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WO/1997/002255A1 |
Bis-oxime derivatives of formula (I) in which A is (a) or (b), where W is oxygen or sulfur, and the other substituents defined as follows: R1 = hydrogen, C1-C4alkyl; cyclopropyl; R2 = hydrogen, C1-C6alkyl; halo(C1-C6) alkyl; C2-C6alkoxya...
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WO/1997/002237A1 |
The invention pertains to fluorobutenic acid oxime esters of formula (I) CF2=CX-CH2-CO-ON=CR1R2 in which: X stands for hydrogen or halogen; R1 and R2 independently of one another stand for hydrogen or (in each case optionally substituted...
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WO/1997/002231A1 |
A process for the preparation of a compound of formula (B), or an addition salt and/or a solvate thereof, wherein Ra and Rd are independently phenyl optionally substituted by one, two or three of halogen, trifluoromethyl, C1-4 alkoxy, C1...
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WO/1997/001530A1 |
Oxime ethers of formula (I) in which a) X is an N atom and Y is an oxygen atom or NH, or b) X is CH and Y is an oxygen atom, in which furthermore R1 is C1-C4alkyl; R2 is hydrogen, C1-C4alkyl or cyclopropyl; and in which R3 and R4 are as ...
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WO/1997/001529A1 |
The present invention provides novel ketimine curing agents. The present invention also provides rapidly curing magnetic recording media prepared using certain ketimine curing agents. More specifically, the invention provides rapidly cur...
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WO/1997/000845A1 |
2,3-Dihalogeno-6-trifluoromethylbenzene derivatives represented by general formula (I) and useful as the starting material of pesticides, drugs, etc., wherein X1 and X2 are the same or different and each represents fluoro or chloro: and ...
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WO/1997/000853A1 |
Compounds of general formula (I), salts thereof or hydrates thereof wherein (a) represents (b) or (c), for example, the compounds (d) and (e), which are useful as a PGD2 antagonist and thus usable in, for example, a remedy for systemic m...
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WO/1997/000856A1 |
Carboxylic acid amide derivatives having formula (I) are disclosed, as well as several processes for preparing the same and their use as fungicides. In formula (I), Ar stands for optionally substituted arylene or heteroarylene; E stands ...
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WO/1997/000866A1 |
Compounds of formula (I) and their possible isomers and isomer mixtures, in which (Z) is a group (a), (b), (c) or (d) and in which the other substituents are as defined herein. They can be used for pest control, in particular as microbic...
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WO/1996/040662A2 |
Linker compounds for formation of stably-linked conjugates are disclosed. Such linker compounds are aminooxy-containing linker compounds useful in forming conjugates having stable oxime linkages. The stably-linked conjugates have utility...
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WO/1996/040149A1 |
The invention provides antioxidant salen-metal complexes, compositions of such antioxidant salen-metal complexes having superoxide activity, catalase activity, and/or peroxidase activity, compositions of salen-metal complexes in a form s...
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WO/1996/040622A1 |
The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises a bis-(2-aryl)hydrazone capable of inhibiting the formation of a...
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WO/1996/040148A1 |
The invention provides antioxidant salen-metal complexes, compositions of such antioxidant salen-metal complexes having superoxide activity, catalase activity, and/or peroxidase activity, compositions of salen-metal complexes in a form s...
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WO/1996/040614A1 |
Compounds having anti-inflammatory and other activities are disclosed. The compounds are derived from diterpene and benzolactan phorboids.
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WO/1996/039392A1 |
The invention concerns phenylpyridazinones of general formula (I), in which R1, R2, R3, R4, R5 and R6 have the meanings specified in the description. Also disclosed are methods of producing these compounds, their use as herbicides and no...
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WO/1996/038408A1 |
A process for producing an N-methyl-methoxyiminoacetamide derivative represented by general formula (I), wherein R3 represents hydrogen, etc.; which comprises reacting an acetal derivative represented by general formula (III), wherein R1...
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WO/1996/038411A1 |
The invention concerns substituted carbamides of general formula (I), several processes for producing them, and their use as fungicides. In the formula, G stands for oxgyen, sulphur or one of the following groups: -Q-CQ-, -CH2-Q-; -Q-CH2...
