The new compounds correspond to formula 1, wherein A is a group OCHR4 or N=CR4; Y isOorNH, R, is C-C6-alkyl; R2 is C1-C6-alkyl or C,-C6-alkyl substituted by 1 to 5 fluorine atoms; R3 is C,-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, C3-C6-cycloalkoxy, C2-C6-alkenyl, C2- C6-alkenyloxy, C2-C6-alkinyl, C2-C6-alkinyloxy, C,-C6-alkoxycarbonyl, CN or halogen, whereby the above-mentioned groups, with the exception of CN and halogen, may be substituted by one or more identical or different substitutents selected from the group comprising halogen, cyano, nitro, C,-C6-alkoxycarbonyl, C,-C6-alkoxy, C,-C6-alkylthio, aminocarbonyl, C,-C6-alkylaminocarbonyl, di-C,-C6-alkylaminocarbonyl, C2-C6-alkenyloxy, C3-C6-cycloalkyl, C3-C6-cycloalkyloxy, heterocyclyl, heterocyclyloxy, aryl, aryloxy, hetaryl, hetaryloxy, whereby the cyclic radicals in turn may be substituted by one or more identical or different substitutents selected from the group comprising halogen, cyano, nitro, Cl-C6- alkyl, C,-C6halogenalkyl, C1-C6-alkoxy, C,-C6-halogenalkoxy, C1-C6-alkoxycarbonyl, Cl-C6- alkylthio, C,-C6-alkylamino, di-C,-C6-alkylamino, C2-C6-alkenyl, optionally substituted benzyl, optionally substituted benzyloxy, optionally substituted aryl, optionally substituted aryloxy, optionally substituted hetaryl and optionally substituted hetaryloxy, whereby the optionally substituted aromatic groups are unsubstituted or mono-to tri-substituted by the same or different substituents selected from halogen, Cj-C6-alkyl, C1-C6-halogenalkyl, C,-C6-alkoxy, C,-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy, C2-C6-alkinyl, C3-C6-alkinyloxy, C,-C6-<BR> alkoxycarbonyl, CN or OCN; or R3 is aryi, hetaryl, heterocyclyl, aryloxy, hetaryloxy or heterocyclyloxy, whereby the above-mentioned groups may be substituted by one or more identical or different substitutents selected from the group comprising halogen, C1-C6-alkoxy, halogen-C,-C6-alkoxy, C,-C6-alkylthio, halogen-C,-C6-alkylthio, C,-C6-alkylsulfinyl,<BR> halogen-C,-C6-alkylsulfinyl, C,-C6-aikylsulfonyl, halogen-C,-C6-alkylsulfonyl,<BR> C,-C6-alkylcarbonyl, halogen-C-C6-alkylcarbonyl, C,-C6-alkoxycarbonyl,<BR> halogen-C,-C6-alkoxycarbonyl, C,-C6-alkylaminocarbonyl, di-(C,-C6-alkyl)-aminocarbonyl, whereby the alkyl groups may be identical or different, C,-C6-alkylaminothiocarbonyl, di-(C,-C6-alkyl)-aminothiocarbonyl,(C,-C6-alkyl)-aminothioca rbonyl, whereby the alkyl groups may be identical or different, C,-C6-alkylamino, di- (C,-C6-alkyl)-amino, N02, an unsubstituted C,-C4-alkylenedioxy group or one which is substituted once to four times by C1-C4-alkyl and/or by halogen, or CN, SF3 and QR5; Q is a direct bond, O, O (C,-C6-alkylene), (C1-C6-alkylene) O, S (=O) p, S (=O) p (C,-C6-alkylene), (C,-C6-alkylene) S (=O) p, C,-Ce-alkylene, C2-C6-alkenylene or C2-C6-alkinylene; Rs is a C2-C6-alkenyl or C2-C6-alkinyl group either unsubstituted or substituted by 1 to 3 halogen atoms, a (C,-C4-alkyl) 3Si group, whereby the alkyl groups may be identical or different, CN, an unsubstituted or mono-to penta-substituted C3-C6-cycloalkyl, aryl, hetaryl or heterocyclyl group, whereby the substituents are selected from the group comprising halogen, C,-C6-alkyl, halogen-C,-C6-alkyl, C,-C6-alkoxy, halogen-C,-C6-alkoxy, phenoxy and CN; p is 0,1 or 2; R4 is methyl, ethyl or cyclopropyl; R6 is hydrogen or methyl.

Formula I should include all the possible isomeric forms, as well as mixtures, e. g. racemic mixtures, and any [E/Z] mixtures.

Alkyl-as a group perse and as a structural element of other groups and compounds, such as halogenalkyl, alkoxy and alkylthio-is either straight-chained, i. e. methyl, ethyl, propyl, butyl, pentyl or hexyl, or branched, e. g. isopropyl, isobutyl, sec.-butyl, tert.-butyl, isopentyl, neopentyl or isohexyl.

Alkenyl-as a group per se se and as a structural element of other groups and compounds, such as halogenalkenyl-is either straight-chained, for example vinyl, 1-methylvinyl, allyl, 1-butenyl or 2-hexenyl, or branched, for example isopropenyl.

Alkinyl-as a group per se and as a structural element of other groups and compounds, such as halogenalkinyl-is either straight-chained, for example propargyl, 2-butinyl or 5- hexinyl, or branched, for example 2-ethinylpropyl or 2-propargylisopropyl.

Alkylenedioxy is-O (alkylene) O-.

Alkylene-as a group per se and as a structural element of other groups and compounds, such as O (alkylene), (alkylene) O, S (=O) p (alkylene), (alkylene) S (=O) p or alkylenedioxy-is either straight-chained, for example-CH2CH2-,-CH2CH2CH2-or-CH2CH2CH2CH2-, or branched, for example-CH (CH3)-,-CH (C2H5)-,-C (CH3) 2-,-CH (CH3) CH2- or -CH (CH3) CH (CH3)-.

Alkenylene is either straight-chained, for example vin-1,2-yiene, all-1, 3-ylene, but-1-en-1,4- ylene or hex-2-en-1,6-ylene, or branched, for example 1-methylvin-1, 2-ylene.

Alkinylene is either straight-chained, for example propargylene, 2-butinylene or 5-hexinylene, or branched, for example 2-ethinylpropylene or 2-propargylisopropylene.

Halogen is fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine, Halogenalkyl may contain identical or different halogen atoms.

Aryl is phenyl or naphthyl, preferably phenyl.

Heteroaryl is a cyclic aromatic group with 5 to 9 ring members in one or two rings, 1 to 3 members of which are hetero atoms, selected from the group oxygen, sulphur and nitrogen.

1 to 2 benzene rings may be condensed onto the heterocycle, whereby the binding to the residual molecule takes place either via the hetero or the benzene moiety.

Examples are benzimidazolyl, benzisoxazolyl, benzisothiazolyl, benzocoumarinyl, benzofuryl, benzothiadiazolyl, benzothiazolyl, benzothienyl, benzoxazolyl, benzoxdiazolyl, quinazolinyl, quinolyl, quinoxalinyl, carbazolyl, dihydrobenzofuryl, furyl, imidazolyl, indazolyl, indolyl, isoquinolinyl, isothiazolyl, isoxazolyl, methylenedioxyphenyl, ethylenedioxyphenyl, naphthyridinyl, oxazolyl, phenanthridinyl, phthalazinyl, pteridinyl, purinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyrazolo [3,4-b] pyridyl, pyridyl, pyrimidinyl, pyrrolyl, tetrazolyl, oxadiazolyl, thiadiazolyl, thiazolyl, thienyl, triazinyl and triazolyl.

Pyridyl, pyrazinyl, pyrimidinyl, thiazolyl, quinolinyl and thienyl are preferred.

Heterocyclyl is a 5-to 7-membered non-aromatic ring with one to three hetero atoms selected from the group comprising N, O and S.

Aromatic 5-and 6-rings are preferred, which have a nitrogen atom as hetero atom and optionally a further hetero atom, preferably nitrogen or sulphur, especially nitrogen.

Thiazolinyl and oxazolinyl are preferred.

Of the compounds of formula 1, those groups are preferred in which: (1) a) A is the group N=CR4; or b) R, is methyl or ethyl, preferably methyl; or c) R2 is methyl, ethyl, fluoromethyl or trifluoroethyl, preferably methyl; or d) R3 is C,-C6-alkyl, C,-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy, C2-C6-alkinyl, C3-C6-alkinyloxy, C3-C6-cycloalkyl, C3-C6-cycloalkyloxy or C,-C6-alkoxycarbonyl, whereby the above-mentioned groups may be partially or totally halogenated; and also CN, OCN or halogen; or e) R3 is phenyl which is unsubstituted or mono-to tri-substituted by identical or different subsituents from halogen, C,-C6-alkyl, C,-C6-halogenalkyl, C,-C6-alkoxy, C,-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy, C2-C6-alkinyl, C3-C6-alkinyloxy,<BR> C,-C6-alkoxycarbonyl, CN, OCN, optionally substituted benzyl, optionally substituted phenyl or optionally substituted phenoxy, whereby the optionally substituted aromatic groups are unsubstituted or mono-to tri-substituted by identical or different subsituents from halogen, C,-C6-alkyl, C,-C6-halogenalkyl, C,-C6-alkoxy, C,-C6- haloalkoxy, C2-C6-alkenyl, C2-C6-alkenyloxy, C2-C6-alkinyl, C3-C6-alkinyloxy, C,-C6- alkoxycarbonyl, CN or OCN; or f) R3 is pyridyl, pyrimidinyl, furyl, thienyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, imidazolyl, pyrazolyl, which are unsubstituted or mono-to tri-substituted by identical or different subsituents from halogen, cyano, nitro, aminocarbonyl, C,- C4-alkyl, C,-C4-halogenalkyl, C,-C4-alkylcarbonyl, C,-C4-alkylsulfonyl, C,-C6-<BR> alkylsulfoxyl, C3-C6-cycloalkyl, optionally substituted arylcarbonyl, C,-C4-alkoxy, C,- C4-halogenalkoxy, C,-C6-alkoxycarbonyl, C,-C6-alkylthio, C,-C6-alkylamino, di-C,-C6- alkylamino, C,-C6-alkylaminocarbonyl, di-C,-C6-alkylaminocarbonyl or C2-C6-alkenyl ; or g) R4 is methyl; or h) R6 is hydrogen.

(2) Compounds of formula 1, wherein: A is N=CR4; Y is O or NH; R, is methyl or ethyl, preferably methyl; R2 is C,-C6-alkyl or C,-C6-alkyl substituted by 1-5 fluorine atoms; R3 is C,-C6-alkyl, C,-C6-alkoxy, C,-C6-alkoxycarbonyl, CN, C3-C6-cycloalkyl, aryl, hetaryl, heterocyclyl, aryloxy, hetaryloxy or heterocyclyloxy, whereby, with the exception of CN, the above-mentioned groups may be substituted; R4 is methyl, ethyl or cyclopropyl; R6 is hydrogen or methyl.

(2a) Of the compounds mentioned under (2), in particular those wherein: R2 is C,-C6-alkyl, fluoromethyl, difluoromethyl or 2,2,2-trifluoroethyl; R3 is C,-C6-alkyl, C,-C6-alkoxy, C,-C6-alkoxycarbonyl, CN, C3-C6-cycloalkyl, phenyl which is unsubstituted or mono-to tri-substituted by halogen, C,-C4-alkyl, C,-C4-haloalkyl, C,-C4-alkoxy, C,-C4-haloalkoxy, C2-C4-alkenyl, C2-C4-alkenyloxy, C2-C6-alkinyl, C3-C6- alkinyloxy, CN, OCN, benzyl, phenyl, or phenyloxy, wherein these aromatic groups are unsubstituted or mono-or di-substituted by halogen, C,-C2-alkyl, C,-C2-haloalkyl or C,-C2- alkoxy.

