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WO/1998/035935A1 |
Novel compounds useful as active ingredients of pesticides are disclosed. Acrylonitrile compounds of formula (I) or their salts, wherein Q is Qa, Qb, Qc or Qd, Y is =C(R�4?)- or =N-, R�1? is alkyl, haloalkyl, etc., each of R�2? and...
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WO/1998/034898A1 |
The invention relates to phenoxyacetic acid derivatives of formula (I), wherein R�1?, R�2?, Xn and A are as defined in the description, A represents a halogen atom, hydroxy, OR�3?, S(O)�k?R�3?, or a group of formula (A-1) or (A...
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WO/1998/009943A1 |
Novel sulfur-containing amino acid derivatives of general formula (I) and exhibiting a high inhibitory activity against LTA�4? hydrases. In said formula (I), R?1� is H, alkyl, (substituted) phenylalkyl, alkanoyl or (substituted) benz...
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WO/1998/008809A1 |
The invention relates to sulfurization of the internucleoside linkages of oligonucleotides. Preferably, the sulfur transfer reagents employed in the method according to the invention are bis(alkoxylthiocarbonyl) tri and tetra sulfides.
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WO/1998/001478A1 |
This invention concerns a free radical polymerization process, selected chain transfer agents employed in the process and polymers made thereby, in which the process comprises preparing polymer of general Formula (A) and Formula (B) comp...
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WO/1997/032844A1 |
The current invention discloses hydroxyamidino derivatives useful as nitric oxide synthase inhibitors.
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WO/1997/029103A2 |
A process of reacting (a) is provided wherein R, R1, R2, R3 and X are selected from (b).
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WO/1997/021673A1 |
A method for achieving improved conversion rates and/or a faster reaction rate, particularly in reaction (a), than those achievable with prior art resins.
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WO/1997/014667A1 |
The invention concerns novel bicyclic cyclopentane-1,3-dione derivatives of formula (I), in which A, B, B', G, Q, X, Y and Z have the meanings indicated in the description, a method of producing said derivatives and their use as pest-con...
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WO/1997/005103A1 |
Phenyl acetic acid derivatives of formula (I) in which: X is NOCH3, CHOCH3 and CHCH3; Y is NMR and O; R, R1 are hydrogen and C1-4 alkyl; R2 is hydrogen, C1-C6 alkyl, C1-C4 alkyl halide and C3-C6 cycloalkyl; R3 is C4-C6 alkyl, substituted...
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WO/1996/021456A1 |
Compounds which inhibit prenyl transferases, particularly farnysyltransferase and geranylgeranyl transferase I, processes for preparing the compounds, pharmaceutical compositions containing the compounds, and methods of use.
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WO/1996/014289A1 |
Fluorobutenyl esters have the formula (I), in which R1 stands for hydrogen or a halogen, and R2 stands for one of the groups (a), (b) or (c), in which V, Y, Z, R3 and R5 have the meanings given in the description. Also disclosed are a pr...
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WO/1996/004793A1 |
A composition comprising (a) a perthioxanthate and/or (b) a combination of (i) a thiocarbonate selected from the group consisting of oligomeric thiocarbonates, monomeric thiocarbonates containing at least 4 sulfur atoms, or combinations ...
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WO/1995/029889A1 |
Compounds of formula (I) in which X is (a) or (b), n is 0, 1, 2, 3, 4 or 5, where if n is greater than 1, the radicals R2 are identical or different; o is 0, 1, 2, 3 or 4, where if o is greater than 1, the radicals R3 are identical or di...
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WO/1995/019167A1 |
A composition suitable for administration to a warm-blooded animal comprising an antisense oligonucleotide to the C-C chemokine family typified by MCP-1 and MIP-1-Alpha which may or may not be labeled with a radionuclide by means of a ch...
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WO/1995/011884A1 |
There are disclosed compounds and methods for inhibiting cataract formation in the lens of the eye of a warm-blooded animal. The compounds generally include derivatives of pantethine or pantetheine where one or more of the alcohol groups...
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WO/1995/011226A1 |
A substituted benzene derivative of formula (I), wherein A is an aryloxy group which may be substituted, an arylthio group which may be substituted or -ON=C(R1)R2, each of R1 and R2 which are independent of each other is an alkyl group w...
