 F F F Br-149 C-C3H5 CF ₃ H H CH ₃ 1-191 C-C4H7 F F F CH ₃ -150 C-C3H5 CF ₃ H H OCH3 1-192 C-C4H7 F F F OCH3-151 C-C3H5 CF ₃ H F H 1-193 C-C4H7 CI H H H-152 C-C3H5 CF ₃ H F F 1-194 C-C4H7 CI H H F-153 C-C3H5 CF ₃ H F CI 1-195 C-C4H7 CI H H CI-154 C-C3H5 CF ₃ H F Br 1-196 C-C4H7 CI H H Br-155 C-C3H5 CF ₃ H F CH ₃ 1-197 C-C4H7 CI H H CH ₃ -156 C-C3H5 CF ₃ H F OCH3 1-198 C-C4H7 CI H H OCH3-157 C-C3H5 CF ₃ F H H 1-199 C-C4H7 CI H F H-158 C-C3H5 CF ₃ F H F I-200 C-C4H7 CI H F F-159 C-C3H5 CF ₃ F H CI 1-201 C-C4H7 CI H F CI-160 C-C3H5 CF ₃ F H Br I-202 C-C4H7 CI H F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-203 C-C4H7 CI H F CH ₃ I-245 C-C4H7 I H H CHs

1-204 C-C4H7 CI H F OCHs I-246 C-C4H7 I H H OCHs

1-205 C-C4H7 CI F H H I-247 C-C4H7 I H F H

1-206 C-C4H7 CI F H F I-248 C-C4H7 I H F F

1-207 C-C4H7 CI F H CI I-249 C-C4H7 I H F CI

1-208 C-C4H7 CI F H Br I-250 C-C4H7 I H F Br

1-209 C-C4H7 CI F H CHs 1-251 C-C4H7 I H F CHs

1-210 C-C4H7 CI F H OCHs I-252 C-C4H7 I H F OCHs

1-21 1 C-C4H7 CI F F H I-253 C-C4H7 I F H H

1-212 C-C4H7 CI F F F I-254 C-C4H7 I F H F

1-213 C-C4H7 CI F F CI I-255 C-C4H7 I F H CI

1-214 C-C4H7 CI F F Br I-256 C-C4H7 I F H Br

1-215 C-C4H7 CI F F CHs I-257 C-C4H7 I F H CHs

1-216 C-C4H7 CI F F OCHs I-258 C-C4H7 I F H OCHs

1-217 C-C4H7 Br H H H I-259 C-C4H7 I F F H

1-218 C-C4H7 Br H H F I-260 C-C4H7 I F F F

1-219 C-C4H7 Br H H CI 1-261 C-C4H7 I F F CI

I-220 C-C4H7 Br H H Br I-262 C-C4H7 I F F Br

1-221 C-C4H7 Br H H CHs I-263 C-C4H7 I F F CHs

I-222 C-C4H7 Br H H OCHs I-264 C-C4H7 I F F OCHs

I-223 C-C4H7 Br H F H I-265 C-C4H7 CHs H H H

I-224 C-C4H7 Br H F F I-266 C-C4H7 CHs H H F

I-225 C-C4H7 Br H F CI I-267 C-C4H7 CHs H H CI

I-226 C-C4H7 Br H F Br I-268 C-C4H7 CHs H H Br

I-227 C-C4H7 Br H F CHs I-269 C-C4H7 CHs H H CHs

I-228 C-C4H7 Br H F OCHs I-270 C-C4H7 CHs H H OCHs

I-229 C-C4H7 Br F H H 1-271 C-C4H7 CHs H F H

I-230 C-C4H7 Br F H F I-272 C-C4H7 CHs H F F

1-231 C-C4H7 Br F H CI I-273 C-C4H7 CHs H F CI

I-232 C-C4H7 Br F H Br I-274 C-C4H7 CHs H F Br

I-233 C-C4H7 Br F H CHs I-275 C-C4H7 CHs H F CHs

I-234 C-C4H7 Br F H OCHs I-276 C-C4H7 CHs H F OCHs

I-235 C-C4H7 Br F F H I-277 C-C4H7 CHs F H H

I-236 C-C4H7 Br F F F I-278 C-C4H7 CHs F H F

I-237 C-C4H7 Br F F CI I-279 C-C4H7 CHs F H CI

I-238 C-C4H7 Br F F Br I-280 C-C4H7 CHs F H Br

I-239 C-C4H7 Br F F CHs 1-281 C-C4H7 CHs F H CHs

I-240 C-C4H7 Br F F OCHs I-282 C-C4H7 CHs F H OCHs

1-241 C-C4H7 I H H H I-283 C-C4H7 CHs F F H

I-242 C-C4H7 I H H F I-284 C-C4H7 CHs F F F

I-243 C-C4H7 I H H CI I-285 C-C4H7 CHs F F CI

I-244 C-C4H7 I H H Br I-286 C-C4H7 CHs F F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-287 C-C4H7 CH ₃ F F CHs I-329 C-C4H7 CFs F H CHs

1-288 C-C4H7 CHs F F OCHs I-330 C-C4H7 CFs F H OCHs

1-289 C-C4H7 OCHs H H H 1-331 C-C4H7 CFs F F H

1-290 C-C4H7 OCHs H H F I-332 C-C4H7 CFs F F F

1-291 C-C4H7 OCHs H H CI I-333 C-C4H7 CFs F F CI

I-292 C-C4H7 OCHs H H Br I-334 C-C4H7 CFs F F Br

I-293 C-C4H7 OCHs H H CHs I-335 C-C4H7 CFs F F CHs

I-294 C-C4H7 OCHs H H OCHs I-336 C-C4H7 CFs F F OCHs

I-295 C-C4H7 OCHs H F H I-337 C2H5 F H H H

I-296 C-C4H7 OCHs H F F I-338 C2H5 F H H F

I-297 C-C4H7 OCHs H F CI I-339 C2H5 F H H CI

I-298 C-C4H7 OCHs H F Br I-340 C2H5 F H H Br

I-299 C-C4H7 OCHs H F CHs 1-341 C2H5 F H H CHs

I-300 C-C4H7 OCHs H F OCHs I-342 C2H5 F H H OCHs

1-301 C-C4H7 OCHs F H H I-343 C2H5 F H F H

I-302 C-C4H7 OCHs F H F I-344 C2H5 F H F F

I-303 C-C4H7 OCHs F H CI I-345 C2H5 F H F CI

I-304 C-C4H7 OCHs F H Br I-346 C2H5 F H F Br

I-305 C-C4H7 OCHs F H CHs I-347 C2H5 F H F CHs

I-306 C-C4H7 OCHs F H OCHs I-348 C2H5 F H F OCHs

I-307 C-C4H7 OCHs F F H I-349 C2H5 F F H H

I-308 C-C4H7 OCHs F F F I-350 C2H5 F F H F

I-309 C-C4H7 OCHs F F CI 1-351 C2H5 F F H CI

1-310 C-C4H7 OCHs F F Br I-352 C2H5 F F H Br

1-31 1 C-C4H7 OCHs F F CHs I-353 C2H5 F F H CHs

1-312 C-C4H7 OCHs F F OCHs I-354 C2H5 F F H OCHs

1-313 C-C4H7 CFs H H H I-355 C2H5 F F F H

1-314 C-C4H7 CFs H H F I-356 C2H5 F F F F

1-315 C-C4H7 CFs H H CI I-357 C2H5 F F F CI

1-316 C-C4H7 CFs H H Br I-358 C2H5 F F F Br

1-317 C-C4H7 CFs H H CHs I-359 C2H5 F F F CHs

1-318 C-C4H7 CFs H H OCHs I-360 C2H5 F F F OCHs

1-319 C-C4H7 CFs H F H 1-361 C2H5 CI H H H

I-320 C-C4H7 CFs H F F I-362 C2H5 CI H H F

1-321 C-C4H7 CFs H F CI I-363 C2H5 CI H H CI

I-322 C-C4H7 CFs H F Br I-364 C2H5 CI H H Br

I-323 C-C4H7 CFs H F CHs I-365 C2H5 CI H H CHs

I-324 C-C4H7 CFs H F OCHs I-366 C2H5 CI H H OCHs

I-325 C-C4H7 CFs F H H I-367 C2H5 CI H F H

I-326 C-C4H7 CFs F H F I-368 C2H5 CI H F F

I-327 C-C4H7 CFs F H CI I-369 C2H5 CI H F CI

I-328 C-C4H7 CFs F H Br I-370 C2H5 CI H F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-371 C2H5 CI H F CH3 1-413 C2H5 I H H CH3

I-372 C2H5 CI H F OCH3 1-414 C2H5 I H H OCH3

I-373 C2H5 CI F H H 1-415 C2H5 I H F H

I-374 C2H5 CI F H F 1-416 C2H5 I H F F

I-375 C2H5 CI F H CI 1-417 C2H5 I H F CI

I-376 C2H5 CI F H Br 1-418 C2H5 I H F Br

I-377 C2H5 CI F H CH ₃ 1-419 C2H5 I H F CH ₃

I-378 C2H5 CI F H OCH3 I-420 C2H5 I H F OCH3

I-379 C2H5 CI F F H 1-421 C2H5 I F H H

I-380 C2H5 CI F F F I-422 C2H5 I F H F

1-381 C2H5 CI F F CI I-423 C2H5 I F H CI

I-382 C2H5 CI F F Br I-424 C2H5 I F H Br

I-383 C2H5 CI F F CH ₃ I-425 C2H5 I F H CH ₃

I-384 C2H5 CI F F OCH3 I-426 C2H5 I F H OCH3

I-385 C2H5 Br H H H I-427 C2H5 I F F H

I-386 C2H5 Br H H F I-428 C2H5 I F F F

I-387 C2H5 Br H H CI I-429 C2H5 I F F CI

I-388 C2H5 Br H H Br I-430 C2H5 I F F Br

I-389 C2H5 Br H H CH ₃ 1-431 C2H5 I F F CH ₃

I-390 C2H5 Br H H OCH3 I-432 C2H5 I F F OCH3

1-391 C2H5 Br H F H I-433 C2H5 CH ₃ H H H

I-392 C2H5 Br H F F I-434 C2H5 CH ₃ H H F

I-393 C2H5 Br H F CI I-435 C2H5 CH3 H H CI

I-394 C2H5 Br H F Br I-436 C2H5 CH3 H H Br

I-395 C2H5 Br H F CH3 I-437 C2H5 CH3 H H CH3

I-396 C2H5 Br H F OCH3 I-438 C2H5 CH ₃ H H OCH3

I-397 C2H5 Br F H H I-439 C2H5 CH ₃ H F H

I-398 C2H5 Br F H F I-440 C2H5 CH ₃ H F F

I-399 C2H5 Br F H CI 1-441 C2H5 CH ₃ H F CI

I-400 C2H5 Br F H Br I-442 C2H5 CH ₃ H F Br

1-401 C2H5 Br F H CH ₃ I-443 C2H5 CH ₃ H F CH ₃

I-402 C2H5 Br F H OCH3 I-444 C2H5 CH ₃ H F OCH3

I-403 C2H5 Br F F H I-445 C2H5 CH ₃ F H H

I-404 C2H5 Br F F F I-446 C2H5 CH ₃ F H F

I-405 C2H5 Br F F CI I-447 C2H5 CH ₃ F H CI

I-406 C2H5 Br F F Br I-448 C2H5 CH ₃ F H Br

I-407 C2H5 Br F F CH ₃ I-449 C2H5 CH ₃ F H CH ₃

I-408 C2H5 Br F F OCH3 I-450 C2H5 CH ₃ F H OCH3

I-409 C2H5 I H H H 1-451 C2H5 CH ₃ F F H

1-410 C2H5 I H H F I-452 C2H5 CH ₃ F F F

1-41 1 C2H5 I H H CI I-453 C2H5 CH ₃ F F CI

1-412 C2H5 I H H Br I-454 C2H5 CH ₃ F F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-455 C2H5 CH ₃ F F CHs I-497 C2H5 CFs F H CHs

1-456 C2H5 CHs F F OCHs I-498 C2H5 CFs F H OCHs

1-457 C2H5 OCHs H H H I-499 C2H5 CFs F F H

1-458 C2H5 OCHs H H F I-500 C2H5 CFs F F F

1-459 C2H5 OCHs H H CI 1-501 C2H5 CFs F F CI

1-460 C2H5 OCHs H H Br I-502 C2H5 CFs F F Br

1-461 C2H5 OCHs H H CHs I-503 C2H5 CFs F F CHs

I-462 C2H5 OCHs H H OCHs I-504 C2H5 CFs F F OCHs

I-463 C2H5 OCHs H F H I-505 OCHs F H H H

I-464 C2H5 OCHs H F F I-506 OCHs F H H F

I-465 C2H5 OCHs H F CI I-507 OCHs F H H CI

I-466 C2H5 OCHs H F Br I-508 OCHs F H H Br

I-467 C2H5 OCHs H F CHs I-509 OCHs F H H CHs

I-468 C2H5 OCHs H F OCHs 1-510 OCHs F H H OCHs

I-469 C2H5 OCHs F H H 1-51 1 OCHs F H F H

I-470 C2H5 OCHs F H F 1-512 OCHs F H F F

1-471 C2H5 OCHs F H CI 1-513 OCHs F H F CI

I-472 C2H5 OCHs F H Br 1-514 OCHs F H F Br

I-473 C2H5 OCHs F H CHs 1-515 OCHs F H F CHs

I-474 C2H5 OCHs F H OCHs 1-516 OCHs F H F OCHs

I-475 C2H5 OCHs F F H 1-517 OCHs F F H H

I-476 C2H5 OCHs F F F 1-518 OCHs F F H F

I-477 C2H5 OCHs F F CI 1-519 OCHs F F H CI

I-478 C2H5 OCHs F F Br I-520 OCHs F F H Br

I-479 C2H5 OCHs F F CHs 1-521 OCHs F F H CHs

I-480 C2H5 OCHs F F OCHs I-522 OCHs F F H OCHs

1-481 C2H5 CFs H H H I-523 OCHs F F F H

I-482 C2H5 CFs H H F I-524 OCHs F F F F

I-483 C2H5 CFs H H CI I-525 OCHs F F F CI

I-484 C2H5 CFs H H Br I-526 OCHs F F F Br

I-485 C2H5 CFs H H CHs I-527 OCHs F F F CHs

I-486 C2H5 CFs H H OCHs I-528 OCHs F F F OCHs

I-487 C2H5 CFs H F H I-529 OCHs CI H H H

I-488 C2H5 CFs H F F I-530 OCHs CI H H F

I-489 C2H5 CFs H F CI 1-531 OCHs CI H H CI

I-490 C2H5 CFs H F Br I-532 OCHs CI H H Br

1-491 C2H5 CFs H F CHs I-533 OCHs CI H H CHs

I-492 C2H5 CFs H F OCHs I-534 OCHs CI H H OCHs

I-493 C2H5 CFs F H H I-535 OCHs CI H F H

I-494 C2H5 CFs F H F I-536 OCHs CI H F F

I-495 C2H5 CFs F H CI I-537 OCHs CI H F CI

I-496 C2H5 CFs F H Br I-538 OCHs CI H F Br No. R ¹ R ³ R ⁵ R ⁶ R ⁷ No. R R ³ R ⁵ R ⁶ R ⁷

1-539 OCHs CI H F CHs 1-581 OCHs I H H CHs

1-540 OCHs CI H F OCHs I-582 OCHs I H H OCHs

1-541 OCHs CI F H H I-583 OCHs I H F H

I-542 OCHs CI F H F I-584 OCHs I H F F

I-543 OCHs CI F H CI I-585 OCHs I H F CI

I-544 OCHs CI F H Br I-586 OCHs I H F Br

I-545 OCHs CI F H CHs I-587 OCHs I H F CHs

I-546 OCHs CI F H OCHs I-588 OCHs I H F OCHs

I-547 OCHs CI F F H I-589 OCHs I F H H

I-548 OCHs CI F F F I-590 OCHs I F H F

I-549 OCHs CI F F CI 1-591 OCHs I F H CI

I-550 OCHs CI F F Br I-592 OCHs I F H Br

1-551 OCHs CI F F CHs I-593 OCHs I F H CHs

I-552 OCHs CI F F OCHs I-594 OCHs I F H OCHs

I-553 OCHs Br H H H I-595 OCHs I F F H

I-554 OCHs Br H H F I-596 OCHs I F F F

I-555 OCHs Br H H CI I-597 OCHs I F F CI

I-556 OCHs Br H H Br I-598 OCHs I F F Br

I-557 OCHs Br H H CHs I-599 OCHs I F F CHs

I-558 OCHs Br H H OCHs I-600 OCHs I F F OCHs

I-559 OCHs Br H F H 1-601 OCHs CHs H H H

I-560 OCHs Br H F F I-602 OCHs CHs H H F

1-561 OCHs Br H F CI I-603 OCHs CHs H H CI

I-562 OCHs Br H F Br I-604 OCHs CHs H H Br

I-563 OCHs Br H F CHs I-605 OCHs CHs H H CHs

I-564 OCHs Br H F OCHs I-606 OCHs CHs H H OCHs

I-565 OCHs Br F H H I-607 OCHs CHs H F H

I-566 OCHs Br F H F I-608 OCHs CHs H F F

I-567 OCHs Br F H CI I-609 OCHs CHs H F CI

I-568 OCHs Br F H Br 1-610 OCHs CHs H F Br

I-569 OCHs Br F H CHs 1-61 1 OCHs CHs H F CHs

I-570 OCHs Br F H OCHs 1-612 OCHs CHs H F OCHs

1-571 OCHs Br F F H 1-613 OCHs CHs F H H

I-572 OCHs Br F F F 1-614 OCHs CHs F H F

I-573 OCHs Br F F CI 1-615 OCHs CHs F H CI

I-574 OCHs Br F F Br 1-616 OCHs CHs F H Br

I-575 OCHs Br F F CHs 1-617 OCHs CHs F H CHs

I-576 OCHs Br F F OCHs 1-618 OCHs CHs F H OCHs

I-577 OCHs I H H H 1-619 OCHs CHs F F H

I-578 OCHs I H H F I-620 OCHs CHs F F F

I-579 OCHs I H H CI 1-621 OCHs CHs F F CI

I-580 OCHs I H H Br I-622 OCHs CHs F F Br No. R R ³ R ⁵ R ⁶ R ⁷

I-665 OCHs CFs F H CHs

I-666 OCHs CFs F H OCHs

I-667 OCHs CFs F F H

I-668 OCHs CFs F F F

I-669 OCHs CFs F F CI

I-670 OCHs CFs F F Br

1-671 OCHs CFs F F CHs

I-672 OCHs CFs F F OCHs

The specific number for each single compound is deductible as follows:

Compound 1.1 .1-3 e.g. comprises the compound of formula 1.1 from Table 1 and line I-3 from Table A; To widen the spectrum of action and to achieve synergistic effects, the pyrimidine compounds of formula (I) may be mixed with a large number of representatives of other herbicidal or growth- regulating active ingredient groups and then applied concomitantly. Suitable components for mixtures are, e.g., herbicides from the classes of the acetamides, amides, aryloxyphenoxypro- pionates, benzamides, benzofuran, benzoic acids, benzothiadiazinones, bipyridylium, carbama- tes, chloroacetamides, chlorocarboxylic acids, cyclohexanediones, dinitroanilines, dinitrophenol, diphenyl ether, glycines, imidazolinones, isoxazoles, isoxazolidinones, nitriles, N-phenylphthal- imides, oxadiazoles, oxazolidinediones, oxyacetamides, phenoxycarboxylic acids, phenylcarba- mates, phenylpyrazoles, phenylpyrazolines, phenylpyridazines, phosphinic acids, phosphoro- amidates, phosphorodithioates, phthalamates, pyrazoles, pyridazinones, pyridines, pyridinecar- boxylic acids, pyridinecarboxamides, pyrimidinediones, pyrimidinyl(thio)benzoates, quinolinecar- boxylic acids, semicarbazones, sulfonylaminocarbonyltriazolinones, sulfonylureas, tetrazoli- nones, thiadiazoles, thiocarbamates, triazines, triazinones, triazoles, triazolinones, triazolo- carboxamides, triazolopyrimidines, triketones, uracils, or ureas.

It may furthermore be beneficial to apply the pyrimidine compounds of formula (I) alone or in combination with other herbicides, or else in the form of a mixture with other crop protection agents, e.g. together with agents for controlling pests or phytopathogenic fungi or bacteria. Also of interest is the miscibility with mineral salt solutions, which are employed for treating nutritional and trace element deficiencies. Other additives such as non-phytotoxic oils and oil concentrates may also be added.

In one embodiment of the present invention the compositions according to the present invention comprise at least one pyrimidine compound of formula (I) (compound A) and at least one further active compound selected from herbicides B, preferably herbicides B of class b1 ) to b15), and safeners C (compound C).

In a preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I. A) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.B) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.C) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of for- mula (I.D) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.E) (corresponds to pyrimidine compound of formula (I)), as defined herein; In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.F) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active com- pound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.G) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.H) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of formula (I.I) (corresponds to pyrimidine compound of formula (I)), as defined herein;

In another preferred embodiment of the invention, the composition comprises as active compound A or component A at least one, preferably exactly one, pyrimidine compound of for- mula (I.J) (corresponds to pyrimidine compound of formula (I)), as defined herein;

Preferred compounds of the formula (I) which, as component A, are constituent of the composition according to the invention are the compounds I .A to I.J, as defined above;

In another embodiment of the present invention the compositions according to the present invention comprise at least one pyrimidine compound of formula (I) and at least one further active compound B (herbicide B).

The further herbicidal compound B (component B) is preferably selected from the herbicides of class b1 ) to b15):

Mixing partners for the composition can be selected from below herbicides B as defined below: B) herbicides of class b1 ) to b15):

b1 ) lipid biosynthesis inhibitors;

b2) acetolactate synthase inhibitors (ALS inhibitors);

b3) photosynthesis inhibitors;

b4) protoporphyrinogen-IX oxidase inhibitors (PPO inhibitors);

b5) bleacher herbicides;

b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSP inhibitors);

b7) glutamine synthetase inhibitors;

b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors);

b9) mitosis inhibitors;

b10) inhibitors of the synthesis of very long chain fatty acids (VLCFA inhibitors);

b1 1 ) cellulose biosynthesis inhibitors;

b12) decoupler herbicides;

b13) auxinic herbicides;

b14) auxin transport inhibitors; and

b15) other herbicides selected from the group consisting of bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin, cumyluron, dalapon, dazomet, difenzoquat, difenzoquat- metilsulfate, dimethipin, DSMA, dymron, endothal and its salts, etobenzanid, flamprop, flam- prop-isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol, flurenol- butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan, indaziflam, maleic hydrazide, mefluidide, metam, methiozolin (CAS 403640-27-7), methyl azide, methyl bromide, methyl-dym- ron, methyl iodide, MSMA, oleic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinocla- mine, triaziflam, tridiphane and 6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (CAS 499223-49-3) and its salts and esters;

including their agriculturally acceptable salts or derivatives;

In one embodiment of the invention, the compositions contain at least one inhibitor of the lipid biosynthesis (herbicide b1 ). These compounds inhibit lipid biosynthesis. Inhibition of the lipid biosynthesis can be affected either through inhibition of acetylCoA carboxylase (hereinafter- termed ACCase herbicides) or through a different mode of action (hereinafter termed non-AC- Case herbicides). The ACCase herbicides belong to the group A of the HRAC classification system whereas the non-ACCase herbicides belong to the group N of the HRAC classification.

In another embodiment of the invention, the compositions contain at least one ALS inhibitor (herbicide b2). The herbicidal activity of these compounds is based on the inhibition of acetolac- tate synthase and thus on the inhibition of the branched chain amino acid biosynthesis. These inhibitors belong to the group B of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one inhibitor of photosynthesis (herbicide b3). The herbicidal activity of these compounds is based either on the inhibition of the photosystem II in plants (so-called PSIl inhibitors, groups C1 , C2 and C3 of HRAC classification) or on diverting the electron transfer in photosystem I in plants (so-called PSI in- hibitors, group D of HRAC classification) and thus on an inhibition of photosynthesis. Amongst these, PSIl inhibitors are preferred.

In another embodiment of the invention, the compositions contain at least one inhibitor of pro- toporphyrinogen-IX-oxidase (herbicide b4). The herbicidal activity of these compounds is based on the inhibition of the protoporphyrinogen-IX-oxidase. These inhibitors belong to the group E of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one bleacher-herbicide (herbicide b5). The herbicidal activity of these compounds is based on the inhibition of the carotenoid biosynthesis. These include compounds which inhibit carotenoid biosynthesis by inhibition of phytoene desaturase (so-called PDS inhibitors, group F1 of HRAC classification), compounds that inhibit the 4-hydroxyphenylpyruvate-dioxygenase (HPPD inhibitors, group F2 of HRAC classification), compounds that inhibit DOXsynthase (group F4 of HRAC class) and compounds which inhibit carotenoid biosynthesis by an unknown mode of action (bleacher - unknown target, group F3 of HRAC classification).

In another embodiment of the invention, the compositions contain at least one EPSP synthase inhibitor (herbicide b6). The herbicidal activity of these compounds is based on the inhibition of enolpyruvyl shikimate 3-phosphate synthase, and thus on the inhibition of the amino acid biosynthesis in plants. These inhibitors belong to the group G of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one glutamine synthetase inhibitor (herbicide b7). The herbicidal activity of these compounds is based on the inhi- bition of glutamine synthetase, and thus on the inhibition of the aminoacid biosynthesis in plants. These inhibitors belong to the group H of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one DHP synthase inhibitor (herbicide b8). The herbicidal activity of these compounds is based on the inhibition of 7,8-dihydropteroate synthase. These inhibitors belong to the group I of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one mitosis inhibitor (herbicide b9). The herbicidal activity of these compounds is based on the disturbance or inhibi- tion of microtubule formation or organization, and thus on the inhibition of mitosis. These inhibitors belong to the groups K1 and K2 of the HRAC classification system. Among these, compounds of the group K1 , in particular dinitroanilines, are preferred.

In another embodiment of the invention, the compositions contain at least one VLCFA inhibitor (herbicide b10). The herbicidal activity of these compounds is based on the inhibition of the syn- thesis of very long chain fatty acids and thus on the disturbance or inhibition of cell division in plants. These inhibitors belong to the group K3 of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one cellulose biosynthesis inhibitor (herbicide b1 1 ). The herbicidal activity of these compounds is based on the inhibition of the biosynthesis of cellulose and thus on the inhibition of the synthesis of cell walls in plants. These inhibitors belong to the group L of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one decoupler herbicide (herbicide b12). The herbicidal activity of these compounds is based on the disruption of the cell membrane. These inhibitors belong to the group M of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one auxinic herbi- cide (herbicide b13). These include compounds that mimic auxins, i.e. plant hormones, and affect the growth of the plants. These compounds belong to the group O of the HRAC classification system.

In another embodiment of the invention, the compositions contain at least one auxin transport inhibitor (herbicide b14). The herbicidal activity of these compounds is based on the inhibition of the auxin transport in plants. These compounds belong to the group P of the HRAC classification system.

As to the given mechanisms of action and classification of the active substances, see e.g. "HRAC, Classification of Herbicides According to Mode of Action", http://www.plantprot.ec- tion.org/hrac/MOA.html).

Preference is given to those compositions according to the present invention comprising at least one herbicide B selected from herbicides of class b1 , b2, b3, b4, b5, b6, b9, b10, b13, and b14.

Specific preference is given to those compositions according to the present invention which comprise at least one herbicide B selected from the herbicides of class b1 , b2, b4, b5, b9, b10, b13, and b14.

Particular preference is given to those compositions according to the present invention which comprise at least one herbicide B selected from the herbicides of class b1 , b2, b4, b5, b9, b10, and b13

Examples of herbicides B which can be used in combination with the compound of formula (I) according to the present invention are:

b1 ) from the group of the lipid biosynthesis inhibitors:

ACC-herbicides such as alloxydim, alloxydim-sodium, butroxydim, clethodim, clodinafop, clodinafop-propargyl, cycloxydim, cyhalofop, cyhalofop-butyl, diclofop, diclofop-methyl, fenoxa- prop, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fluazifop, fluazifop-butyl, fluazifop-P, fluazifop-P-butyl, haloxyfop, haloxyfop-methyl, haloxyfop-P, haloxyfop-P-methyl, metamifop, pi- noxaden, profoxydim, propaquizafop, quizalofop, quizalofop-ethyl, quizalofop-tefuryl, quizalofop- P, quizalofop-P-ethyl, quizalofop-P-tefuryl, sethoxydim, tepraloxydim, tralkoxydim,

4-(4'-Chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-py- ran-3(6H)-one (CAS 1312337-72-6); 4-(2',4'-Dichloro-4-cyclopropyl[1 ,1 '-biphenyl]-3-yl)-5-hy- droxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one (CAS 1312337-45-3); 4-(4'-Chloro-4-ethyl-2'-flu- oro[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6 H)-one (CAS 1033757-93-5); 4-(2',4'-Dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-di one (CAS 1312340-84-3); 5-(Acetyloxy)-4-(4'-chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6- dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one (CAS 1312337-48-6); 5-(Acetyloxy)-4-(2 ^' ,4'-di- chloro-4-cyclopropyl- [1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3 -one; 5- (Acetyloxy)-4-(4'-chloro-4-ethyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H- pyran-3-one (CAS 1312340-82-1 ); 5-(Acetyloxy)-4-(2',4'-dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-3,6- dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one (CAS 1033760-55-2); 4-(4'-Chloro-4-cyclopropyl-2'- fluoro[1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-p yran-3-yl carbonic acid methyl ester (CAS 1312337-51 -1 ); 4-(2 ^' ,4'-Dichloro -4-cyclopropyl- [1 ,1 '-biphenyl]-3-yl)-5,6-dihydro- 2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester; 4-(4'-Chloro-4-ethyl-2'-flu- oro[1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-p yran-3-yl carbonic acid methyl ester (CAS 1312340-83-2); 4-(2',4'-Dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6- tetramethyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester (CAS 1033760-58-5); and non ACC herbicides such as benfuresate, butylate, cycloate, dalapon, dimepiperate, EPTC, esprocarb, ethofumesate, flupropanate, molinate, orbencarb, pebulate, prosulfocarb, TCA, thiobencarb, tio- carbazil, triallate and vernolate;

b2) from the group of the ALS inhibitors:

sulfonylureas such as amidosulfuron, azimsulfuron, bensulfuron, bensulfuron-methyl, chlo- rimuron, chlorimuron-ethyl, chlorsulfuron, cinosulfuron, cyclosulfamuron, ethametsulfuron, ethametsulfuron-methyl, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, flupyrsul- furon-methyl-sodium, foramsulfuron, halosulfuron, halosulfuron-methyl, imazosulfuron, iodosul- furon, iodosulfuron-methyl-sodium, iofensulfuron, iofensulfuron-sodium, mesosulfuron, met- azosulfuron, metsulfuron, metsulfuron-methyl, nicosulfuron, orthosulfamuron, oxasulfuron, primi- sulfuron, primisulfuron-methyl, propyrisulfuron, prosulfuron, pyrazosulfuron, pyrazosulfuron- ethyl, rimsulfuron, sulfometuron, sulfometuron-methyl, sulfosulfuron, thifensulfuron, thifensulfu- ron-methyl, triasulfuron, tribenuron, tribenuron-methyl, trifloxysulfuron, triflusulfuron, triflusulfu- ron-methyl and tritosulfuron,

imidazolinones such as imazamethabenz, imazamethabenz-methyl, imazamox, imazapic, ima- zapyr, imazaquin and imazethapyr, triazolopyrimidine herbicides and sulfonanilides such as cloransulam, cloransulam-methyl, diclosulam, flumetsulam, florasulam, metosulam, penoxsu- lam, pyrimisulfan and pyroxsulam,

pyrimidinylbenzoates such as bispyribac, bispyribac-sodium, pyribenzoxim, pyriftalid, pyrimino- bac, pyriminobac-methyl, pyrithiobac, pyrithiobac-sodium, 4-[[[2-[(4,6-dimethoxy-2-pyrimidi- nyl)oxy]phenyl]methyl]amino]-benzoic acid-1-methylethyl ester (CAS 420138-41 -6), 4-[[[2-[(4,6- dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoic acid propyl ester (CAS 420138-40- 5), N-(4-bromophenyl)-2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzen emethanamine (CAS

420138-01 -8), sulfonylaminocarbonyl-triazolinone herbicides such as flucarbazone, flucarbazone-sodium, propoxycarbazone, propoxycarbazone-sodium, thiencarbazone and thiencarbazone-methyl; and triafamone;

among these, a preferred embodiment of the invention relates to those compositions compris- ing at least one imidazolinone herbicide;

b3) from the group of the photosynthesis inhibitors:

amicarbazone, inhibitors of the photosystem II, e.g. 1 -(6-tert-butylpyrimidin-4-yl)-2-hydroxy-4- methoxy-3-methyl-2H-pyrrol-5-one (CAS 1654744-66-7), 1-(5-tert-butylisoxazol-3-yl)-2-hydroxy- 4-methoxy-3-methyl-2H-pyrrol-5-one (CAS 1637455-12-9), 1 -(5-tert-butylisoxazol-3-yl)-4-chloro- 2-hydroxy-3-methyl-2H-pyrrol-5-one (CAS 1637453-94-1 ), 1-(5-tert-butyl-1 -methyl-pyrazol-3-yl)- 4-chloro-2-hydroxy-3-methyl-2H-pyrrol-5-one (CAS 1654057-29-0), 1-(5-tert-butyl-1 -methyl-py- razol-3-yl)-3-chloro-2-hydroxy-4-methyl-2H-pyrrol-5-one (CAS 1654747-80-4), 4-hydroxy-1-me- thoxy-5-methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin -2-one; (CAS 2023785-78-4), 4-hy- droxy-1 ,5-dimethyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2- one (CAS 2023785-79-5), 5- ethoxy-4-hydroxy-1 -methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2-one (CAS 1701416-69- 4), 4-hydroxy-1 -methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2-one (CAS 1708087-22-2), 4-hydroxy-1 ,5-dimethyl-3-[1 -methyl-5-(trifluoromethyl)pyrazol-3-yl]imidazolidin-2-one (CAS 2023785-80-8), 1-(5-tert-butylisoxazol-3-yl)-4-ethoxy-5-hydroxy-3-methyl-im idazolidin-2-one (CAS 1844836-64-1 ), triazine herbicides, including of chlorotriazine, triazinones, triazindiones, methylthiotriazines and pyridazinones such as ametryn, atrazine, chloridazone, cyanazine, des- metryn, dimethametryn,hexazinone, metribuzin, prometon, prometryn, propazine, simazine, sim- etryn, terbumeton, terbuthylazin, terbutryn and trietazin, aryl urea such as chlorobromuron, chlo- rotoluron, chloroxuron, dimefuron, diuron, fluometuron, isoproturon, isouron, linuron, metam- itron, methabenzthiazuron, metobenzuron, metoxuron, monolinuron, neburon, siduron, tebuthi- uron and thiadiazuron, phenyl carbamates such as desmedipham, karbutilat, phenmedipham, phenmedipham-ethyl, nitrile herbicides such as bromofenoxim, bromoxynil and its salts and esters, ioxynil and its salts and esters, uraciles such as bromacil, lenacil and terbacil, and benta- zon and bentazon-sodium, pyridate, pyridafol, pentanochlor and propanil and inhibitors of the photosystem I such as diquat, diquat-dibromide, paraquat, paraquat-dichloride and paraquat- dimetilsulfate. Among these, a preferred embodiment of the invention relates to those compositions comprising at least one aryl urea herbicide. Among these, likewise a preferred embodiment of the invention relates to those compositions comprising at least one triazine herbicide. Among these, likewise a preferred embodiment of the invention relates to those compositions comprising at least one nitrile herbicide;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen, acifluorfen-sodium, azafenidin, bencarbazone, benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl, chlomethoxyfen, chlorphthalim, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl, flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen, fluorogly- cofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen, halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone, profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfen- trazone, thidiazimin, tiafenacil, trifludimoxazin, ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoro- methyl-2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetat e (CAS 353292- 31-6; S-3100), N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1 A -pyrazole-1 -car- boxamide (CAS 452098-92-9), N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenox y)-5- methyl-1 pyrazole-1-carboxamide (CAS 915396-43-9), N-ethyl-3-(2-chloro-6-fluoro-4-trifluoro- methylphenoxy)-5-methyl-1 A -pyrazole-1-carboxamide (CAS 452099-05-7), N-tetrahydrofurfuryl- 3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1 A -pyrazole-1-carboxamide (CAS 452100-03-7), 3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1 ,4]oxazin-6-yl]-1 ,5-dime- thyl-6-thioxo-[1 ,3,5]triazinan-2,4-dione (CAS 451484-50-7), 2-(2,2,7-trifluoro-3-oxo-4-prop-2- ynyl-3,4-dihydro-2H-benzo[1 ,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1 ,3-dione (CAS

13001 18-96-0), 1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2 -ynyl-3,4-dihydro-2H- benzo[1 ,4]oxazin-6-yl)-1 H-pyrimidine-2,4-dione (CAS 13041 13-05-0), methyl (£)-4-[2-chloro-5- [4-chloro-5-(difluoromethoxy)-1 A -methyl-pyrazol-3-yl]-4-fluoro-phenoxy]-3-methoxy-but-2-eno- ate (CAS 948893-00-3), and 3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1 H-benzimidazol-4-yl]-1-me- thyl-6-(trifluoromethyl)-1 H-pyrimidine-2,4-dione (CAS 212754-02-4);

b5) from the group of the bleacher herbicides:

PDS inhibitors: beflubutamid, diflufenican, fluridone, flurochloridone, flurtamone, norflurazon, picolinafen, and 4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyri midine (CAS 180608-33-7), HPPD inhibitors: benzobicyclon, benzofenap, bicyclopyrone, clomazone, fenquinotrione, isoxaflutole, mesotrione, oxotrione (CAS 1486617-21 -3), pyrasulfotole, pyrazol- ynate, pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione, tolpyralate, topramezone , bleacher, unknown target: aclonifen, amitrole flumeturon,2-chloro-3-methylsulfanyl-N-(1-methyltetrazol-5- yl)-4-(trifluoromethyl)benzamide (CAS 1361 139-71 -0), 2-(2,4-dichlorophenyl)methyl-4,4-dime- thyl-3-isoxazolidone (CAS 81777-95-9) and 2-(2,5-dichlorophenyl)methyl-4,4-dimethyl-3-isoxa- zolidinone (CAS 81778-66-7);

b6) from the group of the EPSP synthase inhibitors: glyphosate, glyphosate-isopropylammo- nium, glyposate-potassium and glyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors: bilanaphos (bialaphos), bilanaphos- sodium, glufosinate, glufosinate-P and glufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors: asulam;

b9) from the group of the mitosis inhibitors:

compounds of group K1 : dinitroanilines such as benfluralin, butralin, dinitramine, ethalfluralin, fluchloralin, oryzalin, pendimethalin, prodiamine and trifluralin, phosphoramidates such as ami- prophos, amiprophos-methyl, and butamiphos, benzoic acid herbicides such as chlorthal, chlor- thal-dimethyl, pyridines such as dithiopyr and thiazopyr, benzamides such as propyzamide and tebutam; compounds of group K2: carbetamide, chlorpropham, flamprop, flamprop-isopropyl, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl and propham ; among these, compounds of group K1 , in particular dinitroanilines are preferred;

b10) from the group of the VLCFA inhibitors:

chloroacetamides such as acetochlor, alachlor, amidochlor, butachlor, dimethachlor, dimethe- namid, dimethenamid-P, metazachlor, metolachlor, metolachlor-S, pethoxamid, pretilachlor, propachlor, propisochlor and thenylchlor, oxyacetanilides such as flufenacet and mefenacet, ac- etanilides such as diphenamid, naproanilide, napropamide and napropamide-M, tetrazolinones such fentrazamide, and other herbicides such as anilofos, cafenstrole, fenoxasulfone, ipfen- carbazone, piperophos, pyroxasulfone and isoxazoline compounds of the formulae 11.1 , II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9

the isoxazoline compounds are known in the art, e.g. from WO 2006/024820, WO

2006/037945, WO 2007/071900 and WO 2007/096576;

among the VLCFA inhibitors, preference is given to chloroacetamides and oxyacetamides; b1 1 ) from the group of the cellulose biosynthesis inhibitors: chlorthiamid, dichlobenil, flupoxam, indaziflam, isoxaben, triaziflam and 1 -cyclohexyl-5-pentafluorphenyloxy-1 ⁴ - [1 ,2,4,6]thiatriazin-3-ylamine (CAS 175899-01 -1 );

b12) from the group of the decoupler herbicides: dinoseb, dinoterb and DNOC and its salts; b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters such as clacyfos, 2,4-DB and its salts and esters, aminocyclopy- rachlor and its salts and esters, aminopyralid and its salts such as aminopyralid-dimethylammo- nium, aminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin, benazolin-ethyl, chloramben and its salts and esters, clomeprop, clopyralid and its salts and esters, dicamba and its salts and esters, dichlorprop and its salts and esters, dichlorprop-P and its salts and esters, flopyrauxifen, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, halauxifen and its salts and esters (CAS 943832-60-8); MCPA and its salts and esters, MCPA-thioethyl, MCPB and its salts and esters, mecoprop and its salts and esters, mecoprop-P and its salts and esters, picloram and its salts and esters, quinclorac, quinmerac, TBA (2,3,6) and its salts and esters, triclopyr and its salts and esters, florpyrauxifen, florpyrauxifen-benzyl (CAS 1390661-72-9) and 4-amino- 3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)picolinic acid (CAS 1629965-65-6);

b14) from the group of the auxin transport inhibitors: diflufenzopyr, diflufenzopyr-sodium, nap- talam and naptalam-sodium;

b15) from the group of the other herbicides: bromobutide, chlorflurenol, chlorflurenol-methyl, cinmethylin, cumyluron, cyclopyrimorate (CAS 499223-49-3 and its salts and esters, dalapon, dazomet, difenzoquat, difenzoquat-metilsulfate, dimethipin, DSMA, dymron, endothal and its salts, etobenzanid, flurenol, flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, inda- nofan, maleic hydrazide, mefluidide, metam, methiozolin (CAS 403640-27-7), methyl azide, methyl bromide, methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone, pelargonic acid, pyributicarb, quinoclamine and tridiphane.