(2b) Of the compounds mentioned under (2a), in particular those wherein: R3 is C,-C4-alkyl, C,-C4-alkoxy, C,-C6-alkoxycarbonyl, or phenyl, which is unsubstituted or mono-to di-substituted by halogen, C,-C2-alkyl, C,-C2-haloalkyl, C,-C2-alkoxy.

(2c) Of the compounds mentioned under (2), in particular those wherein: R3 is C,-C4-alkyl, C,-C4-alkoxy, C,-C6-alkoxycarbonyl, or phenyl, which is unsubstituted or mono-to di-substituted by halogen, C,-C2-alkyl, C,-C2-haloalkyl, C,-C2-alkoxy; R4 is methyl; R6 is methyl.

(3) Compounds of formula 1, wherein: A is OCHR4; Y isOorNH; R, is methyl or ethyl, preferably methyl; R2 is C,-C6-alkyl, preferably methyl; R3 is C,-C6-alkyl, C,-C6-haloalkyl, C2-C6-alkenyl, C,-C6-alkoxy, C2-C6-alkenyloxy, C,-C6- alkoxycarbonyl, CN, C3-C6-cycloalkyl, aryl, hetaryl, heterocyclyl, aryloxy, hetaryloxy or heterocyclyloxy, whereby the hydrocarbon radicals and the cyclic radicals may be substituted as already mentioned above; R4 is methyl, ethyl or cyclopropyl, preferably methyl; R6 is hydrogen or methyl.

(3a) Of the compounds mentioned under (3), in particular those wherein: R3 is C,-C6-alkyl, C,-C6-haloalkyl, C2-C6-alkenyl, C,-C6-alkoxy, C2-C6-alkenyloxy, C,-C6- alkoxycarbonyl, C3-C6-cycloalkyl; R4 is methyl.

(3b) Of the compounds mentioned under (3), in particular those wherein: R3 is phenyl which is unsubstituted or mono-or di-substituted by halogen, C,-C4-alkyl, C,-C4-haloalkyl, C,-C4-alkoxy, C,-C4-haloalkoxy, C2-C4-alkenyl, C2-C4-alkenyloxy, benzyl, phenyl, or phenyloxy, wherein these aromatic groups are unsubstituted or mono-or di- substituted by halogen, C,-C2-alkyl, C,-C2-haloalkyl or C,-C2-alkoxy; R4 is methyl; R6 is hydrogen or methyl.

(3c) Of the compounds mentioned under (3), in particular those wherein: R4 and R6 are methyl.

Compounds of formula I may be produced as follows: A) A compound of formula I may be produced by reacting a compound of the general formula 11 wherein A, R2 and R3 have the significances given for formula 1, with an aldehyde or ketone of the general formula III or with one of its acetal derivatives of the general formula IV wherein Y, R, and R6 have the significances given for formula 1, and Rs is C,-C6-alkyl or the two R5, together with the two oxygen atoms and the carbon to which they are bonded, form a cyclic acetal.

B) A compound of formula 1, wherein Y is NH and A is N=CR4, may be produced by reacting a hydrazone of the general formula V, wherein R, and R6 have the significances given for formula 1, with an aldehyde or a ketone of the general formula VI, wherein R2, R3 and R4 have the significances given for formula 1.

C) A compound of formula 1, wherein A is OCHR4, may be produced by reacting an oxime of the general formula VII wherein Y, R, and R6 have the significances given for formula 1, with a halide of the general formula Vlil wherein R2, R3 and R4 have the significances given for formula I and Hal is a halogen atom such as chlorine, bromine or iodine, especially bromine.

D) A compound of formula I may be produced whereby an oxime of the general formula IX wherein Y, Ri, R3, R6 and A have the significances given for formula I (whereby R3 cannot be halogen), is etherified.

The compounds of formula IX may be obtained whereby either a) a ketone of the general formula X wherein A, Y, R2, R3 and R6 have the significances given for formula 1, is reacted with hydroxylamine or with one of its salts, or b) a compound of the general formula XI wherein Y, Ri, R3, R4 and R6 have the significances given for formula 1, is reacted with nitrous acid or with an alkyl nitrite in the presence of an acid or base, or c) an oxime of the general formula XII wherein A and R3 have the significances given for formula 1, is reacted with an aldehyde or ketone of the general formula III or with an acetal of the general formula IV, as described under A), or d) a ketone oxime of the general formula XIII wherein R3 and R4 have the significances given for formula 1, is reacted with a hydrazone of the general formula V. aa) A compound of formula X, wherein A is OCHR4 and Y, R3, R4 and R6 have the significances given for formula!, may be produced by reacting an oxime of formula VII with a halide of the general formula XXIV wherein Hal is a halogen atom such as chlorine, bromine or iodine, especially bromine.

E) A compound of formula I may be produced by reacting a ketone of the general formula X with an alkoxyamine of the general formula XIV Rz-ONHs XIV wherein R2 has the significances given for formula 1, or with one of its salts.

F) A compound of formula I may be produced by reacting an oxime derivative of the general formula XV wherein A, Y, R"R2, R3 and R6 have the significances given under formula 1, with a methylating agent such as methyl iodide or dimethyl sulphate.

The compounds of formula XV may be obtained whereby either a) a ketone of the general formula XVI wherein A, Y, Ri, R2, R3 and R6 have the significances given under formula 1, is reacted with hydroxylamine or with one of its salts, or b) a phenylacetic acid derivative of the general formula XVII wherein A, Y, Ri, Rs, Rs and R6 have the significances given under formula 1, is reacted with nitrous acid or with an alkyl nitrite. c) A keto derivative of the general formula XVI, wherein Y is O, may be produced whereby an acyl cyanide of the general formula XVIII wherein A, R2, R3 and R6 have the significances given under formula 1, is reacted in a Pinner reaction with an alcohol of the general formula XIX RI-OH XIX wherein R, has the significances given under formula 1. d) A keto derivative of the general formula XVI, wherein Y is NH, may be produced whereby either 1) a keto derivative of the general formula XVI, wherein Y is O, is reacted with an alkylamine of the general formula XX Ri-NH2 XX wherein R, has the significances given under formula 1, or 2) an acid chloride of the general formula XXI wherein A, R2, R3 and R6 have the significances given under formula 1, is reacted with an isocyanide of the general formula XXII R,-NC XXII wherein R, has the significances given under formula I (see EP 547825).

G) A compound of formula I may be produced by reacting a ketone of the general formula XVI, wherein A, Y, Ri, R2, R3 and R6 have the significances given under formula 1, with O-methylhydroxylamine or with one of its salts.

H) A compound of formula 1, wherein Y is NH, may be produced by reacting an ester of the general formula 1, wherein Y is O, with an alkylamine of the general formula XX R1-NH2 XX wherein R, has the significances given under formula 1.

I) A compound of formula 1, wherein Y is NH, may be produced by reacting an oxime ether of the general formula XXIII in the presence of a ruthenium catalyst wherein A, Ri, Rz, Rs and R6 have the significances given under formula 1, with an oxidation agent, for example dimethyl sulphoxide/oxalyl chloride, iodosobenzene, optionally in the presence of a ruthenium catalyst, potassium permanganate, manganese dioxide, tert.-butyl hypochlorite, sodium hypochlorite, tert.-butyl hydroperoxide, N-methylmorpholine-N-oxide.

All the above-described reactions are known per se, for example from WO 96/38408 and EP-A-547.825.

The above-mentioned new intermediates were developed especially for the present invention and similarly form an object of this invention; those of formulae V, IX, X, XV, XVI, XVII, XVIII, XXI and XXIII are of particular importance.

The educts are known or may be produced by known methods.

The compounds of formula I may be used preventatively and/or curatively in the agrarian sector and related fields as active ingredients for controlling plant pests. The active ingredients of formula I according to the invention are notable for their good activity even at low concentrations, for their good plant tolerance and for their environmentally friendly nature. They have very advantageous, especially systemic, properties and may be used to protect a plurality of cultivated plants. Using the active ingredients of formula I on plants or plant parts (fruit, flowers, leaves, stems, tubers, roots) of various crops, the pests appearing can be controlled or destroyed, whereby the parts of plants which grow later also remain protected, e. g. from phytopathogenic micro-organisms.

The compounds I may addition be used as a dressing to treat seeds (fruits, tubers, corms) and plant cuttings to protect against fungal infections and against phytopathogenic fungi occurring in the soil.

The compounds I are effective for example against the following classes of related phyto- pathogenic fungi: Fungi imperfecti (e. g. Botrytis, Pyricularia, Helminthosporium, Fusarium, Septoria, Cercospora and Alternaria); Basidiomycetes (e. g. Rhizoctonia, Hemileia, Puccinia); Ascomycetes (e. g. Venturia and Erysiphe, Podosphaera, Monilinia, Uncinula) and Oomycetes (e. g. Phytophthora, Pythium, Plasmopara).

Target crops for the plant-protecting usage in terms of the invention are for example the following plant cultivars: cereals (wheat, barley, rye, oats, rice, maize, sorghum and related species); beet (sugar beet and fodder beet); pome, stone and berry fruit (apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries and blackberries); legumes (beans, lentils, peas, soya); oil crops (rape, mustard, poppy, olives, sunflowers, coconut, castor oil, cocoa, peanut); cucumber plants (squashes, cucumber, melons); fibre plants (cotton, flax, hemp, jute); citrus fruits (oranges, lemons, grapefruits, mandarines); vegetables (spinach, lettuce, asparagus, cabbage varieties, carrots, onions, tomatoes, potatoes, paprika); laurels (avocado, cinnamonium, camphor) and plants such as tobacco, nuts, coffee, aubergines, sugar cane, tea, pepper, vines, hops, bananas and natural rubber plants, as well as ornamental plants.

In addition, the compounds of formula I according to the invention are valuable active ingredients against insects and pests of the order Acarina, as are present on crop plants and ornamentals in agriculture and in horticulture and in woodland, whilst being tolerated by mammals, fish and plants. The compounds of formula i are especially suitable for the control of pests in crops of cotton, vegetables, fruit and rice, for example spider mites, aphids, caterpillars and plant-and leaf-hoppers in rice. The pests primarily controlled are spider mites such as Panonychus ulmi, aphids such as Aphis craccivora, caterpillars such as those of Heliothis virescens and plant-and leaf-hoppers in rice such as Nilaparvata lugens or Nephotettix cincticeps.

The good pesticidal activity of the compounds I according to the invention corresponds to a mortality of at least 50-60 % of the pests mentioned.

Further areas of application for the active ingredients according to the invention are the protection of stores and material, where the storage matter is protected against putrescence and mould, as well as against insect pests (e. g. corn weevils, mites, maggots etc.). In the hygiene sector, compounds of formula I successfully control animal parasites such as ticks, mites, warble flies etc. on domestic and farm animals. The compounds I are effective against individual or collective stages of development of normally sensitive, but also resistant species of pest. Their activity may be demonstrated in this case for example by the mortality of pests which appear directly or only after some time, for example during moulting, or by reduced oviposition and/or hatching rate.

The compounds I are used in unchanged form or preferably together with customary excipients in formulation techniques. To this end, they are conveniently processed in known manner e. g. into emulsion concentrates, coatable pastes, directly sprayable or diluable solutions, diluted mulsions, wettable poweders, soluble powders, dusts or granules, e. g. by encapsulation into for example polymeric materials. As with the type of medium, the application processes, such as spraying, atomizing, dusting, scattering, coating or pouring are similarly chosen according to the desired aims and the prevailing conditions.