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WO/1993/016992A1 |
Sulfonic acid stilbenes of formula (I) wherein B is -CH=CH- (cis or trans), -CH2CH2- or a bond; X is NH or oxygen; Y is oxygen or sulfur; Z is NH, CH2, oxygen or sulfur; R1 is hydrogen, C1-C4 alkyl, -CH2-Ar, or -Ar wherein Ar is a phenyl...
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WO/1993/009132A1 |
Compounds of formula (I) wherein R1 and A are amino terminal groups: Z is O or N-R2; M is a dipeptide isostere; and D1 and D2 are optionally absent or amino acids; and pharmaceutically acceptable salts thereof, are potent inhibitors of t...
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WO/1993/007116A1 |
Fungicidal compounds having formula (I), wherein W is CH3O.CH=CCO2CH3, CH3ON=CCONR3R4 or CH3ON=CCO2CH3 and stereoisomers thereof; n is 0 or 1; X is oxygen or sulphur; Z is oxygen, sulphur or NR1; R1 is hydrogen or alkyl optionally substi...
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WO/1993/001163A1 |
Constitution: an amino acid derivative represented by the general formula (I): R1NH-CH(R2)-CONH-A-ONO2 and a pharmacologically acceptable salt thereof, wherein R1 represents hydrogen, C1-C7 alkanoyl, C1-C6 alkoxycarbonyl, C6-C10 arylcarb...
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WO/1992/008688A1 |
Compounds represented by formula (I), wherein A represents R, R13 and radicals represented by formulas (A1, A2, A3), B represents radicals represented by formula (II), (values for the variables given herein), are effective as retroviral ...
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WO/1992/008701A1 |
Compounds represented by formula (I) wherein A represents radicals represented by formulae (A1, A2, A3) (values for the variables given herein), are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV prot...
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WO/1991/016299A1 |
A method for control of plant disease, especially fungus, using compounds of formula (I) and novel compounds within the class, wherein: A is C(=O)R, C(=O)OR1, C(=O)SR1, P(=O)QR2Q1R3; C(=O)NHR, SO2R5, SO2NR6R7; Q and Q1 are independently ...
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WO/1991/013028A1 |
Stabilized solid thiocarbonates are produced by a process in which water is evaporated from a stabilized aqueous thiocarbonate solution which contains a stabilizing amount of a sulfide, a polysulfide and/or a base.
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WO/1991/010639A1 |
The present invention relates to hitherto unknown intermediate of formula (I), in which R1 stands for hydrogen or a straight or branched aliphatic C1-C20 carbon chain or an aryl or aralkyl group, aryl and "ar" meaning an aromatic or hete...
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WO/1991/009526A2 |
Oligomeric thiocarbonates such as hexathiodicarbonate salts and thioesters are used as pesticides and preservatives. Certain oligomeric thiocarbonate salts, notably quaternary ammonium hexathiodicarbonates, are prepared. The compounds ar...
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WO/1990/012784A1 |
A method for control of plant disease, especially fungus, using compounds of formula (I) and novel compounds within the class (I), wherein: A is C(=O)R, C(=O)OR?1¿, C(=O)SR?1¿, P(=O)QR?2¿Q?1¿R?3¿; C(=O)NHR, SO¿2?R?5¿, SO¿2?NR?6¿...
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WO/1989/005796A1 |
Novel mercapto-acylamino acids useful in the treatment of hypertension and combinations of mercapto-acylamino acids and atrial natriuretic factors or angiotensin converting enzyme inhibitors useful for treating hypertension are disclosed.
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WO/1989/003383A1 |
This invention relates to monoxanthates and dixanthates of dipropylene glycol and triethylene glycol. These xanthates increase both the rate of plant growth and the concentration of chlorophyll in the plants.
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WO/1988/002363A1 |
The derivatives have the general formula (I) wherein R1 is an optionally mono or polyhalogenated aliphatic acyl group, a benzoyl or phenacetyl group which may carry on the phenyl residue one to three halogeno or alkyl substituents, an al...
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WO/1986/002349A1 |
Lipid derivatives represented by formula (I), (wherein R1 represents alkyl or alkylcarbamoyl, R2 represents H, optionally substituted hydroxy, optionally substituted amino or cyclic amino, R3 represents alkylene, R4 represents H, alkyl o...