Preferred herbicides B that can be used in combination with the pyrimidine compounds of the formula (I) according to the present invention are:

b1 ) from the group of the lipid biosynthesis inhibitors:

clethodim, clodinafop-propargyl, cycloxydim, cyhalofop-butyl, diclofop-methyl, fenoxaprop-P- ethyl, fluazifop-P-butyl, haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop, quizalofop-P-ethyl, quizalofop-P-tefuryl, sethoxydim, tepraloxydim, tralkoxydim, 4-(4'-Chloro-4- cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6 H)-one

(CAS 1312337-72-6); 4-(2',4'-Dichloro-4-cyclopropyl[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetra- methyl-2H-pyran-3(6H)-one (CAS 1312337-45-3); 4-(4'-Chloro-4-ethyl-2'-fluoro[1 ,1 '-biphenyl]-3- yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one (CAS 1033757-93-5); 4-(2',4'-Dichloro-4- ethyl[1 ,1 '-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-di one (CAS 1312340-84-3); 5-(Acetyloxy)-4-(4'-chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetra- methyl-2H-pyran-3-one (CAS 1312337-48-6); 5-(Acetyloxy)-4-(2 ^' ,4'-dichloro-4-cyclopropyl- [1 ,1 '- biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-o ne; 5-(Acetyloxy)-4-(4'-chloro-4- ethyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3 -one (CAS

1312340-82-1 ); 5-(Acetyloxy)-4-(2',4'-dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6- tetramethyl-2H-pyran-3-one (CAS 1033760-55-2); 4-(4'-Chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-bi- phenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran -3-yl carbonic acid methyl ester (CAS 1312337-51-1 ); 4-(2 ^' ,4'-Dichloro -4-cyclopropyl- [1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6- tetramethyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester; 4-(4'-Chloro-4-ethyl-2'-fluoro[1 ,1 '- biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyr an-3-yl carbonic acid methyl ester (CAS 1312340-83-2); 4-(2',4'-Dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetrame- thyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester (CAS 1033760-58-5); benfuresate, dimepiperate, EPTC, esprocarb, ethofumesate, molinate, orbencarb, prosulfocarb, thiobencarb and triallate;

b2) from the group of the ALS inhibitors:

amidosulfuron, azimsulfuron, bensulfuron-methyl, bispyribac-sodium, chlorimuron-ethyl, chlor- sulfuron, cloransulam-methyl, cyclosulfamuron, diclosulam, ethametsulfuron-methyl, ethoxysul- furon, flazasulfuron, florasulam, flucarbazone-sodium, flucetosulfuron, flumetsulam, flupyrsulfu- ron-methyl-sodium, foramsulfuron, halosulfuron-methyl, imazamethabenz-methyl, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl- sodium, iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron, metosulam, met- sulfuron-methyl, nicosulfuron, orthosulfamuron, oxasulfuron, penoxsulam, primisulfuron-methyl, propoxycarbazon-sodium, propyrisulfuron, prosulfuron, pyrazosulfuron-ethyl, pyribenzoxim, py- rimisulfan, pyriftalid, pyriminobac-methyl, pyrithiobac-sodium, pyroxsulam, rimsulfuron, sulfome- turon-methyl, sulfosulfuron, thiencarbazone-methyl, thifensulfuron-methyl, triasulfuron, tribenu- ron-methyl, trifloxysulfuron, triflusulfuron-methyl, tritosulfuron and triafamone;

b3) from the group of the photosynthesis inhibitors:

ametryn, amicarbazone, atrazine, bentazone, bentazone-sodium, bromoxynil and its salts and esters, chloridazone, chlorotoluron, cyanazine, desmedipham, diquat-dibromide, diuron, fluome- turon, hexazinone, ioxynil and its salts and esters, isoproturon, lenacil, linuron, metamitron, methabenzthiazuron, metribuzin, paraquat, paraquat-dichloride, phenmedipham, propanil, pyri- date, simazine, terbutryn, terbuthylazine, thidiazuron, 1-(6-tert-butylpyrimidin-4-yl)-2-hydroxy-4- methoxy-3-methyl-2H-pyrrol-5-one (CAS 1654744-66-7), 1-(5-tert-butylisoxazol-3-yl)-2-hydroxy- 4-methoxy-3-methyl-2H-pyrrol-5-one (CAS 1637455-12-9), 1 -(5-tert-butylisoxazol-3-yl)-4-chloro- 2-hydroxy-3-methyl-2H-pyrrol-5-one (CAS 1637453-94-1 ), 1-(5-tert-butyl-1 -methyl-pyrazol-3-yl)- 4-chloro-2-hydroxy-3-methyl-2H-pyrrol-5-one (CAS 1654057-29-0), 1-(5-tert-butyl-1 -methyl-py- razol-3-yl)-3-chloro-2-hydroxy-4-methyl-2H-pyrrol-5-one (CAS 1654747-80-4), 4-hydroxy-1 - methoxy-5-methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolid in-2-one; (CAS 2023785-78-4), 4- hydroxy-1 ,5-dimethyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2- one (CAS 2023785-79-5), 5- ethoxy-4-hydroxy-1 -methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2-one (CAS 1701416-69- 4), 4-hydroxy-1 -methyl-3-[4-(trifluoromethyl)-2-pyridyl]imidazolidin-2-one (CAS 1708087-22-2), 4-hydroxy-1 ,5-dimethyl-3-[1 -methyl-5-(trifluoromethyl)pyrazol-3-yl]imidazolidin-2-one (CAS 2023785-80-8) and 1 -(5-tert-butylisoxazol-3-yl)-4-ethoxy-5-hydroxy-3-methyl-imi dazolidin-2-one (CAS 1844836-64-1 );

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen-sodium, bencarbazone, benzfendizone, butafenacil, carfentrazone-ethyl, cinidon- ethyl, flufenpyr-ethyl, flumiclorac-pentyl, flumioxazin, fluoroglycofen-ethyl, fomesafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone, pyraflufen, pyraflufen-ethyl, saflufenacil, sul- fentrazone, tiafenacil, trifludimoxazin, ethyl [3-[2-chloro-4-fluoro-5-(1 -methyl-6-trifluoromethyl- 2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetat e (CAS 353292-31 -6; S- 3100), N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1 A -pyrazole-1 -carboxamide (CAS 452098-92-9), N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenox y)-5-methyl-1 H- pyrazole-1-carboxamide (CAS 915396-43-9), N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphe- noxy)-5-methyl-1 A -pyrazole-1 -carboxamide (CAS 452099-05-7), N-tetrahydrofurfuryl-3-(2-chlo- ro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1 A -pyrazole-1-carboxamide (CAS 452100-03-7), 3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1 ,4]oxazin-6-yl]-1 ,5-dimethyl-6-thioxo- [1 ,3,5]triazinan-2,4-dione (CAS 451484-50-7), 2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihy- dro-2H-benzo[1 ,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1 ,3-dione (CAS 13001 18-96-0); 1 - methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-y nyl-3,4-dihydro-2H-benzo[1 ,4]oxazin- 6-yl)-1 H-pyrimidine-2,4-dione (CAS 13041 13-05-0), and 3-[7-chloro-5-fluoro-2-(trifluoromethyl)- 1 H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1 H-pyrimidine-2,4-dione (CAS 212754-02-4); b5) from the group of the bleacher herbicides:

aclonifen, amitrole, beflubutamid, benzobicyclon, bicyclopyrone, clomazone, diflufenican, fenquinotrione, flumeturon, flurochloridone, flurtamone, isoxaflutole, mesotrione, oxotrione (CAS 1486617-21-3), norflurazon, picolinafen, pyrasulfotole, pyrazolynate, sulcotrione, tefuryltrione, tembotrione, tolpyralate, topramezone, 4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)- pyrimidine (CAS 180608-33-7), 2-chloro-3-methylsulfanyl-N-(1 -methyltetrazol-5-yl)-4-(trifluoro- methyl)benzamide (CAS 1361 139-71-0, 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazoli- done (CAS 81777-95-9) and 2-(2,5-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidinone (CAS 81778-66-7);

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium, glyphosate-potassium and glyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors: glufosinate, glufosinate-P, glufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors: asulam;

b9) from the group of the mitosis inhibitors:

benfluralin, dithiopyr, ethalfluralin, flamprop, flamprop-isopropyl, flamprop-methyl, flamprop-M- isopropyl, flamprop-M-methyl, oryzalin, pendimethalin, thiazopyr and trifluralin;

b10) from the group of the VLCFA inhibitors: acetochlor, alachlor, amidochlor, anilofos, buta- chlor, cafenstrole, dimethenamid, dimethenamid-P, fentrazamide, flufenacet, mefenacet, meta- zachlor, metolachlor, S-metolachlor, naproanilide, napropamide, napropamide-M, pretilachlor, fenoxasulfone, ipfencarbazone, pyroxasulfone thenylchlor and isoxazoline-compounds of the formulae 11.1 , II.2, 11.3 , II.4, II.5, II.6, II.7, II.8 and II.9 as mentioned above;

b1 1 ) from the group of the cellulose biosynthesis inhibitors: dichlobenil, flupoxam, indaziflam, isoxaben, triaziflam and 1-cyclohexyl-5-pentafluorphenyloxy-1 ⁴ -[1 ,2,4,6]thiatriazin-3-ylamine (CAS 175899-01 -1 );

b13) from the group of the auxinic herbicides:

2,4-D and its salts and esters, aminocyclopyrachlor and its salts and esters, aminopyralid and its salts such as aminopyralid-dimethylammonium, aminopyralid-tris(2-hydroxypropyl)ammoni- um and its esters, clopyralid and its salts and esters, dicamba and its salts and esters, dichlor- prop-P and its salts and esters, flopyrauxifen, fluroxypyr-meptyl, halauxifen and its salts and esters (CAS 943832-60-8), MCPA and its salts and esters, MCPB and its salts and esters, mecoprop-P and its salts and esters, picloram and its salts and esters, quinclorac, quinmerac, triclopyr and its salts and esters, florpyrauxifen, florpyrauxifen-benzyl (CAS 1390661 -72-9) and 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)picolinic acid (CAS 1629965-65-6);

b14) from the group of the auxin transport inhibitors: diflufenzopyr and diflufenzopyr-sodium; b15) from the group of the other herbicides: bromobutide, cinmethylin, cumyluron, cyclopy- rimorate (CAS 499223-49-3) and its salts and esters, dalapon, difenzoquat, difenzoquat- metilsulfate, DSMA, dymron (= daimuron), indanofan, metam, methylbromide, MSMA, oxazi- clomefone, pyributicarb and tridiphane.

Particularly preferred herbicides B that can be used in combination with the pyrimidine compounds of the formula (I) according to the present invention are:

b1 ) from the group of the lipid biosynthesis inhibitors: clodinafop-propargyl, cycloxydim, cyha- lofop-butyl, fenoxaprop-P-ethyl, pinoxaden, profoxydim, tepraloxydim, tralkoxydim, 4-(4'-Chloro-

4- cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6 H)-one (CAS 1312337-72-6); 4-(2',4'-Dichloro-4-cyclopropyl[1 ,1 '-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetra- methyl-2H-pyran-3(6H)-one (CAS 1312337-45-3); 4-(4'-Chloro-4-ethyl-2'-fluoro[1 ,1 '-biphenyl]-3- yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one (CAS 1033757-93-5); 4-(2',4'-Dichloro-4- ethyl[1 ,1 '-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-di one (CAS 1312340-84-3);

5- (Acetyloxy)-4-(4'-chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetra- methyl-2H-pyran-3-one (CAS 1312337-48-6); 5-(Acetyloxy)-4-(2 ^' ,4'-dichloro-4-cyclopropyl- [1 ,1 '- biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-o ne; 5-(Acetyloxy)-4-(4'-chloro-4- ethyl-2'-fluoro[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3 -one (CAS

1312340-82-1 ); 5-(Acetyloxy)-4-(2',4'-dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6- tetramethyl-2H-pyran-3-one (CAS 1033760-55-2); 4-(4'-Chloro-4-cyclopropyl-2'-fluoro[1 ,1 '-bi- phenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran -3-yl carbonic acid methyl ester (CAS 1312337-51-1 ); 4-(2 ^' ,4'-Dichloro -4-cyclopropyl- [1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6- tetramethyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester; 4-(4'-Chloro-4-ethyl-2'-fluoro[1 ,1 '- biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyr an-3-yl carbonic acid methyl ester (CAS 1312340-83-2); 4-(2',4'-Dichloro-4-ethyl[1 ,1 '-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetrame- thyl-5-oxo-2H-pyran-3-yl carbonic acid methyl ester (CAS 1033760-58-5); esprocarb, prosul- focarb, thiobencarb and triallate;

b2) from the group of the ALS inhibitors: bensulfuron-methyl, bispyribac-sodium, cyclosulfamu- ron, diclosulam, flumetsulam, flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox, imaza- pic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron, iodosulfuron-methyl-sodi- um, iofensulfuron, iofensulfuron-sodium, mesosulfuron, metazosulfuron, nicosulfuron, penoxsu- lam, propoxycarbazon-sodium, propyrisulfuron, pyrazosulfuron-ethyl, pyroxsulam, rimsulfuron, sulfosulfuron, thiencarbazon-methyl, tritosulfuron and triafamone;

b3) from the group of the photosynthesis inhibitors: ametryn, atrazine, diuron, fluometuron, hexazinone, isoproturon, linuron, metribuzin, paraquat, paraquat-dichloride, propanil, terbutryn, terbuthylazine, 1 -(5-tert-butylisoxazol-3-yl)-2-hydroxy-4-methoxy-3-methyl-2H -pyrrol-5-one (CAS 1637455-12-9), 1-(5-tert-butylisoxazol-3-yl)-4-chloro-2-hydroxy-3-methyl-2H -pyrrol-5-one (CAS 1637453-94-1 ), 1-(5-tert-butylisoxazol-3-yl)-4-ethoxy-5-hydroxy-3-methyl-im idazolidin-2- one (CAS 1844836-64-1 );

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors: flumioxazin, oxyfluorfen, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone, trifludimoxazin, ethyl [3-[2-chloro-4-flu- oro-5-(1 -methyl-6-trifluoromethyl-2,4-dioxo-1 ,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyl- oxy]acetate (CAS 353292-31 -6; S-3100, 3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-ben- zo[1 ,4]oxazin-6-yl]-1 ,5-dimethyl-6-thioxo-[1 ,3,5]triazinan-2,4-dione (CAS 451484-50-7), 2-(2,2,7- trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1 ,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole- 1 ,3-dione (CAS 13001 18-96-0), and 1-methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2 - ynyl-3,4-dihydro-2H-benzo[1 ,4]oxazin-6-yl)-1 H-pyrimidine-2,4-dione (CAS 13041 13-05-0);

b5) from the group of the bleacher herbicides: amitrole, bicyclopyrone, clomazone, diflufeni- can, fenquinotrione, flumeturon, flurochloridone, isoxaflutole, mesotrione, oxotrione (CAS 1486617-21-3), picolinafen, sulcotrione, tefuryltrione, tembotrione, tolpyralate, topramezone, 2- chloro-3-methylsulfanyl-N-(1 -methyltetrazol-5-yl)-4-(trifluoromethyl)benzamide (CAS 1361 139- 71-0), 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone (CAS 81777-95-9); and 2-(2,5- dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidinone (CAS 81778-66-7);

b6) from the group of the EPSP synthase inhibitors: glyphosate, glyphosate-isopropylammo- nium and glyphosate-trimesium (sulfosate);

b7) from the group of the glutamine synthase inhibitors: glufosinate, glufosinate-P and glufosinate-ammonium;

b9) from the group of the mitosis inhibitors: pendimethalin and trifluralin;

b10) from the group of the VLCFA inhibitors: acetochlor, cafenstrole, dimethenamid-P, fentra- zamide, flufenacet, mefenacet, metazachlor, metolachlor, S-metolachlor, fenoxasulfone, ipfen- carbazone and pyroxasulfone; likewise, preference is given to isoxazoline compounds of the formulae 11.1 , II.2, 11.3 , II.4, II.5, II.6, II.7, II.8 and II.9 as mentioned above;

b1 1 ) from the group of the cellulose biosynthesis inhibitors: indaziflam, isoxaben and tria- ziflam;

b13) from the group of the auxinic herbicides: 2,4-D and its salts and esters such as clacyfos, and aminocyclopyrachlor and its salts and esters, aminopyralid and its salts and its esters, clopyralid and its salts and esters, dicamba and its salts and esters, flopyrauxifen, fluroxypyr- meptyl, halauxifen, halauxifen-methyl, quinclorac, quinmerac, florpyrauxifen, florpyrauxifen-ben- zyl (CAS 1390661 -72-9) and 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)picolinic acid (CAS 1629965-65-6);

b14) from the group of the auxin transport inhibitors: diflufenzopyr and diflufenzopyr-sodium, b15) from the group of the other herbicides: cinmethylin, dymon (= daimuron), indanofan, oxa- ziclomefone.

Particularly preferred herbicides B are the herbicides B as defined above; in particular, the herbicides B.1 - B.202 listed below in table B:

Table B:

B Herbicide B B Herbicide B

B.1 clethodim B.43 imazosulfuron

B.2 clodinafop-propargyl B.44 iodosulfuron-methyl-sodium

B.3 cycloxydim B.45 iofensulfuron

B.4 cyhalofop-butyl B.46 iofensulfuron-sodium

B.5 fenoxaprop-ethyl B.47 mesosulfuron-methyl

B.6 fenoxaprop-P-ethyl B.48 metazosulfuron

B.7 metamifop B.49 metsulfuron-methyl

B.8 pinoxaden B.50 metosulam

B.9 profoxydim B.51 nicosulfuron

B.10 sethoxydim B.52 penoxsulam

B.1 1 tepraloxydim B.53 propoxycarbazon-sodium

B.12 tralkoxydim B.54 pyrazosulfuron-ethyl

B.13 esprocarb B.55 pyribenzoxim

B.14 ethofumesate B.56 pyriftalid

B.15 molinate B.57 pyroxsulam

B.16 prosulfocarb B.58 propyrisulfuron

B.17 thiobencarb B.59 rimsulfuron

B.18 triallate B.60 sulfosulfuron

B.19 bensulfuron-methyl B.61 thiencarbazone-methyl

B.20 bispyribac-sodium B.62 thifensulfuron-methyl

B.21 cloransulam-methyl B.63 tribenuron-methyl

B.22 chlorsulfuron B.64 tritosulfuron

B.23 clorimuron B.65 triafamone

B.24 cyclosulfamuron B.66 ametryne

B.25 diclosulam B.67 atrazine

B.26 florasulam B.68 bentazon

B.27 flumetsulam B.69 bromoxynil

B.28 flupyrsulfuron-methyl-sodium B.70 bromoxynil-octanoate

B.29 foramsulfuron B.71 bromoxynil-heptanoate

B.30 imazamox B.72 bromoxynil-potassium

B.31 imazamox-ammonium B.73 diuron

B.32 imazapic B.74 fluometuron

B.33 imazapic-ammonium B.75 hexazinone

B.34 imazapic-isopropylammonium B.76 isoproturon

B.35 imazapyr B.77 linuron

B.36 imazapyr-ammonium B.78 metamitron

B.37 imazapyr-isopropylammonium B.79 metribuzin

B.38 imazaquin B.80 propanil

B.39 imazaquin-ammonium B.81 simazin

B.40 imazethapyr B.82 terbuthylazine

B.41 imazethapyr-ammonium B.83 terbutryn

B.42 imazethapyr-isopropylammonium B.84 paraquat-dichloride B Herbicide B B Herbicide B

B.85 acifluorfen B.123 glufosinate-ammonium

B.86 butafenacil B.124 glufosinate-P

B.87 carfentrazone-ethyl B.125 glufosinate-P-ammonium

B.88 flumioxazin B.126 pendimethalin

B.89 fomesafen B.127 trifluralin

B.90 oxadiargyl B.128 acetochlor

B.91 oxyfluorfen B.129 butachlor

B.92 pyraflufen B.130 cafenstrole

B.93 pyraflufen-ethyl B.131 dimethenamid-P

B.94 saflufenacil B.132 fentrazamide

B.95 sulfentrazone B.133 flufenacet

B.96 trifludimoxazin B.134 mefenacet

B.97 ethyl [3-[2-chloro-4-fluoro-5-(1 - B.135 metazachlor

methyl-6-trifluoromethyl-2,4-di- B.136 metolachlor

oxo- 1 ,2 , 3 , 4-tetra h yd ro py ri m i d i n- B.137 S-metolachlor

3-yl)phenoxy]-2-pyridyloxy]ace- B.138 pretilachlor

tate (CAS 353292-31 -6) B.139 fenoxasulfone

B.98 benzobicyclon B.140 indaziflam

B.99 bicyclopyrone B.141 isoxaben

B.100 clomazone B.142 triaziflam

B.101 diflufenican B.143 ipfencarbazone

B.102 flurochloridone B.144 pyroxasulfone

B.103 isoxaflutole B.145 2,4-D

B.104 mesotrione B.146 2,4-D-isobutyl

B.105 norflurazone B.147 2,4-D-dimethylammonium

B.106 picolinafen B.148 2,4-D-N,N,N-

B.107 sulcotrione trimethylethanolammonium

B.108 tefuryltrione B.149 aminopyralid

B.109 tembotrione B.150 aminopyralid-methyl

B.1 10 tolpyralate B.151 aminopyralid-dimethylammonium

B.1 1 1 topramezone B.152 aminopyralid-tris(2-hydroxypro-

B.1 12 topramezone-sodium pyl)ammonium

B.1 13 amitrole B.153 clopyralid

B.1 14 fluometuron B.154 clopyralid-methyl

B.1 15 fenquinotrione B.155 clopyralid-olamine

B.1 16 glyphosate B.156 dicamba

B.1 17 glyphosate-ammonium B.157 dicamba-butotyl

B.1 18 glyphosate-dimethylammonium B.158 dicamba-diglycolamine

B.1 19 glyphosate-isopropylammonium B.159 dicamba-dimethylammonium

B.120 glyphosate-trimesium (sulfosate) B.160 dicamba-diolamine

B.121 glyphosate-potassium B.161 dicamba-isopropylammonium

B.122 glufosinate B.162 dicamba-potassium B Herbicide B B Herbicide B

B.163 dicamba-sodium B.201 2-chloro-3-methylsulfanyl-N-(1 -

B.164 dicamba-trolamine methyltetrazol-5-yl)-4-(trifluoro-

B.165 dicamba-N,N-bis-(3- methyl)benzamide (CAS

aminopropyl)methylamine 1361 139-71 -0)

B.166 dicamba-diethylenetriamine B.202 2-(2,4-dichlorophenyl)methyl-4,4-

B.167 fluroxypyr dimethyl-3-isoxazolidone (CAS

B.168 fluroxypyr-meptyl 81777-95-9)

B.169 halauxifen

B.170 halauxifen-methyl

B.171 MCPA

B.172 MCPA-2-ethylhexyl

B.173 MCPA-dimethylammonium

B.174 quinclorac

B.175 quinclorac-dimethylammonium

B.176 quinmerac

B.177 quinmerac-dimethylammonium

B.178 florpyrauxifen

B.179 florpyrauxifen-benzyl (CAS

1390661 -72-9)

B.180 aminocyclopyrachlor

B.181 aminocyclopyrachlor-potassium

B.182 aminocyclopyrachlor-methyl

B.183 diflufenzopyr

B.184 diflufenzopyr-sodium

B.185 dymron

B.186 indanofan

B.187 oxaziclomefone

B.188 11.1

B.189 W .2

B.190 11.3

B.191 I I .4

B.192 I I .5

B.193 I I .6

B.194 I I .7

B.195 11.8

B.196 i i .g

B.197 4-amino-3-chloro-5-fluoro-6-(7- fluoro-1 H-indol-6-yl)picolinic acid

(CAS 1629965-65-6)

B.198 flopyrauxifen

B.199 oxotrione (CAS 1486617-21 -3)

B.200 cinmethylin In another embodiment of the present invention the compositions according to the present invention comprise at least one pyrimidine compound of formula (I) and at least one safener C.

Safeners are chemical compounds which prevent or reduce damage on useful plants without having a major impact on the herbicidal action of the herbicidal active components of the pre- sent compositions towards unwanted plants. They can be applied either before sowings (e.g. on seed treatments, shoots or seedlings) or in the pre-emergence application or post-emergence application of the useful plant. The safeners and the pyrimidine compounds of formula (I) and/or the herbicides B can be applied simultaneously or in succession.

Suitable safeners are e.g. (quinolin-8-oxy)acetic acids, 1 -phenyl-5-haloalkyl-1 H-1 ,2,4-triazol-3- carboxylic acids, 1 -phenyl-4,5-dihydro-5-alkyl-1 H-pyrazol-3,5-dicarboxylic acids, 4,5-dihydro- 5,5-diaryl-3-isoxazol carboxylic acids, dichloroacetamides, alpha-oximinophenylacetonitriles, acetophenonoximes, 4,6-dihalo-2-phenylpyrimidines, N-[[4-(aminocarbonyl)phenyl]sulfonyl]-2- benzoic amides, 1 ,8-naphthalic anhydride, 2-halo-4-(haloalkyl)-5-thiazol carboxylic acids, phosphorthiolates and N-alkyl-O-phenylcarbamates and their agriculturally acceptable salts and their agriculturally acceptable derivatives such amides, esters, and thioesters, provided they have an acid group.

Examples of preferred safeners C are benoxacor, cloquintocet, cyometrinil, cyprosulfamide, dichlormid, dicyclonon, dietholate, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, mephenate, naphthalic anhydride, oxabetrinil, 4-(dichloroacetyl)-1 -oxa-4- azaspiro[4.5]decane (MON4660, CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxa- zolidine (R-29148, CAS 52836-31-4), metcamifen and BPCMS (CAS 54091 -06-4).

Especially preferred safeners C are benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, naphthalic anhydride, oxabetrinil, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07- 3), 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31-4) and metcamifen.

Particularly preferred safeners C are benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, furilazole, isoxadifen, mefenpyr, naphtalic anhydride, 4-(dichloroace- tyl)-1-oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3), 2,2,5-trimethyl-3-(dichloroace- tyl)-1 ,3-oxazolidine (R-29148, CAS 52836-31 -4) and metcamifen.

Particularly preferred safeners C, which, as component C, are constituent of the composition according to the invention are the safeners C as defined above; in particular the safeners C.1 - C.17 listed below in table C: Table C:

c Safener C

C.1 benoxacor

C.2 cloquintocet

C.3 cloquintocet-mexyl

C.4 cyprosulfamide

C.5 dichlormid

C.6 fenchlorazole

C.7 fenchlorazole-ethyl

C.8 fenclorim C.9 furilazole

C.10 isoxadifen

C.1 1 isoxadifen-ethyl

C.12 mefenpyr

C.13 mefenpyr-diethyl

C.14 naphtalic acid anhydride

C.15 4-(dichloroacetyl)-1 -oxa-4- azaspiro[4.5]decane

(MON4660, CAS 71526-07-3)

C.16 2,2,5-trimethyl-3-(dichloroace- tyl)-1 ,3-oxazolidine (R-29148,

CAS 52836-31 -4)

C.17 metcamifen

The active compounds B of groups b1 ) to b15) and the active compounds C are known herbicides and safeners, see, e.g., The Compendium of Pesticide Common Names (http://www.alan- wood.net/pesticides/); Farm Chemicals Handbook 2000 volume 86, Meister Publishing Com- pany, 2000; B. Hock, C. Fedtke, R. R. Schmidt, Herbizide [Herbicides], Georg Thieme Verlag, Stuttgart 1995; W. H. Ahrens, Herbicide Handbook, 7th edition, Weed Science Society of America, 1994; and K. K. Hatzios, Herbicide Handbook, Supplement for the 7th edition, Weed Science Society of America, 1998. 2,2,5-Trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine [CAS No. 52836-31-4] is also referred to as R-29148. 4-(Dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane [CAS No. 71526-07-3] is also referred to as AD-67 and MON 4660.

The assignment of the active compounds to the respective mechanisms of action is based on current knowledge. If several mechanisms of action apply to one active compound, this substance was only assigned to one mechanism of action.

Active compounds B and C having a carboxyl group can be employed in the form of the acid, in the form of an agriculturally suitable salt as mentioned above or else in the form of an agriculturally acceptable derivative in the compositions according to the invention.

In the case of dicamba, suitable salts include those, where the counterion is an agriculturally acceptable cation. E.g., suitable salts of dicamba are dicamba-sodium, dicamba-potassium, dicamba-methylammonium, dicamba-dimethylammonium, dicamba-isopropylammonium, dicamba-diglycolamine, dicamba-olamine, dicamba-diolamine, dicamba-trolamine, dicamba- N,N-bis-(3-aminopropyl)methylamine and dicamba-diethylenetriamine. Examples of a suitable ester are dicamba-methyl and dicamba-butotyl.

Suitable salts of 2,4-D are 2,4-D-ammonium, 2,4-D-dimethylammonium, 2,4-D-diethylammoni- um, 2,4-D-diethanolammonium (2,4-D-diolamine), 2,4-D-triethanolammonium, 2,4-D-isoprop- ylammonium, 2,4-D-triisopropanolammonium, 2,4-D-heptylammonium, 2,4-D-dodecylammo- nium, 2,4-D-tetradecylammonium, 2,4-D-triethylammonium, 2,4-D-tris(2-hydroxypropyl)ammo- nium, 2,4-D-tris(isopropyl)ammonium, 2,4-D-trolamine, 2,4-D-lithium, 2,4-D-sodium. Examples of suitable esters of 2,4-D are 2,4-D-butotyl, 2,4-D-2-butoxypropyl, 2,4-D-3-butoxypropyl, 2,4-D- butyl, 2,4-D-ethyl, 2,4-D-ethylhexyl, 2,4-D-isobutyl, 2,4-D-isooctyl, 2,4-D-isopropyl, 2,4-D-mep- tyl, 2,4-D-methyl, 2,4-D-octyl, 2,4-D-pentyl, 2,4-D-propyl, 2,4-D-tefuryl and clacyfos. Suitable salts of 2,4-DB are e.g. 2,4-DB-sodium, 2,4-DB-potassium and 2,4-DB-dimethyl- ammonium. Suitable esters of 2,4-DB are e.g. 2,4-DB-butyl and 2,4-DB-isoctyl.

Suitable salts of dichlorprop are e.g. dichlorprop-sodium, dichlorprop-potassium and dichlor- prop-dimethylammonium. Examples of suitable esters of dichlorprop are dichlorprop-butotyl and dichlorprop-isoctyl.

Suitable salts and esters of MCPA include MCPA-butotyl, MCPA-butyl, MCPA-dimethylammo- nium, MCPA-diolamine, MCPA-ethyl, MCPA-thioethyl, MCPA-2-ethylhexyl, MCPA-isobutyl, MCPA-isoctyl, MCPA-isopropyl, MCPA-isopropylammonium, MCPA-methyl, MCPA-olamine, MCPA-potassium, MCPA-sodium and MCPA-trolamine.

A suitable salt of MCPB is MCPB sodium. A suitable ester of MCPB is MCPB-ethyl.

Suitable salts of clopyralid are clopyralid-potassium, clopyralid-olamine and clopyralid-tris-(2- hydroxypropyl)ammonium. Example of suitable esters of clopyralid is clopyralid-methyl.

Examples of a suitable ester of fluroxypyr are fluroxypyr-meptyl and fluroxypyr-2-butoxy-1- methylethyl, wherein fluroxypyr-meptyl is preferred.

Suitable salts of picloram are picloram-dimethylammonium, picloram-potassium, picloram- triisopropanolammonium, picloram-triisopropylammonium and picloram-trolamine. A suitable ester of picloram is picloram-isoctyl.

A suitable salt of triclopyr is triclopyr-triethylammonium. Suitable esters of triclopyr are e.g. triclopyr-ethyl and triclopyr-butotyl.

Suitable salts and esters of chloramben include chloramben-ammonium, chloramben-diola- mine, chloramben-methyl, chloramben-methylammonium and chloramben-sodium. Suitable salts and esters of 2,3,6-TBA include 2,3,6-TBA-dimethylammonium, 2,3,6-TBA-lithium, 2,3,6- TBA-potassium and 2,3,6-TBA-sodium.

Suitable salts and esters of aminopyralid include aminopyralid-potassium, aminopyralid-dime- thylammonium, and aminopyralid-tris(2-hydroxypropyl)ammonium.

Suitable salts of glyphosate are e.g. glyphosate-ammonium, glyphosate-diammonium, glyphoste-dimethylammonium, glyphosate-isopropylammonium, glyphosate-potassium, glypho- sate-sodium, glyphosate-trimesium as well as the ethanolamine and diethanolamine salts, preferably glyphosate-diammonium, glyphosate-isopropylammonium and glyphosate-trimesium (sul- fosate).

A suitable salt of glufosinate is e.g. glufosinate-ammonium.

A suitable salt of glufosinate-P is e.g. glufosinate-P-ammonium.

Suitable salts and esters of bromoxynil are e.g. bromoxynil-butyrate, bromoxynil-heptanoate, bromoxynil-octanoate, bromoxynil-potassium and bromoxynil-sodium.

Suitable salts and esters of ioxonil are e.g. ioxonil-octanoate, ioxonil-potassium and ioxonil- sodium.

Suitable salts and esters of mecoprop include mecoprop-butotyl, mecoprop-dimethylammo- nium, mecoprop-diolamine, mecoprop-ethadyl, mecoprop-2-ethylhexyl, mecoprop-isoctyl, mecoprop-methyl, mecoprop-potassium, mecoprop-sodium and mecoprop-trolamine.

Suitable salts of mecoprop-P are e.g. mecoprop-P-butotyl, mecoprop-P-dimethylammonium, mecoprop-P-2-ethylhexyl, mecoprop-P-isobutyl, mecoprop-P-potassium and mecoprop-P-so- dium.

A suitable salt of diflufenzopyr is e.g. diflufenzopyr-sodium.

A suitable salt of naptalam is e.g. naptalam-sodium. Suitable salts and esters of aminocyclopyrachlor are e.g. aminocyclopyrachlor-dimethylammo- nium, aminocyclopyrachlor-methyl, aminocyclopyrachlor-triisopropanolammonium, aminocyclo- pyrachlor-sodium and aminocyclopyrachlor-potassium.

A suitable salt of quinclorac is e.g. quinclorac-dimethylammonium.

A suitable salt of quinmerac is e.g. quinmerac-dimethylammonium.

A suitable salt of imazamox is e.g. imazamox-ammonium.

Suitable salts of imazapic are e.g. imazapic-ammonium and imazapic-isopropylammonium. Suitable salts of imazapyr are e.g. imazapyr-ammonium and imazapyr-isopropylammonium. A suitable salt of imazaquin is e.g. imazaquin-ammonium.

Suitable salts of imazethapyr are e.g. imazethapyr-ammonium and imazethapyr-isoprop- ylammonium.

A suitable salt of topramezone is e.g. topramezone-sodium.

According to a preferred embodiment of the invention, the composition comprises as herbicidal active compound B or component B at least one, preferably exactly one herbicide B.