Suitable substrates and additives may be solid or liquid and are useful substances in formulation techniques, e. g. natural or regenerated mineral substances, dissolving aids, dispersants, wetting agents, tackifiers, thickeners, binding agents or fertilizers.

The compounds of formula I may be mixed with further active ingredients, e. g. fertilizers, ingredients providing trace elements or other plant protection compositions, especially further fungicides. In doing so, unexpected synergistic effects may occur.

Preferred additions to the mixture are: Azoles, such as azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, imibenconazole, ipconazole, metconazole, myclobutanil, pefurazoate, penconazole, pyrifenox, prochloraz, propiconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizole, triticonazole; pyrimidinyl carbinole, such as ancymidol, fenarimol, nuarimol; 2-amino-pyrimidines, such as bupirimate, dimethirimol, ethirimol; morpholines, such as dodemorph, fenpropidine, fenpropimorph, spiroxamin, tridemorph; anilinopyrimidines, such as cyprodinil, mepanipyrim, pyrimethanil; pyrroles, such as fenpiclonil, fludioxonil; phenylamides, such as benalaxyl, furalaxyl, metalaxyl, r-metalaxyl, ofurace, oxadixyl; benzimidazoles, such as benomyl, carbendazim, debacarb, fuberidazole, thiabendazole; dicarboximides, such as chlozolinate, dichlozoline, iprodione, myclozoline, procymidone, vinclozoline; carboxamides, such as carboxin, fenfuram, flutolanil, mepronil, oxycarboxin, thifluzamide; guanidines, such as guazatine, dodine, iminoctadine; strobilurines, such as azoxystrobin, kresoxim-methyl, metominostrobin, SSF-129, trifloxystrobin; dithiocarbamates, such as ferbam, mancozeb, maneb, metiram, propineb, thiram, zineb, ziram; N-halomethylthio, such as captafol, captan, dichlofluanid, fluoromides, folpet, tolyfluanid; Cu compounds, such as Bordeaux mixture, copper hydroxide, copper oxychloride, copper sulfate, cuprous oxide, mancopper, oxine-copper; nitrophenol-derivatives, such as dinocap, nitrothal-isopropyl; organo-p-derivatives, such as edifenphos, iprobenphos, isoprothiolane, phosdiphen, pyrazophos, tolclofos-methyl; Various others, such as acibenzolar-S-methyl, anilazine, blasticidin-S, chinomethionate, chloroneb, chlorothalonil, cymoxanil, dichlone, diclomezine, dicloran, diethofencarb, dimethomorph, dithianon, etridiazole, famoxadone, fenamidone, fentin, ferimzone, fluazinam, flusulfamide, fenhexamid, fosetyl-aluminium, hymexazol, iprovalicarb, IKF-916, kasugamycin, methasulfocarb, pencycuron, phthalide, polyoxins, probenazole, propamocarb, pyroquilon, quinoxyfen, quintozene, sulfur, triazoxide, tricyclazole, triforine, validamycin.

One preferred method of application of an active ingredient of formula I or of an agrochemical composition containing at least one of these active ingredients is foliar application. The frequency and amount of application depend on the severity of the attack by the pathogen in question. However, the active ingredients I may also reach the plants through the root system via the soil (systemic action) by drenching the locus of the plant with a liquid preparation or by incorporating the substances into the soil in solid form, e. g. in the form of granules (soil application). In rice cultivations, these granules may be dispensed over the flooded paddy field. The compounds I may however also be applied to seed grain to treat seed material (coating), whereby the grains or tubers are either drenched in a liquid preparation of the active ingredient or coated with a solid preparation.

The compositions are produced in known manner, e. g. by intimately mixing and/or grinding the active ingredient with extenders such as solvents, solid carriers and optionally surfactants.

The agrochemical compositions normally contain 0.1 to 99 percent by weight, especially 0.1 to 95 percent by weight, of active ingredient of formula 1,99.9 to 1 percent by weight, especially 99.8 to 5 percent by weight, of a solid or liquid additive and 0 to 25 percent by weight, especially 0.1 to 25 percent by weight, of a surfactant.

Favourable application rates are in general 1 g to 2 kg of active substance (AS) per hectare (ha), preferably 10 g to 1 kg AS/ha, especially 20 g to 600 g AS/ha. For usage as a seed dressing, it is advantageous to use dosages of 10 mg to 1 g active substance per kg of seed grain.

While concentrated compositions are preferred for commercial usage, the end user normally uses diluted compositions.

The compositions may also contain further additives, such as stabilizers, anti-foaming agents, viscosity regulators, binding agents or tackifiers, as well as fertilizers or other active ingredients to achieve special effects.

Preparation Examples 1) Methoxyimino- {2-Ij2-methoxyimino-1-methyl-propylidene)-hydrazonomethylphe nyl}- acetic acid methyl ester A solution of 8.85 g of (2-formylphenyl)-methoximino-acetic acid methyl ester (EP 621277) and 4.61 g of 3-hydrazono-butan-2-one oxime (Polyhedron 4,1761,1985) in 40 ml of pyridine is stirred for 41/2 hours at a bath temperature of 100°C. After cooling, the reaction solution is poured onto ice water, and the precipitated oil is extracted with ethyl acetate.

Purification takes place with ethyl acetate/hexane (1: 2) on silica gel and in this way 9.4 g of <BR> <BR> <BR> (2- [ (2-hydroxyimino-1-methyl-propylidene)-hydrazonomethyl]-pheny l)-methoximino-acetic acid methyl ester are obtained as slightly yellow crystals having a melting point of 148- 149°C. 2.5 g of the above substance, dissolved in 15 ml of dimethylformamide, are added dropwise at 10-20°C to a suspension of 0.44 g of sodium hydride (as a 60% dispersion in mineral oil) in 25 ml of dimethylformamide. After stirring for 15 minutes, 0.64 ml of methyl iodide are added at 10°C and then heated to 40°C over the course of half an hour. The reaction mixture is poured onto ice, mixed with saturated ammonium chloride solution and extracted with ethyl acetate. After drying and concentrating by evaporation, the title compound is obtained in the form of yellow crystals having a melting point of 118-119°C.

2) ( [2- 4-chlorophenyl)-2-methoxyimino-1-methyl-ethylidenel-hvdrazon omethyl phenyl)-methoxyimino-acetic acid methyl ester A solution of 6.12 g of 1- (4-chlorophenyl)-propane-1, 2-dione-1- (O-methyloxime) in 20 ml of ethanol is mixed with 4 ml of hydrazine hydrate. After stirring for 21 hours at room temperature, 80 ml of hexane are added. The precipitated crystals are filtered off, washed with a little hexane and dried. In this way, 4.5 g of 1- (4-chlorophenyl)-2-hydrazono-propan- 1-one O-methyloxime are obtained as white crystals having a melting point of 118-119°C.

A solution of 3.06 g of the above substance and 3.0 g of (2-formylphenyl)-methoxyimino- acetic acid methyl ester (EP 621277) in 30 ml of pyridine is stirred for 18 hours at 90°C.

After cooling, the reaction solution is poured onto ice water and the precipitated oil is extracted with ethyl acetate. Purification takes place with ethyl acetate/hexane (1: 9) on silica gel, and the title compound is obtained as a viscous, yellow oil, which crystallises after some time. (melting point 104-105°C).

3) Methoxyimino- (2- [2-methoxvimino-2- (4-methoxy-phenyl)-1-methyl-ethoxyimino]- methyl}-phenyl)-acetic acid methyl ester 4.84 g of finely ground potassium carbonate are added to a solution of 5.91 g of [2- (hydroxyiminomethyl) phenyl]-methoxyimino-acetic acid methyl ester (EP 499823) and 6.08 g of 2-bromo-1- (4-methoxyphenyl)-propan-1-one, and the suspension is stirred over night at room temperature. The reaction mixture is poured onto water and extracted with ethyl acetate. After purification on silica gel using ethyl acetate/hexane (3: 7), 9.7 g of <BR> <BR> <BR> <BR> methoxyimino-(2-{[2-(4-methoxyphenyl)-1-methyl-2-oxo-ethoxyi mino]-methyl}-phenyl)-acetic acid methyl ester are obtained as a colourless resin.

A solution of 6.0 g of the above substance and 1.67 g of O-methylhydroxylamine hydro- chloride in 30 ml of ethanol is mixed with 1.42 g of pyridine and stirred for 22 hours at room temperature. After adding water, extraction takes place with ethyl acetate, and purification is effected by means of chromatography on silica gel using ethyl acetate/hexane (3: 7). 6.0 g of the title compound are thus obtained in the form of a colourless resin.

4) 2-methOxyimino-2-(2-{rmethOxyimino-2-(4-methoXv-phenVl !-1-methyl-ethOxvimino1- methyl}-phenyl)-. N.-methyl-acetamide a) A solution of 4.27 g of the ester obtained under 3) in 25 ml of ethanolic methylamine (8.03 molar) is stirred over night at room temperature. After distilling off the excess methyl- amine and the solvent, 4.0 g of the title compound are obtained in the form of a slightly yellow resin. b) A solution of 3.0 g of the intermediate obtained under 3) in 20 ml of ethanolic methylamine (8.03 molar) is stirred over night at room temperature. After distilling off the excess methylamine and the solvent and purifying the residue using ethyl acetate/hexane (2: 3) on silica gel, 2.0 g of 2-methOxyimino-2-(2-{[2-(4-methoxy-phenyl)-1-methyl-2-oXo- ethoxyimino]-methyl}-phenyl)-. N.-methyl-acetamide are obtained as a yellowish resin.

A solution of 2 g of the above substance and 0.6 g of O-methylhydroxylamine hydrochloride in 10 ml of ethanol is mixed with 0.5 g of pyridine and stirred for 22 hours at 70°C. After adding water, extraction takes place with ethyl acetate, and purification is effected with ethyl acetate/hexane (2: 3) on silica gel to give 1.8 g of the title compound in the form of a slightly yellow resin.

The compounds of the following tables can be produced in analogous manner.

