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JPH0436147B2 |
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JPH0433834B2 |
Anisotropic compounds of the following formula: (1) wherein is selected from the group consisting of +TR Z represents a covalent bond or a carboxyl group -C(O)O-, R is selected from the group consisting of hydrogen, C1-C12 alkyl, and C1-...
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JPH0432059B2 |
Diphenyl ethers of the formula where Z1, Z2 and Z3 independently of one another are each hyrogen, halogen, nitro, cyano, carboxyl, alkyl of 1 to 4 carbon atoms, or haloalkyl, alkoxy, haloalkoxy, alkylmercapto, haloalkylmercapto, alkylsul...
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JPH0432051B2 |
This invention relates to novel guanidine derivatives of the general formula their isomers at the guanidine group and salts of such compounds. The compounds and their salts are useful as anthelmintics.
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JPH0429661B2 |
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JPH0428829B2 |
Dry soil resistance and nonflame propagating characteristics are insured in textile fibers by applying thereto an aqueous dispersion containing at least 5 weight percent of a perfluoroalkyl ester of a carboxylic acid of from 3 to 30 carb...
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JPH0427976B2 |
Glaucoma can be treated by the application to the eye of a physiologically active amount of a compound of the formula in which: each of R3 and R4 is selected from hydrogen, and alkyl, alkenyl and cycloalkyl radicals, or R3 and R4 togethe...
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JPH0427975B2 |
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JPH0425956B2 |
The invention relates to a new multistage process for the production of 4-amino-6,7-dimethoxy-2-[4-(furo-2-yl)-piperazin-1-yl]-quina
zoline corresponding to the following formula and physiologically compatible salts thereof, which gives ...
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JPH0423770B2 |
Polymerizable monomeric carbamates are disclosed. Polymers comprising recurring units from such carbamates undergo β-elimination in an alkaline environment and are useful in diffusion control layers in diffusion transfer photographic pr...
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JPH0422903B2 |
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JPH0422905B2 |
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JPH0420881B2 |
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JPH0420435B2 |
Novel alpha -aryl-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-benze
neacetontr iles which are effective in destruting and/or preventing the growth of Protozoa; pharmaceutical compositions comprising such compounds as active ingredie...
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JPH0419229B2 |
New cephalosporins are of formula (I) In the formula R and R1 are both H or both hydrolysable or hydrogenolysable gps. or R1 can also be opt. substd. 1-4C alkyl, A is H or an equiv. of an alkali(ne earth) metal or an amine. (I) have anti...
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JPH0419221B2 |
Compounds of the formula I wherein R3 and the NR1R2 group are in a cis-position to each other and wherein Y is OH, R4COO, (R5)2NCOO or R6O either in position 5 or position 7, whereby R4 is an alkyl group having 1-5 carbon atoms or a poss...
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JPH0417947B2 |
A process is disclosed for producing substituted asymmetric ureas, starting from dialkylcarbonates, aromatic amines and aliphatic amines, by a two-step procedure and in the presence of a catalyst selected from among the Lewis' acids and ...
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JPH0415779B2 |
Substituted phenoxyphenylhydroxyamines and pyridyloxyphenylhydroxyamines, and the use thereof for the control of weeds.
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JPH0414643B2 |
The present invention relates to the use of compounds of the formula or pharmacologically acceptable salts thereof, for the preparation of medicaments having immunosuppressive activity.
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JPH0414086B2 |
A process for resolving a racemic modification of beta -adrenergic aryl- or hetaryl-oxypropanolamines such as (+/-)-2-[2-hydroxy-3-[[2-(1_H-indol-3-yl)-1,1-dimethylethyl]
amino]prop oxy]benzonitrile into its individual enantiomers is des...
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JPH049766B2 |
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JPH048427B2 |
(A) Carbacycline derivs. of formulae (X) and (X1) are new. n is 1 or 2. L1 is alpha-R3, beta-R4; beta-R3 or a mixt. of both; R3 and R4 being each H, methyl or fluoro, M1 is alpha-hydroxy, beta-R5 or alpha-R5, beta-hydroxy; R5 being H or ...
