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Matches 351 - 400 out of 1,345

Document Document Title
WO/1996/036618A1
Compounds of formula (Ia) wherein Z is (a), wherein x is an integer from 0 to 4, n is an integer from 0 to 5 and R is defined below; or (b), wherein n is an integer from 0 to 5 and R is defined below; R is selected from the group consist...  
WO/1996/031467A1
Provided is a compound of formula (I). This compound is an intermediate to and is used for preparing the arthropodicidal oxidiazine Compound (II) described in the specification.  
WO/1996/030348A1
The present invention provides an efficient process of reacting a bis-indolyl acid of Formula (II), wherein R1 is a hydrogen or C1-C4 alkyl and R, X, and Y are optional substitutions; to produce a bis-indolyloxallic acid of Formula (III)...  
WO/1996/030377A1
Novel macrocyclic compounds are constructed to include large cyclic structures that are interrupted by at least one ring sytem. Each interrupting ring system includes two bridgehead atoms. Bridgehead atoms are bonded to one or more bridg...  
WO/1996/025406A1
Compounds of formula (I) in which A is possibly substituted alkylene, Ar is possibly substituted arylene or heteroarylene, E is preferably one of the grouping (a), (b), (c), (d), (e), Y1 is oxygen, sulphur or a possibly alkyl-substituted...  
WO/1996/022983A1
The invention relates to novel substituted arylazadioxacyclo alkenes of formula (I), several processes for their production and their use as fungicides.  
WO1996011945A3  
WO/1996/018624A1
The invention concerns novel 1,3,4-oxadiazine derivatives of formula (I) in which Ar1 stands for in each case optionally substituted aryl or hetaryl; Ar2 stands for in each case optionally substituted aryl or hetaryl; and X stands for th...  
WO/1996/016950A1
A HIV-1 protease inhibitor which includes an N-terminal cycle (A) or a C-terminal cycle (B) or both cycles (A) and (B) wherein Y is selected from side chains of Asn or Ile or Val or Glu and alkyl of 1-6 carbon atoms inclusive of linear o...  
WO/1996/015131A1
This invention provides a process for producing a macrocyclic lactone compound, which comprises cultivating Actinoplanes sp. FERM BP-3832, in the presence of L-proline, L-hydroxyproline or L-nipecotic acid, and then isolating a macrocycl...  
WO/1996/013260A1
A compound having formula (I) wherein Me represents a methyl group, having an antibacterial activity.  
WO/1996/011945A2
A process is disclosed for the aromatic sulfonylation, sulfenylation, thiocyanisation and phosphorylation of cyclic depsipeptides with 6 to 24 ring atoms, composed of 'alpha'-hydroxycarboxylic acids and 'alpha'-aminoacids and containing ...  
WO/1996/011191A1
3- and 5-substituted 1,2,3,4-oxatriazole-5-imine compounds of general formula (I), wherein R1 is the same or different groups and represents alkyl or alkoxy groups having 1 to 3 carbon atoms, halogen, trifluoromethyl, nitro, cyano, pheny...  
WO/1995/029171A1
A method for making arthropodicidal oxadiazines and intermediates which are racemic or enantiomerically enriched at their chiral center, the method for making the oxadiazines comprising reaction of an intermediate selected from (II) or (...  
WO/1995/028392A1
The invention provides amphiphilic compounds of the formula (I) Ch-(-L-Ar-(-AH)n)m (where Ch is a hydrophilic chelant moiety or a salt or a chelate thereof); each L is an optionally oxo substituted C2-25-alkylene linker wherein at least ...  
WO/1995/027498A1
The invention concerns the use, to control parasitic protozoans, in particular coccidia, and fish parasites, of cyclic depsipeptides in which the 18-atom ring is made up of amino-acid and hydroxycarboxylic acid units and which have gener...  
WO/1995/026723A1
This invention relates to novel substituted tryptamine and phenalkylamine and related compounds, pharmaceutical compositions thereof and methods of using said compounds and compositions for a number of pharmaceutical indications includin...  
WO/1995/022523A1
A cyclic nitrogenous compound represented by general formula (1) and a herbicide containing the same, exhibiting a high herbicidal activity in a small dose, and having crop selectivity: wherein R1 represents alkyl; R represents hydgrogen...  
WO/1995/022082A1
The invention relates to a colour-photographic recording material which comprises a magenta coupler and, as stabilizer, at least one compound of formula (Ia), (Ib) or (II), where the radicals are as defined in claim 1, and to the novel s...  
WO1995009848A3  
WO/1995/018808A1
Linked polyamine cyclic compounds of general formula V - R - A - R' - W where V and W are independently cyclic polyamine moieties having from 9 to 32 ring members and 3 to 8 amine nitrogens and having either one or more aromatic rings fu...  
WO/1995/018623A1
Novel compounds and libraries of compounds based on nitrogen atoms that are joined together with spanner groups include "letters", i.e. functional groups, that are attached to the nitrogen atoms, to the spanner groups or to both the nitr...  
WO/1995/018116A1
Arthropodicidal compounds, compositions and use of compounds having formula (I) wherein A, E, X, Y, Z, R1, R2, R3, R4, R5, n and m are as defined in the text.  
WO/1995/017093A1
The present invention provides novel cryptophycin compounds having structure (I). The present invention also provides methods for producing cryptophycins from the Nostoc sp. of blue-green algae (cyanobacteria). Pharmaceutical composition...  
WO/1995/016676A1
Arthropodicidal compounds, compositions and use of compounds having formula (I), wherein Q, X, Y, R1 and m are as defined in the text.  