Table 1 Compounds of the general formula 1.1, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 2 Compounds of the general formula 1.1, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 3 Compounds of the general formula 1.1, in which R, is methyl, R2 is ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 4 Compounds of the general formula 1.1, in which R, and R2 are ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 5 Compounds of the general formula 1.1, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 6 Compounds of the general formula 1.1, in which R, is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 7 Compounds of the general formula 1.1, in which R, is methyl, R2 is ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 8 Compounds of the general formula 1.1, in which R, and R2 are ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 9 Compounds of the general formula 1.2, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 10 Compounds of the general formula 1. 2, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 11 Compounds of the general formula 1.2, in which R, is methyl, R2 is ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 12 Compounds of the general formula 1.2, in which R, and R2 are ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 13 Compounds of the general formula 1. 2, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 14 Compounds of the general formula 1.2, in which R, is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 15 Compounds of the general formula 1.2, in which Ri is methyl, R2 is ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 16 Compounds of the general formula 1.2, in which R, and R2 are ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 17 Compounds of the general formula 1.3, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 18 Compounds of the general formula 1.3, in which R, is methyl, R2 is ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 19 Compounds of the general formula 1.3, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 20 Compounds of the general formula 1.3, in which R, is methyl, R2 is ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 21 Compounds of the general formula 1.4, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 22 Compounds of the general formula 1. 4, in which R, is methyl, R2 is ethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 23 Compounds of the general formula 1.4, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 24 Compounds of the general formula 1.4, in which R, is methyl, R2 is ethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 25 Compounds of the general formula 1.1, in which R, is methyl, R2 is fluoromethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 26 Compounds of the general formula 1.1, in which R, is methyl, R2 is difluoromethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 27 Compounds of the general formula 1.1, in which R, is methyl, R2 is 2,2,2-trifluoroethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 28<BR> Compounds of the general formula 1.1, in which R, is ethyl, R2 is fluoromethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 29 Compounds of the general formula 1.1, in which R, is ethyl, R2 is difluoromethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 30 <BR> Compounds of the general formula 1.1, in which R1is ethyl, R2is 2,2,2-trifluoroethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 31 Compounds of the general formula 1.1, in which R, is methyl, R2 is fluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 32 <BR> Compounds of the general formula 1.1, in which R, is methyl, R2 is difluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 33 <BR> Compounds of the general formula 1.1, in which R, is methyl, R2 is 2,2,2-trifluoroethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 34 Compounds of the general formula 1.1, in which R, is ethyl, R2 is fluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 35 Compounds of the general formula 1.1, in which RI is ethyl, R2 is difluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 36 <BR> Compounds of the general formula 1.1, in which R, is ethyl, R2 is 2,2,2-trifluoroethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 37 <BR> Compounds of the general formula 1.3, in which R, is methyl, R2 is fluoromethyl and R6 is<BR> hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 38 Compounds of the general formula 1.3, in which R, is methyl, R2 is difluoromethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 39 Compounds of the general formula 1.3, in which R, is methyl, R2 is 2,2,2-trifluoroethyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 40 Compounds of the general formula 1.3, in which R, is methyl, R2 is fluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 41 Compounds of the general formula 1.3, in which R, is methyl, R2 is difluoromethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 42 Compounds of the general formula 1.3, in which R, is methyl, R2 is 2,2,2-trifluoroethyl and R6 is methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 43 Compounds of the general formula 1.5, in which Ri and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 44 Compounds of the general formula 1.5, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 45 Compounds of the general formula 1. 5, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 46 Compounds of the general formula 1.5, in which R, is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 47 Compounds of the general formula 1.6, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 48 Compounds of the general formula 1.6, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 49 Compounds of the general formula 1.6, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 50 Compounds of the general formula 1. 6, in which R, is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 51 Compounds of the general formula 1.7, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 52 Compounds of the general formula 1.7, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 53 Compounds of the general formula 1.7, in which Rl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 54 Compounds of the general formula 1. 7, in which R, is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 55 Compounds of the general formula 1.8, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 56 Compounds of the general formula 1.8, in which R, is ethyl, R2 is methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 57 Compounds of the general formula 1.8, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 58 Compounds of the general formula 1.8, in which R1 is ethyl, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 59 Compounds of the general formula 1.9, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 60 Compounds of the general formula 1.9, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 61 Compounds of the general formula 1.10, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 62 Compounds of the general formula 1.10, in which R1, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 63 Compounds of the general formula 1.11, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 64 Compounds of the general formula 1.11, in which Ri, R2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table 65 Compounds of the general formula 1.12, in which R, and R2 are methyl and R6 is hydrogen, and R3 corresponds in each case to one of the lines of Table A.

Table 66 Compounds of the general formula 1. 12, in which Ri, ? 2 and R6 are methyl, and R3 corresponds in each case to one of the lines of Table A.

Table A No. R3 No.Rs <BR> <BR> <BR> 1. ............................................................ ............................................................ .................

2. CH2CH3 17. OCH (CH3) CH2CH3 3. (CH2) 2CH3 18. OC (CH3) 3 4. (CH2) 3CH3 19. CH=CH2 5. (CH2) 4CH3 20. CH=CHCH3 6. (CH2) 5CH3 21. CH=C (CH3) 2 7. CH (CH3) 2 22. CH2CH=CH2 8. C (CH3) 3 23. CH2CH=CHCH3 9. CH2CH (CH3) 2 24. OCH2CH=CH2 10. CH (CH3) CH2CH3 25. C=-CH 11. OCH3 26. C-CCH3 12. OCH2CH3 27. C-CC (CH3) 3 13. O (CH2) 2CH3 28. CH2C-CH 14. O (CH2) 3CH3 29. CH2C=CCH3 15. O (CH2) 4CH3 29. CH2C---CCH3 No. R3 30. Ra 31. OCH2C-C-C (CH3) 3 <BR> <BR> <BR> <BR> 32. C (O) OCH3<BR> 33. C (O) OCH2CH3 34. C (O) O (CH2) 2CH3 35. C (O) O (CH2) 3CH3 36. C (O) O (CH2) 4CH3 37. C (O) OCH (CH3) 2 38. C (O) OC (CH3) 3 39. CN 40. ci 41. Br 42. CF3 43. CH2CF3 44. CH2CH2F 45. CH2CN 46. CH20CH3 47. CH20CH2CH3 48. (CH2) 2COOCH3 49. (CH2) 2CONH2 50. (CH2) 2CONHCH3 51. (CH2) 2CON (CH3) 2 52. (CH2) 2SCH3 53. CH20CH2CH=CH2 54.

55.

56. CH=CF2 57. C--C-Br 58. C-C-OCH3 No. R3 .......................................

59. Cyclopropyl 60. Cyclobutyl 61. Cyclopentyl 62. Cyclohexyl 63. Phenyl 64.1-Naphthyl 65.2-Naphthyl 66.2-F-C6H4 67.3-F-C6H4 68.4-F-C6H4 69.2,3-F2-C6H3 71.2,5-F2-C6H3 72.2,6-F2-C6H3 74.3,5-F2-C6H3 75.2-CI-C6H4 76.3-CI-C6H4 77.4-CI-C6H4 78.2,3-CI2-C6H3 79.2,4-CI2-C6H3 80.2,5-CI2-C6H3 81.2,6-CI2-C6H3 82.3,4-CI2-C6H3 83.3,5-CI2-C6H3 84.2,3,4-C13-C6H2 5-C13-C6H2 86.2,3,6-C13-C6H2 88.2,4,6-C13-C6H2 89.3,4,5-CI3-C6H2 90.2-Br-C6H4 No. R3 <BR> <BR> <BR> 91. .................

92.4-Br-C6H4 93.2,3-Br2-C6H3 94.2,4-Br2-C6H3 95.2,5-Br2-C6H3 96.2,6-Br2-C6H3 97.3,4-Br2-C6H3 98.3,5-Br2-C6H3 99.2-F-3-CI-C6H3 <BR> <BR> <BR> <BR> 100. 2-F-4-CI-C6H3<BR> <BR> <BR> <BR> <BR> <BR> 101.2-F-5-CI-C6H3 102.2-F-3-Br-C6H3 103.2-F-4-Br-C6H3 104.2-F-5-Br-C6H3 105.2-CI-3-Br-C6H3 106.2-CI-3-Br-C6H3 107.2-CI-5-Br-C6H3 108.3-F-4-CI-C6H3 109. 3-F-5-CI-C6H3 110.3-F-6-CI-C6H3 111.3-F-4-Br-C6H3 112.3-F-5-Br-C6H3 113.3-F-6-Br-C6H3 114.3-CI-4-Br-C6H3 115.3-CI-5-Br-C6H3 116.3-CI-6-Br-C6H3 117.4-F-5-CI-C6H3 118.4-F-6-CI-C6H3 119.4-F-5-Br-C6H3 120. 4-F-6-Br-C6H3 121.4-CI-5-Br-C6H3 122. 5-F-6-CI-C6H3 No. R3<BR> ,......................<BR> <BR> <BR> <BR> <BR> <BR> <BR> <P>123.................

124.5-CI-6-Br-C6H3 125.3-Br-4-CI-5-Br-C6H2 126.2-CN-C6H4 127.3-CN-C6H4 128.4-CN-C6H4 129.3-OCN-C6H4 130.4-OCN-C6H4 131. 2-CH3O-C6H4 132.3-CH30-C6H4 133.4-CH30-C6H4 134.2,3- (CH30) 2-C6H3 135.2,4- (CH30) 2-C6H3 136.2,5- (CH30) 2-C6H3 137.3,4- (CH30) 2-C6H3 138.3,5- (CH30) 2-C6H3 139.3,4,5- (CH30) 3-C6H2 140.2-C2H50-C6H4 141.3-C2H50-C6H4 142.4-C2H50-C6H4 143.2- (n-C3H70)-C6H4 144. 3-(n-C3H7O)-C6H4 145. 4-(n-C3H7O)-C6H4 146. 2-(i-C3H7O)-C6H4 147. 3-(i-C3H7O)-C6H4 148. 4-(i-C3H7O)-C6H4 149. 4-(n-C4H9O)-C6H4 <BR> <BR> <BR> <BR> <BR> 150. 3-(t-C4H9O)-C6H4<BR> 151. 4-(t-C4H9O)-C6H4 152. 2-Allyl-O-C6H4 153. 3-Allyl-O-C6H4 154.4-Allyl-O-C6H4 No. R3<BR> No. R3<BR> <BR> <BR> <BR> <BR> ............................................................ ........................

156.3-CF3-C6H4 157.4-CF3-C6H4 158.2-Acetyl-C6H4 159.3-Acetyl-C6H4 160.4-Acetyl-C6H4 161.2-Methoxycarbonyl-C6H4 162.3-Methoxycarbonyl-C6H4 163.4-Methoxycarbonyl-C6H4 164.2-Aminocarbonyl-C6H4 165.3-Aminocarbonyl-C6H4 166.4-Aminocarbonyl-C6H4 167.2-Dimethylaminocarbonyl-C6H4 168.3-Dimethylaminocarbonyl-C6H4 169.4-Dimethylaminocarbonyl-C6H4 170.2- (N-Methylaminocarbonyl)-C6H4 171. 3-(N-Methylaminocarbonyl)-C6H4 172. 4-(N-Methylaminocarbonyl)-C6H4 173.2-CH3S-C6H4 174.3-CH3S-C6H4 175.4-CH3S-C6H4 176. 2-CH3SO2-C6H4 177. 3-CH3SO2-C6H4 178. 4-CH3SO2-C6H4 179.2-CF30-C6H4 180.3-CF30-C6H4 181.4-CF30-C6H4 182.2-CHF20-C6H4 183.3-CHF20-C6H4 184.4-CHF20-C6H4 185.3-CF3,4-CF30-C6H3 186.2-CH3NH-C6H4 <BR> <BR> No. R3<BR> No. R3 ......................................

188.4-CH3NH-C6H4 189. 2-(CH3)2N-C6H4 190. 3- (CH3) 2N-C6H4 191. 4-(CH3)2N-C6H4 192.2-Ethoxycarbonyl-C6H4 193.3-Ethoxycarbonyl-C6H4 194.4-Ethoxycarbonyl-C6H4 195.2-CH2FCH2-C6H4 196.3-CH2FCH2-C6H4 197.4-CH2FCH2-C6H4 198.2-CF3CH2-C6H4 199. 3-CF3CH2-C6H4 200.4-CF3CH2-C6H4 201.2-CHF2CF2-C6H4 202.3-CHF2CF2-C6H4 203.4-CHF2CF2-C6H4 204.2-CHF2-C6H4 205.3-CHF2-C6H4 206.4-CHF2-C6H4 207. 2-NO2-C6H4 208. 3-NO2-C6H4 209.4-NO2-C6H4 210.2-CH3-C6H4 211.3-CH3-C6H4 212.4-CH3-C6H4 213.2,3- (CH3) 2-C6H3 214.2,4- (CH3) 2-C6H3 215.2,5- (CH3) 2-C6H3 216.2,6- (CH3) 2-C6H3 217.3,4- (CH3) 2-C6H3 218.3,5- (CH3) 2-C6H3 No. Rs 219.2-C2H5-C6H4 220.3-C2H5-C6H4 221.4-C2H5-C6H4 222.2-i-C3H7-C6H4 223.3-i-C3H7-C6H4 224.4-i-C3H7-C6H4 225. 3-tert.-C4H9-C6H4 226.4-tert.-C4H9-C6H4 227.2-Vinyl-C6H4 228.3-Vinyl-C6H4 229.4-Vinyl-C6H4 230.2-Allyl-C6H4 231.3-Allyl-C6H4 232.4-Allyl-C6H4 233.2-Propargyl-C6H4 234.2-Ethinyl-C6H4 235.3-Propargyloxy-C6H4 236.4-Butinyloxy-C6H4 237.2-C6H5-C6H4 238.3-C6H5-C6H4 239.4-C6H5-C6H4 240.3-CH3-5-t-C4H9-C6H3 241.2-F-4-CH3-C6H3 242.2-F-5-CH3-C6H3 243.2-CH3-4-F-C6H3 244.2-CH3-5-F-C6H3 245.2-CH3-4-CI-C6H3 246.2-F-4-CH3-O-C6H3 247.2-F-4-CH3CH20-C6H3 248.2-F-4-i-C3H7-C6H3 249.4- (4-Chlorophenoxy) phenyl 250.4- (4- No. R3<BR> ..........................................................