According to another preferred embodiment of the invention, the composition comprises as herbicidal active compounds B or component B at least two, preferably exactly two herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as herbicidal active compounds B or component B at least three, preferably exactly three herbi- cides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as safening component C or component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component B at least one, preferably exactly one herbicide B, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises at least two, preferably exactly two, herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises at least three, preferably exactly three, herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1 .1-55), or (1 .1 .1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1.1-55), or (1 .1.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1.1-55), or (1 .1.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1 .1-55), or (1 .1 .1-73), and as component C at least one, preferably exactly one, saf- ener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1 .1-55), or (1 .1 .1-73), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1 .1-55), or (1 .1 .1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .1 ), especially preferred the compound (1.1.1-25), (1.1.1-37), (1.1 .1-31 ), (1 .1.1-49), (1.1.1-61 ), (1 .1 .1-55), or (1 .1 .1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1 .2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .2), especially preferred the compound (1.2.1-25), (1.2.1-37), (1.2.1-31 ), (1 .2.1-49), (1.2.1-61 ), (1 .2.1-55), or (1 .2.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1 .3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .3), especially preferred the compound (1.3.1-25), (1.3.1-37), (1.3.1-31 ), (1 .3.1-49), (1.3.1-61 ), (1 .3.1-55), or (1 .3.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), and at least three, preferably exactly three, herbicides B dif- ferent from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), and as component C at least one, preferably exactly one, saf- ener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1 .4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .4), especially preferred the compound (1.4.1-25), (1.4.1-37), (1.4.1-31 ), (1 .4.1-49), (1.4.1-61 ), (1 .4.1-55), or (1 .4.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), and as component C at least one, preferably exactly one, saf- ener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1 .5.1-37), (1.5.1-31 ), (1 .5.1-49),

(1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .5), especially preferred the compound (1.5.1-25), (1.5.1-37), (1.5.1-31 ), (1 .5.1-49), (1.5.1-61 ), (1 .5.1-55), or (1 .5.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), and as component C at least one, preferably exactly one, saf- ener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1 .6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .6), especially preferred the compound (1.6.1-25), (1.6.1-37), (1.6.1-31 ), (1 .6.1-49), (1.6.1-61 ), (1 .6.1-55), or (1 .6.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1 .7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .7), especially preferred the compound (1.7.1-25), (1.7.1-37), (1.7.1-31 ), (1 .7.1-49), (1.7.1-61 ), (1 .7.1-55), or (1 .7.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), and at least three, preferably exactly three, herbicides B dif- ferent from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), and as component C at least one, preferably exactly one, saf- ener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1 .8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .8), especially preferred the compound (1.8.1-25), (1.8.1-37), (1.8.1-31 ), (1 .8.1-49), (1.8.1-61 ), (1 .8.1-55), or (1 .8.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1 .9.1-37), (1.9.1-31 ), (1 .9.1-49),

(1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .9), especially preferred the compound (1.9.1-25), (1.9.1-37), (1.9.1-31 ), (1 .9.1-49), (1.9.1-61 ), (1 .9.1-55), or (1 .9.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1.10.1-55), or (1 .10.1-73), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1.10.1-25), (1 .10.1-37), (1 .10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .10), especially preferred the compound (1 .10.1-25), (1.10.1-37), (1.10.1-31 ), (1 .10.1- 49), (1.10.1-61 ), (1 .10.1-55), or (1.10.1-73), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one compound of formula (I), preferably of formula (1.31 ), especially preferred the compound (1 .31 .1-25), (1 .31.1-31 ), (1.31 .1-37), (1 .31 .1-49), (1.31 .1-55), or (1 .31.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one compound of formula (I), preferably of formula (1.31 ), especially preferred the compound (1 .31 .1-25), (1 .31.1-31 ), (1.31 .1-37), (1 .31 .1-49),

(1.31 .1-55), or (1 .31.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .31 ), especially preferred the compound (1 .31.1-25), (1.31 .1-31 ), (1.31 .1-37), (1 .31 .1- 49), (1.31 .1-55), or (1 .31.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .31 ), especially preferred the compound (1 .31.1-25), (1.31 .1-31 ), (1.31 .1-37), (1 .31 .1- 49), (1.31 .1-55), or (1 .31.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .31 ), especially preferred the compound (1 .31.1-25), (1.31 .1-31 ), (1.31 .1-37), (1 .31 .1- 49), (1.31 .1-55), or (1 .31.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .31 ), especially preferred the compound (1 .31.1-25), (1.31 .1-31 ), (1.31 .1-37), (1 .31 .1- 49), (1.31 .1-55), or (1 .31.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .31 ), especially preferred the compound (1 .31.1-25), (1.31 .1-31 ), (1.31 .1-37), (1 .31 .1- 49), (1.31 .1-55), or (1 .31.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .37), especially preferred the compound (1 .37.1-25), (1.37.1-31 ), (1.37.1-37), (1 .37.1- 49), (1.37.1-55), or (1 .37.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .38), especially preferred the compound (1 .38.1-25), (1.38.1-31 ), (1.38.1-37), (1 .38.1- 49), (1.38.1-55), or (1 .38.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .39), especially preferred the compound (1 .39.1-25), (1.39.1-31 ), (1.39.1-37), (1 .39.1- 49), (1.39.1-55), or (1 .39.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .46), especially preferred the compound (1 .46.1-25), (1.46.1-31 ), (1.46.1-37), (1 .46.1- 49), (1.46.1-55), or (1 .46.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), and at least two, preferably exactly two, herbicides B different from each other. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .47), especially preferred the compound (1 .47.1-25), (1.47.1-31 ), (1.47.1-37), (1 .47.1- 49), (1.47.1-55), or (1 .47.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .53), especially preferred the compound (1 .53.1-25), (1.53.1-31 ), (1.53.1-37), (1 .53.1- 49), (1.53.1-55), or (1 .53.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .59), especially preferred the compound (1 .59.1-25), (1.59.1-31 ), (1.59.1-37), (1 .59.1- 49), (1.59.1-55), or (1 .59.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .63), especially preferred the compound (1 .63.1-25), (1.63.1-31 ), (1.63.1-37), (1 .63.1- 49), (1.63.1-55), or (1 .63.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .64), especially preferred the compound (1 .64.1-25), (1.64.1-31 ), (1.64.1-37), (1 .64.1- 49), (1.64.1-55), or (1 .64.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .65), especially preferred the compound (1 .65.1-25), (1.65.1-31 ), (1.65.1-37), (1 .65.1- 49), (1.65.1-55), or (1 .65.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 . 72), especially preferred the compound (1.72.1-25), (1.72.1-31 ), (1.72.1-37), (1.72.1- 49), (1.72.1-55), or (1 .72.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .72), especially preferred the compound (1 .72.1-25), (1.72.1-31 ), (1.72.1-37), (1 .72.1- 49), (1.72.1-55), or (1 .72.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .73), especially preferred the compound (1 .73.1-25), (1.73.1-31 ), (1.73.1-37), (1 .73.1- 49), (1.73.1-55), or (1 .73.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), and as component B at least one, preferably exactly one, herbi- cide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .79), especially preferred the compound (1 .79.1-25), (1.79.1-37), (1.79.1-49), (1 .79.1- 31 ), (1.79.1-55), or (1 .79.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37), (1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37),

(1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37),

(1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), and at least three, preferably exactly three, herbicides

B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37),

(1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37), (1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37), (1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .272), especially preferred the compound (1 .272.1-25), (1 .272.1-31 ), (1.272.1-37),

(1.272.1-49), (1 .272.1-55), or (1 .272.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .273), especially preferred the compound (1 .273.1-25), (1 .273.1-31 ), (1.273.1-37), (1.273.1-49), (1 .273.1-55), or (1 .273.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), and at least three, preferably exactly three, herbicides B different from each other. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), at least two, preferably exactly two herbicides B differ- ent from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .584), especially preferred the compound (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), or (1 .584.1-61 ), at least three, preferably exactly three herbicides B dif- ferent from each other, and as component C at least one, preferably exactly one, safener C. According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), and at least three, preferably exactly three, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37), (1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .585), especially preferred the compound (1 .585.1-25), (1 .585.1-31 ), (1.585.1-37),

(1.585.1-49), (1 .585.1-55), or (1 .585.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37), (1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), and as component B at least one, preferably exactly one, herbicide B.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37),

(1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), and at least two, preferably exactly two, herbicides B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37),

(1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), and at least three, preferably exactly three, herbicides

B different from each other.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37),

(1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37), (1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), and as component B at least one, preferably exactly one, herbicide B, and as component C at least one, preferably exactly one safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1 .592), especially preferred the compound (1 .592.1-25), (1 .592.1-31 ), (1.592.1-37), (1.592.1-49), (1 .592.1-55), or (1 .592.1-61 ), at least two, preferably exactly two herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises as component A at least one, preferably exactly one pyrimidine compound of formula (I), preferably of formula (1.592), especially preferred the compound (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), or (1.592.1-61 ), at least three, preferably exactly three herbicides B different from each other, and as component C at least one, preferably exactly one, safener C.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

(1.31. -25), (1 .37. -25), (1 .37. -31), (1 .37. I-37), (1 .37. -49), (1.37.1-55), (1.37. -61), (1 .38. 1-25),

(1.38. -31), (1 .38. -37), (1 .38. -49), (1 .38. I-55), (1 .38. -61), (1.39.1-25), (1.39. -31), (1 .39. 1-37),

(1.39. -49), (1 .39. -55), (1 .39. -61), (1 .46. I-25), (1 .46. -31), (1.46.1-37), (1.46. -49), (1 .46. 1-55),

(1.46. -61), (1 .47. -25), (1 .47. -31), (1 .47. I-37), (1 .47. -49), (1.47.1-55), (1.47. -61), (1 .53. 1-25),

(1.53. -31), (1 .53. -37), (1 .53. -49), (1 .53. I-55), (1 .53. -61), (1.59.1-25), (1.59. -31), (1 .59. 1-37),

(1.59. -49), (1 .59. -55), (1 .59. -61), (1 .63. I-25), (1 .63. -31), (1.63.1-37), (1.63. -49), (1 .63. 1-55),

(1.63. -61), (1 .64. -25), (1 .64. -31), (1 .64. I-37), (1 .64. -49), (1.64.1-55), (1.64. -61), (1 .65. 1-25),

(1.65. -31), (1 .65. -37), (1 .65. -49), (1 .65. I-55), (1 .65. -61), (1.72.1-25), (1.72. -31), (1 .72. 1-37),

(1.72. -49), (1 .72. -55), (1 .72. -61), (1 .73. I-25), (1 .73. -31), (1.73.1-37), (1.73. -49), (1 .73. 1-55),

(1.73. -61), (1 .79. -25), (1 .79. -37), (1 .79. I-49), (1 .79. -31), (1.79.1-55), (1.79. -61), (1 .272.1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b1), in particular selected from the group consisting of clethodim, clodinafop-propargyl, cy- cloxydim, cyhalofop-butyl, fenoxaprop-ethyl, fenoxaprop-P-ethyl, metamifop, pinoxaden, profoxydim, sethoxydim, tepraloxydim, tralkoxydim, esprocarb, ethofumesate, molinate, prosul- focarb, thiobencarb and triallate.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73), (1.31.1-25), (1.37.1-25), (1.37.1-31), (1.37.1-37), (1.37.1-49), (1.37.1-55), (1.37.1-61), (1.38.1-25), (1.38.1-31), (1.38.1-37), (1.38.1-49), (1.38.1-55), (1.38.1-61), (1.39.1-25), (1.39.1-31), (1.39.1-37), 39. I-49), (139. I-55), (139.1-61), (1.46. I-25), (1.46.1-31), (1.46. I-37), (1.46. I-49), (1.46.1-55),

46. 1-61), (1 47. I-25), (1 47. 1-31), (1 .47. I-37), (1 .47. I-49), (1.47. I-55), (1.47. 1-61), (1.53. 1-25),

53. 1-31), (1 53. I-37), (1 53. I-49), (1 .53. I-55), (1 .53. 1-61), (1.59. I-25), (1.59. 1-31), (1.59. 1-37),

59. I-49), (1 59. I-55), (1 59. 1-61), (1 .63. I-25), (1 .63. 1-31), (1.63. I-37), (1.63. I-49), (1.63. 1-55),

63. 1-61), (1 64. I-25), (1 64. 1-31), (1 .64. I-37), (1 .64. I-49), (1.64. I-55), (1.64. 1-61), (1.65. 1-25),

65. 1-31), (1 65. I-37), (1 65. I-49), (1 .65. I-55), (1 .65. 1-61), (1.72. I-25), (1.72. 1-31), (1.72. 1-37),

72. I-49), (1 72. I-55), (1 72. 1-61), (1 .73. I-25), (1 .73. 1-31), (1.73. I-37), (1.73. I-49), (1.73. 1-55),

73. 1-61), (1 79. I-25), (1 79. I-37), (1 .79. I-49), (1 .79. 1-31), (1.79. I-55), (1.79. 1-61), (1.272.1-25),

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b2), in particular selected from the group consisting of bensulfuron-methyl, bispyribac-sodium, cloransulam-methyl, chlorsulfuron, clorimuron, cyclosulfamuron, diclosulam, florasulam, flumet- sulam, flupyrsulfuron-methyl-sodium, foramsulfuron, imazamox, imazamox-ammonium, imaza- pic, imazapic-ammonium, imazapic-isopropylammonium, imazapyr, imazapyr-ammonium, ima- zethapyr-isopropylammonium, imazaquin, imazaquin-ammonium, imazethapyr, imazethapyr- ammonium, imazethapyr-isopropylammonium, imazosulfuron, iodosulfuron-methyl-sodium, io- fensulfuron, iofensulfuron-sodium, mesosulfuron-methyl, metazosulfuron, metsulfuron-methyl, metosulam, nicosulfuron, penoxsulam, propoxycarbazon-sodium, pyrazosulfuron-ethyl, pyriben- zoxim, pyriftalid, pyroxsulam, propyrisulfuron, rimsulfuron, sulfosulfuron, thiencarbazon-methyl, thifensulfuron-methyl, tribenuron-methyl, tritosulfuron and triafamone.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

(1.31. -25), (1.37. -25), (1.37. -31), (1 .37. -37), (1 .37. -49), (1 .37. -55), (1 .37. -61), (1 .38.1 -25),

(1.38. -31), (1.38. -37), (1.38. -49), (1 .38. -55), (1 .38. -61), (1 .39. -25), (1 .39. -31), (1 .39.1 -37),

(1.39. -49), (1.39. -55), (1.39. -61), (1 .46. -25), (1 .46. -31), (1 .46. -37), (1 .46. -49), (1 .46.1 -55),

(1.46. -61), (1.47. -25), (1.47. -31), (1 .47. -37), (1 .47. -49), (1 .47. -55), (1 .47. -61), (1 .53.1 -25),

(1.53. -31), (1.53. -37), (1.53. -49), (1 .53. -55), (1 .53. -61), (1 .59. -25), (1 .59. -31), (1 .59.1 -37),

(1.59. -49), (1.59. -55), (1.59. -61), (1 .63. -25), (1 .63. -31), (1 .63. -37), (1 .63. -49), (1 .63.1 -55),

(1.63. -61), (1.64. -25), (1.64. -31), (1 .64. -37), (1 .64. -49), (1 .64. -55), (1 .64. -61), (1 .65.1 -25),

(1.65. -31), (1.65. -37), (1.65. -49), (1 .65. -55), (1 .65. -61), (1 .72. -25), (1 .72. -31), (1 .72.1 -37),

(1.72. -49), (1.72. -55), (1.72. -61), (1 .73. -25), (1 .73. -31), (1 .73. -37), (1 .73. -49), (1 .73.1 -55),

(1.73. -61), (1.79. -25), (1.79. -37), (1 .79. -49), (1 .79. -31), (1 .79. -55), (1 .79. -61), (1 .272 .1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b3), in particular selected from the group consisting of ametryn, atrazine, bentazon, bromoxynil, bromoxynil-octanoate, bromoxynil-heptanoate, bromoxynil-potassium, diuron, fluometuron, hex- azinone, isoproturon, linuron, metamitron, metribuzin, paraquat-dichloride, propanil, simazin, terbutryn and terbuthylazine.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

(1.31. -25), (1.37. -25), (1.37. -31), (1 .37.1-37), (1 .37. -49), (1 .37.1-55), (1 .37. -61), (1 .38.1 -25),

(1.38. -31), (1.38. -37), (1.38. -49), (1 .38.1-55), (1 .38. -61), (1 .39.1-25), (1 .39. -31), (1 .39.1 -37),

(1.39. -49), (1.39. -55), (1.39. -61), (1 .46.1-25), (1 .46. -31), (1 .46.1-37), (1 .46. -49), (1 .46.1 -55),

(1.46. -61), (1.47. -25), (1.47. -31), (1 .47.1-37), (1 .47. -49), (1 .47.1-55), (1 .47. -61), (1 .53.1 -25),

(1.53. -31), (1.53. -37), (1.53. -49), (1 .53.1-55), (1 .53. -61), (1 .59.1-25), (1 .59. -31), (1 .59.1 -37),

(1.59. -49), (1.59. -55), (1.59. -61), (1 .63.1-25), (1 .63. -31), (1 .63.1-37), (1 .63. -49), (1 .63.1 -55),

(1.63. -61), (1.64. -25), (1.64. -31), (1 .64.1-37), (1 .64. -49), (1 .64.1-55), (1 .64. -61), (1 .65.1 -25),

(1.65. -31), (1.65. -37), (1.65. -49), (1 .65.1-55), (1 .65. -61), (1 .72.1-25), (1 .72. -31), (1 .72.1 -37),

(1.72. -49), (1.72. -55), (1.72. -61), (1 .73.1-25), (1 .73. -31), (1 .73.1-37), (1 .73. -49), (1 .73.1 -55),

(1.73. -61), (1.79. -25), (1.79. -37), (1 .79.1-49), (1 .79. -31), (1 .79.1-55), (1 .79. -61), (1 .272 .1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b4), in particular selected from the group consisting of acifluorfen, butafencil, carfenetrazone- ethyl, flumioxazin, fomesafen, oxadiargyl, oxyfluorfen, pyraflufen, pyraflufen-ethyl, saflufenacil, sulfentrazone, trifludimoxazin, ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-diox o- 1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]aceta te (CAS 353292-31-6; S-3100). According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

[1.31. -25), (1 .37. -25), (1 .37. -31), (1 .37. I-37), (1 .37. -49), (1.37. -55), (1.37. -61), (1 .38. 1-25),

[1.38. -31), (1 .38. -37), (1 .38. -49), (1 .38. I-55), (1 .38. -61), (1.39. -25), (1.39. -31), (1 .39. 1-37),

[1.39. -49), (1 .39. -55), (1 .39. -61), (1 .46. I-25), (1 .46. -31), (1.46. -37), (1.46. -49), (1 .46. 1-55),

[1.46. -61), (1 .47. -25), (1 .47. -31), (1 .47. I-37), (1 .47. -49), (1.47. -55), (1.47. -61), (1 .53. 1-25),

[1.53. -31), (1 .53. -37), (1 .53. -49), (1 .53. I-55), (1 .53. -61), (1.59. -25), (1.59. -31), (1 .59. 1-37),

[1.59. -49), (1 .59. -55), (1 .59. -61), (1 .63. I-25), (1 .63. -31), (1.63. -37), (1.63. -49), (1 .63. 1-55),

[1.63. -61), (1 .64. -25), (1 .64. -31), (1 .64. I-37), (1 .64. -49), (1.64. -55), (1.64. -61), (1 .65. 1-25),

[1.65. -31), (1 .65. -37), (1 .65. -49), (1 .65. I-55), (1 .65. -61), (1.72. -25), (1.72. -31), (1 .72. 1-37),

[1.72. -49), (1 .72. -55), (1 .72. -61), (1 .73. I-25), (1 .73. -31), (1.73. -37), (1.73. -49), (1 .73. 1-55),

[1.73. -61), (1 .79. -25), (1 .79. -37), (1 .79. I-49), (1 .79. -31), (1.79. -55), (1.79. -61), (1 .272.1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b5), in particular selected from the group consisting of amitrole, benzobicyclon, bicyclopyrone, clomazone, diflufenican, fenquintrone, fluometuron, flurochloridone, isoxaflutole, mesotrione, norflurazone, oxotrione (CAS 1486617-21-3), picolinafen, sulcotrione, tefuryltrione, tembotrione, tolpyralate, topramezone, topramezone-sodium, 2-chloro-3-methylsulfanyl-N-(1-methyltetrazol- 5-yl)-4-(trifluoromethyl)benzamide (CAS 1361139-71-0), 2-(2,4-dichlorophenyl)methyl-4,4-dime- thyl-3-isoxazolidone (CAS 81777-95-9) and 2-(2,5-dichlorophenyl)methyl-4,4-dimethyl-3-isoxa- zolidinone (CAS 81778-66-7).

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73), (1.31.1-25), (1.37.1-25), (1.37.1-31), (1.37.1-37), (1.37.1-49), (1.37.1-55), (1.37.1-61), (1.38.1-25), (1.38.1-31), (1.38.1-37), (1.38.1-49), (1.38.1-55), (1.38.1-61), (1.39.1-25), (1.39.1-31), (1.39.1-37), (1.39.1-49), (1.39.1-55), (1.39.1-61), (1.46.1-25), (1.46.1-31), (1.46.1-37), (1.46.1-49), (1.46.1-55), (1.46.1-61), (1.47.1-25), (1.47.1-31), (1.47.1-37), (1.47.1-49), (1.47.1-55), (1.47.1-61), (1.53.1-25), (1.53.1-31), (1.53.1-37), (1.53.1-49), (1.53.1-55), (1.53.1-61), (1.59.1-25), (1.59.1-31), (1.59.1-37), (1.59.1-49), (1.59.1-55), (1.59.1-61), (1.63.1-25), (1.63.1-31), (1.63.1-37), (1.63.1-49), (1.63.1-55), (1.63.1-61), (1.64.1-25), (1.64.1-31), (1.64.1-37), (1.64.1-49), (1.64.1-55), (1.64.1-61), (1.65.1-25), (1.65.1-31), (1.65.1-37), (1.65.1-49), (1.65.1-55), (1.65.1-61), (1.72.1-25), (1.72.1-31), (1.72.1-37), (1.72.1-49), (1.72.1-55), (1.72.1-61), (1.73.1-25), (1.73.1-31), (1.73.1-37), (1.73.1-49), (1.73.1-55), (1.73.1-61), (1.79.1-25), (1.79.1-37), (1.79.1-49), (1.79.1-31), (1.79.1-55), (1.79.1-61), (1.272.1-25), (1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b6), in particular selected from the group consisting of glyphosate, glyphosate-ammonium, glyphosate-dimethylammonium , glyphosate-isopropylammonium and glyphosate-trimesium (sulfosate) and glyphosate-potassium.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

[1.31. -25), (1 .37. -25), (1 37. -31), (1 .37.1-37), (1 .37. -49), (1.37.1-55), (1.37. -61), (1 .38. 1-25),

[1.38. -31), (1 .38. -37), (1 38. -49), (1 .38.1-55), (1 .38. -61), (1.39.1-25), (1.39. -31), (1 .39. 1-37),

[1.39. -49), (1 .39. -55), (1 39. -61), (1 .46.1-25), (1 .46. -31), (1.46.1-37), (1.46. -49), (1 .46. 1-55),

[1.46. -61), (1 .47. -25), (1 47. -31), (1 .47.1-37), (1 .47. -49), (1.47.1-55), (1.47. -61), (1 .53. 1-25),

[1.53. -31), (1 .53. -37), (1 53. -49), (1 .53.1-55), (1 .53. -61), (1.59.1-25), (1.59. -31), (1 .59. 1-37),

[1.59. -49), (1 .59. -55), (1 59. -61), (1 .63.1-25), (1 .63. -31), (1.63.1-37), (1.63. -49), (1 .63. 1-55),

[1.63. -61), (1 .64. -25), (1 64. -31), (1 .64.1-37), (1 .64. -49), (1.64.1-55), (1.64. -61), (1 .65. 1-25),

[1.65. -31), (1 .65. -37), (1 65. -49), (1 .65.1-55), (1 .65. -61), (1.72.1-25), (1.72. -31), (1 .72. 1-37),

[1.72. -49), (1 .72. -55), (1 72. -61), (1 .73.1-25), (1 .73. -31), (1.73.1-37), (1.73. -49), (1 .73. 1-55),

[1.73. -61), (1 .79. -25), (1 79. -37), (1 .79.1-49), (1 .79. -31), (1.79.1-55), (1.79. -61), (1 .272.1-25)

[1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25) , (1.273.1-31),

(1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37),

(1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b7), in particular selected from the group consisting of glufosinate, glufosinate-ammonium, glufosinate-P and glufosinate-P-ammonium.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

[1.31. -25), (1 .37. -25), (1 .37. -31), (1 .37.1-37), (1 .37. -49), (1.37. -55), (1.37. -61), (1 .38. 1-25),

[1.38. -31), (1 .38. -37), (1 .38. -49), (1 .38.1-55), (1 .38. -61), (1.39. -25), (1.39. -31), (1 .39. 1-37),

[1.39. -49), (1 .39. -55), (1 .39. -61), (1 .46.1-25), (1 .46. -31), (1.46. -37), (1.46. -49), (1 .46. 1-55),

[1.46. -61), (1 .47. -25), (1 .47. -31), (1 .47.1-37), (1 .47. -49), (1.47. -55), (1.47. -61), (1 .53. 1-25),

[1.53. -31), (1 .53. -37), (1 .53. -49), (1 .53.1-55), (1 .53. -61), (1.59. -25), (1.59. -31), (1 .59. 1-37),

[1.59. -49), (1 .59. -55), (1 .59. -61), (1 .63.1-25), (1 .63. -31), (1.63. -37), (1.63. -49), (1 .63. 1-55),

[1.63. -61), (1 .64. -25), (1 .64. -31), (1 .64.1-37), (1 .64. -49), (1.64. -55), (1.64. -61), (1 .65. 1-25),

[1.65. -31), (1 .65. -37), (1 .65. -49), (1 .65.1-55), (1 .65. -61), (1.72. -25), (1.72. -31), (1 .72. 1-37),

[1.72. -49), (1 .72. -55), (1 .72. -61), (1 .73.1-25), (1 .73. -31), (1.73. -37), (1.73. -49), (1 .73. 1-55),

[1.73. -61), (1 .79. -25), (1 .79. -37), (1 .79.1-49), (1 .79. -31), (1.79. -55), (1.79. -61), (1 .272.1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b9), in particular selected from the group consisting of pendimethalin and trifluralin.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

[1.31. -25), (1 .37. -25), (1 .37. -31), (1 .37.1-37), (1 .37. -49), (1.37. -55), (1.37. -61), (1 .38. 1-25),

[1.38. -31), (1 .38. -37), (1 .38. -49), (1 .38.1-55), (1 .38. -61), (1.39. -25), (1.39. -31), (1 .39. 1-37),

[1.39. -49), (1 .39. -55), (1 .39. -61), (1 .46.1-25), (1 .46. -31), (1.46. -37), (1.46. -49), (1 .46. 1-55),

[1.46. -61), (1 .47. -25), (1 .47. -31), (1 .47.1-37), (1 .47. -49), (1.47. -55), (1.47. -61), (1 .53. 1-25),

[1.53. -31), (1 .53. -37), (1 .53. -49), (1 .53.1-55), (1 .53. -61), (1.59. -25), (1.59. -31), (1 .59. 1-37),

[1.59. -49), (1 .59. -55), (1 .59. -61), (1 .63.1-25), (1 .63. -31), (1.63. -37), (1.63. -49), (1 .63. 1-55),

[1.63. -61), (1 .64. -25), (1 .64. -31), (1 .64.1-37), (1 .64. -49), (1.64. -55), (1.64. -61), (1 .65. 1-25),

[1.65. -31), (1 .65. -37), (1 .65. -49), (1 .65.1-55), (1 .65. -61), (1.72. -25), (1.72. -31), (1 .72. 1-37),

[1.72. -49), (1 .72. -55), (1 .72. -61), (1 .73.1-25), (1 .73. -31), (1.73. -37), (1.73. -49), (1 .73. 1-55),

[1.73. -61), (1 .79. -25), (1 .79. -37), (1 .79.1-49), (1 .79. -31), (1.79. -55), (1.79. -61), (1 .272.1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b10), in particular selected from the group consisting of acetochlor, butachlor, cafenstrole, dime- thenamid-P, fentrazamide, flufenacet, mefenacet, metazachlor, metolachlor, S-metolachlor, fenoxasulfone, ipfencarbazone and pyroxasulfone. Likewise, preference is given to compositions comprising in addition to a of formula (I), especially an active compound from the group consisting of, at least one and especially exactly one herbicidally active compound from group b10), in particular selected from the group consisting of isoxazoline compounds of the formulae 11.1, II.2, 11.3 , II.4, II.5, II.6, II.7, II.8 and II.9, as defined above.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73), (1.31.1-25), (1.37.1-25), (1.37.1-31), (1.37.1-37), (1.37.1-49), (1.37.1-55), (1.37.1-61), (1.38.1-25), (1.38.1-31), (1.38.1-37), (1.38.1-49), (1.38.1-55), (1.38.1-61), (1.39.1-25), (1.39.1-31), (1.39.1-37), (1.39.1-49), (1.39.1-55), (1.39.1-61), (1.46.1-25), (1.46.1-31), (1.46.1-37), (1.46.1-49), (1.46.1-55), (1.46.1-61), (1.47.1-25), (1.47.1-31), (1.47.1-37), (1.47.1-49), (1.47.1-55), (1.47.1-61), (1.53.1-25), (1.53.1-31), (1.53.1-37), (1.53.1-49), (1.53.1-55), (1.53.1-61), (1.59.1-25), (1.59.1-31), (1.59.1-37), (1.59.1-49), (1.59.1-55), (1.59.1-61), (1.63.1-25), (1.63.1-31), (1.63.1-37), (1.63.1-49), (1.63.1-55), (1.63.1-61), (1.64.1-25), (1.64.1-31), (1.64.1-37), (1.64.1-49), (1.64.1-55), (1.64.1-61), (1.65.1-25), (1.65.1-31), (1.65.1-37), (1.65.1-49), (1.65.1-55), (1.65.1-61), (1.72.1-25), (1.72.1-31), (1.72.1-37), (1.72.1-49), (1.72.1-55), (1.72.1-61), (1.73.1-25), (1.73.1-31), (1.73.1-37), (1.73.1-49), (1.73.1-55), (1.73.1-61), (1.79.1-25), (1.79.1-37), (1.79.1-49), (1.79.1-31), (1.79.1-55), (1.79.1-61), (1.272.1-25), (1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b11), in particular indaziflam, isoxaben and triaziflam.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73), (1.31.1-25), (1.37.1-25), (1.37.1-31), (1.37.1-37), (1.37.1-49), (1.37.1-55), (1.37.1-61), (1.38.1-25), (1.38.1-31), (138. I-37), (138. I-49), (1.38. I-55), (1.38.1-61), (1.39. I-25), (1.39.1-31), (1.39.1 -37),

(1 .39. I-49), (1 39. I-55), (1 39. 1-61), (1 .46. I-25), (1 .46. 1-31), (1 .46. I-37), (1 .46. I-49), (1 .46.1 -55),

(1 .46. 1-61), (1 47. I-25), (1 47. 1-31), (1 .47. I-37), (1 .47. I-49), (1 .47. I-55), (1 .47. 1-61), (1 .53.1 -25),

(1 .53. 1-31), (1 53. I-37), (1 53. I-49), (1 .53. I-55), (1 .53. 1-61), (1 .59. I-25), (1 .59. 1-31), (1 .59.1 -37),

(1 .59. I-49), (1 59. I-55), (1 59. 1-61), (1 .63. I-25), (1 .63. 1-31), (1 .63. I-37), (1 .63. I-49), (1 .63.1 -55),

(1 .63. 1-61), (1 64. I-25), (1 64. 1-31), (1 .64. I-37), (1 .64. I-49), (1 .64. I-55), (1 .64. 1-61), (1 .65.1 -25),

(1 .65. 1-31), (1 65. I-37), (1 65. I-49), (1 .65. I-55), (1 .65. 1-61), (1 .72. I-25), (1 .72. 1-31), (1 .72.1 -37),

(1 .72. I-49), (1 72. I-55), (1 72. 1-61), (1 .73. I-25), (1 .73. 1-31), (1 .73. I-37), (1 .73. I-49), (1 .73.1 -55),

(1 .73. 1-61), (1 79. I-25), (1 79. I-37), (1 .79. I-49), (1 .79. 1-31), (1 .79. I-55), (1 .79. 1-61), (1 .272 .1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b13), in particular selected from the group consisting of 2,4-D, 2,4-D-isobutyl, 2,4-D-dimethyl- ammonium, 2,4-D-N,N,N-trimethylethanolammonium, aminocyclopyrachlor, aminocyclopyra- chlor-potassium, aminocyclopyrachlor-methyl, aminopyralid, aminopyralid-methyl, aminopyralid- dimethylammonium, aminopyralid-tris(2-hydroxypropyl)ammonium, clopyralid, clopyralid-methyl, clopyralid-olamine, dicamba, dicamba-butotyl, dicamba-diglycolamine, dicamba-dimethylammo- nium, dicamba-diolamine, dicamba-isopropylammonium, dicamba-potassium, dicamba-sodium, dicamba-trolamine, dicamba-N,N-bis-(3-aminopropyl)methylamine, dicamba-diethylenetriamine, flopyrauxifen, fluroxypyr, fluroxypyr-meptyl, halauxifen, halauxifen-methyl, MCPA, MCPA-2- ethylhexyl, MCPA-dimethylammonium, quinclorac, quinclorac-dimethylammonium, quinmerac, quinmerac-dimethylammonium, florpyrauxifen, florpyrauxifen-benzyl (CAS 1390661-72-9), and 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)picolini c acid (CAS 1629965-65-6).

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

(1.31. I-25), (1.37. I-25), (1 37. 1-31), (1 37. I-37), (1 37. I-49), (1.37. I-55), (1 37. 1-61), (1 38. I-25),

(1.38. 1-31), (1.38. I-37), (1 38. I-49), (1 38. I-55), (1 38. 1-61), (1.39. I-25), (1 39. 1-31), (1 39. I-37),

(1.39. I-49), (1.39. I-55), (1 39. 1-61), (1 46. I-25), (1 46. 1-31), (1.46. I-37), (1 46. I-49), (1 46. I-55),

(1.46. 1-61), (1.47. I-25), (1 47. 1-31), (1 47. I-37), (1 47. I-49), (1.47. I-55), (1 47. 1-61), (1 53. I-25),

(1.53. 1-31), (1.53. I-37), (1 53. I-49), (1 53. I-55), (1 53. 1-61), (1.59. I-25), (1 59. 1-31), (1 59. I-37),

(1.59. I-49), (1.59. I-55), (1 59. 1-61), (1 63. I-25), (1 63. 1-31), (1.63. I-37), (1 63. I-49), (1 63. I-55),

(1.63. 1-61), (1.64. I-25), (1 64. 1-31), (1 64. I-37), (1 64. I-49), (1.64. I-55), (1 64. 1-61), (1 65. I-25),

(1.65. 1-31), (1.65. I-37), (1 65. I-49), (1 65. I-55), (1 65. 1-61), (1.72. I-25), (1 72. 1-31), (1 72. I-37),

(1.72. I-49), (1.72. I-55), (1 72. 1-61), (1 73. I-25), (1 73. 1-31), (1.73. I-37), (1 73. I-49), (1 73. I-55), (1.73.1-61), (1.79.1-25), (1.79.1-37), (1.79.1-49), (1.79.1-31), (1.79.1-55), (1.79.1-61), (1.272.1-25), (1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b14), in particular selected from the group consisting of diflufenzopyr, diflufenzopyr-sodium, dymron, indanofan and diflufenzopyr-sodium.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1.10.1-25), (1.10.1-37), (1.10.1-31), (1.10.1-49), (1.10.1-61), (1.10.1-55), (1.10.1-73),

(1.31. -25), (1 .37. -25), (1 .37. -31), (1 .37.1-37), (1 .37. -49), (1.37.1-55), (1.37. -61), (1 .38. 1-25),

(1.38. -31), (1 .38. -37), (1 .38. -49), (1 .38.1-55), (1 .38. -61), (1.39.1-25), (1.39. -31), (1 .39. 1-37),

(1.39. -49), (1 .39. -55), (1 .39. -61), (1 .46.1-25), (1 .46. -31), (1.46.1-37), (1.46. -49), (1 .46. 1-55),

(1.46. -61), (1 .47. -25), (1 .47. -31), (1 .47.1-37), (1 .47. -49), (1.47.1-55), (1.47. -61), (1 .53. 1-25),

(1.53. -31), (1 .53. -37), (1 .53. -49), (1 .53.1-55), (1 .53. -61), (1.59.1-25), (1.59. -31), (1 .59. 1-37),

(1.59. -49), (1 .59. -55), (1 .59. -61), (1 .63.1-25), (1 .63. -31), (1.63.1-37), (1.63. -49), (1 .63. 1-55),

(1.63. -61), (1 .64. -25), (1 .64. -31), (1 .64.1-37), (1 .64. -49), (1.64.1-55), (1.64. -61), (1 .65. 1-25),

(1.65. -31), (1 .65. -37), (1 .65. -49), (1 .65.1-55), (1 .65. -61), (1.72.1-25), (1.72. -31), (1 .72. 1-37),

(1.72. -49), (1 .72. -55), (1 .72. -61), (1 .73.1-25), (1 .73. -31), (1.73.1-37), (1.73. -49), (1 .73. 1-55),

(1.73. -61), (1 .79. -25), (1 .79. -37), (1 .79.1-49), (1 .79. -31), (1.79.1-55), (1.79. -61), (1 .272.1-25)

(1.272.1-31), (1.272.1-37), (1.272.1-49), (1.272.1-55), (1.272.1-61), (1.273.1-25), (1.273.1-31), (1.273.1-37), (1.273.1-49), (1.273.1-55), (1.273.1-61), (1.584.1-25), (1.584.1-31), (1.584.1-37), (1.584.1-49), (1.584.1-55), (1.584.1-61), (1.585.1-25), (1.585.1-31), (1.585.1-37), (1.585.1-49), (1.585.1-55), (1.585.1-61), (1.592.1-25), (1.592.1-31), (1.592.1-37), (1.592.1-49), (1.592.1-55), and (1.592.1-61), at least one and especially exactly one herbicidally active compound from group b15), in particular selected from the group consisting of cinmethylin, dymron (= daimuron), indanofan and oxaziclomefone.

According to another preferred embodiment of the invention, the composition comprises, in addition to a pyrimidine compounds of formula (I), especially an active compound from the group consisting of (1.1.1-25), (1.1.1-37), (1.1.1-31), (1.1.1-49), (1.1.1-61), (1.1.1-55), (1.1.1-73), (1.2.1-25), (1.2.1-37), (1.2.1-31), (1.2.1-49), (1.2.1-61), (1.2.1-55), (1.2.1-73), (1.3.1-25), (1.3.1-37), (1.3.1-31), (1.3.1-49), (1.3.1-61), (1.3.1-55), (1.3.1-73), (1.4.1-25), (1.4.1-37), (1.4.1-31), (1.4.1-49), (1.4.1-61), (1.4.1-55), (1.4.1-73), (1.5.1-25), (1.5.1-37), (1.5.1-31), (1.5.1-49), (1.5.1-61), (1.5.1-55), (1.5.1-73), (1.6.1-25), (1.6.1-37), (1.6.1-31), (1.6.1-49), (1.6.1-61), (1.6.1-55), (1.6.1-73), (1.7.1-25), (1.7.1-37), (1.7.1-31), (1.7.1-49), (1.7.1-61), (1.7.1-55), (1.7.1-73), (1.8.1-25), (1.8.1-37), (1.8.1-31), (1.8.1-49), (1.8.1-61), (1.8.1-55), (1.8.1-73), (1.9.1-25), (1.9.1-37), (1.9.1-31), (1.9.1-49), (1.9.1-61), (1.9.1-55), (1.9.1-73), (1 .10.1-25), (1 .10.1-37), (1 .10.1-31 ), (1 .10.1-49), (1 .10.1-61 ), (1 .10.1-55), (1 .10.1-73),

(1.272.1-31 ), (1 .272.1-37), (1.272.1-49), (1 .272.1-55), (1 .272.1-61 ), (1 .273.1-25), (1.273.1-31 ), (1.273.1-37), (1 .273.1-49), (1.273.1-55), (1 .273.1-61 ), (1 .584.1-25), (1 .584.1-31 ), (1.584.1-37), (1.584.1-49), (1 .584.1-55), (1.584.1-61 ), (1 .585.1-25), (1 .585.1-31 ), (1 .585.1-37), (1.585.1-49), (1.585.1-55), (1 .585.1-61 ), (1.592.1-25), (1 .592.1-31 ), (1 .592.1-37), (1 .592.1-49), (1.592.1-55), and (1.592.1-61 ), at least one and especially exactly one safener C, in particular selected from the group consisting of benoxacor, cloquintocet, cyprosulfamide, dichlormid, fenchlorazole, fenclo- rim, furilazole, isoxadifen, mefenpyr, 4-(dichloroacetyl)-1 -oxa-4-azaspiro[4.5]decane (MON4660, CAS 71526-07-3) and 2,2,5-trimethyl-3-(dichloroacetyl)-1 ,3-oxazolidine (R-29148, CAS 52836- 31-4).

Here and below, the term "binary compositions" includes compositions comprising one or more, e.g. 1 , 2 or 3, active compounds of the formula (I) and either one or more, e.g. 1 , 2 or 3, herbicides B or one or more safeners C.

Correspondingly, the term "ternary compositions" includes compositions comprising one or more, e.g. 1 , 2 or 3, active compounds of the formula (I), one or more, e.g. 1 , 2 or 3, herbicides B and one or more, e.g. 1 , 2 or 3, safeners C.

In binary compositions comprising at least one phenylpyrimidine of formula (I) as component A and at least one herbicide B, the weight ratio of the active compounds A:B is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1.

In binary compositions comprising at least one phenylpyrimidine of formula (I) as component A and at least one safener C, the weight ratio of the active compounds A:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1.

In ternary compositions comprising at least one phenylpyrimidine of formula (I) as component A, at least one herbicide B and at least one safener C, the relative proportions by weight of the components A:B are generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1 , the weight ratio of the components A:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1 , and the weight ratio of the components B:C is generally in the range of from 1 :1000 to 1000:1 , preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1. The weight ratio of components A + B to component C is preferably in the range of from 1 :500 to 500:1 , in particular in the range of from 1 :250 to 250:1 and particularly in the range of from 1 :75 to 75:1.

The weight ratios of the individual components in the preferred mixtures mentioned below are within the limits given above, in particular within the preferred limits.

Particularly preferred are the compositions mentioned below comprising the compounds of formula I as defined and the substance(s) as defined in the respective row of table T;

especially preferred comprising as only herbicidal active compounds the compounds of formula I as defined and the substance(s) as defined in the respective row of table T;

most preferably comprising as only active compounds the compounds of formula I as defined and the substance(s) as defined in the respective row of table T.