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WO/1996/038407A1 |
The production of cyclohexanonoxim by the reaction of cyclohexanone with a hydroxyl ammonium salt, i.e. hydroxyl ammonium formiate, and the production of caprolactam by the Beckmann rearrangement of cyclohexanonoxim in a C1-C4 carboxylic...
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WO/1996/037463A1 |
A process for producing an N-methyl-methoxyiminoacetamide derivative represented by general formula (III), wherein R2 represents hydrogen, etc., which comprises reacting a novel 1-alkoxy-4-methoxyimino-2-methyl-3-oxo-1,2,3,4-tetrahydrois...
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WO/1996/036588A1 |
The present invention provides a process for the preparation of substituted aromatic amino compounds which are substituted by at least one -CN multiple bond or a carbonyl group on the aromatic radical or in side chain, by catalytic hydro...
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WO/1996/035669A1 |
Described are (het)aryloxy-, -thio-, aminocrotonates of formula (I) in which the substituents are defined as follows: U is oxygen, sulphur or amino; V is oxygen, sulphur, amino or alkylamino; X, Y, Z, independently of each other, are =N-...
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WO/1996/034851A1 |
The present invention provides a compound of formula (I), (II), (III) or (IV), processes for the preparation of the compounds of the invention, intermediates useful in these processes, a pharmaceutical composition, and methods of using t...
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WO/1996/034937A1 |
N-benzyliminium salts have formula (I), in which R1 and R2 represent independently from each other hydrogen or optionally substituted alkyl, alkenyl, cycloalkyl, aralkyl, heteroaralkyl, aryl or heteroaryl, provided that at least one of t...
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WO/1996/034850A1 |
The present invention provides a compound of formula (I) processes for the preparation of the compounds of the invention, intermediates useful in these processes, a pharmaceutical composition, and methods of using the compounds of the in...
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WO/1996/033164A1 |
Hydroximic acid derivatives of general formula (I), wherein G is either G1 or G2 or G3 or G4 of the formula: R5OC=C(COOR4)-, R5ON=C(COOR4)-, R5ON=C(CONR6R7)-, R5OC=C(CONR6R7)-, X1, X2, X3 are H, halo, HO, mercapto, nitro, SCN, azido, CN,...
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WO/1996/033168A1 |
The present invention presents a benzylsulfide derivative of formula (I) or its salt: wherein R1 is a C1-6 alkyl group, a C1-6 haloalkyl group, a C2-4 alkenyl group, a cyano group, etc., and each of R2 and R3 is a hydrogen atom, a haloge...
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WO/1996/033175A1 |
The current invention discloses amidino derivatives of formula (I) useful as nitric oxide synthase inhibitors wherein R1 is selected from the group consisting of cycloalkyl, heterocyclyl and aryl, which may optionally be substituted; L i...
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WO/1996/032370A1 |
4-Amino-5-oxy-2,6,6-trimethyl-2-cycloheptene compounds represented by general formula (I), pharmacologically acceptable salts thereof, or solvates of these wherein R1 and R2 independently represent each hydrogen, optionally substituted a...
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WO/1996/032373A1 |
Described is a method of preparing essentially pure 'alpha'-bis-oxime isomers of the formula (Ia): R1O-N=CR2-CR3=N-OR4, in which the groups R1O- and R2 are in the cis configuration with respect to the N=C bond, from a mixture of the cis ...
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WO/1996/031464A1 |
The invention concerns hydrazonoacetic acid amides of general formula (I), a process for producing them, and the use of the said amides as pesticides. In the formula shown, the following meanings apply: A stands for a simple bond or opti...
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WO/1996/031463A1 |
The invention pertains to substituted cycloalkenes of general formula (I) and several methods of preparing them, as well as intermediate products and several methods for preparing them. In this formula (I), E stands for methylidene or ni...
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WO/1996/031513A1 |
This invention discloses and claims novel intermediates and procedures for the synthesis of camptothecin derivatives, such as irinotecan, and other compounds related to the synthesis of CPT-11 of formula (I). Related procedures and compo...