Trifluoromethylphenoxy)phenyl 251. 4-(3-Chlorophenoxy)phenyl 252.4- (3- Trifluoromethylphenoxy)phenyl 253.2-Pyridyl 254.3-Pyridyl 255.4-Pyridyl 256.5-CH3-Pyridin-2-yi 257.5-CI-Pyridin-2-yl 258. 6-Cl-Pyridin-2-yl 259.3,5-CI2-Pyridin-2-yl 260.6-CH30-Pyridin-2-yl 261.6-CH3-Pyridin-2-yl 262.6-CI-Pyridin-3-yl 263.6-CH3-Pyridin-3-yl 264.6-CH30-Pyridin-3-yl 265.2-Pyrimidinyl 266.4-CH30-Pyrimidin-2-yl 267.4-C2H50-Pyrimidin-2-yl 268. 4-Cl-Pyrimidin-2-yl 269.4-CH3-Pyrimidin-2-yl 270.5-CH3-Pyrimidin-2-yl 271. 5-Cl-Pyrimidin-2-yl 272.5-CH30-Pyrimidin-2-yl 273.5-C2H50-Pyrimidin-2-yl 274.4-Pyrimidinyl 275.2-CI-Pyrimidin-4-yl 276.2-CH30-Pyrimidin-4-yl 277.2-CH3-Pyrimidin-4-yl 278.6-CI-Pyrimidin-4-yl 279.6-CH3-Pyrimidin-4-yl 280.6-CH30-Pyrimidin-4-yl No. R3 5.Pyrim.diny..

282.2-CH3-Pyrimidin-5-yl 283.2-CI-Pyrimidin-5-yl 284.2-CH30-Pyrimidin-5-yl 285.2-C2H50-Pyrimidin-5-yl 286. 2-Furyl 287.4-C2H5-Fur-2-yl 288.4-CH3-Fur-2-yl 289.4-CI-Fur-2-yl 290.4-CN-Fur-2-yl 291.5-CH3-Fur-2-yl 292.5-CI-Fur-2-yl 293.5-CN-Fur-2-yl 294.3-Furyl 295.5-CH3-Fur-3-yl 296.5-CI-Fur-3-yl 297.5-CN-Fur-3-yl 298.2-Thienyl 299.4-CH3-Thien-2-yl 300. 4-Cl-Thien-2-yl 301.4-CN-Thien-2-yl 302.5-CH3-Thien-2-yl 303. 5-Cl-Thien-2-yl 304.5-CN-Thien-2-yl 305.3-Thienyl 306.5-CH3-Thien-3-yl 307.5-CI-Thien-3-yl 308.5-CN-Thien-3-yl 309.1-Methylpropyl-2-yl 310.1-Methylpropyl-3-yl 311.2-Oxazolyl 312.4-CH3-Oxazol-2-yl .............................

313.4-C!-Oxazo!-2-y! 314.4-CN-Oxazol-2-yl 315.5-CH3-Oxazol-2-yl 316. 5-Cl-Oxazol-2-yl 317.5-CN-Oxazol-2-yl 318.4-Oxazolyl 319. 2-CH3-Oxazol-4-yl 320.2-CI-Oxazol-4-yl 321.2-CN-Oxazol-4-yl 322.5-Oxazolyl 323.2-CH3-Oxazol-5-yl 324. 2-Cl-Oxazol-5-yl 325.2-CN-Oxazol-5-yl 326. 3-lsoxazolyl 327.5-CH3-Isoxazol-3-yl 328.5-CI-Isoxazol-3-yl 329.5-CN-isoxazol-3-yl 330.5-Isoxazolyl 331.3-CH3-Isoxazol-5-yl 332. 3-Cl-lsoxazol-5-yl 333.3-CN-lsoxazol-5-yl 334.2-Thiazolyl 335.4-CH3-Thiazol-2-yl 336.4-CI-Thiazol-2-yl 337.4-CN-Thiazol-2-yl 338.5-CH3-Thiazol-2-yl 339.5-CI-Thiazol-2-yl 340.5-CN-Thiazol-2-yl 341.4-Thiazolyl 342.2-CH3-Thiazol-4-yl 343. 2-Cl-Thiazol-4-yl 344.2-CN-Thiazol-4-yl <BR> <BR> No. R3<BR> <BR> <BR> <BR> <BR> <BR> <BR> 34572-CHsS-Th!azo!-4-y! 346.5-Thiazolyl 347.2-CH3-Thiazol-5-yl 348. 2-Cl-Thiazol-5-yl 349.2-CN-Thiazol-5-yl 350.3-lsothiazolyl 351.5-CH3-lsothiazol-3-yl 352.5-CI-isothiazol-3-yl 353.5-CN-lsothiazol-3-yl 354.5-Isothiazolyl 355.3-CH3-Isothiazol-5-yl 356.3-CI-lsothiazol-5-yl 357.3-CN-isothiazol-5-yl 358.2-lmidazolyl 359.4-CH3-Imidazol-2-yl 360.4-CI-Imidazol-2-yl 361.4-CN-Imidazol-2-yl 362.1-CH3-lmidazol-2-yl 363.1-CH3-4-CI-lmidazol-2-yl 364.1,4- (CH3) 2-Imidazol-2-yl 365.1-CH3-5-CI-Imidazol-2-yl 366.1,5- (CH3) 2-Imidazol-2-yl 367.4-Imidazolyl 368.2-CH3-lmidazol-4-yl 369. 2-Cl-lmidazol-4-yl 370.1-CH3-Imidazol-4-yl 371.1, 2-(CH3)2-lmidazol-4-yl 372.1-CH3-2-CI-lmidazol-4-yl 373.1-CH3-Imidazol-5-yl 374.1-CH3-3-CI-lmidazol-5-yl 375.1,2- (CH3) 2-Imidazol-5-yl 376.3-Pyrazolyl ._..No.'R3-...__..._.

377. Rs 378. 5-Cl-Pyrazol-3-yl 379.5-CN-Pyrazol-3-yl 380.1-CH3-Pyrazol-3-yl 381.1-CH3-4-CI-Pyrazol-3-yl 382.1-CH3-5-CI-Pyrazol-3-yl 383.1, 5-(CH3)2-Pyrazol-3-yl 384.1-CH3-Pyrazol-5-yl 385.1-CH3-3-CI-Pyrazol-5-yl 386.1,3- (CH3) 2-Pyrazol-5-yl 387.4-Pyrazolyl 388. 3-Cl-Pyrazol-4-yl 389.3-CH3-Pyrazol-4-yl 390.1-CH3-Pyrazol-4-yl 391.1-CH3-3-CI-Pyrazol-4-yl 392.1,3- (CH3) 2-Pyrazol-4-yl 393.1,3,4-Oxadiazol-5-yl 394.2-CH3-1,3,4-Oxadiazol-5-yl 4-Oxadiazol-5-yl 396.2-CF3-1,3,4-Oxadiazol-5-yl 4-Oxadiazol-5-yl 398.2-CH30-1,3,4-Oxadiazol-5-yl 399.1,2,4-Oxadiazol-3-yl 400.5-CH3-1,2,4-Oxadiazol-3-yl 4-Oxadiazol-3-yl 4-Oxadiazol-3-yl 403.5-CF3-1,2,4-Oxadiazol-3-yl 404.1,2,4-Triazol-3-yl 405.1-CH3-1,2,4-Triazol-3-yl 406.1-Pyrrolyl 407.3-CH3-Pyrrol-1-yl 408.1-Pyrazolyl No. R3 409. 3-CH3-Pyrazol-1-yl 410.3-CF3-Pyrazol-1-yl 411.4-CH3-Pyrazol-1-yl 412.4-CI-Pyrazol-1-yl 413.4-Ethoxycarbonyi-Pyrazol-1-yl 414.3-CH3-4-Br-Pyrazol-1-yl 415.1-Imidazolyl 416. 4-CH3-lmidazol-1-yl 417.4, 5-Cl2-lmidazol-1-yl 418.2, 4-(CH3)2-lmidazol-1-yl 419.1,2, 4-Triazol-1-yl 420.1,3, 4-Triazol-1-yl 421.3, 5-(CH3) 2-1,2,4-Triazol-1-yl 422.1-Piperidinyl 423.1-Pyrrolidinyl 424.1-Morpholinyl 425.2-#²-Thiazolinyl 426.5-CH3-#²-Thiazolin-2-yl 427.5,5-(CH3)2-#²-Thiazolin-2-yl 428.4, 5-(CH3)2-#²-Thiazolin-2-yl 429.2-#²-Oxazolinyl 430.4-CH3-#²-Oxazolin-2-yl 431.4,4-(CH3) 2-#²-Oxazolin-2-yl 432.

433.

No. Rs 434.

435. Cyclopropoxy 436. Cyclobutoxy 437. Cyclopentoxy 438. Cyclohexyloxy 439. Phenoxy 440.1-Naphthyloxy 441.2-Naphthyloxy 442.2-F-C6H40 443.3-F-C6H40 444.4-F-C6H40 445.2,3-F2-C6H30 446.2,4-F2-C6H30 447.2,5-F2-C6H30 448.2,6-F2-C6H30 449.3,4-F2-C6H30 450.3,5-F2-C6H30 451.2-CI-C6H40 452.3-CI-C6H40 453.4-CI-C6H40 454.2,3-C12-C6H30 455.2,4-C12-C6H30 456.2,5-CI2-C6H30 457.2,6-CI2-C6H30 458.3,4-CI2-C6H30 459.3,5-CI2-C6H30 460.2,3,4-C13-C6H20 461.2,3,5-C13-C6H20 <BR> <BR> No. R3<BR> <BR> No. Rs 462.2,3,5-C!3-CeH20 _......