Particularly preferred are compositions 1 .1 to 1.3653, comprising the compound 1.1.1-25 and the substance(s) as defined in the respective row of table T:

Table T (compositions 1.1 to 1.3653):

comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1 B.1 — 1.29 B.29 — 1 .57 B.57 —

1.2 B.2 — 1.30 B.30 — 1 .58 B.58 —

1.3 B.3 — 1.31 B.31 — 1 .59 B.59 —

1.4 B.4 — 1.32 B.32 — 1 .60 B.60 —

1.5 B.5 — 1.33 B.33 — 1 .61 B.61 —

1.6 B.6 — 1.34 B.34 — 1 .62 B.62 —

1.7 B.7 — 1.35 B.35 — 1 .63 B.63 —

1.8 B.8 — 1.36 B.36 — 1 .64 B.64 —

1.9 B.9 — 1.37 B.37 — 1 .65 B.65 —

1.10 B.10 — 1.38 B.38 — 1 .66 B.66 —

1.1 1 B.1 1 — 1.39 B.39 — 1 .67 B.67 —

1.12 B.12 — 1.40 B.40 — 1 .68 B.68 —

1.13 B.13 — 1.41 B.41 — 1 .69 B.69 —

1.14 B.14 — 1.42 B.42 — 1 .70 B.70 —

1.15 B.15 — 1.43 B.43 — 1 .71 B.71 —

1.16 B.16 — 1.44 B.44 — 1 .72 B.72 —

1.17 B.17 — 1.45 B.45 — 1 .73 B.73 —

1.18 B.18 — 1.46 B.46 — 1 .74 B.74 —

1.19 B.19 — 1.47 B.47 — 1 .75 B.75 —

1.20 B.20 — 1.48 B.48 — 1 .76 B.76 —

1.21 B.21 — 1.49 B.49 — 1 .77 B.77 —

1.22 B.22 — 1.50 B.50 — 1 .78 B.78 —

1.23 B.23 — 1.51 B.51 — 1 .79 B.79 —

1.24 B.24 — 1.52 B.52 — 1 .80 B.80 —

1.25 B.25 — 1.53 B.53 — 1 .81 B.81 —

1.26 B.26 — 1.54 B.54 — 1 .82 B.82 —

1.27 B.27 — 1.55 B.55 — 1 .83 B.83 —

1.28 B.28 — 1.56 B.56 — 1 .84 B.84 — comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.85 B.85 — 1.126 B.126 — 1.167 B.167 —

1.86 B.86 — 1.127 B.127 — 1.168 B.168 —

1.87 B.87 — 1.128 B.128 — 1.169 B.169 —

1.88 B.88 — 1.129 B.129 — 1.170 B.170 —

1.89 B.89 — 1.130 B.130 — 1.171 B.171 —

1.90 B.90 — 1.131 B.131 — 1.172 B.172 —

1.91 B.91 — 1.132 B.132 — 1.173 B.173 —

1.92 B.92 — 1.133 B.133 — 1.174 B.174 —

1.93 B.93 — 1.134 B.134 — 1.175 B.175 —

1.94 B.94 — 1.135 B.135 — 1.176 B.176 —

1.95 B.95 — 1.136 B.136 — 1.177 B.177 —

1.96 B.96 — 1.137 B.137 — 1.178 B.178 —

1.97 B.97 — 1.138 B.138 — 1.179 B.179 —

1.98 B.98 — 1.139 B.139 — 1.180 B.180 —

1.99 B.99 — 1.140 B.140 — 1.181 B.181 —

1.100 B.100 — 1.141 B.141 — 1.182 B.182 —

1.101 B.101 — 1.142 B.142 — 1.183 B.183 —

1.102 B.102 — 1.143 B.143 — 1.184 B.184 —

1.103 B.103 — 1.144 B.144 — 1.185 B.185 —

1.104 B.104 — 1.145 B.145 — 1.186 B.186 —

1.105 B.105 — 1.146 B.146 — 1.187 B.187 —

1.106 B.106 — 1.147 B.147 — 1.188 B.188 —

1.107 B.107 — 1.148 B.148 — 1.189 B.189 —

1.108 B.108 — 1.149 B.149 — 1.190 B.190 —

1.109 B.109 — 1.150 B.150 — 1.191 B.191 —

1.110 B.110 — 1.151 B.151 — 1.192 B.192 —

1.111 B.111 — 1.152 B.152 — 1.193 B.193 —

1.112 B.112 — 1.153 B.153 — 1.194 B.194 —

1.113 B.113 — 1.154 B.154 — 1.195 B.195 —

1.114 B.114 — 1.155 B.155 — 1.196 B.196 —

1.115 B.115 — 1.156 B.156 — 1.197 B.197 —

1.116 B.116 — 1.157 B.157 — 1.198 B.198 —

1.117 B.117 — 1.158 B.158 — 1.199 B.199 —

1.118 B.118 — 1.159 B.159 — 1.200 B.200 —

1.119 B.119 — 1.160 B.160 — 1.201 B.201 —

1.120 B.120 — 1.161 B.161 — 1.202 B.202 —

1.121 B.121 — 1.162 B.162 — 1.203 B.1 C.1

1.122 B.122 — 1.163 B.163 — 1.204 B.2 C.1

1.123 B.123 — 1.164 B.164 — 1.205 B.3 C.1

1.124 B.124 — 1.165 B.165 — 1.206 B.4 C.1

1.125 B.125 — 1.166 B.166 — 1.207 B.5 C.1 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.208 B.6 C.1 1.249 B.47 C.1 1.290 B.88 C.1

1.209 B.7 C.1 1.250 B.48 C.1 1.291 B.89 C.1

1.210 B.8 C.1 1.251 B.49 C.1 1.292 B.90 C.1

1.211 B.9 C.1 1.252 B.50 C.1 1.293 B.91 C.1

1.212 B.10 C.1 1.253 B.51 C.1 1.294 B.92 C.1

1.213 B.11 C.1 1.254 B.52 C.1 1.295 B.93 C.1

1.214 B.12 C.1 1.255 B.53 C.1 1.296 B.94 C.1

1.215 B.13 C.1 1.256 B.54 C.1 1.297 B.95 C.1

1.216 B.14 C.1 1.257 B.55 C.1 1.298 B.96 C.1

1.217 B.15 C.1 1.258 B.56 C.1 1.299 B.97 C.1

1.218 B.16 C.1 1.259 B.57 C.1 1.300 B.98 C.1

1.219 B.17 C.1 1.260 B.58 C.1 1.301 B.99 C.1

1.220 B.18 C.1 1.261 B.59 C.1 1.302 B.100 C.1

1.221 B.19 C.1 1.262 B.60 C.1 1.303 B.101 C.1

1.222 B.20 C.1 1.263 B.61 C.1 1.304 B.102 C.1

1.223 B.21 C.1 1.264 B.62 C.1 1.305 B.103 C.1

1.224 B.22 C.1 1.265 B.63 C.1 1.306 B.104 C.1

1.225 B.23 C.1 1.266 B.64 C.1 1.307 B.105 C.1

1.226 B.24 C.1 1.267 B.65 C.1 1.308 B.106 C.1

1.227 B.25 C.1 1.268 B.66 C.1 1.309 B.107 C.1

1.228 B.26 C.1 1.269 B.67 C.1 1.310 B.108 C.1

1.229 B.27 C.1 1.270 B.68 C.1 1.311 B.109 C.1

1.230 B.28 C.1 1.271 B.69 C.1 1.312 B.110 C.1

1.231 B.29 C.1 1.272 B.70 C.1 1.313 B.111 C.1

1.232 B.30 C.1 1.273 B.71 C.1 1.314 B.112 C.1

1.233 B.31 C.1 1.274 B.72 C.1 1.315 B.113 C.1

1.234 B.32 C.1 1.275 B.73 C.1 1.316 B.114 C.1

1.235 B.33 C.1 1.276 B.74 C.1 1.317 B.115 C.1

1.236 B.34 C.1 1.277 B.75 C.1 1.318 B.116 C.1

1.237 B.35 C.1 1.278 B.76 C.1 1.319 B.117 C.1

1.238 B.36 C.1 1.279 B.77 C.1 1.320 B.118 C.1

1.239 B.37 C.1 1.280 B.78 C.1 1.321 B.119 C.1

1.240 B.38 C.1 1.281 B.79 C.1 1.322 B.120 C.1

1.241 B.39 C.1 1.282 B.80 C.1 1.323 B.121 C.1

1.242 B.40 C.1 1.283 B.81 C.1 1.324 B.122 C.1

1.243 B.41 C.1 1.284 B.82 C.1 1.325 B.123 C.1

1.244 B.42 C.1 1.285 B.83 C.1 1.326 B.124 C.1

1.245 B.43 C.1 1.286 B.84 C.1 1.327 B.125 C.1

1.246 B.44 C.1 1.287 B.85 C.1 1.328 B.126 C.1

1.247 B.45 C.1 1.288 B.86 C.1 1.329 B.127 C.1

1.248 B.46 C.1 1.289 B.87 C.1 1.330 B.128 C.1 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.331 B.129 C.1 1.372 B.170 C.1 1.413 B.9 C.2

1.332 B.130 C.1 1.373 B.171 C.1 1.414 B.10 C.2

1.333 B.131 C.1 1.374 B.172 C.1 1.415 B.11 C.2

1.334 B.132 C.1 1.375 B.173 C.1 1.416 B.12 C.2

1.335 B.133 C.1 1.376 B.174 C.1 1.417 B.13 C.2

1.336 B.134 C.1 1.377 B.175 C.1 1.418 B.14 C.2

1.337 B.135 C.1 1.378 B.176 C.1 1.419 B.15 C.2

1.338 B.136 C.1 1.379 B.177 C.1 1.420 B.16 C.2

1.339 B.137 C.1 1.380 B.178 C.1 1.421 B.17 C.2

1.340 B.138 C.1 1.381 B.179 C.1 1.422 B.18 C.2

1.341 B.139 C.1 1.382 B.180 C.1 1.423 B.19 C.2

1.342 B.140 C.1 1.383 B.181 C.1 1.424 B.20 C.2

1.343 B.141 C.1 1.384 B.182 C.1 1.425 B.21 C.2

1.344 B.142 C.1 1.385 B.183 C.1 1.426 B.22 C.2

1.345 B.143 C.1 1.386 B.184 C.1 1.427 B.23 C.2

1.346 B.144 C.1 1.387 B.185 C.1 1.428 B.24 C.2

1.347 B.145 C.1 1.388 B.186 C.1 1.429 B.25 C.2

1.348 B.146 C.1 1.389 B.187 C.1 1.430 B.26 C.2

1.349 B.147 C.1 1.390 B.188 C.1 1.431 B.27 C.2

1.350 B.148 C.1 1.391 B.189 C.1 1.432 B.28 C.2

1.351 B.149 C.1 1.392 B.190 C.1 1.433 B.29 C.2

1.352 B.150 C.1 1.393 B.191 C.1 1.434 B.30 C.2

1.353 B.151 C.1 1.394 B.192 C.1 1.435 B.31 C.2

1.354 B.152 C.1 1.395 B.193 C.1 1.436 B.32 C.2

1.355 B.153 C.1 1.396 B.194 C.1 1.437 B.33 C.2

1.356 B.154 C.1 1.397 B.195 C.1 1.438 B.34 C.2

1.357 B.155 C.1 1.398 B.196 C.1 1.439 B.35 C.2

1.358 B.156 C.1 1.399 B.197 C.1 1.440 B.36 C.2

1.359 B.157 C.1 1.400 B.198 C.1 1.441 B.37 C.2

1.360 B.158 C.1 1.401 B.199 C.1 1.442 B.38 C.2

1.361 B.159 C.1 1.402 B.200 C.1 1.443 B.39 C.2

1.362 B.160 C.1 1.403 B.201 C.1 1.444 B.40 C.2

1.363 B.161 C.1 1.404 B.202 C.1 1.445 B.41 C.2

1.364 B.162 C.1 1.405 B.1 C.2 1.446 B.42 C.2

1.365 B.163 C.1 1.406 B.2 C.2 1.447 B.43 C.2

1.366 B.164 C.1 1.407 B.3 C.2 1.448 B.44 C.2

1.367 B.165 C.1 1.408 B.4 C.2 1.449 B.45 C.2

1.368 B.166 C.1 1.409 B.5 C.2 1.450 B.46 C.2

1.369 B.167 C.1 1.410 B.6 C.2 1.451 B.47 C.2

1.370 B.168 C.1 1.411 B.7 C.2 1.452 B.48 C.2

1.371 B.169 C.1 1.412 B.8 C.2 1.453 B.49 C.2 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.454 B.50 C.2 1.495 B.91 C.2 1.536 B.132 C.2

1.455 B.51 C.2 1.496 B.92 C.2 1.537 B.133 C.2

1.456 B.52 C.2 1.497 B.93 C.2 1.538 B.134 C.2

1.457 B.53 C.2 1.498 B.94 C.2 1.539 B.135 C.2

1.458 B.54 C.2 1.499 B.95 C.2 1.540 B.136 C.2

1.459 B.55 C.2 1.500 B.96 C.2 1.541 B.137 C.2

1.460 B.56 C.2 1.501 B.97 C.2 1.542 B.138 C.2

1.461 B.57 C.2 1.502 B.98 C.2 1.543 B.139 C.2

1.462 B.58 C.2 1.503 B.99 C.2 1.544 B.140 C.2

1.463 B.59 C.2 1.504 B.100 C.2 1.545 B.141 C.2

1.464 B.60 C.2 1.505 B.101 C.2 1.546 B.142 C.2

1.465 B.61 C.2 1.506 B.102 C.2 1.547 B.143 C.2

1.466 B.62 C.2 1.507 B.103 C.2 1.548 B.144 C.2

1.467 B.63 C.2 1.508 B.104 C.2 1.549 B.145 C.2

1.468 B.64 C.2 1.509 B.105 C.2 1.550 B.146 C.2

1.469 B.65 C.2 1.510 B.106 C.2 1.551 B.147 C.2

1.470 B.66 C.2 1.511 B.107 C.2 1.552 B.148 C.2

1.471 B.67 C.2 1.512 B.108 C.2 1.553 B.149 C.2

1.472 B.68 C.2 1.513 B.109 C.2 1.554 B.150 C.2

1.473 B.69 C.2 1.514 B.110 C.2 1.555 B.151 C.2

1.474 B.70 C.2 1.515 B.111 C.2 1.556 B.152 C.2

1.475 B.71 C.2 1.516 B.112 C.2 1.557 B.153 C.2

1.476 B.72 C.2 1.517 B.113 C.2 1.558 B.154 C.2

1.477 B.73 C.2 1.518 B.114 C.2 1.559 B.155 C.2

1.478 B.74 C.2 1.519 B.115 C.2 1.560 B.156 C.2

1.479 B.75 C.2 1.520 B.116 C.2 1.561 B.157 C.2

1.480 B.76 C.2 1.521 B.117 C.2 1.562 B.158 C.2

1.481 B.77 C.2 1.522 B.118 C.2 1.563 B.159 C.2

1.482 B.78 C.2 1.523 B.119 C.2 1.564 B.160 C.2

1.483 B.79 C.2 1.524 B.120 C.2 1.565 B.161 C.2

1.484 B.80 C.2 1.525 B.121 C.2 1.566 B.162 C.2

1.485 B.81 C.2 1.526 B.122 C.2 1.567 B.163 C.2

1.486 B.82 C.2 1.527 B.123 C.2 1.568 B.164 C.2

1.487 B.83 C.2 1.528 B.124 C.2 1.569 B.165 C.2

1.488 B.84 C.2 1.529 B.125 C.2 1.570 B.166 C.2

1.489 B.85 C.2 1.530 B.126 C.2 1.571 B.167 C.2

1.490 B.86 C.2 1.531 B.127 C.2 1.572 B.168 C.2

1.491 B.87 C.2 1.532 B.128 C.2 1.573 B.169 C.2

1.492 B.88 C.2 1.533 B.129 C.2 1.574 B.170 C.2

1.493 B.89 C.2 1.534 B.130 C.2 1.575 B.171 C.2

1.494 B.90 C.2 1.535 B.131 C.2 1.576 B.172 C.2 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.577 B.173 C.2 1.618 B.12 C.3 1.659 B.53 C.3

1.578 B.174 C.2 1.619 B.13 C.3 1.660 B.54 C.3

1.579 B.175 C.2 1.620 B.14 C.3 1.661 B.55 C.3

1.580 B.176 C.2 1.621 B.15 C.3 1.662 B.56 C.3

1.581 B.177 C.2 1.622 B.16 C.3 1.663 B.57 C.3

1.582 B.178 C.2 1.623 B.17 C.3 1.664 B.58 C.3

1.583 B.179 C.2 1.624 B.18 C.3 1.665 B.59 C.3

1.584 B.180 C.2 1.625 B.19 C.3 1.666 B.60 C.3

1.585 B.181 C.2 1.626 B.20 C.3 1.667 B.61 C.3

1.586 B.182 C.2 1.627 B.21 C.3 1.668 B.62 C.3

1.587 B.183 C.2 1.628 B.22 C.3 1.669 B.63 C.3

1.588 B.184 C.2 1.629 B.23 C.3 1.670 B.64 C.3

1.589 B.185 C.2 1.630 B.24 C.3 1.671 B.65 C.3

1.590 B.186 C.2 1.631 B.25 C.3 1.672 B.66 C.3

1.591 B.187 C.2 1.632 B.26 C.3 1.673 B.67 C.3

1.592 B.188 C.2 1.633 B.27 C.3 1.674 B.68 C.3

1.593 B.189 C.2 1.634 B.28 C.3 1.675 B.69 C.3

1.594 B.190 C.2 1.635 B.29 C.3 1.676 B.70 C.3

1.595 B.191 C.2 1.636 B.30 C.3 1.677 B.71 C.3

1.596 B.192 C.2 1.637 B.31 C.3 1.678 B.72 C.3

1.597 B.193 C.2 1.638 B.32 C.3 1.679 B.73 C.3

1.598 B.194 C.2 1.639 B.33 C.3 1.680 B.74 C.3

1.599 B.195 C.2 1.640 B.34 C.3 1.681 B.75 C.3

1.600 B.196 C.2 1.641 B.35 C.3 1.682 B.76 C.3

1.601 B.197 C.2 1.642 B.36 C.3 1.683 B.77 C.3

1.602 B.198 C.2 1.643 B.37 C.3 1.684 B.78 C.3

1.603 B.199 C.2 1.644 B.38 C.3 1.685 B.79 C.3

1.604 B.200 C.2 1.645 B.39 C.3 1.686 B.80 C.3

1.605 B.201 C.2 1.646 B.40 C.3 1.687 B.81 C.3

1.606 B.202 C.2 1.647 B.41 C.3 1.688 B.82 C.3

1.607 B.1 C.3 1.648 B.42 C.3 1.689 B.83 C.3

1.608 B.2 C.3 1.649 B.43 C.3 1.690 B.84 C.3

1.609 B.3 C.3 1.650 B.44 C.3 1.691 B.85 C.3

1.610 B.4 C.3 1.651 B.45 C.3 1.692 B.86 C.3

1.611 B.5 C.3 1.652 B.46 C.3 1.693 B.87 C.3

1.612 B.6 C.3 1.653 B.47 C.3 1.694 B.88 C.3

1.613 B.7 C.3 1.654 B.48 C.3 1.695 B.89 C.3

1.614 B.8 C.3 1.655 B.49 C.3 1.696 B.90 C.3

1.615 B.9 C.3 1.656 B.50 C.3 1.697 B.91 C.3

1.616 B.10 C.3 1.657 B.51 C.3 1.698 B.92 C.3

1.617 B.11 C.3 1.658 B.52 C.3 1.699 B.93 C.3 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.700 B.94 C.3 1.741 B.135 C.3 1.782 B.176 C.3

1.701 B.95 C.3 1.742 B.136 C.3 1.783 B.177 C.3

1.702 B.96 C.3 1.743 B.137 C.3 1.784 B.178 C.3

1.703 B.97 C.3 1.744 B.138 C.3 1.785 B.179 C.3

1.704 B.98 C.3 1.745 B.139 C.3 1.786 B.180 C.3

1.705 B.99 C.3 1.746 B.140 C.3 1.787 B.181 C.3

1.706 B.100 C.3 1.747 B.141 C.3 1.788 B.182 C.3

1.707 B.101 C.3 1.748 B.142 C.3 1.789 B.183 C.3

1.708 B.102 C.3 1.749 B.143 C.3 1.790 B.184 C.3

1.709 B.103 C.3 1.750 B.144 C.3 1.791 B.185 C.3

1.710 B.104 C.3 1.751 B.145 C.3 1.792 B.186 C.3

1.711 B.105 C.3 1.752 B.146 C.3 1.793 B.187 C.3

1.712 B.106 C.3 1.753 B.147 C.3 1.794 B.188 C.3

1.713 B.107 C.3 1.754 B.148 C.3 1.795 B.189 C.3

1.714 B.108 C.3 1.755 B.149 C.3 1.796 B.190 C.3

1.715 B.109 C.3 1.756 B.150 C.3 1.797 B.191 C.3

1.716 B.110 C.3 1.757 B.151 C.3 1.798 B.192 C.3

1.717 B.111 C.3 1.758 B.152 C.3 1.799 B.193 C.3

1.718 B.112 C.3 1.759 B.153 C.3 1.800 B.194 C.3

1.719 B.113 C.3 1.760 B.154 C.3 1.801 B.195 C.3

1.720 B.114 C.3 1.761 B.155 C.3 1.802 B.196 C.3

1.721 B.115 C.3 1.762 B.156 C.3 1.803 B.197 C.3

1.722 B.116 C.3 1.763 B.157 C.3 1.804 B.198 C.3

1.723 B.117 C.3 1.764 B.158 C.3 1.805 B.199 C.3

1.724 B.118 C.3 1.765 B.159 C.3 1.806 B.200 C.3

1.725 B.119 C.3 1.766 B.160 C.3 1.807 B.201 C.3

1.726 B.120 C.3 1.767 B.161 C.3 1.808 B.202 C.3

1.727 B.121 C.3 1.768 B.162 C.3 1.809 B.1 C.4

1.728 B.122 C.3 1.769 B.163 C.3 1.810 B.2 C.4

1.729 B.123 C.3 1.770 B.164 C.3 1.811 B.3 C.4

1.730 B.124 C.3 1.771 B.165 C.3 1.812 B.4 C.4

1.731 B.125 C.3 1.772 B.166 C.3 1.813 B.5 C.4

1.732 B.126 C.3 1.773 B.167 C.3 1.814 B.6 C.4

1.733 B.127 C.3 1.774 B.168 C.3 1.815 B.7 C.4

1.734 B.128 C.3 1.775 B.169 C.3 1.816 B.8 C.4

1.735 B.129 C.3 1.776 B.170 C.3 1.817 B.9 C.4

1.736 B.130 C.3 1.777 B.171 C.3 1.818 B.10 C.4

1.737 B.131 C.3 1.778 B.172 C.3 1.819 B.11 C.4

1.738 B.132 C.3 1.779 B.173 C.3 1.820 B.12 C.4

1.739 B.133 C.3 1.780 B.174 C.3 1.821 B.13 C.4

1.740 B.134 C.3 1.781 B.175 C.3 1.822 B.14 C.4 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.823 B.15 C.4 1.864 B.56 C.4 1.905 B.97 C.4

1.824 B.16 C.4 1.865 B.57 C.4 1.906 B.98 C.4

1.825 B.17 C.4 1.866 B.58 C.4 1.907 B.99 C.4

1.826 B.18 C.4 1.867 B.59 C.4 1.908 B.100 C.4

1.827 B.19 C.4 1.868 B.60 C.4 1.909 B.101 C.4

1.828 B.20 C.4 1.869 B.61 C.4 1.910 B.102 C.4

1.829 B.21 C.4 1.870 B.62 C.4 1.911 B.103 C.4

1.830 B.22 C.4 1.871 B.63 C.4 1.912 B.104 C.4

1.831 B.23 C.4 1.872 B.64 C.4 1.913 B.105 C.4

1.832 B.24 C.4 1.873 B.65 C.4 1.914 B.106 C.4

1.833 B.25 C.4 1.874 B.66 C.4 1.915 B.107 C.4

1.834 B.26 C.4 1.875 B.67 C.4 1.916 B.108 C.4

1.835 B.27 C.4 1.876 B.68 C.4 1.917 B.109 C.4

1.836 B.28 C.4 1.877 B.69 C.4 1.918 B.110 C.4

1.837 B.29 C.4 1.878 B.70 C.4 1.919 B.111 C.4

1.838 B.30 C.4 1.879 B.71 C.4 1.920 B.112 C.4

1.839 B.31 C.4 1.880 B.72 C.4 1.921 B.113 C.4

1.840 B.32 C.4 1.881 B.73 C.4 1.922 B.114 C.4

1.841 B.33 C.4 1.882 B.74 C.4 1.923 B.115 C.4

1.842 B.34 C.4 1.883 B.75 C.4 1.924 B.116 C.4

1.843 B.35 C.4 1.884 B.76 C.4 1.925 B.117 C.4

1.844 B.36 C.4 1.885 B.77 C.4 1.926 B.118 C.4

1.845 B.37 C.4 1.886 B.78 C.4 1.927 B.119 C.4

1.846 B.38 C.4 1.887 B.79 C.4 1.928 B.120 C.4

1.847 B.39 C.4 1.888 B.80 C.4 1.929 B.121 C.4

1.848 B.40 C.4 1.889 B.81 C.4 1.930 B.122 C.4

1.849 B.41 C.4 1.890 B.82 C.4 1.931 B.123 C.4

1.850 B.42 C.4 1.891 B.83 C.4 1.932 B.124 C.4

1.851 B.43 C.4 1.892 B.84 C.4 1.933 B.125 C.4

1.852 B.44 C.4 1.893 B.85 C.4 1.934 B.126 C.4

1.853 B.45 C.4 1.894 B.86 C.4 1.935 B.127 C.4

1.854 B.46 C.4 1.895 B.87 C.4 1.936 B.128 C.4

1.855 B.47 C.4 1.896 B.88 C.4 1.937 B.129 C.4

1.856 B.48 C.4 1.897 B.89 C.4 1.938 B.130 C.4

1.857 B.49 C.4 1.898 B.90 C.4 1.939 B.131 C.4

1.858 B.50 C.4 1.899 B.91 C.4 1.940 B.132 C.4

1.859 B.51 C.4 1.900 B.92 C.4 1.941 B.133 C.4

1.860 B.52 C.4 1.901 B.93 C.4 1.942 B.134 C.4

1.861 B.53 C.4 1.902 B.94 C.4 1.943 B.135 C.4

1.862 B.54 C.4 1.903 B.95 C.4 1.944 B.136 C.4

1.863 B.55 C.4 1.904 B.96 C.4 1.945 B.137 C.4 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.946 B.138 C.4 1.987 B.179 C.4 1.1028 B.18 C.5

1.947 B.139 C.4 1.988 B.180 C.4 1.1029 B.19 C.5

1.948 B.140 C.4 1.989 B.181 C.4 1.1030 B.20 C.5

1.949 B.141 C.4 1.990 B.182 C.4 1.1031 B.21 C.5

1.950 B.142 C.4 1.991 B.183 C.4 1.1032 B.22 C.5

1.951 B.143 C.4 1.992 B.184 C.4 1.1033 B.23 C.5

1.952 B.144 C.4 1.993 B.185 C.4 1.1034 B.24 C.5

1.953 B.145 C.4 1.994 B.186 C.4 1.1035 B.25 C.5

1.954 B.146 C.4 1.995 B.187 C.4 1.1036 B.26 C.5

1.955 B.147 C.4 1.996 B.188 C.4 1.1037 B.27 C.5

1.956 B.148 C.4 1.997 B.189 C.4 1.1038 B.28 C.5

1.957 B.149 C.4 1.998 B.190 C.4 1.1039 B.29 C.5

1.958 B.150 C.4 1.999 B.191 C.4 1.1040 B.30 C.5

1.959 B.151 C.4 1.1000 B.192 C.4 1.1041 B.31 C.5

1.960 B.152 C.4 1.1001 B.193 C.4 1.1042 B.32 C.5

1.961 B.153 C.4 1.1002 B.194 C.4 1.1043 B.33 C.5

1.962 B.154 C.4 1.1003 B.195 C.4 1.1044 B.34 C.5

1.963 B.155 C.4 1.1004 B.196 C.4 1.1045 B.35 C.5

1.964 B.156 C.4 1.1005 B.197 C.4 1.1046 B.36 C.5

1.965 B.157 C.4 1.1006 B.198 C.4 1.1047 B.37 C.5

1.966 B.158 C.4 1.1007 B.199 C.4 1.1048 B.38 C.5

1.967 B.159 C.4 1.1008 B.200 C.4 1.1049 B.39 C.5

1.968 B.160 C.4 1.1009 B.201 C.4 1.1050 B.40 C.5

1.969 B.161 C.4 1.1010 B.202 C.4 1.1051 B.41 C.5

1.970 B.162 C.4 1.1011 B.1 C.5 1.1052 B.42 C.5

1.971 B.163 C.4 1.1012 B.2 C.5 1.1053 B.43 C.5

1.972 B.164 C.4 1.1013 B.3 C.5 1.1054 B.44 C.5

1.973 B.165 C.4 1.1014 B.4 C.5 1.1055 B.45 C.5

1.974 B.166 C.4 1.1015 B.5 C.5 1.1056 B.46 C.5

1.975 B.167 C.4 1.1016 B.6 C.5 1.1057 B.47 C.5

1.976 B.168 C.4 1.1017 B.7 C.5 1.1058 B.48 C.5

1.977 B.169 C.4 1.1018 B.8 C.5 1.1059 B.49 C.5

1.978 B.170 C.4 1.1019 B.9 C.5 1.1060 B.50 C.5

1.979 B.171 C.4 1.1020 B.10 C.5 1.1061 B.51 C.5

1.980 B.172 C.4 1.1021 B.11 C.5 1.1062 B.52 C.5

1.981 B.173 C.4 1.1022 B.12 C.5 1.1063 B.53 C.5

1.982 B.174 C.4 1.1023 B.13 C.5 1.1064 B.54 C.5

1.983 B.175 C.4 1.1024 B.14 C.5 1.1065 B.55 C.5

1.984 B.176 C.4 1.1025 B.15 C.5 1.1066 B.56 C.5

1.985 B.177 C.4 1.1026 B.16 C.5 1.1067 B.57 C.5

1.986 B.178 C.4 1.1027 B.17 C.5 1.1068 B.58 C.5 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1069 B.59 C.5 1.1110 B.100 C.5 1.1151 B.141 C.5

1.1070 B.60 C.5 1.1111 B.101 C.5 1.1152 B.142 C.5

1.1071 B.61 C.5 1.1112 B.102 C.5 1.1153 B.143 C.5

1.1072 B.62 C.5 1.1113 B.103 C.5 1.1154 B.144 C.5

1.1073 B.63 C.5 1.1114 B.104 C.5 1.1155 B.145 C.5

1.1074 B.64 C.5 1.1115 B.105 C.5 1.1156 B.146 C.5

1.1075 B.65 C.5 1.1116 B.106 C.5 1.1157 B.147 C.5

1.1076 B.66 C.5 1.1117 B.107 C.5 1.1158 B.148 C.5

1.1077 B.67 C.5 1.1118 B.108 C.5 1.1159 B.149 C.5

1.1078 B.68 C.5 1.1119 B.109 C.5 1.1160 B.150 C.5

1.1079 B.69 C.5 1.1120 B.110 C.5 1.1161 B.151 C.5

1.1080 B.70 C.5 1.1121 B.111 C.5 1.1162 B.152 C.5

1.1081 B.71 C.5 1.1122 B.112 C.5 1.1163 B.153 C.5

1.1082 B.72 C.5 1.1123 B.113 C.5 1.1164 B.154 C.5

1.1083 B.73 C.5 1.1124 B.114 C.5 1.1165 B.155 C.5

1.1084 B.74 C.5 1.1125 B.115 C.5 1.1166 B.156 C.5

1.1085 B.75 C.5 1.1126 B.116 C.5 1.1167 B.157 C.5

1.1086 B.76 C.5 1.1127 B.117 C.5 1.1168 B.158 C.5

1.1087 B.77 C.5 1.1128 B.118 C.5 1.1169 B.159 C.5

1.1088 B.78 C.5 1.1129 B.119 C.5 1.1170 B.160 C.5

1.1089 B.79 C.5 1.1130 B.120 C.5 1.1171 B.161 C.5

1.1090 B.80 C.5 1.1131 B.121 C.5 1.1172 B.162 C.5

1.1091 B.81 C.5 1.1132 B.122 C.5 1.1173 B.163 C.5

1.1092 B.82 C.5 1.1133 B.123 C.5 1.1174 B.164 C.5

1.1093 B.83 C.5 1.1134 B.124 C.5 1.1175 B.165 C.5

1.1094 B.84 C.5 1.1135 B.125 C.5 1.1176 B.166 C.5

1.1095 B.85 C.5 1.1136 B.126 C.5 1.1177 B.167 C.5

1.1096 B.86 C.5 1.1137 B.127 C.5 1.1178 B.168 C.5

1.1097 B.87 C.5 1.1138 B.128 C.5 1.1179 B.169 C.5

1.1098 B.88 C.5 1.1139 B.129 C.5 1.1180 B.170 C.5

1.1099 B.89 C.5 1.1140 B.130 C.5 1.1181 B.171 C.5

1.1100 B.90 C.5 1.1141 B.131 C.5 1.1182 B.172 C.5

1.1101 B.91 C.5 1.1142 B.132 C.5 1.1183 B.173 C.5

1.1102 B.92 C.5 1.1143 B.133 C.5 1.1184 B.174 C.5

1.1103 B.93 C.5 1.1144 B.134 C.5 1.1185 B.175 C.5

1.1104 B.94 C.5 1.1145 B.135 C.5 1.1186 B.176 C.5

1.1105 B.95 C.5 1.1146 B.136 C.5 1.1187 B.177 C.5

1.1106 B.96 C.5 1.1147 B.137 C.5 1.1188 B.178 C.5

1.1107 B.97 C.5 1.1148 B.138 C.5 1.1189 B.179 C.5

1.1108 B.98 C.5 1.1149 B.139 C.5 1.1190 B.180 C.5

1.1109 B.99 C.5 1.1150 B.140 C.5 1.1191 B.181 C.5 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1192 B.182 C.5 1.1233 B.21 C.6 1.1274 B.62 C.6

1.1193 B.183 C.5 1.1234 B.22 C.6 1.1275 B.63 C.6

1.1194 B.184 C.5 1.1235 B.23 C.6 1.1276 B.64 C.6

1.1195 B.185 C.5 1.1236 B.24 C.6 1.1277 B.65 C.6

1.1196 B.186 C.5 1.1237 B.25 C.6 1.1278 B.66 C.6

1.1197 B.187 C.5 1.1238 B.26 C.6 1.1279 B.67 C.6

1.1198 B.188 C.5 1.1239 B.27 C.6 1.1280 B.68 C.6

1.1199 B.189 C.5 1.1240 B.28 C.6 1.1281 B.69 C.6

1.1200 B.190 C.5 1.1241 B.29 C.6 1.1282 B.70 C.6

1.1201 B.191 C.5 1.1242 B.30 C.6 1.1283 B.71 C.6

1.1202 B.192 C.5 1.1243 B.31 C.6 1.1284 B.72 C.6

1.1203 B.193 C.5 1.1244 B.32 C.6 1.1285 B.73 C.6

1.1204 B.194 C.5 1.1245 B.33 C.6 1.1286 B.74 C.6

1.1205 B.195 C.5 1.1246 B.34 C.6 1.1287 B.75 C.6

1.1206 B.196 C.5 1.1247 B.35 C.6 1.1288 B.76 C.6

1.1207 B.197 C.5 1.1248 B.36 C.6 1.1289 B.77 C.6

1.1208 B.198 C.5 1.1249 B.37 C.6 1.1290 B.78 C.6

1.1209 B.199 C.5 1.1250 B.38 C.6 1.1291 B.79 C.6

1.1210 B.200 C.5 1.1251 B.39 C.6 1.1292 B.80 C.6

1.1211 B.201 C.5 1.1252 B.40 C.6 1.1293 B.81 C.6

1.1212 B.202 C.5 1.1253 B.41 C.6 1.1294 B.82 C.6

1.1213 B.1 C.6 1.1254 B.42 C.6 1.1295 B.83 C.6

1.1214 B.2 C.6 1.1255 B.43 C.6 1.1296 B.84 C.6

1.1215 B.3 C.6 1.1256 B.44 C.6 1.1297 B.85 C.6

1.1216 B.4 C.6 1.1257 B.45 C.6 1.1298 B.86 C.6

1.1217 B.5 C.6 1.1258 B.46 C.6 1.1299 B.87 C.6

1.1218 B.6 C.6 1.1259 B.47 C.6 1.1300 B.88 C.6

1.1219 B.7 C.6 1.1260 B.48 C.6 1.1301 B.89 C.6

1.1220 B.8 C.6 1.1261 B.49 C.6 1.1302 B.90 C.6

1.1221 B.9 C.6 1.1262 B.50 C.6 1.1303 B.91 C.6

1.1222 B.10 C.6 1.1263 B.51 C.6 1.1304 B.92 C.6

1.1223 B.11 C.6 1.1264 B.52 C.6 1.1305 B.93 C.6

1.1224 B.12 C.6 1.1265 B.53 C.6 1.1306 B.94 C.6

1.1225 B.13 C.6 1.1266 B.54 C.6 1.1307 B.95 C.6

1.1226 B.14 C.6 1.1267 B.55 C.6 1.1308 B.96 C.6

1.1227 B.15 C.6 1.1268 B.56 C.6 1.1309 B.97 C.6

1.1228 B.16 C.6 1.1269 B.57 C.6 1.1310 B.98 C.6

1.1229 B.17 C.6 1.1270 B.58 C.6 1.1311 B.99 C.6

1.1230 B.18 C.6 1.1271 B.59 C.6 1.1312 B.100 C.6

1.1231 B.19 C.6 1.1272 B.60 C.6 1.1313 B.101 C.6

1.1232 B.20 C.6 1.1273 B.61 C.6 1.1314 B.102 C.6 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1315 B.103 C.6 1.1356 B.144 C.6 1.1397 B.185 C.6

1.1316 B.104 C.6 1.1357 B.145 C.6 1.1398 B.186 C.6

1.1317 B.105 C.6 1.1358 B.146 C.6 1.1399 B.187 C.6

1.1318 B.106 C.6 1.1359 B.147 C.6 1.1400 B.188 C.6

1.1319 B.107 C.6 1.1360 B.148 C.6 1.1401 B.189 C.6

1.1320 B.108 C.6 1.1361 B.149 C.6 1.1402 B.190 C.6

1.1321 B.109 C.6 1.1362 B.150 C.6 1.1403 B.191 C.6

1.1322 B.110 C.6 1.1363 B.151 C.6 1.1404 B.192 C.6

1.1323 B.111 C.6 1.1364 B.152 C.6 1.1405 B.193 C.6

1.1324 B.112 C.6 1.1365 B.153 C.6 1.1406 B.194 C.6

1.1325 B.113 C.6 1.1366 B.154 C.6 1.1407 B.195 C.6

1.1326 B.114 C.6 1.1367 B.155 C.6 1.1408 B.196 C.6

1.1327 B.115 C.6 1.1368 B.156 C.6 1.1409 B.197 C.6

1.1328 B.116 C.6 1.1369 B.157 C.6 1.1410 B.198 C.6

1.1329 B.117 C.6 1.1370 B.158 C.6 1.1411 B.199 C.6

1.1330 B.118 C.6 1.1371 B.159 C.6 1.1412 B.200 C.6

1.1331 B.119 C.6 1.1372 B.160 C.6 1.1413 B.201 C.6

1.1332 B.120 C.6 1.1373 B.161 C.6 1.1414 B.202 C.6

1.1333 B.121 C.6 1.1374 B.162 C.6 1.1415 B.1 C.7

1.1334 B.122 C.6 1.1375 B.163 C.6 1.1416 B.2 C.7

1.1335 B.123 C.6 1.1376 B.164 C.6 1.1417 B.3 C.7

1.1336 B.124 C.6 1.1377 B.165 C.6 1.1418 B.4 C.7

1.1337 B.125 C.6 1.1378 B.166 C.6 1.1419 B.5 C.7

1.1338 B.126 C.6 1.1379 B.167 C.6 1.1420 B.6 C.7

1.1339 B.127 C.6 1.1380 B.168 C.6 1.1421 B.7 C.7

1.1340 B.128 C.6 1.1381 B.169 C.6 1.1422 B.8 C.7

1.1341 B.129 C.6 1.1382 B.170 C.6 1.1423 B.9 C.7

1.1342 B.130 C.6 1.1383 B.171 C.6 1.1424 B.10 C.7

1.1343 B.131 C.6 1.1384 B.172 C.6 1.1425 B.11 C.7

1.1344 B.132 C.6 1.1385 B.173 C.6 1.1426 B.12 C.7

1.1345 B.133 C.6 1.1386 B.174 C.6 1.1427 B.13 C.7

1.1346 B.134 C.6 1.1387 B.175 C.6 1.1428 B.14 C.7

1.1347 B.135 C.6 1.1388 B.176 C.6 1.1429 B.15 C.7

1.1348 B.136 C.6 1.1389 B.177 C.6 1.1430 B.16 C.7

1.1349 B.137 C.6 1.1390 B.178 C.6 1.1431 B.17 C.7

1.1350 B.138 C.6 1.1391 B.179 C.6 1.1432 B.18 C.7

1.1351 B.139 C.6 1.1392 B.180 C.6 1.1433 B.19 C.7

1.1352 B.140 C.6 1.1393 B.181 C.6 1.1434 B.20 C.7

1.1353 B.141 C.6 1.1394 B.182 C.6 1.1435 B.21 C.7

1.1354 B.142 C.6 1.1395 B.183 C.6 1.1436 B.22 C.7

1.1355 B.143 C.6 1.1396 B.184 C.6 1.1437 B.23 C.7 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1438 B.24 C.7 1.1479 B.65 C.7 1.1520 B.106 C.7