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WO/1985/000167A1 |
The present invention relates particularly to chemical compounds having the formula (I), R1-CO-NR3- ADA BD-S-R2 wherein R1 is a radical corresponding to an amino acid R1-COOH, ADA BD is an alkylene radical at C2 or C3 which may be substi...
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WO/1984/000032A1 |
1-amino-4-oxy-3-(mercapto-alkyl)-(unbranched chain)-benzenes, having particularly the formula (I) wherein R and R2 are hydrogen or an alkyl residue with 1 to 6 atoms of carbon, R' is hydrogen, an alkyl residue with 1 to 6 atoms of carbon...
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WO/1983/003603A1 |
Alcoxycarbonyl-dithiocarbamate, respectively alcoxycarbonyl-thiolcarbamate used as active substances and having the formula (I) wherein R1 and R2, which may be the same or different, are hydrogen, a saturated or unsaturated straight or b...
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WO/1983/002448A1 |
Process for the preparation of peptides including higher polypeptides utilizing indenylmethoxycarbonyl blocking groups and products produced thereby.
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WO/1982/004251A1 |
A process for preparing DL-cysteine by reacting (Beta)-halogenoalanine with trithiocarbonate and decomposing the resulting trithiocarbonic acid mono (aminocarboxyethyl) ester. This process is an industrially excellent process for prepari...
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JP7422076B2 |
The problem of the present invention is to provide a compound which can form a composition having excellent patterning accuracy and heat resistance. The present invention is a compound represented by the following general formula (1). (I...
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JP2023164361A |
To provide: ionizable lipid compounds or pharmaceutically acceptable salts, isotopic variants, tautomers or stereoisomers thereof; nanoparticle pharmaceutical compositions comprising the compounds; and application of the compounds and th...
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JP2023544882A |
Glioblastoma is one of the most deadly brain tumors. The difficulty in treating glioblastoma is related to, among other things, the sensitivity of the brain to drugs, the limited brain penetration of chemotherapeutic agents, and the resi...
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JP7303817B2 |
A process for preparing an S,S′-dialkyldithiocarbonate from a dialkyl disulfide and from a particular metal catalyst, in the presence of carbon monoxide is described in addition to the use of S,S′-dialkyldithiocarbonates as reagents ...
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JP7235737B2 |
Suggested is a semiconductor nano-sized light emitting material having a ligand.
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JP2023027526A |
To provide a photosensitive surface treatment agent, a laminate, a transistor, a pattern formation method, and a transistor manufacturing method.A photosensitive surface treatment agent comprises a compound represented by the formula (1)...
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JP7042283B2 |
Provided are new alkenyl carbonothioates of formula (I), their manufacture and their use as flavours and fragrances. Also provided are flavour and fragrance compositions and edible products, in particular coffee products, comprising the ...
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JP7041925B2 |
The objective of the present invention is to provide a method for producing a carbonate derivative in a safe and efficient manner. The method for producing a carbonate derivative according to the present invention is characterized in com...
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JP2022039516A |
To provide a method for producing a bis(thiocarbonyl) disulfide compound useful as a reversible addition-fragmentation chain-transfer polymerization agent (RAFT agent) in an industrial manner and at low cost.The present invention disclos...
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JP2022007984A |
To provide a novel agricultural chemical, in particular a herbicide.The present invention discloses a ketone or oxime compound represented by formula (1): [where B is B-1, B-2 or B-3, Q is an oxygen atom, NOR7 or the like, R6 is a hydrog...
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JP6950872B2 |
There is provided novel agricultural chemicals, in particular herbicides. A ketone or oxime compound or a salt thereof of Formula (1):wherein B is a ring of any one of B-1, B-2, or B-3, Q is an oxygen atom, a sulfur atom, NOR7, etc., R6 ...
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JP6850892B2 |
Provided is a process for synthesizing a functionalized cyclic dithiocarbamate.
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JP2021038205A |
To provide a novel agrochemical, particularly a herbicide.The present invention relates to a ketone or oxime compound represented by formula (1) and a herbicide containing the same [where B is B-1, B-2, B-3, Q is an oxygen atom or NOR7, ...
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