463.2,4, 5-Cl3-C6H2O 464.2,4,6-CI3-C6H20 465.3,4,5-CI3-C6H20 466.2-Br-C6H40 467.3-Br-C6H40 468.4-Br-C6H40 469.2,3-Br2-C6H30 470.2,4-Br2-C6H30 471.2,5-Br2-C6H30 472.2,6-Br2-C6H30 473.3,4-Br2-C6H30 474.3,5-Br2-C6H30 475.2-F-3-CI-C6H30 476.2-F-4-CI-C6H30 477.2-F-5-CI-C6H30 478.2-F-3-Br-C6H30 479.2-F-4-Br-C6H30 480.2-F-5-Br-C6H30 481.2-CI-3-Br-C6H30 482.2-CI-4-Br-C6H30 483.2-CI-5-Br-C6H30 484. 3-F-4-Cl-C6H3O 485. 3-F-5-Cl-C6H3O 486. 3-F-6-Cl-C6H3O 487.3-F-4-Br-C6H30 488.3-F-5-Br-C6H30 489.3-F-6-Br-C6H30 490.3-CI-4-Br-C6H30 491. 3-Cl-5-Br-C6H3O 492.3-CI-6-Br-C6H30 493. 4-F-5-Cl-C6H3O <BR> No. R3 494. 4-F-6-Cl-C6H3O 495. 4-F-5-Br-C6H3O 496.4-F-6-Br-C6H30 497.4-CI-5-Br-C6H30 498. 5-F-6-Cl-C6H3O 499.5-F-6-Br-C6H30 500.5-CI-6-Br-C6H30 501.3-Br-4-CI-5-Br-C6H20 502.2-CN-C6H40 503.3-CN-C6H40 504.4-CN-C6H40 505.4-Dimethylaminocarbonyl-C6H40 506. 2-(N-Methylaminocarbonyl)-C6H4O 507.3- (N-Methylaminocarbonyl)-C6H40 508.4- (N-Methylaminocarbonyl)-C6H40 509.2-CH3S-C6H40 510.3-CH3S-C6H40 511.4-CH3S-C6H40 512.2-CH3S02-C6H40 513.3-CH3S02-C6H40 514.4-CH3S02-C6H40 515.2-CF30-C6H40 516.3-CF30-C6H40 517.4-CF30-C6H40 518. 2-CHF2O-C6H4O 519. 4-CHF2O-C6H4O 520. 4-CHF2O-C6H4O 521.3-CF3,4-CF30-C6H30 522.2-CH3NH-C6H40 523.3-CH3NH-C6H40 524.4-CH3NH-C6H40 525.2- (CH3) 2N-C6H40 No. R3 52673-(CH3)2N-C6H40 527.4- (CH3) 2N-C6H40 528.2-Ethoxycarbonyl-C6H40 529.3-Ethoxycarbonyl-C6H40 530.4-Ethoxycarbonyl-C6H40 531.2-CH2FCH2-C6H40 532.3-CH2FCH2-C6H40 533.4-CH2FCH2-C6H40 534.2-CF3CH2-C6H40 535.3-CF3CH2-C6H40 536.4-CF3CH2-C6H40 537.2-CHF2CF2-C6H40 538.3-CHF2CF2-C6H40 539.4-CHF2CF2-C6H40 540.2-CHF2-C6H40 541.3-CHF2-C6H40 542.4-CHF2-C6H40 543.2-CH30-C6H40 544.3-CH30-C6H40 545.4-CH30-C6H40 546.2,3- (CH30) 2-C6H30 547.2,4- (CH30) 2-C6H30 548.2, 5-(CH3O)2-C6H3O 549.3,4- (CH30) 2-C6H30 550.3,5- (CH30) 2-C6H30 551.3,4,5- (CH30) 3-C6H20 552.2-C2H50-C6H40 553.3-C2H50-C6H40 554.4-C2H50-C6H40 555. 2-(n-C3H7O)-C6H4O 556. 3-(n-C3H7O)-C6H4O 557. 4-(n-C3H7O)-C6H4O No. R3 558. 2-(i-C3H7O)-C6H4O 559. 3-(i-C3H7O)-C6H4O 560. 4-(i-C3H7O)-C6H4O 561.4- (n-C4H90)-C6H40 562. 3-(t-C4H9O)-C6H4O 563.4- (t-C4H90)-C6H40 564.2-Allyl-O-C6H40 565.3-Allyl-O-C6H40 566.4-Allyl-O-C6H40 567.2-CF3-C6H40 568.3-CF3-C6H40 569.4-CF3-C6H40 570.2-Acetyl-C6H40 571.3-Acetyl-C6H40 572.4-Acetyl-C6H40 573.2-Methoxycarbonyl-C6H40 574.3-Methoxycarbonyl-C6H40 575.4-Methoxycarbonyl-C6H40 576.2-Aminocarbonyl-C6H40 577.3-Aminocarbonyl-C6H40 578.4-Aminocarbonyl-C6H40 579.2-Dimethylaminocarbonyl-C6H40 580.3-Dimethylaminocarbonyl-C6H40 581. 2-NO2-C6H4O 582. 3-NO2-C6H4O 583. 4-NO2-C6H4O 584.2-CH3-C6H40 585.3-CH3-C6H40 586.4-CH3-C6H40 587.2,3- (CH3) 2-C6H30 588.2,4- (CH3) 2-C6H30 589.2,5- (CH3) 2-C6H30 No. Rs 590.gjo 591.3,4- (CH3) 2-C6H30 593.2-C2H5-C6H40 594.3-C2H5-C6H40 595.4-C2H5-C6H40 596.2-i-C3H7-C6H40 597.3-i-C3H7-C6H40 598.4-i-C3H7-C6H40 599.3-tert.-C4H9-C6H40 600.4-tert.-C4H9-C6H40 601.2-Vinyl-C6H40 602.3-Vinyl-C6H40 603.4-Vinyl-C6H40 604. 2-Allyl-C6H4O 605.3-Allyl-C6H40 606.4-Allyl-C6H40 607.2-C6H5-C6H40 608.3-C6H5-C6H40 609.4-C6H5-C6H40 610. 3-CH3-5-t-C4H9-C6H3O 611.2-F-4-CH3-C6H30 612.2-F-5-CH3-C6H30 613.2-CH3-4-F-C6H30 614.2-CH3-5-F-C6H30 615.2-CH3-4-CI-C6H30 616.2-Pyridyloxy 617.3-Pyridyloxy 618.4-Pyridyloxy 619.2-Pyrimidinyloxy 620.4-Pyrimidinyloxy 621.5-Pyrimidinyloxy No.Rs 622.1-CH3-P!per!d!ny!-3-oxy 623.1-CH3-Piperidinyl-4-oxy Details relating to physical data in the Tables which follow °=mp. in°Celsius<BR> Number = chemical shift of R4 in'H-NMR (. 8. in ppm); *cis-trans isomers Table 67: Compounds of formula No. YPiR2Rs?4Phys.data Phys.dama 67. 1. O CH3 CH3 CH3 CH3 118-119° 67.2.0 CH3 CH2CH3 CH3 CH3 78-81° 67.3. O CH3 (CH2) 2CH3 CH3 CH3 2.08/2.20 (R3&P4) 67.4.0 CH3 CH2F CH3 CH3 120-122° 67.5.0 CH3 CH2CF3 CH3 CH3 98-99° 67.6.0 CH3 CH3 4-CH3-C6H4 CH3 113-115° 67.7.0 CH3 CH3 4-CH3CH2-C6H4 CH3 117-118° 67.8.0 CH3 CH3 4-F-C6H4 CH3 101-103° 67.9.0 CH3 CH3 4-CI-C6H4 CH3 104-105° 67.10. O CH3 CH3 4-Br-C6H4 CH3 124-127° 67.11.0 CH3 CH3 4-CH30-C6H4 CH3 118-120° 67.12.0 CH3 CH3 3-CF3-C6H4 CH3 112-113° 67.13. O CH3 CH34-CH3CH2O-C6H4 CH3 109-111° Table 68: Compounds of formula No. Y R, R2 R3 R4 Phys. data .

68.1.0 CH3 CH3 CH3 CH3 1.40 57* 68.3.0 CH3 CH3 2, 4- (CI) 2-C6H3 CH3 1. 46/1.54* 68.4.0 CH2CH3 CH3 2, 4-(CI) 2-C6H3 CH3 1.56 68.5. O CH3 CH3 4-CH3O-C6H4 CH3 1. 43/1.57* 68.6.0 CH3 CH2CH3 2, 4- (F) 2-C6H3 CH3 1. 43/1.58* 57* 68.8. O CH3 CH3 2-F-4-CH3CH2O-C6H3 CH3 1. 42/1.57* 68.9. O CH3 CH3 2-F-4-i-C3H7O-C6H3 CH3 1. 42/1.57* 68.10.0 CH3 CH3 2, 5- (CH3) 2-C6H3 CH3 1. 43/1.54* 68.11.0 CH3 CH2CH3 4-(4-chlorophenoxy)-CH3 1. 44/1.59* C6H4 68.12. NH CH3 CH3 CH3 CH3 1.37 68.13. NH CH3 CH3 4-CI-C6H4 CH3 1.35/1.53* 68.14. NH CH3 CH3 2,4- (Cl)2-C6H3 CH3 1. 51 68.15. NH CH3 CH3 4-CH30-C6H4 CH3 1.36/1.53* 68.16. NH CH3 CH2CH3 2,4-(F)2-C6H3 CH3 1. 38/1.56* 68.17. NH CH3 CH3 2-F-4-CH30-C6H3 CH3 1.35/1.54* <BR> <BR> <BR> 68. 18. NH CH3 CH3 2-F-4-CH3CH20-C6H3 CH3 1.41/1.54* 68.19. NH CH3 CH3 2-F-4-i-C3H7-C6H3 CH3 1. 35/1.54* 68.20. NH CH3 CH3 2,5-(CH3)2-C6H5 CH3 1. 31/1.51* 68.21. NH CH3 CH2CH3 4-(4-chlorophenoxy)- CH3 1.37/1. 56* C6H4 Table 69: Intermediate products of formula 11 No.AR2RsR4Phys.data<BR> <BR> <BR> <BR> <BR> <BR> ...............................