1.1439 B.25 C.7 1.1480 B.66 C.7 1.1521 B.107 C.7

1.1440 B.26 C.7 1.1481 B.67 C.7 1.1522 B.108 C.7

1.1441 B.27 C.7 1.1482 B.68 C.7 1.1523 B.109 C.7

1.1442 B.28 C.7 1.1483 B.69 C.7 1.1524 B.110 C.7

1.1443 B.29 C.7 1.1484 B.70 C.7 1.1525 B.111 C.7

1.1444 B.30 C.7 1.1485 B.71 C.7 1.1526 B.112 C.7

1.1445 B.31 C.7 1.1486 B.72 C.7 1.1527 B.113 C.7

1.1446 B.32 C.7 1.1487 B.73 C.7 1.1528 B.114 C.7

1.1447 B.33 C.7 1.1488 B.74 C.7 1.1529 B.115 C.7

1.1448 B.34 C.7 1.1489 B.75 C.7 1.1530 B.116 C.7

1.1449 B.35 C.7 1.1490 B.76 C.7 1.1531 B.117 C.7

1.1450 B.36 C.7 1.1491 B.77 C.7 1.1532 B.118 C.7

1.1451 B.37 C.7 1.1492 B.78 C.7 1.1533 B.119 C.7

1.1452 B.38 C.7 1.1493 B.79 C.7 1.1534 B.120 C.7

1.1453 B.39 C.7 1.1494 B.80 C.7 1.1535 B.121 C.7

1.1454 B.40 C.7 1.1495 B.81 C.7 1.1536 B.122 C.7

1.1455 B.41 C.7 1.1496 B.82 C.7 1.1537 B.123 C.7

1.1456 B.42 C.7 1.1497 B.83 C.7 1.1538 B.124 C.7

1.1457 B.43 C.7 1.1498 B.84 C.7 1.1539 B.125 C.7

1.1458 B.44 C.7 1.1499 B.85 C.7 1.1540 B.126 C.7

1.1459 B.45 C.7 1.1500 B.86 C.7 1.1541 B.127 C.7

1.1460 B.46 C.7 1.1501 B.87 C.7 1.1542 B.128 C.7

1.1461 B.47 C.7 1.1502 B.88 C.7 1.1543 B.129 C.7

1.1462 B.48 C.7 1.1503 B.89 C.7 1.1544 B.130 C.7

1.1463 B.49 C.7 1.1504 B.90 C.7 1.1545 B.131 C.7

1.1464 B.50 C.7 1.1505 B.91 C.7 1.1546 B.132 C.7

1.1465 B.51 C.7 1.1506 B.92 C.7 1.1547 B.133 C.7

1.1466 B.52 C.7 1.1507 B.93 C.7 1.1548 B.134 C.7

1.1467 B.53 C.7 1.1508 B.94 C.7 1.1549 B.135 C.7

1.1468 B.54 C.7 1.1509 B.95 C.7 1.1550 B.136 C.7

1.1469 B.55 C.7 1.1510 B.96 C.7 1.1551 B.137 C.7

1.1470 B.56 C.7 1.1511 B.97 C.7 1.1552 B.138 C.7

1.1471 B.57 C.7 1.1512 B.98 C.7 1.1553 B.139 C.7

1.1472 B.58 C.7 1.1513 B.99 C.7 1.1554 B.140 C.7

1.1473 B.59 C.7 1.1514 B.100 C.7 1.1555 B.141 C.7

1.1474 B.60 C.7 1.1515 B.101 C.7 1.1556 B.142 C.7

1.1475 B.61 C.7 1.1516 B.102 C.7 1.1557 B.143 C.7

1.1476 B.62 C.7 1.1517 B.103 C.7 1.1558 B.144 C.7

1.1477 B.63 C.7 1.1518 B.104 C.7 1.1559 B.145 C.7

1.1478 B.64 C.7 1.1519 B.105 C.7 1.1560 B.146 C.7 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1561 B.147 C.7 1.1602 B.188 C.7 1 .1643 B.27 C.8

1.1562 B.148 C.7 1.1603 B.189 C.7 1 .1644 B.28 C.8

1.1563 B.149 C.7 1.1604 B.190 C.7 1 .1645 B.29 C.8

1.1564 B.150 C.7 1.1605 B.191 C.7 1 .1646 B.30 C.8

1.1565 B.151 C.7 1.1606 B.192 C.7 1 .1647 B.31 C.8

1.1566 B.152 C.7 1.1607 B.193 C.7 1 .1648 B.32 C.8

1.1567 B.153 C.7 1.1608 B.194 C.7 1 .1649 B.33 C.8

1.1568 B.154 C.7 1.1609 B.195 C.7 1 .1650 B.34 C.8

1.1569 B.155 C.7 1.1610 B.196 C.7 1 .1651 B.35 C.8

1.1570 B.156 C.7 1.161 1 B.197 C.7 1 .1652 B.36 C.8

1.1571 B.157 C.7 1.1612 B.198 C.7 1 .1653 B.37 C.8

1.1572 B.158 C.7 1.1613 B.199 C.7 1 .1654 B.38 C.8

1.1573 B.159 C.7 1.1614 B.200 C.7 1 .1655 B.39 C.8

1.1574 B.160 C.7 1.1615 B.201 C.7 1 .1656 B.40 C.8

1.1575 B.161 C.7 1.1616 B.202 C.7 1 .1657 B.41 C.8

1.1576 B.162 C.7 1.1617 B.1 C.8 1 .1658 B.42 C.8

1.1577 B.163 C.7 1.1618 B.2 C.8 1 .1659 B.43 C.8

1.1578 B.164 C.7 1.1619 B.3 C.8 1 .1660 B.44 C.8

1.1579 B.165 C.7 1.1620 B.4 C.8 1 .1661 B.45 C.8

1.1580 B.166 C.7 1.1621 B.5 C.8 1 .1662 B.46 C.8

1.1581 B.167 C.7 1.1622 B.6 C.8 1 .1663 B.47 C.8

1.1582 B.168 C.7 1.1623 B.7 C.8 1 .1664 B.48 C.8

1.1583 B.169 C.7 1.1624 B.8 C.8 1 .1665 B.49 C.8

1.1584 B.170 C.7 1.1625 B.9 C.8 1 .1666 B.50 C.8

1.1585 B.171 C.7 1.1626 B.10 C.8 1 .1667 B.51 C.8

1.1586 B.172 C.7 1.1627 B.1 1 C.8 1 .1668 B.52 C.8

1.1587 B.173 C.7 1.1628 B.12 C.8 1 .1669 B.53 C.8

1.1588 B.174 C.7 1.1629 B.13 C.8 1 .1670 B.54 C.8

1.1589 B.175 C.7 1.1630 B.14 C.8 1 .1671 B.55 C.8

1.1590 B.176 C.7 1.1631 B.15 C.8 1 .1672 B.56 C.8

1.1591 B.177 C.7 1.1632 B.16 C.8 1 .1673 B.57 C.8

1.1592 B.178 C.7 1.1633 B.17 C.8 1 .1674 B.58 C.8

1.1593 B.179 C.7 1.1634 B.18 C.8 1 .1675 B.59 C.8

1.1594 B.180 C.7 1.1635 B.19 C.8 1 .1676 B.60 C.8

1.1595 B.181 C.7 1.1636 B.20 C.8 1 .1677 B.61 C.8

1.1596 B.182 C.7 1.1637 B.21 C.8 1 .1678 B.62 C.8

1.1597 B.183 C.7 1.1638 B.22 C.8 1 .1679 B.63 C.8

1.1598 B.184 C.7 1.1639 B.23 C.8 1 .1680 B.64 C.8

1.1599 B.185 C.7 1.1640 B.24 C.8 1 .1681 B.65 C.8

1.1600 B.186 C.7 1.1641 B.25 C.8 1 .1682 B.66 C.8

1.1601 B.187 C.7 1.1642 B.26 C.8 1 .1683 B.67 C.8 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1684 B.68 C.8 1.1725 B.109 C.8 1.1766 B.150 C.8

1.1685 B.69 C.8 1.1726 B.110 C.8 1.1767 B.151 C.8

1.1686 B.70 C.8 1.1727 B.111 C.8 1.1768 B.152 C.8

1.1687 B.71 C.8 1.1728 B.112 C.8 1.1769 B.153 C.8

1.1688 B.72 C.8 1.1729 B.113 C.8 1.1770 B.154 C.8

1.1689 B.73 C.8 1.1730 B.114 C.8 1.1771 B.155 C.8

1.1690 B.74 C.8 1.1731 B.115 C.8 1.1772 B.156 C.8

1.1691 B.75 C.8 1.1732 B.116 C.8 1.1773 B.157 C.8

1.1692 B.76 C.8 1.1733 B.117 C.8 1.1774 B.158 C.8

1.1693 B.77 C.8 1.1734 B.118 C.8 1.1775 B.159 C.8

1.1694 B.78 C.8 1.1735 B.119 C.8 1.1776 B.160 C.8

1.1695 B.79 C.8 1.1736 B.120 C.8 1.1777 B.161 C.8

1.1696 B.80 C.8 1.1737 B.121 C.8 1.1778 B.162 C.8

1.1697 B.81 C.8 1.1738 B.122 C.8 1.1779 B.163 C.8

1.1698 B.82 C.8 1.1739 B.123 C.8 1.1780 B.164 C.8

1.1699 B.83 C.8 1.1740 B.124 C.8 1.1781 B.165 C.8

1.1700 B.84 C.8 1.1741 B.125 C.8 1.1782 B.166 C.8

1.1701 B.85 C.8 1.1742 B.126 C.8 1.1783 B.167 C.8

1.1702 B.86 C.8 1.1743 B.127 C.8 1.1784 B.168 C.8

1.1703 B.87 C.8 1.1744 B.128 C.8 1.1785 B.169 C.8

1.1704 B.88 C.8 1.1745 B.129 C.8 1.1786 B.170 C.8

1.1705 B.89 C.8 1.1746 B.130 C.8 1.1787 B.171 C.8

1.1706 B.90 C.8 1.1747 B.131 C.8 1.1788 B.172 C.8

1.1707 B.91 C.8 1.1748 B.132 C.8 1.1789 B.173 C.8

1.1708 B.92 C.8 1.1749 B.133 C.8 1.1790 B.174 C.8

1.1709 B.93 C.8 1.1750 B.134 C.8 1.1791 B.175 C.8

1.1710 B.94 C.8 1.1751 B.135 C.8 1.1792 B.176 C.8

1.1711 B.95 C.8 1.1752 B.136 C.8 1.1793 B.177 C.8

1.1712 B.96 C.8 1.1753 B.137 C.8 1.1794 B.178 C.8

1.1713 B.97 C.8 1.1754 B.138 C.8 1.1795 B.179 C.8

1.1714 B.98 C.8 1.1755 B.139 C.8 1.1796 B.180 C.8

1.1715 B.99 C.8 1.1756 B.140 C.8 1.1797 B.181 C.8

1.1716 B.100 C.8 1.1757 B.141 C.8 1.1798 B.182 C.8

1.1717 B.101 C.8 1.1758 B.142 C.8 1.1799 B.183 C.8

1.1718 B.102 C.8 1.1759 B.143 C.8 1.1800 B.184 C.8

1.1719 B.103 C.8 1.1760 B.144 C.8 1.1801 B.185 C.8

1.1720 B.104 C.8 1.1761 B.145 C.8 1.1802 B.186 C.8

1.1721 B.105 C.8 1.1762 B.146 C.8 1.1803 B.187 C.8

1.1722 B.106 C.8 1.1763 B.147 C.8 1.1804 B.188 C.8

1.1723 B.107 C.8 1.1764 B.148 C.8 1.1805 B.189 C.8

1.1724 B.108 C.8 1.1765 B.149 C.8 1.1806 B.190 C.8 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1807 B.191 C.8 1.1848 B.30 C.9 1.1889 B.71 C.9

1.1808 B.192 C.8 1.1849 B.31 C.9 1.1890 B.72 C.9

1.1809 B.193 C.8 1.1850 B.32 C.9 1.1891 B.73 C.9

1.1810 B.194 C.8 1.1851 B.33 C.9 1.1892 B.74 C.9

1.1811 B.195 C.8 1.1852 B.34 C.9 1.1893 B.75 C.9

1.1812 B.196 C.8 1.1853 B.35 C.9 1.1894 B.76 C.9

1.1813 B.197 C.8 1.1854 B.36 C.9 1.1895 B.77 C.9

1.1814 B.198 C.8 1.1855 B.37 C.9 1.1896 B.78 C.9

1.1815 B.199 C.8 1.1856 B.38 C.9 1.1897 B.79 C.9

1.1816 B.200 C.8 1.1857 B.39 C.9 1.1898 B.80 C.9

1.1817 B.201 C.8 1.1858 B.40 C.9 1.1899 B.81 C.9

1.1818 B.202 C.8 1.1859 B.41 C.9 1.1900 B.82 C.9

1.1819 B.1 C.9 1.1860 B.42 C.9 1.1901 B.83 C.9

1.1820 B.2 C.9 1.1861 B.43 C.9 1.1902 B.84 C.9

1.1821 B.3 C.9 1.1862 B.44 C.9 1.1903 B.85 C.9

1.1822 B.4 C.9 1.1863 B.45 C.9 1.1904 B.86 C.9

1.1823 B.5 C.9 1.1864 B.46 C.9 1.1905 B.87 C.9

1.1824 B.6 C.9 1.1865 B.47 C.9 1.1906 B.88 C.9

1.1825 B.7 C.9 1.1866 B.48 C.9 1.1907 B.89 C.9

1.1826 B.8 C.9 1.1867 B.49 C.9 1.1908 B.90 C.9

1.1827 B.9 C.9 1.1868 B.50 C.9 1.1909 B.91 C.9

1.1828 B.10 C.9 1.1869 B.51 C.9 1.1910 B.92 C.9

1.1829 B.11 C.9 1.1870 B.52 C.9 1.1911 B.93 C.9

1.1830 B.12 C.9 1.1871 B.53 C.9 1.1912 B.94 C.9

1.1831 B.13 C.9 1.1872 B.54 C.9 1.1913 B.95 C.9

1.1832 B.14 C.9 1.1873 B.55 C.9 1.1914 B.96 C.9

1.1833 B.15 C.9 1.1874 B.56 C.9 1.1915 B.97 C.9

1.1834 B.16 C.9 1.1875 B.57 C.9 1.1916 B.98 C.9

1.1835 B.17 C.9 1.1876 B.58 C.9 1.1917 B.99 C.9

1.1836 B.18 C.9 1.1877 B.59 C.9 1.1918 B.100 C.9

1.1837 B.19 C.9 1.1878 B.60 C.9 1.1919 B.101 C.9

1.1838 B.20 C.9 1.1879 B.61 C.9 1.1920 B.102 C.9

1.1839 B.21 C.9 1.1880 B.62 C.9 1.1921 B.103 C.9

1.1840 B.22 C.9 1.1881 B.63 C.9 1.1922 B.104 C.9

1.1841 B.23 C.9 1.1882 B.64 C.9 1.1923 B.105 C.9

1.1842 B.24 C.9 1.1883 B.65 C.9 1.1924 B.106 C.9

1.1843 B.25 C.9 1.1884 B.66 C.9 1.1925 B.107 C.9

1.1844 B.26 C.9 1.1885 B.67 C.9 1.1926 B.108 C.9

1.1845 B.27 C.9 1.1886 B.68 C.9 1.1927 B.109 C.9

1.1846 B.28 C.9 1.1887 B.69 C.9 1.1928 B.110 C.9

1.1847 B.29 C.9 1.1888 B.70 C.9 1.1929 B.111 C.9 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.1930 B.1 12 C.9 1.1971 B.153 C.9 1 .2012 B.194 C.9

1.1931 B.1 13 C.9 1.1972 B.154 C.9 1 .2013 B.195 C.9

1.1932 B.1 14 C.9 1.1973 B.155 C.9 1 .2014 B.196 C.9

1.1933 B.1 15 C.9 1.1974 B.156 C.9 1 .2015 B.197 C.9

1.1934 B.1 16 C.9 1.1975 B.157 C.9 1 .2016 B.198 C.9

1.1935 B.1 17 C.9 1.1976 B.158 C.9 1 .2017 B.199 C.9

1.1936 B.1 18 C.9 1.1977 B.159 C.9 1 .2018 B.200 C.9

1.1937 B.1 19 C.9 1.1978 B.160 C.9 1 .2019 B.201 C.9

1.1938 B.120 C.9 1.1979 B.161 C.9 1 .2020 B.202 C.9

1.1939 B.121 C.9 1.1980 B.162 C.9 1 .2021 B.1 C.10

1.1940 B.122 C.9 1.1981 B.163 C.9 1 .2022 B.2 C.10

1.1941 B.123 C.9 1.1982 B.164 C.9 1 .2023 B.3 C.10

1.1942 B.124 C.9 1.1983 B.165 C.9 1 .2024 B.4 C.10

1.1943 B.125 C.9 1.1984 B.166 C.9 1 .2025 B.5 C.10

1.1944 B.126 C.9 1.1985 B.167 C.9 1 .2026 B.6 C.10

1.1945 B.127 C.9 1.1986 B.168 C.9 1 .2027 B.7 C.10

1.1946 B.128 C.9 1.1987 B.169 C.9 1 .2028 B.8 C.10

1.1947 B.129 C.9 1.1988 B.170 C.9 1 .2029 B.9 C.10

1.1948 B.130 C.9 1.1989 B.171 C.9 1 .2030 B.10 C.10

1.1949 B.131 C.9 1.1990 B.172 C.9 1 .2031 B.1 1 C.10

1.1950 B.132 C.9 1.1991 B.173 C.9 1 .2032 B.12 C.10

1.1951 B.133 C.9 1.1992 B.174 C.9 1 .2033 B.13 C.10

1.1952 B.134 C.9 1.1993 B.175 C.9 1 .2034 B.14 C.10

1.1953 B.135 C.9 1.1994 B.176 C.9 1 .2035 B.15 C.10

1.1954 B.136 C.9 1.1995 B.177 C.9 1 .2036 B.16 C.10

1.1955 B.137 C.9 1.1996 B.178 C.9 1 .2037 B.17 C.10

1.1956 B.138 C.9 1.1997 B.179 C.9 1 .2038 B.18 C.10

1.1957 B.139 C.9 1.1998 B.180 C.9 1 .2039 B.19 C.10

1.1958 B.140 C.9 1.1999 B.181 C.9 1 .2040 B.20 C.10

1.1959 B.141 C.9 1.2000 B.182 C.9 1 .2041 B.21 C.10

1.1960 B.142 C.9 1.2001 B.183 C.9 1 .2042 B.22 C.10

1.1961 B.143 C.9 1.2002 B.184 C.9 1 .2043 B.23 C.10

1.1962 B.144 C.9 1.2003 B.185 C.9 1 .2044 B.24 C.10

1.1963 B.145 C.9 1.2004 B.186 C.9 1 .2045 B.25 C.10

1.1964 B.146 C.9 1.2005 B.187 C.9 1 .2046 B.26 C.10

1.1965 B.147 C.9 1.2006 B.188 C.9 1 .2047 B.27 C.10

1.1966 B.148 C.9 1.2007 B.189 C.9 1 .2048 B.28 C.10

1.1967 B.149 C.9 1.2008 B.190 C.9 1 .2049 B.29 C.10

1.1968 B.150 C.9 1.2009 B.191 C.9 1 .2050 B.30 C.10

1.1969 B.151 C.9 1.2010 B.192 C.9 1 .2051 B.31 C.10

1.1970 B.152 C.9 1.201 1 B.193 C.9 1 .2052 B.32 C.10 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2053 B.33 C.10 1.2094 B.74 C.10 1.2135 B.115 C.10

1.2054 B.34 C.10 1.2095 B.75 C.10 1.2136 B.116 C.10

1.2055 B.35 C.10 1.2096 B.76 C.10 1.2137 B.117 C.10

1.2056 B.36 C.10 1.2097 B.77 C.10 1.2138 B.118 C.10

1.2057 B.37 C.10 1.2098 B.78 C.10 1.2139 B.119 C.10

1.2058 B.38 C.10 1.2099 B.79 C.10 1.2140 B.120 C.10

1.2059 B.39 C.10 1.2100 B.80 C.10 1.2141 B.121 C.10

1.2060 B.40 C.10 1.2101 B.81 C.10 1.2142 B.122 C.10

1.2061 B.41 C.10 1.2102 B.82 C.10 1.2143 B.123 C.10

1.2062 B.42 C.10 1.2103 B.83 C.10 1.2144 B.124 C.10

1.2063 B.43 C.10 1.2104 B.84 C.10 1.2145 B.125 C.10

1.2064 B.44 C.10 1.2105 B.85 C.10 1.2146 B.126 C.10

1.2065 B.45 C.10 1.2106 B.86 C.10 1.2147 B.127 C.10

1.2066 B.46 C.10 1.2107 B.87 C.10 1.2148 B.128 C.10

1.2067 B.47 C.10 1.2108 B.88 C.10 1.2149 B.129 C.10

1.2068 B.48 C.10 1.2109 B.89 C.10 1.2150 B.130 C.10

1.2069 B.49 C.10 1.2110 B.90 C.10 1.2151 B.131 C.10

1.2070 B.50 C.10 1.2111 B.91 C.10 1.2152 B.132 C.10

1.2071 B.51 C.10 1.2112 B.92 C.10 1.2153 B.133 C.10

1.2072 B.52 C.10 1.2113 B.93 C.10 1.2154 B.134 C.10

1.2073 B.53 C.10 1.2114 B.94 C.10 1.2155 B.135 C.10

1.2074 B.54 C.10 1.2115 B.95 C.10 1.2156 B.136 C.10

1.2075 B.55 C.10 1.2116 B.96 C.10 1.2157 B.137 C.10

1.2076 B.56 C.10 1.2117 B.97 C.10 1.2158 B.138 C.10

1.2077 B.57 C.10 1.2118 B.98 C.10 1.2159 B.139 C.10

1.2078 B.58 C.10 1.2119 B.99 C.10 1.2160 B.140 C.10

1.2079 B.59 C.10 1.2120 B.100 C.10 1.2161 B.141 C.10

1.2080 B.60 C.10 1.2121 B.101 C.10 1.2162 B.142 C.10

1.2081 B.61 C.10 1.2122 B.102 C.10 1.2163 B.143 C.10

1.2082 B.62 C.10 1.2123 B.103 C.10 1.2164 B.144 C.10

1.2083 B.63 C.10 1.2124 B.104 C.10 1.2165 B.145 C.10

1.2084 B.64 C.10 1.2125 B.105 C.10 1.2166 B.146 C.10

1.2085 B.65 C.10 1.2126 B.106 C.10 1.2167 B.147 C.10

1.2086 B.66 C.10 1.2127 B.107 C.10 1.2168 B.148 C.10

1.2087 B.67 C.10 1.2128 B.108 C.10 1.2169 B.149 C.10

1.2088 B.68 C.10 1.2129 B.109 C.10 1.2170 B.150 C.10

1.2089 B.69 C.10 1.2130 B.110 C.10 1.2171 B.151 C.10

1.2090 B.70 C.10 1.2131 B.111 C.10 1.2172 B.152 C.10

1.2091 B.71 C.10 1.2132 B.112 C.10 1.2173 B.153 C.10

1.2092 B.72 C.10 1.2133 B.113 C.10 1.2174 B.154 C.10

1.2093 B.73 C.10 1.2134 B.114 C.10 1.2175 B.155 C.10 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2176 B.156 C.10 1.2217 B.197 C.10 1.2258 B.36 C.11

1.2177 B.157 C.10 1.2218 B.198 C.10 1.2259 B.37 C.11

1.2178 B.158 C.10 1.2219 B.199 C.10 1.2260 B.38 C.11

1.2179 B.159 C.10 1.2220 B.200 C.10 1.2261 B.39 C.11

1.2180 B.160 C.10 1.2221 B.201 C.10 1.2262 B.40 C.11

1.2181 B.161 C.10 1.2222 B.202 C.10 1.2263 B.41 C.11

1.2182 B.162 C.10 1.2223 B.1 C.11 1.2264 B.42 C.11

1.2183 B.163 C.10 1.2224 B.2 C.11 1.2265 B.43 C.11

1.2184 B.164 C.10 1.2225 B.3 C.11 1.2266 B.44 C.11

1.2185 B.165 C.10 1.2226 B.4 C.11 1.2267 B.45 C.11

1.2186 B.166 C.10 1.2227 B.5 C.11 1.2268 B.46 C.11

1.2187 B.167 C.10 1.2228 B.6 C.11 1.2269 B.47 C.11

1.2188 B.168 C.10 1.2229 B.7 C.11 1.2270 B.48 C.11

1.2189 B.169 C.10 1.2230 B.8 C.11 1.2271 B.49 C.11

1.2190 B.170 C.10 1.2231 B.9 C.11 1.2272 B.50 C.11

1.2191 B.171 C.10 1.2232 B.10 C.11 1.2273 B.51 C.11

1.2192 B.172 C.10 1.2233 B.11 C.11 1.2274 B.52 C.11

1.2193 B.173 C.10 1.2234 B.12 C.11 1.2275 B.53 C.11

1.2194 B.174 C.10 1.2235 B.13 C.11 1.2276 B.54 C.11

1.2195 B.175 C.10 1.2236 B.14 C.11 1.2277 B.55 C.11

1.2196 B.176 C.10 1.2237 B.15 C.11 1.2278 B.56 C.11

1.2197 B.177 C.10 1.2238 B.16 C.11 1.2279 B.57 C.11

1.2198 B.178 C.10 1.2239 B.17 C.11 1.2280 B.58 C.11

1.2199 B.179 C.10 1.2240 B.18 C.11 1.2281 B.59 C.11

1.2200 B.180 C.10 1.2241 B.19 C.11 1.2282 B.60 C.11

1.2201 B.181 C.10 1.2242 B.20 C.11 1.2283 B.61 C.11

1.2202 B.182 C.10 1.2243 B.21 C.11 1.2284 B.62 C.11

1.2203 B.183 C.10 1.2244 B.22 C.11 1.2285 B.63 C.11

1.2204 B.184 C.10 1.2245 B.23 C.11 1.2286 B.64 C.11

1.2205 B.185 C.10 1.2246 B.24 C.11 1.2287 B.65 C.11

1.2206 B.186 C.10 1.2247 B.25 C.11 1.2288 B.66 C.11

1.2207 B.187 C.10 1.2248 B.26 C.11 1.2289 B.67 C.11

1.2208 B.188 C.10 1.2249 B.27 C.11 1.2290 B.68 C.11

1.2209 B.189 C.10 1.2250 B.28 C.11 1.2291 B.69 C.11

1.2210 B.190 C.10 1.2251 B.29 C.11 1.2292 B.70 C.11

1.2211 B.191 C.10 1.2252 B.30 C.11 1.2293 B.71 C.11

1.2212 B.192 C.10 1.2253 B.31 C.11 1.2294 B.72 C.11

1.2213 B.193 C.10 1.2254 B.32 C.11 1.2295 B.73 C.11

1.2214 B.194 C.10 1.2255 B.33 C.11 1.2296 B.74 C.11

1.2215 B.195 C.10 1.2256 B.34 C.11 1.2297 B.75 C.11

1.2216 B.196 C.10 1.2257 B.35 C.11 1.2298 B.76 C.11 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2299 B.77 C.11 1.2340 B.118 C.11 1.2381 B.159 C.11

1.2300 B.78 C.11 1.2341 B.119 C.11 1.2382 B.160 C.11

1.2301 B.79 C.11 1.2342 B.120 C.11 1.2383 B.161 C.11

1.2302 B.80 C.11 1.2343 B.121 C.11 1.2384 B.162 C.11

1.2303 B.81 C.11 1.2344 B.122 C.11 1.2385 B.163 C.11

1.2304 B.82 C.11 1.2345 B.123 C.11 1.2386 B.164 C.11

1.2305 B.83 C.11 1.2346 B.124 C.11 1.2387 B.165 C.11

1.2306 B.84 C.11 1.2347 B.125 C.11 1.2388 B.166 C.11

1.2307 B.85 C.11 1.2348 B.126 C.11 1.2389 B.167 C.11

1.2308 B.86 C.11 1.2349 B.127 C.11 1.2390 B.168 C.11

1.2309 B.87 C.11 1.2350 B.128 C.11 1.2391 B.169 C.11

1.2310 B.88 C.11 1.2351 B.129 C.11 1.2392 B.170 C.11

1.2311 B.89 C.11 1.2352 B.130 C.11 1.2393 B.171 C.11

1.2312 B.90 C.11 1.2353 B.131 C.11 1.2394 B.172 C.11

1.2313 B.91 C.11 1.2354 B.132 C.11 1.2395 B.173 C.11

1.2314 B.92 C.11 1.2355 B.133 C.11 1.2396 B.174 C.11

1.2315 B.93 C.11 1.2356 B.134 C.11 1.2397 B.175 C.11

1.2316 B.94 C.11 1.2357 B.135 C.11 1.2398 B.176 C.11

1.2317 B.95 C.11 1.2358 B.136 C.11 1.2399 B.177 C.11

1.2318 B.96 C.11 1.2359 B.137 C.11 1.2400 B.178 C.11

1.2319 B.97 C.11 1.2360 B.138 C.11 1.2401 B.179 C.11

1.2320 B.98 C.11 1.2361 B.139 C.11 1.2402 B.180 C.11

1.2321 B.99 C.11 1.2362 B.140 C.11 1.2403 B.181 C.11

1.2322 B.100 C.11 1.2363 B.141 C.11 1.2404 B.182 C.11

1.2323 B.101 C.11 1.2364 B.142 C.11 1.2405 B.183 C.11

1.2324 B.102 C.11 1.2365 B.143 C.11 1.2406 B.184 C.11

1.2325 B.103 C.11 1.2366 B.144 C.11 1.2407 B.185 C.11

1.2326 B.104 C.11 1.2367 B.145 C.11 1.2408 B.186 C.11

1.2327 B.105 C.11 1.2368 B.146 C.11 1.2409 B.187 C.11

1.2328 B.106 C.11 1.2369 B.147 C.11 1.2410 B.188 C.11

1.2329 B.107 C.11 1.2370 B.148 C.11 1.2411 B.189 C.11

1.2330 B.108 C.11 1.2371 B.149 C.11 1.2412 B.190 C.11

1.2331 B.109 C.11 1.2372 B.150 C.11 1.2413 B.191 C.11

1.2332 B.110 C.11 1.2373 B.151 C.11 1.2414 B.192 C.11

1.2333 B.111 C.11 1.2374 B.152 C.11 1.2415 B.193 C.11

1.2334 B.112 C.11 1.2375 B.153 C.11 1.2416 B.194 C.11

1.2335 B.113 C.11 1.2376 B.154 C.11 1.2417 B.195 C.11

1.2336 B.114 C.11 1.2377 B.155 C.11 1.2418 B.196 C.11

1.2337 B.115 C.11 1.2378 B.156 C.11 1.2419 B.197 C.11

1.2338 B.116 C.11 1.2379 B.157 C.11 1.2420 B.198 C.11

1.2339 B.117 C.11 1.2380 B.158 C.11 1.2421 B.199 C.11 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2422 B.200 C.1 1 1.2463 B.39 C.12 1 .2504 B.80 C.12

1.2423 B.201 C.1 1 1.2464 B.40 C.12 1 .2505 B.81 C.12

1.2424 B.202 C.1 1 1.2465 B.41 C.12 1 .2506 B.82 C.12

1.2425 B.1 C.12 1.2466 B.42 C.12 1 .2507 B.83 C.12

1.2426 B.2 C.12 1.2467 B.43 C.12 1 .2508 B.84 C.12

1.2427 B.3 C.12 1.2468 B.44 C.12 1 .2509 B.85 C.12

1.2428 B.4 C.12 1.2469 B.45 C.12 1 .2510 B.86 C.12

1.2429 B.5 C.12 1.2470 B.46 C.12 1 .251 1 B.87 C.12

1.2430 B.6 C.12 1.2471 B.47 C.12 1 .2512 B.88 C.12

1.2431 B.7 C.12 1.2472 B.48 C.12 1 .2513 B.89 C.12

1.2432 B.8 C.12 1.2473 B.49 C.12 1 .2514 B.90 C.12

1.2433 B.9 C.12 1.2474 B.50 C.12 1 .2515 B.91 C.12

1.2434 B.10 C.12 1.2475 B.51 C.12 1 .2516 B.92 C.12

1.2435 B.1 1 C.12 1.2476 B.52 C.12 1 .2517 B.93 C.12

1.2436 B.12 C.12 1.2477 B.53 C.12 1 .2518 B.94 C.12

1.2437 B.13 C.12 1.2478 B.54 C.12 1 .2519 B.95 C.12

1.2438 B.14 C.12 1.2479 B.55 C.12 1 .2520 B.96 C.12

1.2439 B.15 C.12 1.2480 B.56 C.12 1 .2521 B.97 C.12

1.2440 B.16 C.12 1.2481 B.57 C.12 1 .2522 B.98 C.12

1.2441 B.17 C.12 1.2482 B.58 C.12 1 .2523 B.99 C.12

1.2442 B.18 C.12 1.2483 B.59 C.12 1 .2524 B.100 C.12

1.2443 B.19 C.12 1.2484 B.60 C.12 1 .2525 B.101 C.12

1.2444 B.20 C.12 1.2485 B.61 C.12 1 .2526 B.102 C.12

1.2445 B.21 C.12 1.2486 B.62 C.12 1 .2527 B.103 C.12

1.2446 B.22 C.12 1.2487 B.63 C.12 1 .2528 B.104 C.12

1.2447 B.23 C.12 1.2488 B.64 C.12 1 .2529 B.105 C.12

1.2448 B.24 C.12 1.2489 B.65 C.12 1 .2530 B.106 C.12

1.2449 B.25 C.12 1.2490 B.66 C.12 1 .2531 B.107 C.12

1.2450 B.26 C.12 1.2491 B.67 C.12 1 .2532 B.108 C.12

1.2451 B.27 C.12 1.2492 B.68 C.12 1 .2533 B.109 C.12

1.2452 B.28 C.12 1.2493 B.69 C.12 1 .2534 B.1 10 C.12

1.2453 B.29 C.12 1.2494 B.70 C.12 1 .2535 B.1 1 1 C.12

1.2454 B.30 C.12 1.2495 B.71 C.12 1 .2536 B.1 12 C.12

1.2455 B.31 C.12 1.2496 B.72 C.12 1 .2537 B.1 13 C.12

1.2456 B.32 C.12 1.2497 B.73 C.12 1 .2538 B.1 14 C.12

1.2457 B.33 C.12 1.2498 B.74 C.12 1 .2539 B.1 15 C.12

1.2458 B.34 C.12 1.2499 B.75 C.12 1 .2540 B.1 16 C.12

1.2459 B.35 C.12 1.2500 B.76 C.12 1 .2541 B.1 17 C.12

1.2460 B.36 C.12 1.2501 B.77 C.12 1 .2542 B.1 18 C.12

1.2461 B.37 C.12 1.2502 B.78 C.12 1 .2543 B.1 19 C.12

1.2462 B.38 C.12 1.2503 B.79 C.12 1 .2544 B.120 C.12 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2545 B.121 C.12 1.2586 B.162 C.12 1 .2627 B.1 C.13

1.2546 B.122 C.12 1.2587 B.163 C.12 1 .2628 B.2 C.13

1.2547 B.123 C.12 1.2588 B.164 C.12 1 .2629 B.3 C.13

1.2548 B.124 C.12 1.2589 B.165 C.12 1 .2630 B.4 C.13

1.2549 B.125 C.12 1.2590 B.166 C.12 1 .2631 B.5 C.13

1.2550 B.126 C.12 1.2591 B.167 C.12 1 .2632 B.6 C.13

1.2551 B.127 C.12 1.2592 B.168 C.12 1 .2633 B.7 C.13

1.2552 B.128 C.12 1.2593 B.169 C.12 1 .2634 B.8 C.13

1.2553 B.129 C.12 1.2594 B.170 C.12 1 .2635 B.9 C.13

1.2554 B.130 C.12 1.2595 B.171 C.12 1 .2636 B.10 C.13

1.2555 B.131 C.12 1.2596 B.172 C.12 1 .2637 B.1 1 C.13

1.2556 B.132 C.12 1.2597 B.173 C.12 1 .2638 B.12 C.13

1.2557 B.133 C.12 1.2598 B.174 C.12 1 .2639 B.13 C.13

1.2558 B.134 C.12 1.2599 B.175 C.12 1 .2640 B.14 C.13

1.2559 B.135 C.12 1.2600 B.176 C.12 1 .2641 B.15 C.13

1.2560 B.136 C.12 1.2601 B.177 C.12 1 .2642 B.16 C.13

1.2561 B.137 C.12 1.2602 B.178 C.12 1 .2643 B.17 C.13

1.2562 B.138 C.12 1.2603 B.179 C.12 1 .2644 B.18 C.13

1.2563 B.139 C.12 1.2604 B.180 C.12 1 .2645 B.19 C.13

1.2564 B.140 C.12 1.2605 B.181 C.12 1 .2646 B.20 C.13

1.2565 B.141 C.12 1.2606 B.182 C.12 1 .2647 B.21 C.13

1.2566 B.142 C.12 1.2607 B.183 C.12 1 .2648 B.22 C.13

1.2567 B.143 C.12 1.2608 B.184 C.12 1 .2649 B.23 C.13

1.2568 B.144 C.12 1.2609 B.185 C.12 1 .2650 B.24 C.13

1.2569 B.145 C.12 1.2610 B.186 C.12 1 .2651 B.25 C.13

1.2570 B.146 C.12 1.261 1 B.187 C.12 1 .2652 B.26 C.13

1.2571 B.147 C.12 1.2612 B.188 C.12 1 .2653 B.27 C.13

1.2572 B.148 C.12 1.2613 B.189 C.12 1 .2654 B.28 C.13

1.2573 B.149 C.12 1.2614 B.190 C.12 1 .2655 B.29 C.13

1.2574 B.150 C.12 1.2615 B.191 C.12 1 .2656 B.30 C.13

1.2575 B.151 C.12 1.2616 B.192 C.12 1 .2657 B.31 C.13

1.2576 B.152 C.12 1.2617 B.193 C.12 1 .2658 B.32 C.13

1.2577 B.153 C.12 1.2618 B.194 C.12 1 .2659 B.33 C.13

1.2578 B.154 C.12 1.2619 B.195 C.12 1 .2660 B.34 C.13

1.2579 B.155 C.12 1.2620 B.196 C.12 1 .2661 B.35 C.13

1.2580 B.156 C.12 1.2621 B.197 C.12 1 .2662 B.36 C.13

1.2581 B.157 C.12 1.2622 B.198 C.12 1 .2663 B.37 C.13

1.2582 B.158 C.12 1.2623 B.199 C.12 1 .2664 B.38 C.13

1.2583 B.159 C.12 1.2624 B.200 C.12 1 .2665 B.39 C.13

1.2584 B.160 C.12 1.2625 B.201 C.12 1 .2666 B.40 C.13

1.2585 B.161 C.12 1.2626 B.202 C.12 1 .2667 B.41 C.13 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2668 B.42 C.13 1.2709 B.83 C.13 1 .2750 B.124 C.13

1.2669 B.43 C.13 1.2710 B.84 C.13 1 .2751 B.125 C.13

1.2670 B.44 C.13 1.271 1 B.85 C.13 1 .2752 B.126 C.13

1.2671 B.45 C.13 1.2712 B.86 C.13 1 .2753 B.127 C.13

1.2672 B.46 C.13 1.2713 B.87 C.13 1 .2754 B.128 C.13

1.2673 B.47 C.13 1.2714 B.88 C.13 1 .2755 B.129 C.13

1.2674 B.48 C.13 1.2715 B.89 C.13 1 .2756 B.130 C.13

1.2675 B.49 C.13 1.2716 B.90 C.13 1 .2757 B.131 C.13

1.2676 B.50 C.13 1.2717 B.91 C.13 1 .2758 B.132 C.13

1.2677 B.51 C.13 1.2718 B.92 C.13 1 .2759 B.133 C.13

1.2678 B.52 C.13 1.2719 B.93 C.13 1 .2760 B.134 C.13

1.2679 B.53 C.13 1.2720 B.94 C.13 1 .2761 B.135 C.13

1.2680 B.54 C.13 1.2721 B.95 C.13 1 .2762 B.136 C.13

1.2681 B.55 C.13 1.2722 B.96 C.13 1 .2763 B.137 C.13

1.2682 B.56 C.13 1.2723 B.97 C.13 1 .2764 B.138 C.13

1.2683 B.57 C.13 1.2724 B.98 C.13 1 .2765 B.139 C.13

1.2684 B.58 C.13 1.2725 B.99 C.13 1 .2766 B.140 C.13

1.2685 B.59 C.13 1.2726 B.100 C.13 1 .2767 B.141 C.13

1.2686 B.60 C.13 1.2727 B.101 C.13 1 .2768 B.142 C.13

1.2687 B.61 C.13 1.2728 B.102 C.13 1 .2769 B.143 C.13

1.2688 B.62 C.13 1.2729 B.103 C.13 1 .2770 B.144 C.13

1.2689 B.63 C.13 1.2730 B.104 C.13 1 .2771 B.145 C.13

1.2690 B.64 C.13 1.2731 B.105 C.13 1 .2772 B.146 C.13

1.2691 B.65 C.13 1.2732 B.106 C.13 1 .2773 B.147 C.13

1.2692 B.66 C.13 1.2733 B.107 C.13 1 .2774 B.148 C.13

1.2693 B.67 C.13 1.2734 B.108 C.13 1 .2775 B.149 C.13

1.2694 B.68 C.13 1.2735 B.109 C.13 1 .2776 B.150 C.13

1.2695 B.69 C.13 1.2736 B.1 10 C.13 1 .2777 B.151 C.13

1.2696 B.70 C.13 1.2737 B.1 1 1 C.13 1 .2778 B.152 C.13

1.2697 B.71 C.13 1.2738 B.1 12 C.13 1 .2779 B.153 C.13

1.2698 B.72 C.13 1.2739 B.1 13 C.13 1 .2780 B.154 C.13

1.2699 B.73 C.13 1.2740 B.1 14 C.13 1 .2781 B.155 C.13

1.2700 B.74 C.13 1.2741 B.1 15 C.13 1 .2782 B.156 C.13

1.2701 B.75 C.13 1.2742 B.1 16 C.13 1 .2783 B.157 C.13

1.2702 B.76 C.13 1.2743 B.1 17 C.13 1 .2784 B.158 C.13

1.2703 B.77 C.13 1.2744 B.1 18 C.13 1 .2785 B.159 C.13

1.2704 B.78 C.13 1.2745 B.1 19 C.13 1 .2786 B.160 C.13

1.2705 B.79 C.13 1.2746 B.120 C.13 1 .2787 B.161 C.13

1.2706 B.80 C.13 1.2747 B.121 C.13 1 .2788 B.162 C.13

1.2707 B.81 C.13 1.2748 B.122 C.13 1 .2789 B.163 C.13

1.2708 B.82 C.13 1.2749 B.123 C.13 1 .2790 B.164 C.13 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2791 B.165 C.13 1.2832 B.4 C.14 1 .2873 B.45 C.14