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JPH04500815A |
The invention relates to new 2-amino-7-carbamoyl-1,2,3,4-tetrahydronaphthalenes, a process for preparing them and their use as drugs.
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JPH046181B2 |
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JPH044311B2 |
A compound of the formula where R is selected from the group consisting of CH3-CO-(CH2)2-O-, +TR The compounds are useful in treating depression.
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JPH043382B2 |
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JPH043381B2 |
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JPH043380B2 |
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JPH041737B2 |
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JPH04982B2 |
Novel prodrug forms of known non-steroidai anti-inflammatory agents and a process for preparing them are disclosed, said prodrugs having the structural formula wherein R-@- is the acyl residue of a non-steroidal anti-inflammatory agent c...
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JPH0380147B2 |
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JPH0380182B2 |
The invention relates to new 3-nitro-4-aminophenols of the formula (I) (1) in which R denotes hydrogen or halogen, preferably chlorine or bromine, and R' denotes hydrogen or alkyl, hydroxyalkyl, dihydroxyalkyl or halogenohydroxyalkyl whi...
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JPH03291259A |
PURPOSE: To readily obtain the title compound containing a new compound useful as an intermediate for production of carbapenem based antibiotic used in a medicine in good yield by reacting a specific enolate compound used as a nucleophil...
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JPH0379339B2 |
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JPH0379340B2 |
1,1,1-azidodinitro compounds such as 1,1,1-azidodinitroethane are prepared by reacting the corresponding 1,1,1-trinitromethyl compound with lithium azide in the presence of a dipolar aprotic solvent. 1,1,1-azidodinitro compounds are also...
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JPH0356127Y2 |
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JPH0377178B2 |
This invention relates to a new method for preparing N-mono-acylated gem-diamino derivatives of general formula I from an aminoacid, hydroxyacid, peptide or depsipeptide residue with the terminal -NH2 or -OH groups protected P-(A)n-NH-@H...
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JPH0374817B2 |
A heat-developable color light-sensitive material comprising a support having thereon at least: (1) a light-sensitive silver-halide, (2) a coupler capable of coupling with an oxidation product of a developing agent, (3) a hydrophilic bin...
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JPH0374643B2 |
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JPH0374654B2 |
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JPH0374218B2 |
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JPH03258756A |
NEW MATERIAL:An alkoxyamine derivative expressed by formula I (R1 is 3-5C alkyl; R2 is lower alkyl; n is 2, 3 or 4; either one of A and B is O and the other is -NH-). EXAMPLE: N-[4-(2-Ethylbutyl)phenoxy]propyl-O-ethylhydroxyamine. USE: U...
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JPH0372056B2 |
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JPH0369338B2 |
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JPH0365339B2 |
The invention relates to compounds of the formulawhere Y is -OH; halogen;-NHCH3; R1SO3-, where R1 is a straight chain or branched chain alkyl group having 1 to 5 carbon atoms, or aryl; and R2 is -C(CH3)3 or -O-C(CH3)3. Processes for prep...
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JPH0362644B2 |
Hydroxylammonium salts are prepared by an improved process, wherein nitric oxide is reduced catalytically with hydrogen in a dilute aqueous solution of a mineral acid in the presence of a suspended supported platinum catalyst and at elev...
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JPH0361661B2 |
This invention discloses a number of novel odorant oximes having from 11 to 14 carbon atoms, processes for making same, and odorant compositions containing same.
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JPH0361664B2 |
1-[2-(2,4-Dichlorophenyl)-pentyl]-1H-1,2,4-triazole can be produced, in a novel, simple, economical and isomer-free form, by reacting 2-(2,4-dichlorophenyl)-valeronitrile, in the presence of hydrogen, an acid and a hydrogenation catalyst...
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JPH0359897B2 |
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JPH0359899B2 |
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