69.2. N=CR4 CH3 4-CH3CH2-C6H4 CH3 92-95° 69.3. N=CR4 CH3 4-F-C6H4 CH3 134-136° 69.4. N=CR4 CH3 4-CI-C6H4 CH3 118-119° 69.5. N=CR4 CH3 4-Br-C6H4 CH3 127-129° 69.6. N=CR4 CH3 4-CH30-C6H4 CH3 87-90° 69.7. N=CR4 CH3 4-CH3CH20-C6H4 CH3 92-94° 69.8. N=CR4 CH3 3-CF3-C6H4 CH3 96-98° 69.9. N=CR4 CH3 CH3 CH3 94-970 69.10. N=CR4 CH3 OCH (CH3) 2 CH3 Table 70: Intermediate products of formula X No. Y A R1 R3 R4 R6 Phys. data 70.1.0 OCHR4 CH3 CH3 CH3 H 1. 39 70.2. O OCHR4 CH3 4-CI-C6H4 CH3 H 1. 55 70.3. O OCHR4 CH3 4-CH3O-C6H4 CH3 H 1. 55 70.4.0 OCHR4 CH3 2, 4- (F) 2-C6H3 CH3 H 1.53 70.5.0 OCHR4 CH2CH3 2,4- (CI) 2-C6H3 CH3 H 1.53 70.6.0 OCHR4 CH3 2-F-4-CH30-C6H3 CH3 H 1.53 70.7.0 OCHR4 CH3 2-F-4-CH3CH20-C6H3 CH3 H 1,54 70.8.0 OCHR4 CH3 2-F-4-i-C3H70-C6H3 CH3 H 1.53 70.9.0 OCHR4 CH3 2, 5- (CH3) 2-C6H3 CH3 H 1.47 70.10.0 OCHR4 CH3 4-(4-chlorophenoxy)-C6H4 CH3 H 1.57 70.11. NH OCHR4 CH3 4-CH30-C6H4 CH3 H 1.56 Table 71: Intermediate products of formula IX No. y A R, R3 R4 R6 Phys. data 71.1. O N=CR4 CH3 CH3 CH3 H 148-149° 71.2.0 OCHR4 CH3 CH3 CH3 H 1.41 71.3. O N=CR4 CH3 4-CH3-C6H4CH3 H 71.4. O N=CR4 CH3 4-CH3CH2-C6H4CH3 H 71.5.0 N=CR4 CH3 4-F-C6H4 CH3 H No. y A R, R3 R4 R6 Phys. data 71.6.0 N=CR4 CH3 4-CI-C6H4 CH3 H 71.7. O N=CR4 CH3 4-Br-C6H4CH3 H 71.8.0 N=CR4 CH3 4-CH30-C6H4 CH3 H 71.9. O N=CR4 CH3 4-CH3CH2O-C6H4CH3 H 71.10. O N=CR4 CH3 3-CF3-C6H4CH3 H 71.11.0 N=CR4 CH3 OCH3 CH3 H 71.12.0 N=CR4 CH3 OCH (CH3) 2 CH3 H 71.13. O N=CR4 CH34-CH3-C6H4 CH3 CH3 71.14. O N=CR4 CH34-CH3CH2-C6H4 CH3 CH3 71.15.0 N=CR4 CH3 4-F-C6H4 CH3 CH3 71.16. O N=CRa CH3 4-CI-CsH4 CH3 CH3 71.17. ON=CR4 CH3 4-Br-C6H4 CH3 CH3 71.18. O N=CR4 CH34-CH3O-C6H4 CH3 CH3 71.19. O N=CR4 CH34-CH3CH2O-C6H4 CH3 CH3 71.20. ON=CR4 CH3 3-CF3-C6H4 CH3 CH3 71.21.0 N=CR4 CH3 CH3 CH3 CH3 71.22.0 N=CR4 CH3 OCH (CH3) 2 CH3 CH3 Table 72: Intermediate products of formula XV No Y A R, R2 R3 R4 R6 72.1. O N=CR4 CH3 CH3 4-CH3-C6H4CH3 H 72.2. O N=CR4 CH3 CH3 4-CH3CH2-C6H4CH3 H 72.3. O N=CR4 CH3 CH3 4-F-C6H4CH3 H No Y A R1 R2 R3 R4 R6 72.4. O N=CR4 CH3 CH3 4-CI-C6Ha CH3 H 72.5.0 N=CR4 CH3 CH3 4-Br-C6H4 CH3 H 72.6.0 N=CR4 CH3 CH3 4-CH30-C6H4 CH3 H 72.7.0 N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 H 72.8.0 N=CR4 CH3 CH3 3-CF3-C6H4 CH3 H 72.9.0 N=CR4 CH3 CH3 CH3 CH3 H 72.10.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 H 72.11.0 N=CR4 CH3 CH3 4-CH3-C6H4 CH3 CH3 72.12.0 N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 CH3 <BR> <BR> <BR> <BR> <BR> 72. 13. 0 N=CR4 CH3 CH3 4-F-C6H4 CH3 CH 72.14.0 N=CR4 CH3 CH3 4-CI-C6H4 CH3 CH 72.15.0 N=CR4 CH3 CH3 4-Br-C6H4 CH3 CH3 72.16.0 N=CR4 CH3 CH3 4-CH30-C6H4 CH3 CH3 72.17.0 N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 CH3 72.18.0 N=CR4 CH3 CH3 3-CF3-C6H4 CH3 CH3 72.19.0 N=CR4 CH3 CH3 CH3 CH3 CH3 72.20.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 CH3 72.21. NH N=CR4 CH3 CH3 4-CH3-C6H4 CH3 H 72.22. NH N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 H 72.23. NH N=CR4 CH3 CH3 4-F-C6H4 CH3 H 72.24. NH N=CR4 CH3 CH3 4-CI-C6H4 CH3 H 72.25. NH N=CR4 CH3 CH3 4-Br-C6H4 CH3 H 72.26. NH N=CR4 CH3 CH3 4-CH30-C6H4 CH3 H 72.27. NH N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 H 72.28. NH N=CR4 CH3 CH3 3-CF3-C6H4 CH3 H 72.29. NH N=CR4 CH3 CH3 CH3 CH3 H 72.30. NH N=CR4 CH3 CH3 OCH (CH3) 2 CH3 H 72.31. NH N=CR4 CH3 CH3 4-CH3-C6H4 CH3 CH3 72.32. NH N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 CH3 72.33. NH N=CR4 CH3 CH3 4-F-C6H4 CH3 CH3 72.34. NH N=CR4 CH3 CH3 4-CI-C6H4 CH3 CH 72.35. NH N=CR4 CH3 CH3 4-Br-C6H4 CH3 CH3 No Y A R, R2 R3 R4 R6 72.36. NH N=CR4 CH3 CH3 4-CH30-C6H4 CH3 CH3 72.37. NH N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 CH3 72.38. NH N=CR4 CH3 CH3 3-CF3-C6H4 CH3 CH3 72.39. NH N=CR4 CH3 CH3 CH3 CH3 CH3 72.40. NH N=CR4 CH3 CH3 OCH (CH3) 2 CH3 CH3 Table 73: Intermediate products of formula XVI No Y A R, R2 R3 R4 R6 73.1. O N=CR4 CH3 CH3 4-CH3-C6H4CH3 H 73.2. O N=CR4 CH3 CH3 4-CH3CH2-C6H4CH3 H 73.3. O N=CR4 CH3 CH3 4-F-C6H4CH3 H 73.4. O N=CR4 CH3 CH3 4-CI-C6Ha CH3 H 73.5. O N=CR4 CH3 CH3 4-Br-C6H4CH3 H 73.6.0 N=CR4 CH3 CH3 4-CH30-C6H4 CH3 H 73.7. O N=CR4 CH3 CH34-CH3CH20-C6H4 CH3 H 73.8. O N=CR4 CH3 CH3 3-CF3-C6H4CH3 H 73.9.0 N=CR4 CH3 CH3 CH3 CH3 H 73.10.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 H 73.11. O N=CR4 CH3 CH34-CH3-C6H4 CH3 CH3 73.12. O N=CR4 CH3 CH34-CH3CH2-C6H4 CH3 CH3 73.13.0 N=CR4 CH3 CH3 4-F-C6H4 CH3 CH3 73.14. O N=CRa CH3 CH3 4-CI-C6Ha CH3 CH3 73.15. ON=CR4 CH3 CH3 4-Br-C6H4 CH3 CH3 73.16.0 N=CR4 CH3 CH3 4-CH30-C6H4 CH3 CH3 73.17. O N=CR4 CH3 CH34-CH3CH2O-C6H4 CH3 CH3 73.18. ON=CR4 CH3 CH3 3-CF3-C6H4 CH3 CH3 73.19.0 N=CR4 CH3 CH3 CH3 CH3 CH3 73.20.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 CH3 73.21. NH N=CR4 CH3 CH3 4-CH3-C6H4 CH3 H 73.22. NH N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 H No Y A R, R2 R3 R4 R6 73.23. NH N=CR4 CH3 CH3 4-F-C6H4 CH3 H 73.24. NH N=CR4 CH3 CH3 4-CI-C6H4 CH3 H 73.25. NH N=CR4 CH3 CH3 4-Br-C6H4 CH3 H 73.26. NH N=CR4 CH3 CH3 4-CH30-C6H4 CH3 H 73.27. NH N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 H 73.28. NH N=CR4 CH3 CH3 3-CF3-C6H4 CH3 H 73.29. NH N=CR4 CH3 CH3 CH3 CH3 H 73.30. NH N=CR4 CH3 CH3 OCH (CH3) 2 CH3 H 73.31. NH N=CR4 CH3 CH3 4-CH3-C6H4 CH3 CH3 73.32. NH N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 CH3 73.33. NH N=CR4 CH3 CH3 4-F-C6H4 CH3 CH3 73.34. NH N=CR4 CH3 CH3 4-CI-C6H4 CH3 CH3 73.35. NH N=CR4 CH3 CH3 4-Br-C6H4 CH3 CH3 73.36. NH N=CR4 CH3 CH3 4-CH30-C6H4 CH3 CH3 73.37. NH N=CR4 CH3 CH3 4-CH3CH20-C6H4 CH3 CH3 73.38. NH N=CR4 CH3 CH3 3-CF3-C6H4 CH3 CH3 73.39. NH N=CR4 CH3 CH3 CH3 CH3 CH3 73.40. NH N=CR4 CH3 CH3 OCH (CH3) 2 CH3 CH3 Table 74: Intermediate products of formula XVII No Y A Ri R2 R3 R4 R6 74.1.0 N=CR4 CH3 CH3 4-CH3-C6H4 CH3 H 74.2.0 N=CR4 CH3 CH3 4-CH3CH2-C6H4 CH3 H 74.3.0 N=CR4 CH3 CH3 4-F-C6H4 CH3 H 74.4.0 N=CR4 CH3 CH3 4-CI-C6H4 CH3 H 74.5.0 N=CR4 CH3 CH3 4-Br-C6H4 CH3 H 74.6.0 N=CR4 CH3 CH3 4-CH30-C6H4 CH3 H 74.7. O N=CR4 CH3 CH3 4-CH3CH2O-C6H4CH3 H <BR> <BR> <BR> 74. 8. 0 N=CR4 CH3 CH3 3-CF3-C6H4 CH3 H 74.9.0 N=CR4 CH3 CH3 CH3 CH3 H 74.10.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 H 74.11. O N=CR4 CH3 CH3 4-CH3-C6H4 CH3 CH3 74.12. O N=CR4 CH3 CH34-CH3CH2-C6H4 CH3 CH3 74.13.0 N=CR4 CH3 CH3 4-F-C6H4 CH3 CH3 74.14.0 N=CR4 CH3 CH3 4-CI-C6H4 CH3 CH3 74.15. ON=CR4 CH3 CH3 4-Br-C6H4 CH3 CH3 74.16. O N=CR4 CH3 CH34-CH3O-C6H4 CH3 CH3 74.17. O N=CR4 CH3 CH34-CH3CH2O-C6H4 CH3 CH3 74.18. ON=CR4 CH3 CH3 3-CF3-C6H4 CH3 CH3 74.19.0 N=CR4 CH3 CH3 CH3 CH3 CH3 74.20.0 N=CR4 CH3 CH3 OCH (CH3) 2 CH3 CH3 Table 75: Intermediate products of formula XVIII No A R2 R3 R4 R6 75.1. N=CR4 CH3 4-CH3-C6H4 CH3 H 75.2. N=CR4 CH3 4-CH3CH2-C6H4 CH3 H 75.3. N=CR4 CH3 4-F-C6H4 CH3 H 75.4. N=CR4 CH3 4-CI-C6H4 CH3 H 75.5. N=CR4 CH3 4-Br-C6H4 CH3 H 75.6. N=CR4 CH3 4-CH30-C6H4 CH3 H 75.7. N=CR4 CH3 4-CH3CH20-C6H4 CH3 H 75.8. N=CR4 CH3 3-CF3-C6H4 CH3 H 75.9. N=CR4 CH3 CH3 CH3 H 75. 10. N=CR4 CH3 OCH (CH3) 2 CH3 H 75.11. N=CR4 CH3 4-CH3-C6H4 CH3 CH3 75.12. N=CR4 CH3 4-CH3CH2-C6H4 CH3 CH3 75.13. N=CR4 CH3 4-F-C6H4 CH3 CH3 <BR> <BR> <BR> 75. 14. N=CR4 CH3 4-CI-C6Ha CH3 CH3<BR> <BR> <BR> 75. 15. N=CR4 CH3 4-Br-CsH4 CH3 CH3 75.16. N=CR4 CH3 4-CH30-C6H4 CH3 CH3 75.17. N=CR4 CH3 4-CH3CH20-C6H4 CH3 CH3 75.18. N=CR4 CH3 3-CF3-C6H4 CH3 CH3 75.19. N=CR4 CH3 CH3 CH3 CH3 75.20. N=CR4 CH3 OCH (CH3) 2 CH3 CH3 Table 76: Intermediate products of formula XXI No A R2 R3 R4 R6 76.1. N=CR4 CH3 4-CH3-C6H4 CH3 H 76.2. N=CR4 CH3 4-CH3CH2-C6H4 CH3 H 76.3. N=CR4 CH3 4-F-C6H4 CH3 H 76.4. N=CR4 CH3 4-CI-C6H4 CH3 H 76.5. N=CR4 CH3 4-Br-C6H4 CH3 H 76.6. N=CR4 CH3 4-CH30-C6H4 CH3 H 76.7. N=CR4 CH3 4-CH3CH20-C6H4 CH3 H 76. 8. N=CR4 CH3 3-CF3-C6H4 CH3 H 76.9. N=CR4 CH3 CH3 CH3 H 76.10. N=CR4 CH3 OCH (CH3) 2 CH3 H 76.11. N=CR4 CH3 4-CH3-C6H4 CH3 CH3 76.12. N=CR4 CH3 4-CH3CH2-C6H4 CH3 CH3 76. 13. N=CR4 CH3 4-F-C6H4 CH3 CH3 76.14. N=CR4 CH3 4-CI-C6H4 CH3 CH3 76.15. N=CR4 CH3 4-Br-C6H4 CH3 CH3 76.16. N=CR4 CH3 4-CH30-C6H4 CH3 CH3 76.17. N=CR4 CH3 4-CH3CH20-C6H4 CH3 CH3 76.18. N=CR4 CH3 3-CF3-C6H4 CH3 CH3 76.19. N=CR4 CH3 CH3 CH3 CH3 76.20. N=CR4 CH3 OCH (CH3) 2 CH3 CH3 Formulations may be prepared analogously to those described for example in WO 97/33890.

