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JPS5913507B2 |
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JPS5913502B2 |
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JPS5913500B2 |
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JPS5913501B2 |
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JPS59508B2 |
Compounds of the formulae:
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JPS5857431B2 |
Compounds of the formulae:
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JPS5817745B2 |
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JPS57188516A |
The invention relates to sulphenamide compounds of Formula (I) as defined herein and to methods for their preparation. Also included in the invention are compositions containing said sulphenamide compounds; and the use of said compounds ...
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JPS57185262A |
Novel sulphenamides of the general formula I in which R<1>, R<2> and R<3> are as defined in the description, a process for their preparation, their utilisation as medicines, in particular their utilisation as lipoxygenase inhibitors, med...
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JPS5747669B2 |
Thiocarbamylsulfenamides are prepared in high yields in a process comprising the reaction of a monohaloamine with tri- or tetrathiocarbonate salt. The compounds have particular utility as accelerators in the vulcanization of unsaturated ...
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JPS57112375A |
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JPS5653536B2 |
2-Substituted-5-carboxamidobenzoic acids and the pharmaceutically acceptable salts thereof as hypolipemic agents.
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JPS56158766A |
The present invention provides 5.6;8,9-tetrahydro-7H-di- benz(d,f)azonine derivatives of the formula:wherein R1 and R2, which are the same or different, are hydrogen or halogen atoms or lower alkyl or lower alkoxy radicals, R3 is a hydro...
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JPS56100766A |
NEW MATERIAL:A geldanamycin derivative of formula I(R is halogen). EXAMPLE: 19-Bromogeldanamycin. USE: The compound has remarkable effect to suppress the growth of experimental tumor cell W-2K-11 which has been widely recognized as a mod...
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JPS563870B2 |
The compounds of the general formula (I) in which X = halogen atom, methyl or methoxy groups; n = 2, 3 or 4; A = together with a nitrogen atom a partially or completely saturated heterocycle which is optionally substituted by 1 to 2 meth...
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JPS55160764A |
The invention relates to novel guanidine derivatives, particularly to substituted guanidines of the formula (I) having hypoglycaemic activity, for the oral treatment of hyperglycaemia in mammals, especially for the oral treatment of Diab...
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JPS5542981B2 |
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JPS5542982B2 |
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JPS55124745A |
The invention relates to 11-aminoundecanoic acids and 11-aminoundeca-4,8-dienoic acids and the esters of these acids. They have the formula I (I) wherein R1 and R3 are e.g. hydrogen and R2 and R4 are e.g. methyl and E is e.g. the radical...
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JPS5438119B1 |
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JPS54116088A |
Disclosed are catalysts for the polymerization of higher lactam monomers. The catalysts comprise an essentially homogenic binary mixture of lauric-lactam and a salt of lauric-lactam. The inventive catalyst can be stored at room temperatu...
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JPS5420492B2 |
1325528 Aminophenyl - cycloamidine derivatives BAYER AG 11 June 1971 [13 June 1970] 27494/71 Heading C2C Novel aminophenyl-cycloamidine derivatives (1) wherein R is a hydrogen atom or a straight or branched chain alkyl, alkenyl or alkyny...
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JPS5416496B1 |
1325528 Aminophenyl - cycloamidine derivatives BAYER AG 11 June 1971 [13 June 1970] 27494/71 Heading C2C Novel aminophenyl-cycloamidine derivatives (1) wherein R is a hydrogen atom or a straight or branched chain alkyl, alkenyl or alkyny...
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JPS5470299A |
PURPOSE: The acylation of maytansinol with a specific compound is effected in the presence of a carbodiimide to produce maytansine derivatives useful as carcinostatic agent or antiactynomyces agent with industrial advantage. CONSTITUTION...
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JPS549195B2 |
Procedure for obtaining phenoxypropylamine derivatives of general formula **(See formula)** where R is hydrogen or an alkyl radical and R1 is hydrogen, an alkyl, cycloalkyl, aralkyl, or aryl radical, or R and R1 together are a divalent, ...
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JPS549196B2 |
Procedure for obtaining phenoxypropylamine derivatives of general formula **(See formula)** where R is hydrogen or an alkyl moiety and R7 is hydrogen, an alkyl, cycloalkyl, aralkyl, or aryl moiety, or R and R1 together are a bivalent hyd...
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JPS549194B2 |
Procedure for obtaining phenoxypropylamine derivatives of general formula, where R is hydrogen or an alkyl moiety and R1 is hydrogen, an alkyl, cycloalkyl, aralkyl, or aryl moiety, or R and R1 together are a bivalent hydrocarbon moiety, ...
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JPS53124281A |
PURPOSE: Cis-8-(O-dimethylthiocarbamyl)-3,6,11-trimethyl-2,6-methano1
,2,3,4,5,6-hexahydro-3-benzazocine of formula I.
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JPS5382763A |
PURPOSE: To easily and economically remove coloring impurities, which cause bad influences to the polymerization and the properties of the obtd. resins, by treatment of cyanonrborbornene with active arcbon at ≤100°C.
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JPS5382768A |
PURPOSE: N-Acylpolylactams obtd. by reaction of trivalent or more multivalent alcohol with cpd. I(X is halogen;R is 1-12C org. gp. ) and cpd. II (M is H or alkali metal;R1 is 2-11C org. gp. ), e. g. cpd. III(R" is trivalent or mo re mult...
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JPS5319599B2 |
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JPS533398B2 |
Procedure for obtaining dibenzazezines, of general formula: **(See formula)** wherein R1 and R2 are the same or different, and represent a member chosen from the group consisting of a hydrogen atom, a hydroxy group, a lower alkoxy group,...
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JPS532877B2 |
Title cpds. of formula (I): (where R1 and R2 are H, OH, alkoxy, aralkoxy, CH2OH or R1 + R2 is alkylenedioxy; R3, R4 and R5 are H, OH, alkoxy or adjacent pairs form alkylene dioxy and R6 is H, alkyl, alkenyl aralkyl or cycloalkyl, but R1-...
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JPS532878B2 |
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JPS535160A |
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JPS52125162A |
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JPS52118425A |
Novel thiocarbamates and sulphoxides of the formula I are used for controlling undesired plant growth. The symbols in formula I have the meaning given in the claims. A herbicide contains the compounds of the formula I besides an inert ca...
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JPS5232890B2 |
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JPS5295651A |
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JPS5283747A |
PURPOSE: Nitrosourea derivatives expressed by the formula I: [R1 is halogen, substituted alkyl, (substituted) alkenyl, (substituted) aryl, (substituted) heterocyclic group; n is an integer, 2-10]. For example, 1-(β-chloroethyl)-3-(Np-ch...
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JPS5278865A |
of the disclosure: Compounds of the formula in which R4 represents an alkyl radical having from 1 to 4 carbon atoms, R5 represents a linear or branched alkylene radical having from 1 to 10 carbon atoms in the chain which may be substitut...
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JPS5222846B2 |
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JPS5265285A |
Prepn. if of benzazocine derivs. of formula (I), in racemic or optically active forms when R4 is not = R5 and/or R2 is not = R3, and their acid. addn. salts. Method comprises reacting cpds. of formula (II) with alcohols R2R3CHOH at 100-2...
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JPS51143662A |
PURPOSE: A process for preparing nitrosourea derivatives used as carcinostatic agents,by acylating novel mercuric salts of nitrosourea derivatives.
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JPS51125273A |
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JPS51110586A |
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JPS51108083A |
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JPS5198285A |
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JPS5191252A |
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JPS5188984A |
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