1.2792 B.166 C.13 1.2833 B.5 C.14 1 .2874 B.46 C.14

1.2793 B.167 C.13 1.2834 B.6 C.14 1 .2875 B.47 C.14

1.2794 B.168 C.13 1.2835 B.7 C.14 1 .2876 B.48 C.14

1.2795 B.169 C.13 1.2836 B.8 C.14 1 .2877 B.49 C.14

1.2796 B.170 C.13 1.2837 B.9 C.14 1 .2878 B.50 C.14

1.2797 B.171 C.13 1.2838 B.10 C.14 1 .2879 B.51 C.14

1.2798 B.172 C.13 1.2839 B.1 1 C.14 1 .2880 B.52 C.14

1.2799 B.173 C.13 1.2840 B.12 C.14 1 .2881 B.53 C.14

1.2800 B.174 C.13 1.2841 B.13 C.14 1 .2882 B.54 C.14

1.2801 B.175 C.13 1.2842 B.14 C.14 1 .2883 B.55 C.14

1.2802 B.176 C.13 1.2843 B.15 C.14 1 .2884 B.56 C.14

1.2803 B.177 C.13 1.2844 B.16 C.14 1 .2885 B.57 C.14

1.2804 B.178 C.13 1.2845 B.17 C.14 1 .2886 B.58 C.14

1.2805 B.179 C.13 1.2846 B.18 C.14 1 .2887 B.59 C.14

1.2806 B.180 C.13 1.2847 B.19 C.14 1 .2888 B.60 C.14

1.2807 B.181 C.13 1.2848 B.20 C.14 1 .2889 B.61 C.14

1.2808 B.182 C.13 1.2849 B.21 C.14 1 .2890 B.62 C.14

1.2809 B.183 C.13 1.2850 B.22 C.14 1 .2891 B.63 C.14

1.2810 B.184 C.13 1.2851 B.23 C.14 1 .2892 B.64 C.14

1.281 1 B.185 C.13 1.2852 B.24 C.14 1 .2893 B.65 C.14

1.2812 B.186 C.13 1.2853 B.25 C.14 1 .2894 B.66 C.14

1.2813 B.187 C.13 1.2854 B.26 C.14 1 .2895 B.67 C.14

1.2814 B.188 C.13 1.2855 B.27 C.14 1 .2896 B.68 C.14

1.2815 B.189 C.13 1.2856 B.28 C.14 1 .2897 B.69 C.14

1.2816 B.190 C.13 1.2857 B.29 C.14 1 .2898 B.70 C.14

1.2817 B.191 C.13 1.2858 B.30 C.14 1 .2899 B.71 C.14

1.2818 B.192 C.13 1.2859 B.31 C.14 1 .2900 B.72 C.14

1.2819 B.193 C.13 1.2860 B.32 C.14 1 .2901 B.73 C.14

1.2820 B.194 C.13 1.2861 B.33 C.14 1 .2902 B.74 C.14

1.2821 B.195 C.13 1.2862 B.34 C.14 1 .2903 B.75 C.14

1.2822 B.196 C.13 1.2863 B.35 C.14 1 .2904 B.76 C.14

1.2823 B.197 C.13 1.2864 B.36 C.14 1 .2905 B.77 C.14

1.2824 B.198 C.13 1.2865 B.37 C.14 1 .2906 B.78 C.14

1.2825 B.199 C.13 1.2866 B.38 C.14 1 .2907 B.79 C.14

1.2826 B.200 C.13 1.2867 B.39 C.14 1 .2908 B.80 C.14

1.2827 B.201 C.13 1.2868 B.40 C.14 1 .2909 B.81 C.14

1.2828 B.202 C.13 1.2869 B.41 C.14 1 .2910 B.82 C.14

1.2829 B.1 C.14 1.2870 B.42 C.14 1 .291 1 B.83 C.14

1.2830 B.2 C.14 1.2871 B.43 C.14 1 .2912 B.84 C.14

1.2831 B.3 C.14 1.2872 B.44 C.14 1 .2913 B.85 C.14 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.2914 B.86 C.14 1.2955 B.127 C.14 1.2996 B.168 C.14

1.2915 B.87 C.14 1.2956 B.128 C.14 1.2997 B.169 C.14

1.2916 B.88 C.14 1.2957 B.129 C.14 1.2998 B.170 C.14

1.2917 B.89 C.14 1.2958 B.130 C.14 1.2999 B.171 C.14

1.2918 B.90 C.14 1.2959 B.131 C.14 1.3000 B.172 C.14

1.2919 B.91 C.14 1.2960 B.132 C.14 1.3001 B.173 C.14

1.2920 B.92 C.14 1.2961 B.133 C.14 1.3002 B.174 C.14

1.2921 B.93 C.14 1.2962 B.134 C.14 1.3003 B.175 C.14

1.2922 B.94 C.14 1.2963 B.135 C.14 1.3004 B.176 C.14

1.2923 B.95 C.14 1.2964 B.136 C.14 1.3005 B.177 C.14

1.2924 B.96 C.14 1.2965 B.137 C.14 1.3006 B.178 C.14

1.2925 B.97 C.14 1.2966 B.138 C.14 1.3007 B.179 C.14

1.2926 B.98 C.14 1.2967 B.139 C.14 1.3008 B.180 C.14

1.2927 B.99 C.14 1.2968 B.140 C.14 1.3009 B.181 C.14

1.2928 B.100 C.14 1.2969 B.141 C.14 1.3010 B.182 C.14

1.2929 B.101 C.14 1.2970 B.142 C.14 1.3011 B.183 C.14

1.2930 B.102 C.14 1.2971 B.143 C.14 1.3012 B.184 C.14

1.2931 B.103 C.14 1.2972 B.144 C.14 1.3013 B.185 C.14

1.2932 B.104 C.14 1.2973 B.145 C.14 1.3014 B.186 C.14

1.2933 B.105 C.14 1.2974 B.146 C.14 1.3015 B.187 C.14

1.2934 B.106 C.14 1.2975 B.147 C.14 1.3016 B.188 C.14

1.2935 B.107 C.14 1.2976 B.148 C.14 1.3017 B.189 C.14

1.2936 B.108 C.14 1.2977 B.149 C.14 1.3018 B.190 C.14

1.2937 B.109 C.14 1.2978 B.150 C.14 1.3019 B.191 C.14

1.2938 B.110 C.14 1.2979 B.151 C.14 1.3020 B.192 C.14

1.2939 B.111 C.14 1.2980 B.152 C.14 1.3021 B.193 C.14

1.2940 B.112 C.14 1.2981 B.153 C.14 1.3022 B.194 C.14

1.2941 B.113 C.14 1.2982 B.154 C.14 1.3023 B.195 C.14

1.2942 B.114 C.14 1.2983 B.155 C.14 1.3024 B.196 C.14

1.2943 B.115 C.14 1.2984 B.156 C.14 1.3025 B.197 C.14

1.2944 B.116 C.14 1.2985 B.157 C.14 1.3026 B.198 C.14

1.2945 B.117 C.14 1.2986 B.158 C.14 1.3027 B.199 C.14

1.2946 B.118 C.14 1.2987 B.159 C.14 1.3028 B.200 C.14

1.2947 B.119 C.14 1.2988 B.160 C.14 1.3029 B.201 C.14

1.2948 B.120 C.14 1.2989 B.161 C.14 1.3030 B.202 C.14

1.2949 B.121 C.14 1.2990 B.162 C.14 1.3031 B.1 C.15

1.2950 B.122 C.14 1.2991 B.163 C.14 1.3032 B.2 C.15

1.2951 B.123 C.14 1.2992 B.164 C.14 1.3033 B.3 C.15

1.2952 B.124 C.14 1.2993 B.165 C.14 1.3034 B.4 C.15

1.2953 B.125 C.14 1.2994 B.166 C.14 1.3035 B.5 C.15

1.2954 B.126 C.14 1.2995 B.167 C.14 1.3036 B.6 C.15 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.3037 B.7 C.15 1.3078 B.48 C.15 1.3119 B.89 C.15

1.3038 B.8 C.15 1.3079 B.49 C.15 1.3120 B.90 C.15

1.3039 B.9 C.15 1.3080 B.50 C.15 1.3121 B.91 C.15

1.3040 B.10 C.15 1.3081 B.51 C.15 1.3122 B.92 C.15

1.3041 B.11 C.15 1.3082 B.52 C.15 1.3123 B.93 C.15

1.3042 B.12 C.15 1.3083 B.53 C.15 1.3124 B.94 C.15

1.3043 B.13 C.15 1.3084 B.54 C.15 1.3125 B.95 C.15

1.3044 B.14 C.15 1.3085 B.55 C.15 1.3126 B.96 C.15

1.3045 B.15 C.15 1.3086 B.56 C.15 1.3127 B.97 C.15

1.3046 B.16 C.15 1.3087 B.57 C.15 1.3128 B.98 C.15

1.3047 B.17 C.15 1.3088 B.58 C.15 1.3129 B.99 C.15

1.3048 B.18 C.15 1.3089 B.59 C.15 1.3130 B.100 C.15

1.3049 B.19 C.15 1.3090 B.60 C.15 1.3131 B.101 C.15

1.3050 B.20 C.15 1.3091 B.61 C.15 1.3132 B.102 C.15

1.3051 B.21 C.15 1.3092 B.62 C.15 1.3133 B.103 C.15

1.3052 B.22 C.15 1.3093 B.63 C.15 1.3134 B.104 C.15

1.3053 B.23 C.15 1.3094 B.64 C.15 1.3135 B.105 C.15

1.3054 B.24 C.15 1.3095 B.65 C.15 1.3136 B.106 C.15

1.3055 B.25 C.15 1.3096 B.66 C.15 1.3137 B.107 C.15

1.3056 B.26 C.15 1.3097 B.67 C.15 1.3138 B.108 C.15

1.3057 B.27 C.15 1.3098 B.68 C.15 1.3139 B.109 C.15

1.3058 B.28 C.15 1.3099 B.69 C.15 1.3140 B.110 C.15

1.3059 B.29 C.15 1.3100 B.70 C.15 1.3141 B.111 C.15

1.3060 B.30 C.15 1.3101 B.71 C.15 1.3142 B.112 C.15

1.3061 B.31 C.15 1.3102 B.72 C.15 1.3143 B.113 C.15

1.3062 B.32 C.15 1.3103 B.73 C.15 1.3144 B.114 C.15

1.3063 B.33 C.15 1.3104 B.74 C.15 1.3145 B.115 C.15

1.3064 B.34 C.15 1.3105 B.75 C.15 1.3146 B.116 C.15

1.3065 B.35 C.15 1.3106 B.76 C.15 1.3147 B.117 C.15

1.3066 B.36 C.15 1.3107 B.77 C.15 1.3148 B.118 C.15

1.3067 B.37 C.15 1.3108 B.78 C.15 1.3149 B.119 C.15

1.3068 B.38 C.15 1.3109 B.79 C.15 1.3150 B.120 C.15

1.3069 B.39 C.15 1.3110 B.80 C.15 1.3151 B.121 C.15

1.3070 B.40 C.15 1.3111 B.81 C.15 1.3152 B.122 C.15

1.3071 B.41 C.15 1.3112 B.82 C.15 1.3153 B.123 C.15

1.3072 B.42 C.15 1.3113 B.83 C.15 1.3154 B.124 C.15

1.3073 B.43 C.15 1.3114 B.84 C.15 1.3155 B.125 C.15

1.3074 B.44 C.15 1.3115 B.85 C.15 1.3156 B.126 C.15

1.3075 B.45 C.15 1.3116 B.86 C.15 1.3157 B.127 C.15

1.3076 B.46 C.15 1.3117 B.87 C.15 1.3158 B.128 C.15

1.3077 B.47 C.15 1.3118 B.88 C.15 1.3159 B.129 C.15 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.3160 B.130 C.15 1.3201 B.171 C.15 1 .3242 B.10 C.16

1.3161 B.131 C.15 1.3202 B.172 C.15 1 .3243 B.1 1 C.16

1.3162 B.132 C.15 1.3203 B.173 C.15 1 .3244 B.12 C.16

1.3163 B.133 C.15 1.3204 B.174 C.15 1 .3245 B.13 C.16

1.3164 B.134 C.15 1.3205 B.175 C.15 1 .3246 B.14 C.16

1.3165 B.135 C.15 1.3206 B.176 C.15 1 .3247 B.15 C.16

1.3166 B.136 C.15 1.3207 B.177 C.15 1 .3248 B.16 C.16

1.3167 B.137 C.15 1.3208 B.178 C.15 1 .3249 B.17 C.16

1.3168 B.138 C.15 1.3209 B.179 C.15 1 .3250 B.18 C.16

1.3169 B.139 C.15 1.3210 B.180 C.15 1 .3251 B.19 C.16

1.3170 B.140 C.15 1.321 1 B.181 C.15 1 .3252 B.20 C.16

1.3171 B.141 C.15 1.3212 B.182 C.15 1 .3253 B.21 C.16

1.3172 B.142 C.15 1.3213 B.183 C.15 1 .3254 B.22 C.16

1.3173 B.143 C.15 1.3214 B.184 C.15 1 .3255 B.23 C.16

1.3174 B.144 C.15 1.3215 B.185 C.15 1 .3256 B.24 C.16

1.3175 B.145 C.15 1.3216 B.186 C.15 1 .3257 B.25 C.16

1.3176 B.146 C.15 1.3217 B.187 C.15 1 .3258 B.26 C.16

1.3177 B.147 C.15 1.3218 B.188 C.15 1 .3259 B.27 C.16

1.3178 B.148 C.15 1.3219 B.189 C.15 1 .3260 B.28 C.16

1.3179 B.149 C.15 1.3220 B.190 C.15 1 .3261 B.29 C.16

1.3180 B.150 C.15 1.3221 B.191 C.15 1 .3262 B.30 C.16

1.3181 B.151 C.15 1.3222 B.192 C.15 1 .3263 B.31 C.16

1.3182 B.152 C.15 1.3223 B.193 C.15 1 .3264 B.32 C.16

1.3183 B.153 C.15 1.3224 B.194 C.15 1 .3265 B.33 C.16

1.3184 B.154 C.15 1.3225 B.195 C.15 1 .3266 B.34 C.16

1.3185 B.155 C.15 1.3226 B.196 C.15 1 .3267 B.35 C.16

1.3186 B.156 C.15 1.3227 B.197 C.15 1 .3268 B.36 C.16

1.3187 B.157 C.15 1.3228 B.198 C.15 1 .3269 B.37 C.16

1.3188 B.158 C.15 1.3229 B.199 C.15 1 .3270 B.38 C.16

1.3189 B.159 C.15 1.3230 B.200 C.15 1 .3271 B.39 C.16

1.3190 B.160 C.15 1.3231 B.201 C.15 1 .3272 B.40 C.16

1.3191 B.161 C.15 1.3232 B.202 C.15 1 .3273 B.41 C.16

1.3192 B.162 C.15 1.3233 B.1 C.16 1 .3274 B.42 C.16

1.3193 B.163 C.15 1.3234 B.2 C.16 1 .3275 B.43 C.16

1.3194 B.164 C.15 1.3235 B.3 C.16 1 .3276 B.44 C.16

1.3195 B.165 C.15 1.3236 B.4 C.16 1 .3277 B.45 C.16

1.3196 B.166 C.15 1.3237 B.5 C.16 1 .3278 B.46 C.16

1.3197 B.167 C.15 1.3238 B.6 C.16 1 .3279 B.47 C.16

1.3198 B.168 C.15 1.3239 B.7 C.16 1 .3280 B.48 C.16

1.3199 B.169 C.15 1.3240 B.8 C.16 1 .3281 B.49 C.16

1.3200 B.170 C.15 1.3241 B.9 C.16 1 .3282 B.50 C.16 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.3283 B.51 C.16 1.3324 B.92 C.16 1.3365 B.133 C.16

1.3284 B.52 C.16 1.3325 B.93 C.16 1.3366 B.134 C.16

1.3285 B.53 C.16 1.3326 B.94 C.16 1.3367 B.135 C.16

1.3286 B.54 C.16 1.3327 B.95 C.16 1.3368 B.136 C.16

1.3287 B.55 C.16 1.3328 B.96 C.16 1.3369 B.137 C.16

1.3288 B.56 C.16 1.3329 B.97 C.16 1.3370 B.138 C.16

1.3289 B.57 C.16 1.3330 B.98 C.16 1.3371 B.139 C.16

1.3290 B.58 C.16 1.3331 B.99 C.16 1.3372 B.140 C.16

1.3291 B.59 C.16 1.3332 B.100 C.16 1.3373 B.141 C.16

1.3292 B.60 C.16 1.3333 B.101 C.16 1.3374 B.142 C.16

1.3293 B.61 C.16 1.3334 B.102 C.16 1.3375 B.143 C.16

1.3294 B.62 C.16 1.3335 B.103 C.16 1.3376 B.144 C.16

1.3295 B.63 C.16 1.3336 B.104 C.16 1.3377 B.145 C.16

1.3296 B.64 C.16 1.3337 B.105 C.16 1.3378 B.146 C.16

1.3297 B.65 C.16 1.3338 B.106 C.16 1.3379 B.147 C.16

1.3298 B.66 C.16 1.3339 B.107 C.16 1.3380 B.148 C.16

1.3299 B.67 C.16 1.3340 B.108 C.16 1.3381 B.149 C.16

1.3300 B.68 C.16 1.3341 B.109 C.16 1.3382 B.150 C.16

1.3301 B.69 C.16 1.3342 B.110 C.16 1.3383 B.151 C.16

1.3302 B.70 C.16 1.3343 B.111 C.16 1.3384 B.152 C.16

1.3303 B.71 C.16 1.3344 B.112 C.16 1.3385 B.153 C.16

1.3304 B.72 C.16 1.3345 B.113 C.16 1.3386 B.154 C.16

1.3305 B.73 C.16 1.3346 B.114 C.16 1.3387 B.155 C.16

1.3306 B.74 C.16 1.3347 B.115 C.16 1.3388 B.156 C.16

1.3307 B.75 C.16 1.3348 B.116 C.16 1.3389 B.157 C.16

1.3308 B.76 C.16 1.3349 B.117 C.16 1.3390 B.158 C.16

1.3309 B.77 C.16 1.3350 B.118 C.16 1.3391 B.159 C.16

1.3310 B.78 C.16 1.3351 B.119 C.16 1.3392 B.160 C.16

1.3311 B.79 C.16 1.3352 B.120 C.16 1.3393 B.161 C.16

1.3312 B.80 C.16 1.3353 B.121 C.16 1.3394 B.162 C.16

1.3313 B.81 C.16 1.3354 B.122 C.16 1.3395 B.163 C.16

1.3314 B.82 C.16 1.3355 B.123 C.16 1.3396 B.164 C.16

1.3315 B.83 C.16 1.3356 B.124 C.16 1.3397 B.165 C.16

1.3316 B.84 C.16 1.3357 B.125 C.16 1.3398 B.166 C.16

1.3317 B.85 C.16 1.3358 B.126 C.16 1.3399 B.167 C.16

1.3318 B.86 C.16 1.3359 B.127 C.16 1.3400 B.168 C.16

1.3319 B.87 C.16 1.3360 B.128 C.16 1.3401 B.169 C.16

1.3320 B.88 C.16 1.3361 B.129 C.16 1.3402 B.170 C.16

1.3321 B.89 C.16 1.3362 B.130 C.16 1.3403 B.171 C.16

1.3322 B.90 C.16 1.3363 B.131 C.16 1.3404 B.172 C.16

1.3323 B.91 C.16 1.3364 B.132 C.16 1.3405 B.173 C.16 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.3406 B.174 C.16 1.3447 B.13 C.17 1 .3488 B.54 C.17

1.3407 B.175 C.16 1.3448 B.14 C.17 1 .3489 B.55 C.17

1.3408 B.176 C.16 1.3449 B.15 C.17 1 .3490 B.56 C.17

1.3409 B.177 C.16 1.3450 B.16 C.17 1 .3491 B.57 C.17

1.3410 B.178 C.16 1.3451 B.17 C.17 1 .3492 B.58 C.17

1.341 1 B.179 C.16 1.3452 B.18 C.17 1 .3493 B.59 C.17

1.3412 B.180 C.16 1.3453 B.19 C.17 1 .3494 B.60 C.17

1.3413 B.181 C.16 1.3454 B.20 C.17 1 .3495 B.61 C.17

1.3414 B.182 C.16 1.3455 B.21 C.17 1 .3496 B.62 C.17

1.3415 B.183 C.16 1.3456 B.22 C.17 1 .3497 B.63 C.17

1.3416 B.184 C.16 1.3457 B.23 C.17 1 .3498 B.64 C.17

1.3417 B.185 C.16 1.3458 B.24 C.17 1 .3499 B.65 C.17

1.3418 B.186 C.16 1.3459 B.25 C.17 1 .3500 B.66 C.17

1.3419 B.187 C.16 1.3460 B.26 C.17 1 .3501 B.67 C.17

1.3420 B.188 C.16 1.3461 B.27 C.17 1 .3502 B.68 C.17

1.3421 B.189 C.16 1.3462 B.28 C.17 1 .3503 B.69 C.17

1.3422 B.190 C.16 1.3463 B.29 C.17 1 .3504 B.70 C.17

1.3423 B.191 C.16 1.3464 B.30 C.17 1 .3505 B.71 C.17

1.3424 B.192 C.16 1.3465 B.31 C.17 1 .3506 B.72 C.17

1.3425 B.193 C.16 1.3466 B.32 C.17 1 .3507 B.73 C.17

1.3426 B.194 C.16 1.3467 B.33 C.17 1 .3508 B.74 C.17

1.3427 B.195 C.16 1.3468 B.34 C.17 1 .3509 B.75 C.17

1.3428 B.196 C.16 1.3469 B.35 C.17 1 .3510 B.76 C.17

1.3429 B.197 C.16 1.3470 B.36 C.17 1 .351 1 B.77 C.17

1.3430 B.198 C.16 1.3471 B.37 C.17 1 .3512 B.78 C.17

1.3431 B.199 C.16 1.3472 B.38 C.17 1 .3513 B.79 C.17

1.3432 B.200 C.16 1.3473 B.39 C.17 1 .3514 B.80 C.17

1.3433 B.201 C.16 1.3474 B.40 C.17 1 .3515 B.81 C.17

1.3434 B.202 C.16 1.3475 B.41 C.17 1 .3516 B.82 C.17

1.3435 B.1 C.17 1.3476 B.42 C.17 1 .3517 B.83 C.17

1.3436 B.2 C.17 1.3477 B.43 C.17 1 .3518 B.84 C.17

1.3437 B.3 C.17 1.3478 B.44 C.17 1 .3519 B.85 C.17

1.3438 B.4 C.17 1.3479 B.45 C.17 1 .3520 B.86 C.17

1.3439 B.5 C.17 1.3480 B.46 C.17 1 .3521 B.87 C.17

1.3440 B.6 C.17 1.3481 B.47 C.17 1 .3522 B.88 C.17

1.3441 B.7 C.17 1.3482 B.48 C.17 1 .3523 B.89 C.17

1.3442 B.8 C.17 1.3483 B.49 C.17 1 .3524 B.90 C.17

1.3443 B.9 C.17 1.3484 B.50 C.17 1 .3525 B.91 C.17

1.3444 B.10 C.17 1.3485 B.51 C.17 1 .3526 B.92 C.17

1.3445 B.1 1 C.17 1.3486 B.52 C.17 1 .3527 B.93 C.17

1.3446 B.12 C.17 1.3487 B.53 C.17 1 .3528 B.94 C.17 comp. herbisafener comp. herbisafener comp. herbisafener no. cide B C no. cide B C no. cide B C

1.3529 B.95 C.17 1.3570 B.136 C.17 1.3611 B.177 C.17

1.3530 B.96 C.17 1.3571 B.137 C.17 1.3612 B.178 C.17

1.3531 B.97 C.17 1.3572 B.138 C.17 1.3613 B.179 C.17

1.3532 B.98 C.17 1.3573 B.139 C.17 1.3614 B.180 C.17

1.3533 B.99 C.17 1.3574 B.140 C.17 1.3615 B.181 C.17

1.3534 B.100 C.17 1.3575 B.141 C.17 1.3616 B.182 C.17

1.3535 B.101 C.17 1.3576 B.142 C.17 1.3617 B.183 C.17

1.3536 B.102 C.17 1.3577 B.143 C.17 1.3618 B.184 C.17

1.3537 B.103 C.17 1.3578 B.144 C.17 1.3619 B.185 C.17

1.3538 B.104 C.17 1.3579 B.145 C.17 1.3620 B.186 C.17

1.3539 B.105 C.17 1.3580 B.146 C.17 1.3621 B.187 C.17

1.3540 B.106 C.17 1.3581 B.147 C.17 1.3622 B.188 C.17

1.3541 B.107 C.17 1.3582 B.148 C.17 1.3623 B.189 C.17

1.3542 B.108 C.17 1.3583 B.149 C.17 1.3624 B.190 C.17

1.3543 B.109 C.17 1.3584 B.150 C.17 1.3625 B.191 C.17

1.3544 B.110 C.17 1.3585 B.151 C.17 1.3626 B.192 C.17

1.3545 B.111 C.17 1.3586 B.152 C.17 1.3627 B.193 C.17

1.3546 B.112 C.17 1.3587 B.153 C.17 1.3628 B.194 C.17

1.3547 B.113 C.17 1.3588 B.154 C.17 1.3629 B.195 C.17

1.3548 B.114 C.17 1.3589 B.155 C.17 1.3630 B.196 C.17

1.3549 B.115 C.17 1.3590 B.156 C.17 1.3631 B.197 C.17

1.3550 B.116 C.17 1.3591 B.157 C.17 1.3632 B.198 C.17

1.3551 B.117 C.17 1.3592 B.158 C.17 1.3633 B.199 C.17

1.3552 B.118 C.17 1.3593 B.159 C.17 1.3634 B.200 C.17

1.3553 B.119 C.17 1.3594 B.160 C.17 1.3635 B.201 C.17

1.3554 B.120 C.17 1.3595 B.161 C.17 1.3636 B.202 C.17

1.3555 B.121 C.17 1.3596 B.162 C.17 1.3637 — C.1

1.3556 B.122 C.17 1.3597 B.163 C.17 1.3638 — C.2

1.3557 B.123 C.17 1.3598 B.164 C.17 1.3639 — C.3

1.3558 B.124 C.17 1.3599 B.165 C.17 1.3640 — C.4

1.3559 B.125 C.17 1.3600 B.166 C.17 1.3641 — C.5

1.3560 B.126 C.17 1.3601 B.167 C.17 1.3642 — C.6

1.3561 B.127 C.17 1.3602 B.168 C.17 1.3643 — C.7

1.3562 B.128 C.17 1.3603 B.169 C.17 1.3644 — C.8

1.3563 B.129 C.17 1.3604 B.170 C.17 1.3645 — C.9

1.3564 B.130 C.17 1.3605 B.171 C.17 1.3646 — C.10

1.3565 B.131 C.17 1.3606 B.172 C.17 1.3647 — C.11

1.3566 B.132 C.17 1.3607 B.173 C.17 1.3648 — C.12

1.3567 B.133 C.17 1.3608 B.174 C.17 1.3649 — C.13

1.3568 B.134 C.17 1.3609 B.175 C.17 1.3650 — C.14

1.3569 B.135 C.17 1.3610 B.176 C.17 1.3651 — C.15 comp. herbisafener comp. herbisafener

no. cide B C no. cide B C

1.3652 C.16 1.3653 C.17

The specific number for each single composition is deductible as follows:

Composition 1 .203 e.g. comprises the compound (1.1 .1-25), clethodim (B.1 ) and benoxacor (C.1 ) (see table B, entry B.1 and table C, entry C.1 ).

Also preferred are compositions 2.1 to 2.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .1.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 3.1 to 3.3653 which differ from compositions 1 .1 to 1.3653 wherein they additionally comprise B.2 as further herbicide B.

Also preferred are compositions 4.1 to 4.3653 which differ from compositions 1 .1 to 1.3653 wherein they additionally comprise B.8 as further herbicide B.

Also preferred are compositions 5.1 to 5.3653 which differ from compositions 1 .1 to 1.3653 wherein they additionally comprise B.30 as further herbicide B.

Also preferred are compositions 6.1 to 6.3653 which differ from compositions 1 .1 to 1.3653 wherein they additionally comprise B.32 as further herbicide B.

Also preferred are compositions 7.1 to 7.3653 which differ from the corresponding compositions 1 .1 to 1 .3653 wherein they additionally comprise B.35 as further herbicide B.

Also preferred are compositions 8.1 to 8.3653 which differ from the corresponding composi- tions 1 .1 to 1 .3653 wherein they additionally comprise B.38 as further herbicide B.

Also preferred are compositions 9.1 to 9.3653 which differ from the corresponding compositions 1 .1 to 1 .3653 wherein they additionally comprise B.40 as further herbicide B.

Also preferred are compositions 10.1 to 10.3653 which differ from the corresponding compositions 1 .1 to 1 .3653 wherein they additionally comprise B.51 as further herbicide B.

Also preferred are compositions 1 1 .1 to 1 1.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.55 as further herbicide B.

Also preferred are compositions 12.1 to 12.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.56 as further herbicide B.

Also preferred are compositions 13.1 to 13.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.64 as further herbicide B.

Also preferred are compositions 14.1 to 14.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.66 as further herbicide B.

Also preferred are compositions 15.1 to 15.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.67 as further herbicide B.

Also preferred are compositions 16.1 to 16.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.68 as further herbicide B.

Also preferred are compositions 17.1 to 17.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.69 as further herbicide B.

Also preferred are compositions 18.1 to 18.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.73 as further herbicide B.

Also preferred are compositions 19.1 to 19.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.76 as further herbicide B.

Also preferred are compositions 20.1 to 20.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.81 as further herbicide B.

Also preferred are compositions 21 .1 to 21.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.82 as further herbicide B.

Also preferred are compositions 22.1 to 22.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.85 as further herbicide B.

Also preferred are compositions 23.1 to 23.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.88 as further herbicide B.

Also preferred are compositions 24.1 to 24.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.89 as further herbicide B.

Also preferred are compositions 25.1 to 25.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.94 as further herbicide B.

Also preferred are compositions 26.1 to 26.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.95 as further herbicide B.

Also preferred are compositions 27.1 to 27.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.98 as further herbicide B.

Also preferred are compositions 28.1 to 28.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.100 as further herbicide B.

Also preferred are compositions 29.1 to 29.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.103 as further herbicide B.

Also preferred are compositions 30.1 to 30.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.103 and B.67 as further herbicides B.

Also preferred are compositions 31 .1 to 31.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.103 and B.76 as further herbicides B.

Also preferred are compositions 32.1 to 32.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.103 and B.82 as further herbicides B.

Also preferred are compositions 33.1 to 33.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.104 as further herbicide B.

Also preferred are compositions 34.1 to 34.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.104 and B.67 as further herbicides B.

Also preferred are compositions 35.1 to 35.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.104 and B.76 as further herbicides B.

Also preferred are compositions 36.1 to 36.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.104 and B.82 as further herbicides B.

Also preferred are compositions 37.1 to 37.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.106 as further herbicide B.

Also preferred are compositions 38.1 to 38.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.107 as further herbicide B.

Also preferred are compositions 39.1 to 39.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B. 107 and B.67 as further herbicides B.

Also preferred are compositions 40.1 to 40.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B. 107 and B.76 as further herbicides B.

Also preferred are compositions 41 .1 to 41.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B. 107 and B.82 as further herbicides B.

Also preferred are compositions 42.1 to 42.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.109 as further herbicide B.

Also preferred are compositions 43.1 to 43.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 1 1 as further herbicide B.

Also preferred are compositions 44.1 to 44.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 1 1 and B.67 as further herbicides B.

Also preferred are compositions 45.1 to 45.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 1 1 and B.76 as further herbicides B.

Also preferred are compositions 46.1 to 46.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 1 1 and B.82 as further herbicides B.

Also preferred are compositions 47.1 to 47.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B. 1 16 as further herbicide B.

Also preferred are compositions 48.1 to 48.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.67 as further herbicides B.

Also preferred are compositions 49.1 to 49.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.94 as further herbicides B.

Also preferred are compositions 50.1 to 50.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.103 as further herbicides B.

Also preferred are compositions 51 .1 to 51.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.128 as further herbicides B.

Also preferred are compositions 52.1 to 52.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.104 as further herbicides B.

Also preferred are compositions 53.1 to 53.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.107 as further herbicides B.

Also preferred are compositions 54.1 to 54.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.1 16 and B.1 1 1 as further herbicides B.

Also preferred are compositions 55.1 to 55.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.122 as further herbicide B.

Also preferred are compositions 56.1 to 56.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.126 as further herbicide B.

Also preferred are compositions 57.1 to 57.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.128 as further herbicide B.

Also preferred are compositions 58.1 to 58.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.131 as further herbicide B.

Also preferred are compositions 59.1 to 59.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.132 as further herbicide B.

Also preferred are compositions 60.1 to 60.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.133 as further herbicide B.

Also preferred are compositions 61 .1 to 61.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.135 as further herbicide B.

Also preferred are compositions 62.1 to 62.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.137 as further herbicide B.

Also preferred are compositions 63.1 to 63.3653 which differ from compositions 1 1.1 to 1.3653 wherein they additionally comprise B.138 as further herbicide B.

Also preferred are compositions 64.1 to 64.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.140 as further herbicide B.

Also preferred are compositions 65.1 to 65.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.145 as further herbicide B.

Also preferred are compositions 66.1 to 66.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.153 as further herbicide B.

Also preferred are compositions 67.1 to 67.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.156 as further herbicide B.

Also preferred are compositions 68.1 to 68.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.171 as further herbicide B.

Also preferred are compositions 69.1 to 69.3653 which differ from compositions 1 .1 to 1 .3653 wherein they additionally comprise B.174 as further herbicide B.

Also preferred are compositions 70.1 to 70.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.1.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 71 .1 to 71.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.1.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 72.1 to 72.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.1.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 73.1 to 73.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .1.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 74.1 to 74.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.1.1-73) instead of compound (1.1.1-25).

Also preferred are compositions 76.1 to 76.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 77.1 to 77.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 78.1 to 78.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 79.1 to 79.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .2.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 80.1 to 80.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 81 .1 to 81.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 82.1 to 82.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.2.1-73) instead of compound (1.1.1-25).

Also preferred are compositions 83.1 to 83.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.3.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 84.1 to 84.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .3.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 85.1 to 85.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.3.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 86.1 to 86.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .3.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 87.1 to 87.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.3.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 88.1 to 88.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.3.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 89.1 to 89.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.3.1-73) instead of compound (1.1.1-25).

Also preferred are compositions 90.1 to 90.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.4.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 91 .1 to 91.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .4.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 92.1 to 92.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.4.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 93.1 to 93.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.4.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 94.1 to 94.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.4.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 95.1 to 95.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.4.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 96.1 to 96.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1 .4.1-73) instead of compound (1.1.1-25).

Also preferred are compositions 97.1 to 97.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.5.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 98.1 to 98.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.5.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 99.1 to 99.3653 which differ from compositions 1 .1 to 1 .3653 wherein they comprise compound (1.5.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 100.1 to 100.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .5.1-49) instead of compound (1 .1.1-25).

Also preferred are compositions 101.1 to 101.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .5.1-61 ) instead of compound (1 .1.1-25).

Also preferred are compositions 102.1 to 102.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .5.1-55) instead of compound (1 .1.1-25).

Also preferred are compositions 103.1 to 103.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .5.1-73) instead of compound (1 .1.1-25).

Also preferred are compositions 104.1 to 104.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .6.1-25) instead of compound (1 .1.1-25).

Also preferred are compositions 105.1 to 105.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .6.1-37) instead of compound (1 .1.1-25).

Also preferred are compositions 105.1 to 106.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .6.1-31 ) instead of compound (1 .1.1-25).

Also preferred are compositions 107.1 to 107.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .6.1-49) instead of compound (1 .1.1-25).

Also preferred are compositions 108.1 to 108.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .6.1-61 ) instead of compound (1 .1.1-25).

Also preferred are compositions 109.1 to 09.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .6.1-55) instead of compound (1 .1.1-25).

Also preferred are compositions 1 10.1 to 10.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .6.1-73) instead of compound (1 .1.1-25).

Also preferred are compositions 1 1 1.1 to 1 1.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-25) instead of compound (1 .1.1-25).

Also preferred are compositions 1 12.1 to 12.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-37) instead of compound (1 .1.1-25). Also preferred are compositions 1 13.1 to 13.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-31 ) instead of compound (1 .1.1-25).

Also preferred are compositions 1 14.1 to 14.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-49) instead of compound (1 .1.1-25).

Also preferred are compositions 1 15.1 to 15.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-61 ) instead of compound (1 .1.1-25).

Also preferred are compositions 1 16.1 to 16.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-55) instead of compound (1 .1.1-25).

Also preferred are compositions 1 17.1 to 18.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .7.1-73) instead of compound (1 .1.1-25). Also preferred are compositions 1 19.1 to 19.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-25) instead of compound (1 .1.1-25).

Also preferred are compositions 120.1 to 20.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-37) instead of compound (1 .1.1-25).

Also preferred are compositions 121.1 to 21.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-31 ) instead of compound (1 .1.1-25).

Also preferred are compositions 122.1 to 22.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-49) instead of compound (1 .1.1-25).

Also preferred are compositions 123.1 to 23.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-61 ) instead of compound (1 .1.1-25). Also preferred are compositions 124.1 to 24.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-55) instead of compound (1 .1.1-25).

Also preferred are compositions 125.1 to 25.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .8.1-73) instead of compound (1 .1.1-25).

Also preferred are compositions 126.1 to 26.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-25) instead of compound (1 .1.1-25).

Also preferred are compositions 127.1 to 27.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-37) instead of compound (1 .1.1-25).

Also preferred are compositions 128.1 to 28.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-31 ) instead of compound (1 .1.1-25). Also preferred are compositions 129.1 to 29.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-49) instead of compound (1 .1.1-25).

Also preferred are compositions 130.1 to 30.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-61 ) instead of compound (1 .1.1-25).

Also preferred are compositions 131.1 to 31.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-55) instead of compound (1 .1.1-25).

Also preferred are compositions 132.1 to 32.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .9.1-73) instead of compound (1 .1.1-25).

Also preferred are compositions 133.1 to 33.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 134.1 to 34.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 135.1 to 35.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 136.1 to 36.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-49) instead of compound (1 .1 .1-25).

Also preferred are compositions 137.1 to 37.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-61 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 138.1 to 38.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-55) instead of compound (1 .1 .1-25).

Also preferred are compositions 139.1 to 39.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .10.1-73) instead of compound (1 .1 .1-25).

Also preferred are compositions 140.1 to 40.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 141.1 to 41.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 142.1 to 42.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 143.1 to 43.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-49) instead of compound (1 .1 .1-25).

Also preferred are compositions 144.1 to 44.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-55) instead of compound (1 .1 .1-25).

Also preferred are compositions 145.1 to 45.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .31 .1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 146.1 to 46.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 147.1 to 47.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 148.1 to 48.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 149.1 to 49.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-49) instead of compound (1 .1 .1-25).

Also preferred are compositions 150.1 to 50.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 151.1 to 51.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .37.1-61 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 152.1 to 52.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .38.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 153.1 to 53.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .38.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 154.1 to 54.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .38.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 155.1 to 56.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .38.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 157.1 to 57.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .38.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 158.1 to 58.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .38.1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 159.1 to 59.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 160.1 to 60.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 161.1 to 61.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 162.1 to 62.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 163.1 to 63.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 164.1 to 64.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .39.1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 165.1 to 65.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 166.1 to 66.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 167.1 to 67.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 168.1 to 68.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 169.1 to 69.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 170.1 to 70.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .46.1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 171.1 to 71.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .47.1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 172.1 to 72.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .47.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 173.1 to 73.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .47.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 174.1 to 74.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .47.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 175.1 to 75.3653 which differ from compositions 1 .1 to .3653 wherein they comprise compound ( .47.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 176.1 to 76.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .47.1-61 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 177.1 to 77.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 178.1 to 78.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 179.1 to 79.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 180.1 to 80.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-49) instead of compound (1 .1 .1-25).