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WO/1996/030329A1 |
The invention relates to substituted benzenes and derivatives thereof, useful as neuraminidase inhibitors, to pharmaceutical compositions comprising such compounds, and to methods of using these compounds for treating viral and other inf...
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WO/1996/029305A1 |
Compounds of formula (I) wherein either a) Z is N, Y is O or NH and W is O, S, SO or SO2, or b) Z is CH, Y is O and W is S, SO or SO2; and R is alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, phenyl or heterocyclyl, each of which is o...
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WO/1996/028402A1 |
The present invention relates to a process for stereoselective or regioselective chemical synthesis which generally comprises reacting a nucleophile and a chiral or prochiral cyclic substrate in the presence of a non-racemic chiral catal...
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WO/1996/025525A1 |
Alternative equilibrium modifiers for use with aldoxime extractants, such as hydroxyl aryl aldoxime extractants, employed in the process for extraction of metal values, particularly copper values, in the extraction from aqueous solutions...
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WO/1996/025398A1 |
The invention relates to novel substituted heterocyclic compounds, several processes for their production and their use as fungicides, and novel intermediate products, several processes for their production and their use as fungicides.
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WO/1996/024601A1 |
The present invention relates to a transition metal cationic chiral non-racemic complex containing a substituted or unsubstituted tetradentate or quinquedentatate ligand derived from two salicylaldimine units, the cationic complex includ...
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WO/1996/023763A1 |
The invention relates to novel alkoximino acetic acid amides, a process for their production and their use as pest-control agents.
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WO/1996/022967A1 |
A process for producing aromatic or heteroaromatic hydroxylamines of the general formula (I) in which R1 is an unsubstituted or substituted aryl radical or an unsubstituted or substituted hetaryl radical from the pyridine or quinoline gr...
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WO/1996/023010A2 |
Disclosed herein are processes for polymerizing ethylene, acyclic olefins, and/or selected cyclic olefins, and optionally selected olefinic esters or carboxylic acids, and other monomers. The polymerizations are catalysed by selected tra...
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WO/1996/021355A1 |
Pesticidal compounds having general formula (I) or a salt thereof is provided, in which n represents an integer from 0 to 4; m represents an integer 0 or 1; each R independently represents a halogen atom or a nitro, cyano, hydroxyl, alky...
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WO/1996/021450A2 |
The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging). Accordingly, a composition is disclosed which comprises a dioone bis[hydrazone] capable of inhibiting the formation of a...
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WO/1996/021354A1 |
Pesticidal as a pesticide against whitefly, Lepidoptera and certain fungi is provided of compound of general formula (I) or a salt thereof is provided, in which n represents an integer from 0 to 4; m represents an integer 0 or 1; each R ...
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WO/1996/020930A1 |
Acetylenes substituted with a phenyl or heteroaryl group and with a 5,6,7,8-tetrahydronaphthyl or 7,8-dihydronaphthyl group have retinoid-like biological activity. The 5,6,7,8-tetrahydronaphthyl or 7,8-dihydronaphthyl group is substitute...
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WO/1996/020164A1 |
A process for producing a compound represented by general formula (I) (E-isomer), wherein R1 and R2 are the same or different and each represents hydrogen or alkyl; and R represents hydrogen or alkyl which comprises eliminating the prote...
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WO/1996/019438A1 |
A novel process for producing chiral hydroxylamines for use as intermediates to make chiral hydroxyureas, which process comprises a tandem condensation-cyclization reaction between a dimethylsulfoxonium methylide and an appropriately sub...
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WO/1996/019463A1 |
A heteroaromatic oxazole compound represented by general formula (I) of a pharmaceutically acceptable salt thereof: wherein Z represents oxygen; one of R and R1 represents a group represented by formula (a), (wherein R3 represents lower ...
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WO/1996/019462A1 |
An oxazole derivative represented by general formula (I) or a medicinally acceptable salt thereof, each being excellent in antipyretic, analgesic, antiphlogistic, and particularly selective cyclooxygenase-2 (COX-2) inhibitory effects and...
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WO/1996/018402A1 |
The present invention is directed to cobalt compounds that can exchange or bind functional moieties such as histidine on a protein's surface resulting in the inactivation of a biological activity of the protein due to the complexing of t...
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