Biological Examples Example B-1: Effect against Puccinia araminis on wheat a) Residual protective action Wheat plants are sprayed to drip point, 6 days after sowing, with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and infected 24 hours later with a uredospore suspension of the fungus. After an incubation period of 48 hours (conditions: 95 to 100 % relative atmospheric humidity at 20°), the plants are placed in a greenhouse at 22°. 12 days after infection, the fungal attack is evaluated. b) Systemic action An aqueous spray liquor prepared from wettable powder of the active ingredient (0.006 % active substance, based on the volume of soil) is poured onto wheat plants 5 days after sowing. Care is taken that the spray liquor does not come into contact with the parts of the plant that are above ground. 48 hours later, the plants are infected with a uredospore suspension of the fungus. After an incubation period of 48 hours (conditions: 95 to 100 % relative atmospheric humidity at 20°), the plants are placed in a greenhouse at 22°. 12 days after infection, the fungal attack is evaluated.

Compounds from the tables show good effect.

Example B-2: Effect against Phytophthora infestans on tomatoes a) Residual protective action Tomato plants are sprayed to drip point, after cultivation for 3 weeks, with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and infected 24 hours later with a sporangia suspension of the fungus. Evaluation of the fungal attack takes place 5 days after infection, during which period conditions of 90 to 100 % relative atmospheric humidity and a temperature of 20° are maintained. b) Systemic action An aqueous spray liquor prepared from wettable powder of the active ingredient (0.006 % active substance, based on the volume of soil) is poured onto tomato plants which have been cultivated for three weeks. Care is taken that the spray liquor does not come into contact with the parts of the plant that are above ground. 48 hours later, the plants are infected with a sporangia suspension of the fungus. Evaluation of the fungal attack takes place 5 days after infection, during which period conditions of 90 to 100 % relative atmospheric humidity and a temperature of 20° are maintained.

Compounds from the tables show good effect.

Example B-3: Residual protective action against Cercospora arachidicola on peanuts Peanut plants of 10 to 15 cm height are sprayed to drip point with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and infected 48 hours later with a conidia suspension of the fungus. The plants are incubated for 72 hours at 21 ° and at high atmospheric humidity and subsequently placed in a greenhouse until the typical leaf spots appear. Evaluation of the efficacy of the active substance takes place 12 days after infection and is based on the number and size of the leaf spots.

Compounds from the tables show good effect.

Example B-4: Effect against Plasmopara viticola on vines Vine seedlings at the 4 to 5 leaf stage are sprayed to drip point with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and infected 24 hours later with a sporangia suspension of the fungus. Evaluation of the fungal attack takes place 6 days after infection, during which period conditions of 95 to 100 % relative atmospheric humidity and a temperature of 20° are maintained.

Compounds from the tables show good effect.

Example B-5: Effect against Colletotrichum laaenarium on cucumbers Cucumber plants are sprayed after cultivation for 2 weeks with a spray liquor prepared from wettable powder of the active ingredient (concentration 0.002%). After 2 days, the plants are infected with a spore suspension (1.5x105 spores/ml) of the fungus and incubated for 36 hours at 23°C and at high atmospheric humidity. Incubation is then continued at normal atmospheric humidity and at ca. 22°C. The fungal attack occurring is evaluated 8 days after infection.

Compounds from the tables show good effect.

Example B-6: Residual protective action against Venturia inaequalis on appies Apple cuttings with fresh shoots of 10 to 20 cm length are sprayed to drip point with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and infected 24 hours later with a conidia suspension of the fungus. The plants are incubated for 5 days at 90 to 100 % relative atmospheric humidity and placed in a greenhouse at 20 to 24° for a further 10 days. 12 days after infection, the fungal attack is evaluated.

Compounds from the tables show good effect.

Example B-7: Effect against Ervsiphe graminis on barley a) Residual protective action Barley plants of approximately 8 cm height are sprayed to drip point with an aqueous spray liquor prepared from wettable powder of the active ingredient (0.02 % active substance), and dusted 3 to 4 hours later with conidia of the fungus. The infected plants are placed in a greenhouse at 22°. 12 days after infection, the fungal attack is evaluated.

Compounds from the tables show good effect. b) Systemic action An aqueous spray liquor prepared from wettable powder of the active ingredient (0.002 % active substance, based on the volume of soil) is poured onto barley plants of approximately 8 cm height. Care is taken that the spray liquor does not come into contact with the parts of the plant that are above ground. 48 hours later, the plants are dusted with conidia of the fungus. The infected plants are placed in a greenhouse at 22°. 12 days after infection, the fungal attack is evaluated.

Compounds from the tables show good effect.

Example B-8: Effect against Podosphaera leucotricha on apple shoots Apple cuttings with fresh shoots of ca. 15 cm length are sprayed with a spray liquor (0.06% active substance). After 24 hours, the treated plants are infected with a conidia suspension of the fungus and placed in climate-controlled chamber at 70% relative atmospheric humidity and 20°C. 12 days after infection, the fungal attack is evaluated.

Compounds from the tables show good effect.

Bioloqical Examp ! es: B. Insecticidal action Example B-9: Effect against Aphis craccivora Pea seedlings are infected with Aphis craccivora, subsequently sprayed with a spray liquor containing 100 ppm active ingredient, and then incubated at 20°. Using a comparison between the number of dead leaf aphids on the treated and the untreated plants 3 and 6 days later, the percentage reduction in population (% action) is determined.

Compounds from the tables show good effect in this test, i. e. a death rate of more than 80%.

Example B-10: Effect against Diabrotica balteata Maize seedlings are sprayed with an aqueous emulsion spray liquor containing 400 ppm active ingredient. After the spray coating has begun to dry, the seedlings are colonized with 10 larvae of the second stage of Diabrotica balteata and then placed in a plastic container.

Using a comparison between the number of dead larvae on the treated and the untreated plants 6 days later, the percentage reduction in population (% action) is determined.

Compounds from the tables show good effect in this test.

Example B-11: Effect against Heliothis virescens Young soya plants are sprayed with an aqueous emulsion spray liquor containing 100 ppm active ingredient. After the spray coating has begun to dry, the plants are colonized with 10 grubs of the first stage of Heliothis virescens and then placed in a plastic container.

Using a comparison between the number of dead grubs and the feeding damage on the treated and the untreated plants 6 days later, the percentage reduction in population and in feeding damage (% action) is determined.

Compounds from the tables show good effect in this test.

Example B-12: Effect against Spodoptera littoralis Young soya plants are sprayed with an aqueous emulsion spray liquor containing 100 ppm active ingredient. After the spray coating has begun to dry, the plants are colonized with 10 grubs of the third stage of Spodoptera littoralis and then placed in a plastic container.

Using a comparison between the number of dead grubs and the feeding damage on the treated and the untreated plants 3 days later, the percentage reduction in population and in feeding damage (% action) is determined.

Compounds from the tables show good effect in this test.

Example B-13: Effect against Nilaparvata luaens Rice plants are sprayed with an aqueous emulsion spray liquor containing 100 ppm active ingredient. After the spray coating has begun to dry, the rice plants are colonized with plant- and leaf-hopper larvae of the second and third stage. Evaluation takes place 21 days later.

Using a comparison between the number of surviving plant-and leaf-hoppers on the treated and the untreated plants, the percentage reduction in population (% action) is determined.

Compounds from the tables show over 90% effect.

Example B-14: Effect against Plutella Mlostelia grubs Young cabbage plants are sprayed with an aqueous emulsion spray liquor containing 100 ppm active ingredient. After the spray coating has begun to dry, the cabbage plants are colonized with 10 grubs of the third stage of Plutella xylostella and placed in a plastic container. Evaluation takes place 3 days later. Using a comparison between the number of dead grubs and the feeding damage on the treated and the untreated plants, the percentage reduction in population and in feeding damage (% action) is determined.

Compounds from the tables show good effect.

Example B-15: Effect against Musca domestica A sugar cube is treated with a solution of the test substance so that, after drying over night, the concentration of test substance in the sugar is 250 ppm. This treated cube is placed on an aluminium dish with a wet cotton-wool pad and 10 Musca domestica adults of an OP- resistant strain, covered with a beaker and incubated at 25°C. After 24 hours, the mortality rate is determined.

Compounds from the tables show good effect.

Biological Examples: C. Acaricidal action B-16: Effect against Tetranychus urticae Young bean plants are colonized with a mixed population of Tetranychus urticae and sprayed one day later with an aqueous emulsion spray liquor containing 400 ppm active ingredient. The plants are subsequently incubated for 6 days at 25°C and then evaluated.

Using a comparison between the number of dead eggs, larvae and adults on the treated and the untreated plants, the percentage reduction in population (% action) is determined.

Compounds from the tables show good effect.

Example B-17: Effect on mixed populations of Tetranychus cinnabarinus Dilution series.

Bush beans at the second leaf stage are colonized with a mixed population (eggs, larvae/nymphs, adults) of an OP-tolerant strain of Tetranychus cinnabarinus. 24 hours after infection, the products are applied to the plants at dosages of 200.100,50 mqAS/I in an automatic spray cabin. The substances are formulated and diluted with water to the corresponding dosages. The test is evaluated 2 and 7 days after application for the percentage mortality of eggs, larvae/nymphs and adults. Compounds from the tables exhibit over 70% mortality in dilutions up to 50 mg AS/litre.

Example B-18: Effect against Boophilus microplus Adult female ticks which have sucked themselves full are adhered to a PVC plate, covered with a cotton-wool pad, and then 10 ml of test solution containing 125 ppm active ingredient is poured on. The cotton-wool pad is removed and the ticks are incubated for 4 weeks to lay eggs. The effect is shown either as mortality or sterility of females or as ovicidal action of eggs.