Also preferred are compositions 181.1 to 81.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-55) instead of compound (1 .1 .1-25).

Also preferred are compositions 182.1 to 82.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .53.1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 183.1 to 83.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 184.1 to 84.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 185.1 to 85.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 186.1 to 86.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-49) instead of compound (1 .1 .1-25).

Also preferred are compositions 187.1 to 87.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 188.1 to 88.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .59.1-61 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 189.1 to 89.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 190.1 to 90.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 191.1 to 91.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-37) instead of compound (1 .1 .1-25).

Also preferred are compositions 192.1 to 92.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 193.1 to 93.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-55) instead of compound (1 .1 .1-25).

Also preferred are compositions 194.1 to 94.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .63.1-61 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 195.1 to 95.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .64.1-25) instead of compound (1 .1 .1-25).

Also preferred are compositions 196.1 to 96.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .64.1-31 ) instead of compound (1 .1 .1-25).

Also preferred are compositions 197.1 to 97.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound ( .64.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 198.1 to 198.3653 which differ from compositions .3653 wherein they comprise compound (1 .64.1-49) instead of compound (1 .1 .1-25) Also preferred are compositions 199.1 to 199.3653 which differ from compositions .3653 wherein they comprise compound (1 .64.1-55) instead of compound (1 .1 .1-25) Also preferred are compositions 200.1 to 200.3653 which differ from compositions .3653 wherein they comprise compound (1 .64.1-61 ) instead of compound (1 .1 .1-25) Also preferred are compositions 201.1 to 201.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-25) instead of compound (1 .1 .1-25) Also preferred are compositions 202.1 to 202.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-31 ) instead of compound (1 .1 .1-25) Also preferred are compositions 203.1 to 203.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-37) instead of compound (1 .1 .1-25) Also preferred are compositions 204.1 to 204.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-49) instead of compound (1 .1 .1-25) Also preferred are compositions 205.1 to 205.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-55) instead of compound (1 .1 .1-25) Also preferred are compositions 206.1 to 206.3653 which differ from compositions .3653 wherein they comprise compound (1 .65.1-61 ) instead of compound (1 .1 .1-25) Also preferred are compositions 207.1 to 207.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-25) instead of compound (1 .1 .1-25) Also preferred are compositions 208.1 to 208.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-31 ) instead of compound (1 .1 .1-25) Also preferred are compositions 209.1 to 209.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-37) instead of compound (1 .1 .1-25) Also preferred are compositions 210.1 to 210.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-49) instead of compound (1 .1 .1-25) Also preferred are compositions 21 1.1 to 21 1.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-55) instead of compound (1 .1 .1-25) Also preferred are compositions 212.1 to 212.3653 which differ from compositions .3653 wherein they comprise compound (1 .72.1-61 ) instead of compound (1 .1 .1-25) Also preferred are compositions 213.1 to 213.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-25) instead of compound (1 .1 .1-25) Also preferred are compositions 214.1 to 214.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-31 ) instead of compound (1 .1 .1-25) Also preferred are compositions 215.1 to 215.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-37) instead of compound (1 .1 .1-25) Also preferred are compositions 216.1 to 216.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-49) instead of compound (1 .1 .1-25) Also preferred are compositions 217.1 to 217.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-55) instead of compound (1 .1 .1-25) Also preferred are compositions 218.1 to 218.3653 which differ from compositions .3653 wherein they comprise compound (1 .73.1-61 ) instead of compound (1 .1 .1-25) Also preferred are compositions 219.1 to 219.3653 which differ from compositions .3653 wherein they comprise compound (1 .79.1-25) instead of compound (1 .1 .1-25). Also preferred are compositions 220.1 to 220.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .79.1-31 ) instead of compound (1 .1 .1-25). Also preferred are compositions 221.1 to 221.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .79.1-37) instead of compound (1 .1 .1-25). Also preferred are compositions 222.1 to 222.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .79.1-49) instead of compound (1 .1 .1-25). Also preferred are compositions 223.1 to 223.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .79.1-55) instead of compound (1 .1 .1-25). Also preferred are compositions 224.1 to 224.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .79.1-61 ) instead of compound (1 .1 .1-25). Also preferred are compositions 225.1 to 225.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-25) instead of compound (1.1.1-25). Also preferred are compositions 226.1 to 226.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-31 ) instead of compound (1.1.1-25). Also preferred are compositions 227.1 to 227.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-37) instead of compound (1.1.1-25). Also preferred are compositions 228.1 to 228.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-49) instead of compound (1.1.1-25). Also preferred are compositions 229.1 to 229.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-55) instead of compound (1.1.1-25). Also preferred are compositions 230.1 to 230.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .272.1-61 ) instead of compound (1.1.1-25). Also preferred are compositions 231.1 to 231.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-25) instead of compound (1.1.1-25). Also preferred are compositions 232.1 to 232.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-31 ) instead of compound (1.1.1-25). Also preferred are compositions 233.1 to 234.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-37) instead of compound (1.1.1-25). Also preferred are compositions 235.1 to 235.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-49) instead of compound (1.1.1-25). Also preferred are compositions 236.1 to 236.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-55) instead of compound (1.1.1-25). Also preferred are compositions 237.1 to 237.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .273.1-61 ) instead of compound (1.1.1-25). Also preferred are compositions 238.1 to 238.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .584.1-25) instead of compound (1.1.1-25). Also preferred are compositions 239.1 to 239.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .584.1-31 ) instead of compound (1.1.1-25). Also preferred are compositions 240.1 to 240.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .584.1-37) instead of compound (1.1.1-25). Also preferred are compositions 241.1 to 241.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .584.1-49) instead of compound (1.1.1-25). Also preferred are compositions 242.1 to 242.3653 which differ from compositions 1 . .3653 wherein they comprise compound 1 .584.1-55) instead of compound (1.1.1-25). Also preferred are compositions 243.1 to 243.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .584.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 244.1 to 244.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 245.1 to 245.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 246.1 to 246.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 247.1 to 247.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 248.1 to 248.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 249.1 to 249.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .585.1-61 ) instead of compound (1.1.1-25).

Also preferred are compositions 250.1 to 250.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-25) instead of compound (1.1.1-25).

Also preferred are compositions 251.1 to 251.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-31 ) instead of compound (1.1.1-25).

Also preferred are compositions 252.1 to 252.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-37) instead of compound (1.1.1-25).

Also preferred are compositions 253.1 to 253.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-49) instead of compound (1.1.1-25).

Also preferred are compositions 254.1 to 254.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-55) instead of compound (1.1.1-25).

Also preferred are compositions 255.1 to 255.3653 which differ from compositions 1 .1 to 1.3653 wherein they comprise compound (1 .592.1-61 ) instead of compound (1.1.1-25).

The invention also relates to agrochemical compositions comprising at least an auxiliary and at least one pyrimidine compound of formula (I) according to the invention.

An agrochemical composition comprises a pesticidal effective amount of a pyrimidine compound of formula (I). The term "effective amount" denotes an amount of the composition or of the compounds I, which is sufficient for controlling unwanted plants, especially for controlling unwanted plants in cultivated plants and which does not result in a substantial damage to the treated plants. Such an amount can vary in a broad range and is dependent on various factors, such as the plants to be controlled, the treated cultivated plant or material, the climatic conditions and the specific pyrimidine compound of formula (I) used.

The pyrimidine compounds of formula (I), their N-oxides, salts or derivatives can be converted into customary types of agrochemical compositions, e. g. solutions, emulsions, suspensions, dusts, powders, pastes, granules, pressings, capsules, and mixtures thereof. Examples for agrochemical composition types are suspensions (e.g. SC, OD, FS), emulsifiable concentrates (e.g. EC), emulsions (e.g. EW, EO, ES, ME), capsules (e.g. CS, ZC), pastes, pastilles, wettable powders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g. WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gel formulations for the treatment of plant propagation materials such as seeds (e.g. GF). These and further agrochemical compositions types are defined in the "Catalogue of pesticide formulation types and international coding system", Technical Monograph No. 2, 6 ^th Ed. May 2008, CropLife International.

The agrochemical compositions are prepared in a known manner, such as described by Mollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001 ; or Knowles, New devel- opments in crop protection product formulation, Agrow Reports DS243, T&F Informa, London, 2005.

Suitable auxiliaries are solvents, liquid carriers, solid carriers or fillers, surfactants, disper- sants, emulsifiers, wetters, adjuvants, solubilizers, penetration enhancers, protective colloids, adhesion agents, thickeners, humectants, repellents, attractants, feeding stimulants, compatibil- izers, bactericides, anti-freezing agents, anti-foaming agents, colorants, tackifiers and binders. Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil fractions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic, and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, benzylalcohol, cyclohexanol; glycols; DMSO; ketones, e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N-methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.

Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharides, e.g. cellulose, starch; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of vegetable origin, e.g. cereal meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.

Suitable surfactants are surface-active compounds, such as anionic, cationic, non-ionic, and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as emulsifier, dispersant, solubilizer, wetter, penetration enhancer, protective colloid, or adjuvant. Examples of surfactants are listed in McCutcheon's, Vol.1 : Emulsifiers & Detergents, McCutcheon's Directories, Glen Rock, USA, 2008 (International Ed. or North American Ed.).

Suitable anionic surfactants are alkali, alkaline earth or ammonium salts of sulfonates, sul- fates, phosphates, carboxylates, and mixtures thereof. Examples of sulfonates are alkylaryl- sulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine sulfonates, sulfonates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates or sulfosuccinamates. Examples of sul- fates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acid esters. Examples of phosphates are phosphate esters. Examples of carboxylates are alkyl carboxylates, and carboxylated alcohol or alkylphenol ethoxylates.

Suitable nonionic surfactants are alkoxylates, N-substituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric surfactants, and mixtures thereof. Examples of alkoxylates are compounds such as alcohols, alkylphenols, amines, amides, arylphenols, fatty acids, or fatty acid esters which have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide. Examples of N-substituted fatty acid amides are fatty acid glucamides or fatty acid alkanolamides. Examples of esters are fatty acid esters, glycerol esters, or monoglycerides. Examples of sugar- based surfactants are sorbitans, ethoxylated sorbitans, sucrose, and glucose esters, or al- kylpoly-glucosides. Examples of polymeric surfactants are home- or copolymers of vinylpyrroli- done, vinylalcohols, or vinylacetate.

Suitable cationic surfactants are quaternary surfactants, e.g. quaternary ammonium com- pounds with one or two hydrophobic groups, or salts of long-chain primary amines. Suitable amphoteric surfactants are alkylbetains and imidazolines. Suitable block polymers are block polymers of the A-B or A-B-A type comprising blocks of polyethylene oxide and polypropylene oxide, or of the A-B-C type comprising alkanol, polyethylene oxide and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or polyeth- yleneamines.

Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity themselves, and which improve the biological performance of the pyrimidine compounds of formula (I) on the target. Examples are surfactants, mineral or vegetable oils, and other auxiliaries. Further examples are listed by Knowles, Adjuvants, and additives, Agrow Reports DS256, T&F Informa UK, 2006, chapter 5.

Suitable thickeners are polysaccharides (e.g. xanthan gum, carboxymethylcellulose), inorganic clays (organically modified or unmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazoli- nones and benzisothiazolinones.

Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea, and glycerin.

Suitable anti-foaming agents are silicones, long chain alcohols, and salts of fatty acids.

Suitable colorants (e.g. in red, blue, or green) are pigments of low water solubility and water- soluble dyes. Examples are inorganic colorants (e.g. iron oxide, titan oxide, iron hexacyanofer- rate) and organic colorants (e.g. alizarin-, azo-, and phthalocyanine colorants).

Suitable tackifiers or binders are polyvinylpyrrolidone, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or synthetic waxes, and cellulose ethers.

Examples for agrochemical composition types and their preparation are:

i) Water-soluble concentrates (SL, LS)

10-60 wt% of a pyrimidine compound of formula (I) according to the invention and 5-15 wt% wetting agent (e.g. alcohol alkoxylates) are dissolved in water and/or in a water-soluble solvent (e.g. alcohols) ad 100 wt%. The active substance dissolves upon dilution with water.

ii) Dispersible concentrates (DC)

5-25 wt% of a pyrimidine compound of formula (I) according to the invention and 1 -10 wt% dis- persant (e. g. polyvinylpyrrolidone) are dissolved in organic solvent (e.g. cyclohexanone) ad 100 wt%. Dilution with water gives a dispersion.

iii) Emulsifiable concentrates (EC)

15-70 wt% of a pyrimidine compound of formula (I) according to the invention and 5-10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in water-insoluble organic solvent (e.g. aromatic hydrocarbon) ad 100 wt%. Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40 wt% of a pyrimidine compound of formula (I) according to the invention and 1 -10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in 20-40 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). This mixture is introduced into water ad 100 wt% by means of an emulsifying machine and made into a homogeneous emulsion. Dilution with water gives an emulsion.

v) Suspensions (SC, OD, FS)

In an agitated ball mill, 20-60 wt% of a pyrimidine compound of formula (I) according to the invention are comminuted with addition of 2-10 wt% dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate), 0,1-2 wt% thickener (e.g. xanthan gum) and water ad 100 wt% to give a fine active substance suspension. Dilution with water gives a stable suspension of the active substance. For FS type composition up to 40 wt% binder (e.g. polyvinylalco- hoi) is added.

vi) Water-dispersible granules and water-soluble granules (WG, SG)

50-80 wt% of a pyrimidine compound of formula (I) according to the invention are ground finely with addition of dispersants and wetting agents (e.g. sodium lignosulfonate and alcohol ethoxylate) ad 100 wt% and prepared as water-dispersible or water-soluble granules by means of technical appliances (e. g. extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active substance.

vii) Water-dispersible powders and water-soluble powders (WP, SP, WS)

50-80 wt% of a pyrimidine compound of formula (I) according to the invention are ground in a rotor-stator mill with addition of 1 -5 wt% dispersants (e.g. sodium lignosulfonate), 1-3 wt% wet- ting agents (e.g. alcohol ethoxylate) and solid carrier (e.g. silica gel) ad 100 wt%. Dilution with water gives a stable dispersion or solution of the active substance.

viii) Gel (GW, GF)

In an agitated ball mill, 5-25 wt% of a pyrimidine compound of formula (I) according to the invention are comminuted with addition of 3-10 wt% dispersants (e.g. sodium lignosulfonate), 1 -5 wt% thickener (e.g. carboxymethylcellulose) and water ad 100 wt% to give a fine suspension of the active substance. Dilution with water gives a stable suspension of the active substance. iv) Microemulsion (ME)

5-20 wt% of a pyrimidine compound of formula (I) according to the invention are added to 5-30 wt% organic solvent blend (e.g. fatty acid dimethylamide and cyclohexanone), 10-25 wt% sur- factant blend (e.g. alcohol ethoxylate and arylphenol ethoxylate), and water ad 100 %. This mixture is stirred for 1 h to produce spontaneously a thermodynamically stable microemulsion. iv) Microcapsules (CS)

An oil phase comprising 5-50 wt% of a pyrimidine compound of formula (I) according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), 2-15 wt% acrylic monomers (e.g. methylmethacrylate, methacrylic acid, and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radical initiator results in the formation of poly(meth)acrylate microcapsules. Alternatively, an oil phase comprising 5-50 wt% of a pyrimidine compound of formula (I) according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), and an iso- cyanate monomer (e.g. diphenylmethene-4,4'-diisocyanate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). The addition of a polyamine (e.g. hexameth- ylenediamine) results in the formation of polyurea microcapsules. The monomers amount to 1 - 10 wt%. The wt% relate to the total CS composition. ix) Dustable powders (DP, DS)

1-10 wt% of a pyrimidine compound of formula (I) according to the invention are ground finely and mixed intimately with solid carrier (e.g. finely divided kaolin) ad 100 wt%.

x) Granules (GR, FG)

0.5-30 wt% of a pyrimidine compound of formula (I) according to the invention is ground finely and associated with solid carrier (e.g. silicate) ad 100 wt%. Granulation is achieved by extrusion, spray-drying or the fluidized bed.

xi) Ultra-low volume liquids (UL)

1-50 wt% of a pyrimidine compound of formula (I) according to the invention are dissolved in organic solvent (e.g. aromatic hydrocarbon) ad 100 wt%.

The agrochemical compositions types i) to xi) may optionally comprise further auxiliaries, such as 0,1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0,1 -1 wt% anti-foaming agents, and 0,1-1 wt% colorants.

The agrochemical compositions comprising generally comprise between 0.01 and 95%, prefer- ably between 0.1 and 90%, and in particular between 0.5 and 75%, by weight of the pyrimidine compound of formula (I). The pyrimidine compounds of formula (I) are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).

Solutions for seed treatment (LS), suspoemulsions (SE), flowable concentrates (FS), powders for dry treatment (DS), water-dispersible powders for slurry treatment (WS), water-soluble pow- ders (SS), emulsions (ES), emulsifiable concentrates (EC) and gels (GF) are usually employed for the purposes of treatment of plant propagation materials, particularly seeds. The agrochemical compositions in question give, after two-to-tenfold dilution, active substance concentrations of from 0.01 to 60% by weight, preferably from 0.1 to 40% by weight, in the ready-to-use preparations. Application can be carried out before or during sowing.

Methods for applying pyrimidine compounds of formula (I) and agrochemical compositions thereof, on to plant propagation material, especially seeds, include dressing, coating, pelleting, dusting, soaking and in-furrow application methods of the propagation material. Preferably, pyrimidine compounds of formula (I) and agrochemical compositions thereof, are applied on to the plant propagation material by a method such that germination is not induced, e. g. by seed dressing, pelleting, coating and dusting.

Various types of oils, wetters, adjuvants, fertilizer, or micronutrients, and further pesticides (e.g. herbicides, insecticides, fungicides, growth regulators, safeners) may be added to the pyrimidine compounds of formula (I) and the agrochemical compositions comprising them as pre- mix or, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the agrochemical compositions according to the invention in a weight ratio of 1 :100 to 100:1 , preferably 1 :10 to 10:1.

The user applies the pyrimidine compound of formula (I) according to the invention and the agrochemical compositions comprising them usually from a pre-dosage device, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system. Usually, the agrochemical compo- sition is made up with water, buffer, and/or further auxiliaries to the desired application concentration and the ready-to-use spray liquor or the agrochemical composition according to the invention is thus obtained. Usually, 20 to 2000 liters, preferably 50 to 400 liters, of the ready-to- use spray liquor are applied per hectare of agricultural useful area.

According to one embodiment, either individual components of the agrochemical composition according to the invention or partially premixed components, e. g. components comprising py- rimidine compounds of formula (I) may be mixed by the user in a spray tank and further auxiliaries and additives may be added, if appropriate.

In a further embodiment, individual components of the agrochemical composition according to the invention such as parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate.

In a further embodiment, either individual components of the agrochemical composition according to the invention or partially premixed components, e. g components comprising pyrimi- dine compounds of formula (I) can be applied jointly (e.g. after tank mix) or consecutively.

The pyrimidine compounds of formula (I), are suitable as herbicides. They are suitable as such or as an appropriately formulated composition (agrochemical composition).

The pyrimidine compounds of formula (I), or the agrochemical compositions comprising the pyrimidine compounds of formula (I), control vegetation on non-crop areas very efficiently, especially at high rates of application. They act against broad-leaved weeds and grass weeds in crops such as wheat, rice, maize, soya, and cotton without causing any significant damage to the crop plants. This effect is mainly observed at low rates of application.

The pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, are applied to the plants mainly by spraying the leaves. Here, the application can be carried out using, e.g., water as carrier by customary spraying techniques using spray liquor amounts of from about 100 to 1000 l/ha (e.g. from 300 to 400 l/ha). The pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, may also be applied by the low-volume or the ultra-low-volume method, or in the form of micro granules.

Application of the pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, can be done before, during, and/or after, preferably during and/or after, the emergence of the undesirable plants.

The pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, can be applied pre-, post-emergence or pre-plant, or together with the seed of a crop plant. It is also possible to apply the pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, by applying seed, pretreated with the pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, of a crop plant. If the active ingredients are less well tolerated by certain crop plants, application techniques may be used in which the herbicidal compositions are sprayed, with the aid of the spraying equipment, in such a way that as far as possible they do not come into contact with the leaves of the sensitive crop plants, while the active ingredients reach the leaves of undesirable plants growing underneath, or the bare soil surface (post-directed, lay-by).

In a further embodiment, the pyrimidine compounds of formula (I), or the agrochemical compositions comprising them, can be applied by treating seed. The treatment of seeds comprises essentially all procedures familiar to the person skilled in the art (seed dressing, seed coating, seed dusting, seed soaking, seed film coating, seed multilayer coating, seed

encrusting, seed dripping and seed pelleting) based on the pyrimidine compounds of formula (I), or the agrochemical compositions prepared therefrom. Here, the herbicidal compositions can be applied diluted or undiluted.

The term "seed" comprises seed of all types, such as, e.g., corns, seeds, fruits, tubers, seedlings and similar forms. Here, preferably, the term seed describes corns and seeds. The seed used can be seed of the useful plants mentioned above, but also the seed of transgenic plants or plants obtained by customary breeding methods.

When employed in plant protection, the amounts of active substances applied, i.e. the pyrimidine compounds of formula (I) without formulation auxiliaries, are, depending on the kind of ef- feet desired, from 0.001 to 2 kg per ha, preferably from 0.005 to 2 kg per ha, more preferably from 0.05 to 0.9 kg per ha and in particular from 0.1 to 0.75 kg per ha.

In another embodiment of the invention, the application rate of the pyrimidine compounds of formula (I) is from 0.001 to 3 kg/ha, preferably from 0.005 to 2.5 kg/ha and in particular from 0.01 to 2 kg/ha of active substance (a.s.).

In another preferred embodiment of the invention, the rates of application of the pyrimidine compounds of formula (I) according to the present invention (total amount of pyrimidine compounds of formula (I)) are from 0.1 g/ha to 3000 g/ha, preferably 10 g/ha to 1000 g/ha, depending on the control target, the season, the target plants and the growth stage.

In another preferred embodiment of the invention, the application rates of the pyrimidine com- pounds of formula (I) are in the range from 0.1 g/ha to 5000 g/ha and preferably in the range from 1 g/ha to 2500 g/ha or from 5 g/ha to 2000 g/ha.

In another preferred embodiment of the invention, the application rate of the pyrimidine compounds of formula (I) is 0.1 to 1000 g/ha, preferablyl to 750 g/ha, more preferably 5 to 500 g/ha.

In treatment of plant propagation materials such as seeds, e. g. by dusting, coating or drenching seed, amounts of active substance of from 0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to 100 g, and most preferably from 5 to 100 g, per 100 kilogram of plant propagation material (preferably seeds) are generally required.

In another embodiment of the invention, to treat the seed, the amounts of active substances applied, i.e. the pyrimidine compounds of formula (I) are generally employed in amounts of from 0.001 to 10 kg per 100 kg of seed.

When used in the protection of materials or stored products, the amount of active substance applied depends on the kind of application area and on the desired effect. Amounts customarily applied in the protection of materials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meter of treated material.

Depending on the application method in question, the compounds of formula (I), or the agrochemical compositions comprising them, can additionally be employed in a further number of crop plants for eliminating undesirable plants. Examples of suitable crops are the following: Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis, Avena sativa, Beta vulgaris spec, altissima, Beta vulgaris spec, rapa, Brassica napus var. napus, Brassica napus var. napobrassica, Brassica rapa var. silvestris, Brassica oleracea, Brassica nigra, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossy- pium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vul- gare, Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec, Manihot esculenta, Medicago sativa, Musa spec, Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus spec, Pistacia vera, Pisum sativum, Prunus avium, Prunus persica, Pyrus communis, Prunus armeniaca, Prunus cerasus, Prunus dulcis and Prunus domestica, Ribes sylvestre, Ricinus communis, Saccharum officinarum, Secale cereale, Sinapis alba, Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticale, Triticum durum, Vicia faba, Vitis vinifera, and Zea mays.

Preferred crops are Arachis hypogaea, Beta vulgaris spec, altissima, Brassica napus var. napus, Brassica oleracea, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cynodon dactylon, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hordeum vulgare, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec, Medicago sativa, Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa , Phaseolus lunatus, Phaseolus vulgaris, Pistacia vera, Pisum sativum, Prunus dulcis, Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (s. vulgare), Triticale, Triticum aestivum, Triticum durum, Vicia faba, Vitis vinifera, and Zea mays.

Especially preferred crops are crops of cereals, corn, soybeans, rice, oilseed rape, cotton, potatoes, peanuts, or permanent crops.

The pyrimidine compounds of formula (I) according to the invention, or the agrochemical compositions comprising them, can also be used in genetically modified plants. The term "genetically modified plants" is to be understood as plants whose genetic material has been modified by the use of recombinant DNA techniques to include an inserted sequence of DNA that is not native to that plant species' genome or to exhibit a deletion of DNA that was native to that species' genome, wherein the modification(s) cannot readily be obtained by cross breeding, mutagenesis or natural recombination alone. Often, a particular genetically modified plant will be one that has obtained its genetic modification(s) by inheritance through a natural breeding or propagation process from an ancestral plant whose genome was the one directly treated by use of a recombinant DNA technique. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include but are not limited to targeted post-translational modification of protein(s), oligo- or polypeptides, e. g., by inclusion therein of amino acid mutation(s) that permit, decrease, or promote glycosylation or polymer additions such as prenylation, acety- lation farnesylation, or PEG moiety attachment.

Plants that have been modified by breeding, mutagenesis or genetic engineering, e.g. have been rendered tolerant to applications of specific classes of herbicides, such as auxin herbicides such as dicamba or 2,4-D; bleacher herbicides such as hydroxyphenylpyruvate dioxygen- ase (HPPD) inhibitors or phytoene desaturase (PDS) inhibitors; acetolactate synthase (ALS) in- hibitors such as sulfonyl ureas or imidazolinones; enolpyruvyl shikimate 3-phosphate synthase (EPSP) inhibitors such as glyphosate; glutamine synthetase (GS) inhibitors such as glufosinate; protoporphyrinogen-IX oxidase inhibitors; lipid biosynthesis inhibitors such as acetyl CoA carboxylase (ACCase) inhibitors; or oxynil (i. e. bromoxynil or ioxynil) herbicides as a result of conventional methods of breeding or genetic engineering; furthermore, plants have been made re- sistant to multiple classes of herbicides through multiple genetic modifications, such as resistance to both glyphosate and glufosinate or to both glyphosate and a herbicide from another class such as ALS inhibitors, HPPD inhibitors, auxin herbicides, or ACCase inhibitors. These herbicide resistance technologies are, e.g., described in Pest Management Science 61 , 2005, 246; 61 , 2005, 258; 61 , 2005, 277; 61 , 2005, 269; 61 , 2005, 286; 64, 2008, 326; 64, 2008, 332; Weed Science 57, 2009, 108; Australian Journal of Agricultural Research 58, 2007, 708; Science 316, 2007, 1 185; and references quoted therein. Several cultivated plants have been rendered tolerant to herbicides by mutagenesis and conventional methods of breeding, e. g., Clearfield® summer rape (Canola, BASF SE, Germany) being tolerant to imidazolinones, e. g., ima- zamox, or ExpressSun® sunflowers (DuPont, USA) being tolerant to sulfonyl ureas, e. g., tribe- nuron. Genetic engineering methods have been used to render cultivated plants such as soybean, cotton, corn, beets and rape, tolerant to herbicides such as glyphosate, imidazolinones, and glufosinate, some of which are under development or commercially available under the brands or trade names RoundupReady® (glyphosate tolerant, Monsanto, USA), Cultivance® (imidazolinone tolerant, BASF SE, Germany), and LibertyLink® (glufosinate tolerant, Bayer CropScience, Germany).

Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus thuringiensis, such as delta-endotoxins, e. g., CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, CrylllB(bl ) or Cry9c; vegetative insecticidal proteins (VIP), e. g., VIP1 , VIP2, VIP3, or VIP3A; insecticidal proteins of bacteria colonizing nematodes, e. g., Photorhabdus spp. or Xenorhabdus spp.; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such as Streptomycetes toxins, plant lectins, such as pea or barley lectins; ag- glutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cys- tatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxy-steroid oxidase, ec- dysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-re- ductase; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hor- mone esterase; diuretic hormone receptors (helicokinin receptors); stilbene synthase, bibenzyl synthase, chitinases or glucanases. In the context of the present invention these insecticidal proteins or toxins are to be understood expressly also as including pre-toxins, hybrid proteins, truncated or otherwise modified proteins. Hybrid proteins are characterized by a new combination of protein domains, (see, e. g., WO 02/015701 ). Further examples of such toxins or genet- ically modified plants capable of synthesizing such toxins are disclosed, e. g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/18810, and WO

03/52073. The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g., in the publications mentioned above.

These insecticidal proteins contained in the genetically modified plants impart to the plants pro- ducing these proteins tolerance to harmful pests from all taxonomic groups of arthropods, especially to beetles (Coeloptera), two-winged insects (Diptera), and moths (Lepidoptera) and to nematodes (Nematoda). Genetically modified plants capable to synthesize one or more insecticidal proteins are, e. g., described in the publications mentioned above, and some of which are commercially available such as YieldGard® (corn cultivars producing the CrylAb toxin), Yield- Gard® Plus (corn cultivars producing CrylAb and Cry3Bb1 toxins), Starlink® (corn cultivars producing the Cry9c toxin), Herculex® RW (corn cultivars producing Cry34Ab1 , Cry35Ab1 and the enzyme Phosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cotton cultivars producing the CrylAc toxin), Bollgard® I (cotton cultivars producing the CrylAc toxin), Bollgard® II (cotton cultivars producing CrylAc and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing a VIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt1 1 (e. g., Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the CrylAb toxin and PAT enzyme), MIR604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the CrylAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).

Furthermore, plants are also covered that are by the use of recombinant DNA techniques ca- pable to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens. Examples of such proteins are the so-called "pathogene- sis-related proteins" (PR proteins, see, e.g., EP-A 392 225), plant disease resistance genes (e. g., potato culti-vars, which express resistance genes acting against Phytophthora infestans derived from the Mexican wild potato, Solanum bulbocastanum) or T4-lyso-zym (e.g., potato culti- vars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylovora). The methods for producing such genetically modi-fied plants are generally known to the person skilled in the art and are described, e.g., in the publications mentioned above.

Furthermore, plants are also covered that are by the use of recombinant DNA techniques ca- pable to synthesize one or more proteins to increase the productivity (e.g., bio-mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.

Furthermore, plants are also covered that contain by the use of recombinant DNA techniques a modified amount of ingredients or new ingredients, specifically to improve human or animal nutrition, e. g., oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e. g., Nexera® rape, Dow AgroSciences, Canada).

Furthermore, plants are also covered that contain by the use of recombinant DNA techniques a modified amount of ingredients or new ingredients, specifically to improve raw material pro- duction, e.g., potatoes that produce increased amounts of amylopectin (e.g. Amflora® potato, BASF SE, Germany).

The preparation of the pyrimidine compounds of formula (I) is illustrated by the following examples.

A Preparation examples

Example 1 : 3-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoic acid:

1.1 5-(2-chlorophenyl)-2-cyclopropyl-4-CH3-pyrimidine:

A solution of 1-(2-Chlorophenyl)2-propanone (31 g) in dimethylformamiddimethylacetal (60 ml.) was stirred for 2 h at 125°C. TLC showed that the SM was consumed (PE: EtOAc = 1 :1 ). The mixture was concentrated to give (E)-3-(2-chlorophenyl)-4-(dimethylamino)but-3-en-2-one (41 g, 99.5%) as a yellow oil and used directly without purification. To a solution of the crude (E)-3-(2-chlorophenyl)-4-(dimethylamino)but-3-en-2-one (33.6 g) in EtOH (600 ml.) was added cyclopropanecarboxamidine hydrochloride (45 g) and t-BuOK (42 g). The resulting mixture was stirred for 16 h at 90°C. TLC (PE: EtOAc=3:1 ) showed that the SM was consumed. The mixture was filtered, and the filtrate was concentrated, purified by column (gradient EtOAc: PE = from 0:1 to 1 : 10) to give 5-(2-chlorophenyl)-2-cyclopropyl-4-CH ₃ -pyrimidine (29 g, 79.23%) as a yellow oil.

¹ H NMR CDCI3 400MHz: δ: 1.04 - 1.1 1 (m, 2 H); 1.16 - 1.23 (m, 2 H); 2.19 - 2.36 (m, 1 H); 2.3 (s, 3H); 7.17 - 7.23 (m, 1 H) 7.30 - 7.41 (m, 2 H) 7.43 - 7.56 (m, 1 H) 8.28 (s, 1 H).

1.2 ethyl 3-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoate:

To a solution of 5-(2-chlorophenyl)-2-cyclopropyl-4-CH3-pyrimidine (3 g) in THF (60 mL) was added LDA (8 mL) dropwise at -78°C 10 min later, glyoxalic acid ethylester (1 .6 g) in THF was added dropwise. The mixture was stirred at -78°C for 1 h. aq. NH ₄ CI (60 mL) was added. The mixture was extracted with EtOAc, dried over Na2S0 ₄ and concentrated. The crude was purified by column (PE:EtOAc = 50:1 to 2:1 ) to give ethyl 3-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin- 4-yl]-2-OH-propanoate (3 g, 47.2%) as a yellow oil.

¹ H NMR: CDCIs 400MHz δ ppm 1.1 1 - 1.19 (m, 4 H); 1 .23 (m, 3 H); 2.19 - 2.34 (m, 1 H); 2.89 - 3.06 (m, 1 H); 3.08 - 3.17 (m, 1 H); 4.10 - 4.27 (m, 3 H); 4.32 - 4.41 (m, 1 H); 4.46 - 4.55 (m, 1 H); 4.58 - 4.70 (m, 1 H); 7.20 - 7.26 (m, 1 H); 7.33 - 7.42 (m, 2 H); 7.51 (d, 1 H); 8.35 (s, 1 H).

1.3 3-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoic acid:

A solution of ethyl 3-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoate (1 g) in MeOH (30ml) and THF (30 mL) and H ₂ 0 (10 mL) was cooled to 0 °C Then LiOH-H ₂ 0 (0.36 g) in H2O was added. The mixture was stirred at 20 °C for 15 h. The mixture was concentrated. The residue was adjusted to pH=2-3 with 1 N HCI, and extracted with EtOAc. The organic layer was dried over Na2S0 ₄ and concentrated. The crude product was purified by prep-HPLC to give 3- [5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-propa noic acid (0.6 g, 66.7%) as a yellow oil.

H NMR: CDCI3 400MHz δ ppm 1.36 (m, 4 H); 2.44 (m, 1 H); 3.06 - 3.38 (m, 2 H); 4.55 (m, 1 H); 7.29 (m, 1 H); 7.39 - 7.51 (m, 2 H); 7.53 - 7.60 (m, 1 H); 8.60 (s, 1 H); 9.06 (br. s., 1 H). Example 2 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-pro pane-1 ,2-diol:

2.1 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-pro pan-2-ol:

To a solution of 5-(2-chlorophenyl)-2-cyclopropyl-4-CH3-pyrimidine (1.3 g) in THF (30 mL) was added 2M LDA solution in THF (3.5 mL) dropwise at -78°C. 10 min later, CH3COCH3 (0.4 g) in THF was added dropwise. Then the mixture was stirred at -78°C for 1 h. aq. NH ₄ CI (30 mL) was added. The mixture was extracted with EtOAc, dried over Na2S0 ₄ and concentrated. The crude product was purified by column chromatography (PE:EtOAc = 50:1 to 5:1 ) to give 1 -[5-(2- chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-propan-2-o l (1 .1 g, 68.8%) as a yellow oil. H NMR: CDCI3 400MHz δ ppm 1.09 (s, 3 H); 1 .14 - 1 .22 (m, 5 H); 2.24 - 2.38 (m, 1 H); 2.54 - 2.66 (m, 1 H); 2.69 - 2.79 (m, 1 H) ; 6.08 (s, 1 H) ; 7.18 (m, 1 H) ; 7.32 - 7.45 (m, 2 H) ; 7.52 (m, 1 H) ; 8.37 (s, 1 H).

2.2 5-(2-chlorophenyl)-2-cyclopropyl-4-(2-CH3-prop-1 -enyl)pyrimidine:

To a solution of 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-pro pan-2-ol (1 .1 g) in toluene (30 mL) was added PPTS (0.18 g). The mixture was stirred at 100°C for 10 h. Brine (30 mL) was added. Then the mixture was extracted with EtOAc, dried over Na2S0 ₄ and concentrated. The crude was purified by column (PE:EtOAc = 50:1 to 30:1 ) to give 5-(2-chlorophenyl)-2- cyclopropyl-4-(2-CH3-prop-1 -enyl)pyrimidine (0.8 g, 81 .6%) as a yellow oil.

2.3 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-pro pane-1 ,2-diol: To a solution of 5-(2-chlorophenyl)-2-cyclopropyl-4-(2-CH ₃ -prop-1 -enyl)pyrimidine (0.45 g) in THF (10 mL) was added NMO (0.35 g) and K ₂ 0s0 ₄ -2H ₂ 0 (0.049 g). Then the mixture was stirred at 30°C for 12 h. The mixture was concentrated in vacuum. The crude product was purified by column chromatography (PE: EtOAc = 50:1 to 5:1 ) to give -[5-(2-chlorophenyl)-2- cyclopropyl-pyrimidin-4-yl]-2-CH3-propane-1 ,2-diol (0.2 g, 41.9%) as a yellow oil.

¹ H NMR: CDCIs 400MHz δ ppm (2 rotamers) 0.95 - 1.33 (m, 2x 10 H) ; 2.38 - 2.55 (m, 2x1 H) ; 4.33 (s, 1 H); 4.35 (s, 1 H) ; 5.86 (br, 2x 2 H) ; 7.23 (m, 2x1 H) ; 7.39 - 7.47 (m, 2x2 H) ; 7.54 - 7.58 (m, 2x1 H) ; 8.52 - 8.66 (s, 1 H) ; 8.68 - 8.69 (s, 1 H).

Example 3 methyl 2-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoate:

3.1 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine:

To a solution of 5-bromo-2-cyclopropyl-pyrimidine (5.3 g) in dry dioxane (40 ml) was added 2- chloro-phenylboronic acid (8.5 g), K ₂ C0 ₃ (7.4 g) and Pd(dppf)CI ₂ .xCH ₂ CI ₂ (550 mg) under N ₂ . The resulting mixture was heated at 100°C overnight. Then the mixture was diluted with water, extracted with EtOAc. The combined organic layers were washed with brine, dried over anhydrous Na ₂ S0 ₄ , filtered and concentrated to give crude product (8 g), which was purified by column (PE:EtOAc = 5:1 ) to afford 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine (4 g, 60%). H NMR: CDCIs 400MHz δ 8.69 (s, 2 H), 7.2 - 7.6 (m, 4 H), 2.35 (br s, 1 H), 1.05 - 1 .30 (m, 4 H).

3.2 methyl 2-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoate:

To a solution of 2,2,6,6-tetramethylpiperidine (1.6 g) in dry THF (50 mL) was added dropwise n-BuLi (10.8 mL) at-78°C under N ₂ . The resulting mixture was stirred at -78°C for 1 h. Then 5-(2- chlorophenyl)-2-cyclopropyl-pyrimidine (1 g) in 10 mL THF was added dropwised at-78°C. After stirred for 5min, methlypyruvate (2.2 g) was added. The mixture was stirred while warming from -78°C to room temperature. Then aq. NH ₄ CI was added at 0 °C. The mixture was extracted with EtOAc. The combined organic layers were washed with saturated brine, dried over anhydrous Na ₂ S0 ₄ , filtered, concentrated and purified by column chromatography (PE:EtOAc = 10:1 ) to give methyl 2-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-OH-pro panoate (200 mg, 14%) as a white solid.

¹ H NMR: MeOD 400MHz (2 rotamers) δ 8.35 (s, 1 H), 8.29 (s, 1 H), 7.2 - 7.5 (m, 2x4 H), 3.66 - 3.73 (2s, 2x 3H), 2.18 - 2.38 (m, 2x1 H), 1 .63 (s, 3 H), 1.53 (s, 3 H), 1.06 - 1.25 (m, 2x4 H). Example 4: 5-(2-chlorophenyl)-2-cyclopropyl-4-(3-CH ₃ -2-furyl)pyrimidine:

4.1 a 2-(2-chlorophenyl)-1-(3-CH ₃ -2-furyl)ethanone:

To a solution of N-methoxy-N,3-dimethyl-furan-2-carboxamide (1 .5 g) in dry THF (60 mL) under Argon is added at -78°C chloro-[(2-chlorophenyl)-CH ₃ ]magnesium (CAS 29874-00-8) drop wise. The reaction mixture is stirred for 1 h at -78°C warmed to room temperature and stirred for 16 h. The reaction was quenched with brine (60 mL), extracted with ethyl acetate, dried and concentrated. The product was purified by column chromatography (gradient cyclo- hexane/ethyl acetate = from 1 :0 to 3:2) to give 2-(2-chlorophenyl)-1 -(3-CH3-2-furyl)ethanone (1.05 g, 50.5 %).