WO/1995/013351A1
Novel bleach catalysts, a method for bleaching substrates using these catalysts and detergent compositions containing same are reported. The bleaches are of the quaternary oxaziridinium salt-type. Substrates such as fabrics may be bleach...  
WO/1995/009848A2
This invention relates to dichelants, in particular compounds having two macrocyclic chelant groups linked by a bridge containing an ester or amide bond, especially compounds of formula (V) (wherein each X which may be the same or differ...  
WO/1995/007272A1
A compound represented by general formula (I) or a salt thereof, having an excellent helminthicidal activity as a vermicide for humans and animals, wherein A represents appropriately substituted benzyl; Aa, B and D represent each lower a...  
WO/1995/006643A1
Herbicidally active compounds of formula (I), wherein RA, X, U, W, Q, m, n and p are as defined in the text, compositions containing said compounds and methods for making and using them.  
WO/1995/004728A1
New azadioxacycloalkenes have the formula (I), in which A stands for optionally substituted alkane diyl (alkylene); Ar stands for optionally substituted arylene or heteroarylene; E stands for one of the following groupings (a), (b), (c),...  
WO/1995/001979A1
The present invention relates to novel heterocyclic compounds having general formula (1) wherein: X is O, S, Se, or NR2; Y1, Y2, Y3, Y4 independently are N or CR2; Z is O, S, Se, NR2 or C = N; and A is (a) or (b) wherein W is O, S, NH or...  
WO/1994/025424A1
Described are fullerene derivatives of the formula (I) in which the symbols are as defined as follows: F is a fullerene unit of the formula C(20+2m) in which m = 20, 25, 28 or 29; E1 and E2, when they are the same or different, are COOH,...  
WO/1994/019334A1
A novel PF1022 derivative as a cyclic depsipeptide, represented by general formula (I), or a salt thereof, having the vermifugal activity against various parasites living in man, domestic and pet animals, and the like and thus being usef...  
WO/1994/019481A1
A novel compound B1371A represented by formula (I) or a novel compound B1371B represented by formula (II), each having a cysteine protease activity, a process for producing the same, and a bacterium producing the same. The compounds are ...  
WO/1994/013660A1
The amount of chiral doping substances in FLC mixtures may be reduced by introducing chiral complex ligands and macrocycles into the FLC mixture or on the orientation layer.  
WO1993025543A3  
WO/1994/010173A1
Disclosed are novel anellated triazole compounds of formula (I), in which RA, m, n, X X, V, W and Q have the meaning stated in the specification; a method of their preparation; and their use as herbicides.  
WO/1994/003442A1
3- and 5-substituted 1,2,3,4-oxatriazole-5-imine compounds of general formula (I) wherein R1 is the same or different groups and represents alkyl or alkoxy groups having 1 to 3 carbon atoms, halogen, trifluoromethyl, nitro, cyano, phenyl...  
WO/1993/025543A2
The invention concerns the use, to control endoparasites in medical and veterinary practice, of cyclic depsipeptides with 18 ring atoms and having general formula (I), in which R?1¿ to R?6¿ are as defined in the description, plus optic...  
WO/1993/019045A1
Substituted amides, agricultural compositions containing them and a method to control arthropods in agronomic and nonagronomic environments, the amides having formula (I) wherein X is oxygen or sulfur and Q, G and Y are as defined in the...  
WO/1993/019053A1
A compound represented by general formula (I) or a salt thereof, excellent in parasiticidal activity as an enthelmintic for animal and man, wherein A represents benzyl which is appropriately substituted or phenyl which may be appropriate...  
WO/1993/018038A1
Insecticidal compounds of the formula (I) wherein G, X, Y and Q are as defined in the text, agricultural compositions containing them and a method for using the compounds to control arthropods in agronomic and nonagronomic environments.  
WO/1993/011117A1
Novel N-[2-(cyclic alkyl)phenyl]pyrazole-4-carboxamides useful as fungicides, methods of using said compounds, and fungicidal compositions containing them.  
WO/1993/005028A1
Crown ether compounds which can function as receptor molecules for species such as alcohols, especially for ethanol, and other materials capable of forming hydrogen bonds. The compounds are based on 1,7-diaza-12-crown-4 group, substitute...  
WO/1993/004142A1
Decomposable complex ligands may be stabilized by derivating them with blocking secondary or tertiary carbonic or sulfonic acids. Orientation layers and liquid crystal mixtures may be added to these stabilized derivates that cause in FLC...  
WO/1992/020682A1
Substituted anilides of formula (I), wherein Q is one of (Q-1), (Q-2) and (Q-3), and R?1� to R?5�, Y, Z and Z?1� are as defined in the text, arthropodicidal compositions containing such compounds; and a method for controlling arthr...  
WO/1992/013847A1
The present invention relates to hitherto unknown 3-substituted 1,2,3,4-oxatriazole-5-imine compounds which have proved to have biological effects making them suitable for treatment of cardiovascular diseases (blood clots), angina pector...  
WO/1992/011249A1
Arthropodicidal carboxanilides of formulae (I) and (II) wherein Q, X, X?1¿, Y and G are as defined in the text, arthropodicidal compositions containing said compounds and a method for using the compounds to control arthropods.  
WO1991012243A3  
WO/1991/012243A2
A monomer and polymers resulting therefrom, the monomer comprising (I), wherein n = 1 or 2; m = 1 or 2; R' = H or CH3; X = -O-, -CH2, -NR-; R = H, -alkyl, -aryl, -CH2(CH2)y-C = N, -CH2O alkyl, -(CH2)yOH, -CH2CH(OH)CH3 wherein y = 1 - 12;...  

Matches 351 - 400 out of 1,345