1H NMR CDCI3 400MHz: δ 7.46 - 7.36 (m, 2H), 7.30 - 7.19 (m, 3H), 6.41 (d, J = 1 .7 Hz, 1 H), 4.33 (s, 2H), 2.39 (s, 3H).

4.1 b 2-(2-chlorophenyl)-1-(3-CH ₃ -2-furyl)ethanone:

To a suspension of NaH (60 %, 1 .61 g) in dry DMF (60 mL) under Argon is added at -10°C 2- (3-CH3-2-furyl)-2-morpholino-acetonitrile (7.6 g). The reaction is stirred for 30 min. followed by addition of a solution of 1 -(bromomethyl)-2-chloro-benzene (6.88 g) in dry DMF. The reaction is warmed to room temperature and stirred for 16 h. The mixture is poured into a saturated aq. ammonium chloride solution, extracted with ethyl acetate, washed with water and aq. LiCI solution (10 %), dried and concentrated. The residue is dissolved in a mixture of methanol and water (7:3) and CuS0 ₄ (16.7 g) is added. The reaction mixture is stirred for 1 .5 h at 60°C. After concentration of the mixture, water is added, the mixture is extracted with ethyl acetate, washed with saturated aq. sodium sulfite solution and brine, dried and concentrated. The product is purified by column chromatography (gradient cyclohexane/ethyl acetate = from 1 :0 to 3:2) to give 2-(2-chlorophenyl)-1 -(3-CH ₃ -2-furyl)ethanone (5.0 g, 63.6 %).

1H NMR CDCI3 400MHz: δ 7.46 - 7.36 (m, 2H), 7.30 - 7.19 (m, 3H), 6.41 (d, J = 1 .7 Hz, 1 H), 4.33 (s, 2H), 2.39 (s, 3H).

4.2 2-(2-chlorophenyl)-3-(dimethylamino)-1 -(3-CH ₃ -2-furyl)prop-2-en-1-one:

A solution of 2-(2-chlorophenyl)-1-(3-CH3-2-furyl)ethanone (1 .05 g) in dimethylformamide- dimethylacetal (6 ml.) was stirred for 16 h at 65°C. TLC showed that the SM was consumed. The mixture was concentrated and purified by column chromatography (gradient cyclohexane/ethyl acetate = from 1 :0 to 1 :9) to give 2-(2-chlorophenyl)-3-(dimethylamino)-1 -(3-CH ₃ -2- furyl)prop-2-en-1 -one (700 mg, 54.0 %).

H NMR CDCI3 400MHz: δ 7.68 (s, 1 H), 7.42 - 7.34 (m, 1 H), 7.29 - 7.16 (m, 3H), 7.13 (d, J = 1.7 Hz, 1 H), 6.25 (d, J = 1.7 Hz, 1 H), 2.78 (s, 6H), 2.32 (s, 3H).

4.3 5-(2-chlorophenyl)-2-cyclopropyl-4-(3-CH ₃ -2-furyl)pyrimidine:

To a solution of 2-(2-chlorophenyl)-3-(dimethylamino)-1-(3-CH3-2-furyl)prop-2 -en-1 -one (4.9 g) in EtOH (100 ml.) was added cyclopropanecarboxamidine hydrochloride (2.24 g) and NaOEt (21 %, 6.93 g). The resulting mixture was stirred for 16 h at reflux. TLC (PE: EtOAc=3:1 ) showed that the SM was consumed. The mixture was filtered, and the filtrate was concentrated, purified by column (gradient EtOAc: PE = from 0:1 to 1 :0) to give 5-(2-chlorophenyl)-2-cyclopropyl-4- CH3-pyrimidine (4.0 g, 73 %) as a yellow solid.

¹ H NMR CDCI3 400MHz: δ 8.38 (s, 1 H), 7.52 - 7.36 (m, 1 H), 7.37 - 7.17 (m, 3H), 7.05 (d, J = 1.7 Hz, 1 H), 6.27 (d, J = 1.7 Hz, 1 H), 2.43 (s, 3H), 2.37 - 2.28 (m, 1 H), 1.27 - 1.21 (m, 2H), 1.14 - 1 .08 (m, 2H).

Example 5: N-acetyl-5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carbo xamide:

5.1 5-Bromo-2-cyclopropyl-pyrimidine-4-carboxylic acid:

NaH (60% purity, 41 .9 g) is added in portions to EtOH (800 mL) at 0 °C. The resulting mixture is warmed to ambient temperature and the cyclopropanecarboxamidine hydrochlorid (93.5 g) is added in portions. The reaction is warmed to 50 °C and maintained at this temperature for 0.5 h and then cooled to ambient temperature before mucobromic acid (100 g) is added in EtOH while keeping the internal temperature below 55 °C. The mixture is allowed to cool to ambient temperature and stirred for additional 16 h. All solid components are removed by filtration and the resulting solution is concentrated under reduced pressure. Aq. HCI (1 mol/L) is added, the aqueous phase is washed with EtOAc (3x), the combined organic extracts are dried over MgS04 and the solid parts removed by filtration. The residue is concentrated under reduced pressure and the resulting solid titrated with (ίΡ Ο. The solids are collected by filtration and dried yielding the title compound (68.0 g, yield 72 %) as a colorless solid.

1 H NMR (400 MHz, CDCI ₃ ): δ = 8.91 (s, 1 H), 2.38 - 2.26 (m, 1 H), 1.34 - 1 .14 (m, 4H) ppm; MS (ESI) m/z 244.9 [M + H+]. 5.2 Methyl 5-bromo-2-cyclopropyl-pyrimidine-4-carboxylate:

5-Bromo-2-cyclopropyl-pyrimidine-4-carboxylic acid (91 .0 g) is dissolved in MeOH (1200 ml.) and cone, sulfuric acid (20 ml.) is added dropwise at ambient temperature. The reaction is heated to reflux and stirred for 16 h. The resulting mixture is cooled to ambient temperature and neutralized with aq. sat. NaHCC>3. The residue is parted between EtOAc and aq. sat. NaHCC>3, the phases are separated, the aq. phase is extracted with EtOAc and the combined organics are dried over MgS0 ₄ . Solid parts are removed by filtration and the organic phase is concentrated under reduced pressure. Column chromatography of the resulting crude product (ISCO- CombiFlash Rf, cyclohexane/EtOAc) yields the title compound (1.48 g, yield 63%) as a colorless solid.

H NMR (400 MHz, CDCI ₃ ): δ = 8.74 (s, 1 H), 4.01 (s, 3H), 2.33 - 2.22 (m, 1 H), 1 .21 - 1 .06 (m, 4H) ppm; MS (ESI) m/z 246.9 [M + H ⁺ ].

5.3 methyl 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxylate:

A mixture of methyl 5-bromo-2-cyclopropyl-pyrimidine-4-carboxylate (8.00 g), 2-(chlorophe- nyl)boronic acid (5.1 1 g), K3PO4 (8.89 g) and PdC dppf (4.19 g) in dioxane (120ml_) and water is heated under reflux under an atmosphere of argon for 5 h. Water and EtOAc are added, the phases are separated and organic phase is dried over MgS0 ₄ . The solids are removed via filtration and resulting solution is concentrated under reduced pressure. Column chromatography of the crude product (ISCO-CombiFlash Rf) yields the title compound (3.00 g, yield 48%).

¹ H NMR (400 MHz, CDCI3): δ 8.60 (s, 1 H), 7.52 - 7.44 (m, 1 H), 7.49 - 7.47 (m, 1 H), 7.39 - 7.34 (m, 2H), 7.26 - 7.24 (m, 1 H), 3.79 (s, 3H), 2.45 - 2.39 (m, 1 H), 1 .28 - 1 .24 (m, 2H), 1 .19 - 1 .14 (m, 2H) ppm; MS (ESI) m/z 289.1 [M + H ⁺ ].

5.4 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxylic acid:

Methyl 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxylate (3.00 g) is dissolved in THF and lithiumhydroxid (373 mg) followed by water until the base is completely dissolved. The resulting mixture is stirred for 2 hours at ambient temperature; the volatiles are removed under reduced pressure and the remains are then acidified to pH = 1 - 2 with aqueous hydrochloric acid. The aq. phase is extracted with EtOAc and the combined organics are dried over MgS0 ₄ . Solid parts are removed by filtration and the organic phase is concentrated under reduced pressure yielding the title compound (2.00 g, yield 70%) as a colorless solid.

H NMR (400 MHz, CDCI ₃ ): δ 10.94 (brs, 1 H), 8.67 (s, 1 H), 7.51 - 7.49 (m, 1 H), 7.42 - 7.35 (m, 1 H), 7.24 - 7.22 (m, 1 H), 2.45 - 2.39 (m, 1 H), 1.29 - 1 .22 (m, 4H) ppm; MS (ESI) m/z 275.0 [M + H ⁺ ].

5.5: 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxamide:

To a solution of 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxylic acid (1 .0 g) in DCM (15 ml.) are added DMF (2 drops) and oxalyl chloride (924 mg) and the mixture is stirred for 16 h at room temperature. This mixture is added to a mixture of a 2 M solution of ammonia in dioxane (3.64 ml.) and triethylamine (1 .1 1 ml.) in DCM (10 ml_). The combined mixtures are stirred for 16 h at room temperature. After addition of water the mixture was stirred for 5 minutes and separated. The organic phase was concentrated and purified by column chromatography yielding 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxamide (696 mg 70 %).

¹ H NMR (400 MHz, Chloroform-d) δ 8.67 (s, 1 H), 7.52 - 7.47 (m, 1 H), 7.43 - 7.31 (m, 2H), 7.25 - 7.20 (m, 1 H), 2.48 - 2.35 (m, 1 H), 1.34 - 1 .21 (m, 4H). 5.6: N-acetyl-5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carbo xamide:

To a solution of 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxamide (230 mg) in dry THF (10 mL) is added a 1 M solution of LiHMDS in THF (0.84 mL) at -20°C. After stirring for 10 min. at -20°C acetic anhydride (129 mg) is added and the reaction is warmed to room temperature and stirred for 16 h. Water is added, the aq. phase is extracted with ethyl acetate. The combined organic extracts are washed with water and brine, dried and concentrated.

Purification by column chromatography (gradient EtOAc: CH = from 0:1 to 1 :4) yielded N-acetyl- 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carboxamide (30 mg, 1 1 %).

H NMR (400 MHz, Chloroform-d) δ 10.25 (s, 1 H), 8.60 (d, J = 0.9 Hz, 1 H), 7.56 - 7.45 (m, 1 H), 7.45 - 7.34 (m, 2H), 7.33 - 7.18 (m, 1 H), 2.48 (s, 3H), 2.44 - 2.36 (m, 1 H), 1 .32 - 1.19 (m, 6H).

Example 6: ethyl 2-[5-(2-chlorophenyl)-2-methoxy-pyrimidin-4-yl]acetate:

To a solution of 5-(2-chlorophenyl)-2-methoxy-4-CH3-pyrimidine (1.0 g) in dry THF (25 mL) is added a 1 M solution of LiHMDS (8.52 mL) at 0 °C and the mixture is stirred for 30 min. at 0 °C. To this mixture is added diethylcarbonate (2.1 1 g) and the mixture is slowly warmed to room temperature and stirred for 22 h. Saturated aq. Ammonium chloride solution is added and the mixtures is extracted 3 times with ethyl acetate. The organic phase was concentrated and purified by column chromatography yielding ethyl 2-[5-(2-chlorophenyl)-2-methoxy-pyrimidin-4- yl]acetate (900 mg, 95% purity, 65 % yield).

1H NMR DMSO-d6 500MHz: 8.48 (s, 1 H), 7.65 - 7.60 (m, 1 H), 7.53 - 7.43 (m, 2H), 7.42 - 7.37 (m, 1 H), 4.01 - 3.90 (m, 5H), 3.71 - 3.50 (m, 2H), 1 .07 (t, J = 7.1 Hz, 3H).

Example 7: methyl 2-[5-(2-bromophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2-CH3-pro panoate: To a solution of methyl 2-[5-(2-bromophenyl)-2-cyclopropyl-pyrimidin-4-yl]acetate (800 mg) in dry THF (30 mL) is added iodomethane (1 .31 g) at -78 °C, followed by addition of potassium tert-butanolate (776 mg). The mixture is stirred for 1 h at -78 °C. The mixture is slowly warmed to room temperature and stirred for 65 h at room temperature. Reaction control shows conversion to mono- and di-methyl product. Another portion of Iodomethane (1 .31 g) and potassium tert-butanolate (776 mg) is added and the mixture is stirred 16 h at room

temperature. After addition of water, the mixture is extracted with ethyl acetate, washed with saturated aq. sodium bicarbonate solution, dried and concentrated. The product is purified by column chromatography to give methyl 2-[5-(2-bromophenyl)-2-cyclopropyl-pyrimidin-4-yl]-2- CHs-propanoate (210 mg, 24.3 %).

H NMR (400 MHz, Chloroform-d) δ 8.22 (s, 1 H), 7.68 (dd, J = 7.9, 1 .3 Hz, 1 H), 7.34 (td, J = 7.5, 1.3 Hz, 1 H), 7.30 - 7.22 (m, 1 H), 7.19 (dd, J = 7.5, 1 .8 Hz, 1 H), 3.48 (s, 3H), 2.33 - 2.24 (m, 1 H), 1.48 (s, 3H), 1.37 (s, 3H), 1.23 - 1 .14 (m, 2H), 1 .15 - 1 .04 (m, 2H).

Example 7: [5-(2-Chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]methanol:

DIBAIH (1 N in THF, 38.8 mL) is added dropwise to a solution of methyl 5-(2-chlorophenyl)-2- cyclopropyl-pyrimidine-4-carboxylate (5.60 g) in THF (50 mL) at 0 °C. Upon completion of the addition the reaction mixture is warmed to ambient temperature and stirred for 2 h. EtOAc (50 mL) is slowly added and the mixture is stirred for 15 min before aq. NaOH (2 mol/L) is added at 0 °C until the phases are clear. The phases are separated and the aq. phase is extracted with EtOAc (2x). The combined organics are dried over MgS0 ₄ , solid parts are removed by filtration and the organic phase is concentrated under reduced pressure yielding the title compound (4.00 g, yield 79%). H NMR (400 MHz, CDCI ₃ ): δ 8.36 (s, 1 H), 7.53 - 7.51 (m, 1 H), 7.42 -7.34 (m, 2H), 7.21 - 7.17 (m, 1 H), 4.46 (d, J = 22.0 Hz, 2H), 2.42 - 2.35 (m, 1 H), 1 .27 - 1 .23 (m, 2H), 1 .20 - 1.15 (m, 2H) ppm; MS (ESI) m/z 261 .0 [M + H ⁺ ].

Example 8: 2-[5-(2-chloro-4-fluorophenyl)-2-cyclopropyl-pyrimidin-4-yl] propan-2-ol

MeMgBr (3N in Et.20, 2.18 mL) is added dropwise to a solution of methyl 5-(2-chlorophenyl)-2- cyclopropyl-pyrimidine-4-carboxylate (1.00 g) in Et^O (20 mL) at -20 °C. Upon completion of the addition the reaction mixture is warmed to 0 °C and stirred for 1 h. EtOAc and aq. sat. NH ₄ CI is added and the phases are separated. The organic phase is dried over MgS0 ₄ , solid parts are removed by filtration and the organic phase is concentrated under reduced pressure.

Purification by column chromatography (ISCO-CombiFlash Rf, reversed phase, MeCN/water)) yields the title compound (810 mg, 95%) as a colorless oil.

H NMR (400 MHz, DMSO-d ₆ ): δ 8.22 (s, 1 H), 7.48 (dd, J = 9.0, 2.6 Hz, 1 H), 7.40 (dd, J = 8.6, 6.3 Hz, 1 H), 7.23 (td, J = 8.6, 2.6 Hz, 1 H), 4.84 (s, 1 H), 2.33 - 2.17 (m, 1 H), 1 .37 (s, 3H), 1.35 (s, 3H), 1 .13 - 0.98 (m, 4H) ppm; MS (ESI) m/z 307.0 [M + H ⁺ ].

Example 9: 1-[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]ethanol:

9.1 : 5-(2-chlorophenyl)-2-cyclopropyl-pyrimidine-4-carbaldehyde

A mixture of [5-(2-Chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]methanol (2.00 g) and MnC>2 (8.00 g) in chloroform (20 mL) are heated under reflux for 16 h. Solid parts are removed by filtration and the organic phase is concentrated under reduced pressure. Purification by column chromatography (ISCO-CombiFlash Rf, cyclohexane/EtOAc) yields the title compound (1.50 g, 76%).

¹ H NMR (400 MHz, CDCI3): δ 9.95 (s, 1 H), 8.64 (s,1 H), 7.51 - 7.48 (m, 1 H), 7.44 - 7.36 (m, 2H), 7.26 - 7.24 (m, 1 H), 2.48 - 2.41 (m, 1 H), (tt, J = 8.1 , 4.8 Hz, 1 H), 1 .31 - 1.26 (m, 2H), 1.23

- 1 .17 (m, 2H) ppm; MS (ESI) m/z 259.0 [M + H ⁺ ].

9.2: 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4-yl]ethanol:

MeMgBr (3N in Et ₂ 0, 33.4 mL) is added dropwise to a solution of 5-(2-chlorophenyl)-2- cyclopropyl-pyrimidine-4-carbaldehyde (23.6 g) in Et^O (200 mL) at -10 °C. Upon completion of the addition the reaction mixture is warmed to 25 °C and stirred for 1 h. EtOAc and aq. sat. NH4CI are added and the phases are separated. The organic phase is dried over MgS0 ₄ , solid parts are removed by filtration and the organic phase is concentrated under reduced pressure. Purification by column chromatography (ISCO-CombiFlash Rf, reversed phase, MeCN/water)) yields the title compound (17.9 g, 68%) as a colorless oil.

H NMR (400 MHz, CDCI3, 2 rotamers): δ 8.37 (s, 1 H), 8.31 (s, 1 H), 7.55 - 7.50 (m, 2H), 7.42

- 7.33 (m, 4 H), 7.25 - 7.16 (m, 2H), 4.79 - 4.69 (m, 1 H), 4.36 - 4.33 (m, 1 H), 2.38 - 2.32 (m, 2H), 1.25 - 1 .22 (m, 4H), 1 .18 - 1 .12 (m, 10H) ppm; MS (ESI) m/z 275.0 [M + H ⁺ ].

Example 10: 5-(2-chlorophenyl)-2-cyclopropyl-4-(1-methoxyethyl)pyrimidin e:

NaH (21 .2 mg) is added to a solution of 1 -[5-(2-chlorophenyl)-2-cyclopropyl-pyrimidin-4- yl]ethanol (210 mg) in DMF (5 mL) at 0 °C. The mixture is warmed to 25 °C and stirred for 30 min before Mel (52.6 μί) is added. The reaction is stirred for 2 h at 25 °C. Water and EtOAc are and the phases are separated. The organic phase is dried over MgS0 ₄ , solid parts are removed by filtration and the organic phase is concentrated under reduced pressure. Purification by column chromatography (ISCO-CombiFlash Rf, reversed phase, MeCN/water)) yields the title compound (80.0 mg, 36%) as a colorless oil. H NMR (400 MHz, CDCI ₃ , 2 rotamers): δ 8.46 (s, 1 H), 8.33 (s, 1 H), 7.65 - 7.60 (m, 2H), 7.53

- 7.39 (m, 6H), 4.15 - 4.08 (m, 2H), 3.00 (s, 3H), 2.93 (s, 3H), 2.31 - 2.25 (m, 2H), 1.34 (d, J =

XX Hz, 3H), 1 .25 (d, J = 6.4 Hz, 3H), 1.12 - 1 .05 (m, 8H) ppm; MS (ESI) m/z 289.0 [M + H ⁺ ]. Below listed are the meaning of abbreviations used in preparation process above.

CH cyclohexane

EtOH ethanol

DCM dichloromethane

DMF dimethylformamide

PE petrol ether

TLC thin layer chromatography

EtOAc ethylacetate

SM starting material

LDA lithium diisopropylamide

LiHMDS lithium bis(trimethylsilyl)amide

MeOH methanol

NaHMDS sodium bis(trimethylsilyl)amide

THF tetrahydrofuran

Prep-HPLC preparative high pressure liquid chromatography

NMO N-methylmorpholine-N-oxide

PPTS pyridinium p-tolouolsulfonate

LAH Lithium aluminium hydride

DIBAIH Diisobutylaluminium hydride

PCC Pyridinium Chlorochromate. With appropriate modification of the starting materials, the procedures given in the synthesis examples below were used to obtain further compounds of formula I. The compounds obtained in this manner are listed in the Table X that follows, together with physical data.

The products shown below were characterized by melting point determination, by the masses ([m/z]) or retention time (RT; [min.]) determined by HPLC-MS or HPLC spectrometry.

HPLC-MS = high performance liquid chromatography-coupled mass spectrometry; HPLC methods:

Method: Column: Phenomenex Kinetex 1 .7 μηη XB-C18 100A; 50 x 2.1 mm; mobile phase: A: water + 0.1 % trifluoroacetic acid (TFA); B: acetonitrile + 0.1 % TFA; gradient: 5-100% B in 1 .50 minutes; 100% B 0.25 min; flow: 0.8-1.Oml/min in 1.51 minutes at 60°C.MS: quadrupole elec- trospray ionization, 80 V (positive mode).

Table X:

B Use examples

The herbicidal activity of the pyrimidine compounds of formula (I) was demonstrated by the following greenhouse experiments:

The culture containers used were plastic flowerpots containing loamy sand with approximately 3.0% of humus as the substrate. The seeds of the test plants were sown separately for each species.

For the pre-emergence treatment, the active ingredients, which had been suspended or emulsified in water, were applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with transparent plastic hoods until the plants had rooted. This cover caused uniform germination of the test plants, unless this had been impaired by the active ingredients.

For the post-emergence treatment, the test plants were first grown to a height of 3 to 15 cm, depending on the plant habit, and only then treated with the active ingredients which had been suspended or emulsified in water. For this purpose, the test plants were either sown directly and grown in the same containers, or they were first grown separately as seedlings and transplanted into the test containers a few days prior to treatment.

Depending on the species, the plants were kept at 10 - 25°C or 20 - 35°C, respectively.

The test period extended over 2 to 4 weeks. During this time, the plants were tended, and their response to the individual treatments was evaluated.

Evaluation was carried out using a scale from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial moieties, and 0 means no damage, or normal course of growth. A good herbicidal activity is given at values of at least 70 and a very good herbicidal activity is given at values of at least 85.

The plants used in the greenhouse experiments were of the following species:

At an application rate of 1000 g/ha, Ex.1 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and good herbicidal activity against AVEFA and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.2 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY, and good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG. At an application rate of 2000 g/ha, Ex.4 applied by the post-emergence method showed very good herbicidal activity against SETVI, AVEFA and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against AGSST, APESV and ECHCG.

At an application rate of 1819 g/ha, Ex.5 applied by the post-emergence method showed very good herbicidal activity against SETVI, AVEFA and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.6 applied by the post-emergence method showed very good herbicidal activity against ECHCG and APESV, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.7 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.8 applied by the post-emergence method showed very good herbicidal activity against MATIN, ABUTH and AMARE.

At an application rate of 1856 g/ha, Ex.9 applied by the post-emergence method showed very good herbicidal activity against ECHCG, AVEFA and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV, and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.10 applied by the post-emergence method showed very good herbicidal activity against SETVI, ABUTH and AMARE, and applied by the pre-emergence method showed very good herbicidal activity against AGSST, MATIN and SETFA.

At an application rate of 2000 g/ha, Ex.1 1 applied by the pre-emergence method showed very good herbicidal activity against SETFA and good herbicidal activity against ECHCG.

At an application rate of 250 g/ha, Ex.13 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG and POLCO, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV.

At an application rate of 250 g/ha, Ex.14 applied by the post-emergence method showed good herbicidal activity against LOLMU, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.15 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY, and good herbicidal activity against AMARE, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.16 applied by the post-emergence method showed good herbicidal activity against AMARE, and applied by the pre-emergence method showed very good herbicidal activity against SETFA.

At an application rate of 2000 g/ha, Ex.17 applied by the pre-emergence method showed very good herbicidal activity against AGSST, ECHCG and SETFA. At an application rate of 2000 g/ha, example 19 applied by the post-emergence method showed very good herbicidal activity against AMARE and ABUTH.

At an application rate of 2000 g/ha, Ex.20 applied by the post-emergence method showed good herbicidal activity against AMARE and MATIN, and applied by the pre-emergence method showed good herbicidal activity against ECHCG. At an application rate of 1000 g/ha, Ex.21 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.22 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.24 applied by the post-emergence method showed very good herbicidal activity against ECHCG and SETVI, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.25 applied by the post-emergence method showed very good herbicidal activity against MATIN, and applied by the pre-emergence method showed very good herbicidal activity against AGSST and POAAN.

At an application rate of 2000 g/ha, Ex.26 applied by the post-emergence method showed very good herbicidal activity against ECHCG and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.27 applied by the post-emergence method showed very good herbicidal activity against AMARE, ECHCG and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against AGSST, ECHCG and APESV.

At an application rate of 1 163 g/ha, Ex.28 applied by the post-emergence method, showed very good herbicidal activity against AMARE, and good herbicidal activity against ABUTH.

At an application rate of 2000 g/ha, Ex.29 applied by the post-emergence method showed very good herbicidal activity against MATIN and AMARE.

At an application rate of 2000 g/ha, Ex.30 applied by the post-emergence method showed very good herbicidal activity against SETVI and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.31 applied by the post-emergence method showed very good herbicidal activity against SETVI and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.32 applied by the post-emergence method, showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.33 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.34 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and good herbicidal activity against ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV, and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.35 applied by the post-emergence method showed very good herbicidal activity against AMARE, ECHCG and ALOMY, and applied by the pre-emer- gence method showed very good herbicidal activity against AGSST, ECHCG and APESV..

At an application rate of 2000 g/ha, Ex.36 applied by the post-emergence method showed very good herbicidal activity against MATIN, and applied by the pre-emergence method showed very good herbicidal activity against AGSST and POAAN. At an application rate of 2000 g/ha, Ex.37 applied by the pre-emergence method showed good herbicidal activity against SETFA.

At an application rate of 1000 g/ha, Ex.38 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.39 applied by the post-emergence method showed very good herbicidal activity against AMARE and ABUTH, and applied by the pre-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.40 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.41 applied by the post-emergence method showed very good herbicidal activity against MATIN and ALOMY.

At an application rate of 1000 g/ha, Ex.42 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.44 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ECHCG.

At an application rate of 1000 g/ha, Ex.47 applied by the post-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 1000 g/ha, Ex.49 applied by the post-emergence method showed very good herbicidal activity against ALOMY and SETVI, and good herbicidal activity against

ECHCG, and applied by the pre-emergence method showed good herbicidal activity against APESV and ECHCG.

At an application rate of 500 g/ha, Ex.50 applied by the post-emergence method showed very good herbicidal activity against AMARE and SETVI.

At an application rate of 1000 g/ha, Ex.51 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.52 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.54 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.55 applied by the post-emergence method showed very good herbicidal activity against SETVI and AMARE.

At an application rate of 1000 g/ha, Ex.58 applied by the post-emergence method showed very good herbicidal activity against SETVI, and good herbicidal activity against AVEFA.

At an application rate of 1000 g/ha, Ex.59 applied by the post-emergence method showed very good herbicidal activity against SETVI, and good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG, and good herbicidal activity against SETFA.

At an application rate of 1000 g/ha, Ex.60 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY.

At an application rate of 500 g/ha, Ex.62 applied by the post-emergence method showed very good herbicidal activity against SETVI. At an application rate of 1000 g/ha, Ex.63 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.65 applied by the post-emergence method showed very good herbicidal activity against AMARE and ECHCG.

At an application rate of 2000 g/ha, Ex.66 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.67 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA, and good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.70 applied by the post-emergence method showed very good herbicidal activity against ALOMY and SETVI.

At an application rate of 2000 g/ha, Ex.71 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA, and good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.73 applied by the post-emergence method showed good herbicidal activity against ALOMY.

At an application rate of 2000 g/ha, Ex.74 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.76 applied by the post-emergence method showed very good herbicidal activity against SETVI, and good herbicidal activity against ALOMY.

At an application rate of 1000 g/ha, Ex.77 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY.

At an application rate of 1000 g/ha, Ex.78 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.79 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY.

At an application rate of 1000 g/ha, Ex.81 applied by the post-emergence method showed very good herbicidal activity against AVEFA and ALOMY.

At an application rate of 2000 g/ha, Ex.85 applied by the post-emergence method showed very good herbicidal activity against ABUTH, and good herbicidal activity against AMARE.

At an application rate of 1000 g/ha, Ex.86 applied by the post-emergence method showed very good herbicidal activity against SETVI, and good activity against ABUTH and AMARE, and ap- plied by the pre-emergence method showed good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.87 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and applied by the pre-emergence method showed good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.88 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.89 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and good activity against AVEFA, and applied by the pre-emergence method showed good herbicidal activity against APESV. At an application rate of 2000 g/ha, Ex.90 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.92 applied by the post-emergence method showed good herbicidal activity against ALOMY, SETVI and ECHCG.

At an application rate of 2000 g/ha, Ex.93 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.94 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.95 applied by the post-emergence method showed very good herbicidal activity against ALOMY and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.96 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.97 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 500 g/ha, Ex.98 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.99 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.101 applied by the post-emergence method showed very good herbicidal activity against ABUTH, and AMARE.

At an application rate of 2000 g/ha, Ex.102 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.103 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.104 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV, and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.105 applied by the post-emergence method showed very good herbicidal activity against APESV, and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against ALOMY, and ECHCG.

At an application rate of 2000 g/ha, Ex.106 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA, and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 500 g/ha, Ex.108 applied by the post-emergence method showed good herbicidal activity against ALOMY, and showed very good herbicidal activity against POLCO.

At an application rate of 1000 g/ha, Ex.1 10 applied by the post-emergence method showed good herbicidal activity against ECHCG. At an application rate of 1000 g/ha, Ex.1 12 applied by the post-emergence method showed good herbicidal activity against ECHCG.

At an application rate of 500 g/ha, Ex.1 14 applied by the post-emergence method showed very good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.1 19 applied by the post-emergence method showed good herbicidal activity against SETVI, and showed very good herbicidal activity against ALOMY.

At an application rate of 1000 g/ha, Ex.120 applied by the post-emergence method showed good herbicidal activity against ALOMY.

At an application rate of 500 g/ha, Ex.121 applied by the post-emergence method showed very good herbicidal activity against LOLMU, ECHCG, POLCO and ALOMY.

At an application rate of 2000 g/ha, Ex.123 applied by the post-emergence method showed good herbicidal activity against SETVI, and very good herbicidal activity against AMARE.

At an application rate of 500 g/ha, Ex.125 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.126 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.127 applied by the post-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.128 applied by the post-emergence method showed very good herbicidal activity against AVEFA, and ECHCG, and good herbicidal activity against ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.129 applied by the post-emergence method showed very good herbicidal activity against AMARE, ALOMY, and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.131 applied by the post-emergence method showed very good herbicidal activity against AMARE, and ECHCG.

At an application rate of 2000 g/ha, Ex.132 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and good herbicidal activity against AMARE.

At an application rate of 500 g/ha, Ex.135 applied by the post-emergence method showed good herbicidal activity against ALOMY.

At an application rate of 1000 g/ha, Ex.141 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.143 applied by the post-emergence method showed very good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.146 applied by the post-emergence method showed very good herbicidal activity against ABUTH, SETVI and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.147 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA, and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.150 applied by the post-emergence method showed very good herbicidal activity against AMARE and ECHCG, and good herbicidal activity against ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV, and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.153 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA, and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.154 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA, and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.155 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and ECHCG.

At an application rate of 2000 g/ha, Ex.157 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.159 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA, and applied by the pre-emergence method showed good herbicidal activity against APESV, and ECHCG.

At an application rate of 2000 g/ha, Ex.164 applied by the post-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.21 1 applied by the post-emergence method showed good herbicidal activity against ALOMY and very good herbicidal activity against ECHCG, and applied by the pre-emergence method showed good herbicidal activity against APESV, and POAAN.

At an application rate of 2000 g/ha, Ex.213 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AFEFA and ECHCG, and applied by the pre- emergence method showed good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 2000 g/ha, Ex.214 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and ECHCG, and applied by the pre- emergence method showed good herbicidal activity against APESV and ECHCG, and good herbicidal activity against POAAN.

At an application rate of 2000 g/ha, Ex.215 applied by the post-emergence method showed very good herbicidal activity against ALOMY and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.216 applied by the post-emergence method showed very good herbicidal activity against ALOMY and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.219 applied by the post-emergence method showed good herbicidal activity against SETVI.

At an application rate of 1000 g/ha, Ex.220 applied by the pre-emergence method showed good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.221 applied by the post-emergence method showed very good herbicidal activity against ABUTH, AGSST and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 2000 g/ha, Ex.222 applied by the post-emergence method showed very good herbicidal activity against ABUTH, AMARE and MATIN. At an application rate of 2000 g/ha, Ex.223 applied by the post-emergence method showed very good herbicidal activity against ABUTH, AMARE and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 2000 g/ha, Ex.224 applied by the post-emergence method showed very good herbicidal activity against ALOMY and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.225 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV, ECHCG and POAAN. At an application rate of 500 g/ha, Ex.226 applied by the post-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 1000 g/ha, Ex.228 applied by the post-emergence method showed good herbicidal activity against ABUTH and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 1000 g/ha, Ex.229 applied by the pre-emergence method showed very good herbicidal activity against APESV and good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.230 applied by the post-emergence method showed good herbicidal activity against MATIN.

At an application rate of 2000 g/ha, Ex.231 applied by the post-emergence method showed very good herbicidal activity against ECHCG and good herbicidal activity against MATIN.

At an application rate of 2000 g/ha, Ex.232 applied by the post-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.233 applied by the pre-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.234 applied by the post-emergence method showed good herbicidal activity against POAAN, and applied by the pre-emergence method showed very good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.236 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.237 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.238 applied by the post-emergence method showed good herbicidal activity against ALOMY, and very good herbicidal activity against ALOMY, AMARE and ECHCG.

At an application rate of 2000 g/ha, Ex.240 applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.241 applied by the post-emergence method showed good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and POAAN.

At an application rate of 1000 g/ha, Ex.243 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG. At an application rate of 500 g/ha, Ex.244 applied by the post-emergence method showed good herbicidal activity against ALOMY, POAAN, and POLCO, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 1000 g/ha, Ex.245 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and good herbicidal activity against ECHCG.

At an application rate of 500 g/ha, Ex.246 applied by the pre-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 500 g/ha, Ex.247 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AGSST, and AMARE, and applied by the pre-emergence method showed very good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 2000 g/ha, Ex.248 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG, and SETVI, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV, ECHCG and POAAN.

At an application rate of 2000 g/ha, Ex.250 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 500 g/ha, Ex.251 applied by the pre-emergence method showed very good herbicidal activity against AMARE.

At an application rate of 1000 g/ha, Ex.252 applied by the post-emergence method showed very good herbicidal activity against ABUTH.

At an application rate of 1000 g/ha, Ex.253 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AMARE, and good herbicidal activity against ABUTH.

At an application rate of 1000 g/ha, Ex.254 applied by the post-emergence method showed very good herbicidal activity against ECHCG and AMARE, and good herbicidal activity against ALOMY.

At an application rate of 500 g/ha, Ex.255 applied by the post-emergence method showed good herbicidal activity against AMARE.

At an application rate of 2000 g/ha, Ex.256 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.257 applied by the post-emergence method showed good herbicidal activity against MATIN.

At an application rate of 2000 g/ha, Ex.259 applied by the post-emergence method showed very good herbicidal activity against ALOMY, POAAN and ECHCG, and applied by the pre- emergence method showed good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.260 applied by the post-emergence method showed very good herbicidal activity against ALOMY, and good herbicidal activity against AVEFA and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against ECHCG and MATIN, and good herbicidal activity against APESV. At an application rate of 1000 g/ha, Ex.261 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.262 applied by the post-emergence method showed very good herbicidal activity against AMARE, SETVI and ECHCG, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.263 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 500 g/ha, Ex.264 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA.

At an application rate of 250 g/ha, Ex.265 applied by the post-emergence method showed good herbicidal activity against ALOMY and CHEAL, and very good herbicidal activity against AMARE.

At an application rate of 1000 g/ha, Ex.266 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and ABUTH, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.267 applied by the post-emergence method showed very good herbicidal activity against ECHCG, POAAN and ABUTH, and applied by the pre- emergence method showed very good herbicidal activity against POAAN and ECHCG.

At an application rate of 1000 g/ha, Ex.268 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against POAAN and ECHCG.

At an application rate of 1000 g/ha, Ex.269 applied by the post-emergence method showed very good herbicidal activity against ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against SETFA.

At an application rate of 1000 g/ha, Ex.270 applied by the post-emergence method showed very good herbicidal activity against ALOMY and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.271 applied by the post-emergence method showed good herbicidal activity against ECHCG, very good herbicidal activity against SETVI.

At an application rate of 2000 g/ha, Ex.272 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and SETVI, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.273 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and SETVI, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.274 applied by the post-emergence method showed very good herbicidal activity against ALOMY and ECHCG, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.276 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and ABUTH, and applied by the pre- emergence method showed very good herbicidal activity against APESV. At an application rate of 1000 g/ha, Ex.211 applied by the post-emergence method showed very good herbicidal activity against ALOMY, SETVI and ECHCG, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.278 applied by the post-emergence method showed very good herbicidal activity against AMARE, ABUTH and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.279 applied by the post-emergence method showed very good herbicidal activity against AMARE, ABUTH and ALOMY, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.281 applied by the post-emergence method showed good herbicidal activity against AMARE, ABUTH and ALOMY, and very good herbicidal activity against ABUTH.

At an application rate of 2000 g/ha, Ex.282 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and SETVI, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.283 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.284 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.285 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and ABUTH, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.286 applied by the post-emergence method showed very good herbicidal activity against ECHCG, AMARE and ABUTH, and applied by the pre- emergence method showed very good herbicidal activity against AMARE, APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.287 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.288 applied by the post-emergence method showed very good herbicidal activity against ALOMY.

At an application rate of 2000 g/ha, Ex.289 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and SETVI, and applied by the pre-emer- gence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 2000 g/ha, Ex.290 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AVEFA and ECHCG, and applied by the pre- emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 500 g/ha, Ex.291 applied by the post-emergence method showed good herbicidal activity against ALOMY, AVEFA and LOLMU, and applied by the pre-emer- gence method showed very good herbicidal activity against POAAN, APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.292 applied by the post-emergence method showed very good herbicidal activity against ECHCG and SETVI, and good herbicidal activity against ALOMY, and applied by the pre-emergence method showed very good herbicidal activity against APESV and ECHCG.

At an application rate of 1000 g/ha, Ex.293 applied by the post-emergence method showed good herbicidal activity against ABUTH, and applied by the pre-emergence method showed very good herbicidal activity against SETFA, and good herbicidal activity against ECHCG.

At an application rate of 2000 g/ha, Ex.294 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ABUTH and ECHCG, and applied by the pre- emergence method showed good herbicidal activity against APESV.

At an application rate of 2000 g/ha, Ex.295 applied by the post-emergence method showed very good herbicidal activity against ALOMY and AVEFA, and applied by the pre-emergence method showed very good herbicidal activity against APESV, AMARE and ECHCG.

At an application rate of 1000 g/ha, Ex.296 applied by the post-emergence method showed very good herbicidal activity against ABUTH.

At an application rate of 2000 g/ha, Ex.297 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG and AVEFA, and applied by the pre- emergence method showed very good herbicidal activity against APESV, and good herbicidal activity against ECHCG and ABUTH.

At an application rate of 1000 g/ha, Ex.309 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG and AMARE, and very good herbicidal activity against APESV.

At an application rate of 500 g/ha, Ex.310 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and POLCO, and very good herbicidal activity against ALOMY, ECHCG and APESV.

At an application rate of 500 g/ha, Ex.31 1 applied by the post-emergence method showed very good herbicidal activity against ALOMY, AMARE and POLCO, and very good herbicidal activity against ALOMY, ECHCG and APESV.

At an application rate of 500 g/ha, Ex.312 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG and POLCO, and very good herbicidal activity against ALOMY, ECHCG and APESV.

At an application rate of 1000 g/ha, Ex.313 applied by the post-emergence method showed very good herbicidal activity against ALOMY, ECHCG and SETVI, and very good herbicidal activity against ECHCG and APESV.

At an application rate of 1000 g/ha, Ex.314 applied by the post-emergence method showed very good herbicidal activity against AMARE, ECHCG and SETVI, and very good herbicidal ac- tivity against ECHCG and APESV.

At an application rate of 2000 g/ha, Ex.315 applied by the post-emergence method showed very good herbicidal activity against AMARE, ECHCG and ALOMY, and very good herbicidal activity against ECHCG and APESV.