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Matches 1,001 - 1,050 out of 1,113

Document Document Title
JPS5528968A
PURPOSE: The oxidation of a tertiary amine with hydrogen peroxide is carried out in the presence of a carbonate salt or carbon dioxide and in the presence or absence of a chelating reagent to produce quantitatively amine oxide in a short...  
JPS5515477A  
JPS55376B2  
JPS5441567B2  
JPS5440531B2  
JPS5440530B2  
JPS54151949A
The pharmaceutical compositions contain cis- and trans-N-(2-aminocyclopentyl)-N-acylanilides of the general formula and their pharmacologically acceptable acid addition salts. The substituents are defined in Claim 1. These pharmaceutical...  
JPS54128546A
Compounds of the formula [wherein p is zero or one; Q is oxygen or sulphur; R is alkyl, cycloalkyl, vinyl, ethoxy or methoxymethyl. R1 is hydrogen, alkyl, dimethylaminoalkyl, aralkyl or alkenylmethyl; and Y and Z are each hydrogen, halog...  
JPS54122233A  
JPS54106451A  
JPS5479230A
New salts of alpha -isocyanocarboxylic acid of the formula wherein R is alkyl or phenyl, R1 is hydrogen, alkyl or phenylalkyl or R and R1 together represent an alkylene chain with at least 2 carbon atoms, and R2 is an alkali metal ion ar...  
JPS5462317A
Alkyl amine oxides have been found to exhibit valuable insecticidal and/or ovicidal activity.  
JPS5444651A
New geminally disubstituted indenes are of general formula I (I) wherein each of R1 and R2 is hydrogen or R1 and R2 together form a direct bond or an alkylene group -(CH2)n-, in which n is an integer from 1 to 4, R3 is hydrogen, C1-3-alk...  
JPS5348197B2  
JPS53149944A
2-AMinobenzylamines (I): (where Hal = Cl or Br; R1 = H, Cl or Br; R2 = cyclohexyl, hydroxycyclohexyl, morpholinocarbonylmethyl or isopropylaminocarbonylmethyl gp.; R3 = H or methyl and R4 = H, or, if R2 = isopropylaminocarbonylmethyl or ...  
JPS53141243A
Compounds having the formula and the pharmaceutically acceptable salts thereof, wherein R1 is alkanoyl; R2 is alkyl; R3 is alkylamino, dialkylamino, a 1-piperazinyl group, 4-aryl-1,2,3,6-tetrahydro-1-pyridinyl, or N-alkyl-N-(pyridinylalk...  
JPS53119841A
PURPOSE: Phenylglyoxal derivatives of formula I, e.g. 2-benzyloxyphenylglyoxal hydrate.  
JPS53116347A
Novel N-(aminocycloheptyl)-N-alkanoyl anilides of the formula in which the substituents are described in Claim 1, are prepared. These compounds are obtained by acylating an appropriately substituted N-[2-(disubstituted amino)-cycloheptyl...  
JPS53116339A
2-AMinobenzylamines (I): (where Hal = Cl or Br; R1 = H, Cl or Br; R2 = cyclohexyl, hydroxycyclohexyl, morpholinocarbonylmethyl or isopropylaminocarbonylmethyl gp.; R3 = H or methyl and R4 = H, or, if R2 = isopropylaminocarbonylmethyl or ...  
JPS5336453B2  
JPS5336452B2  
JPS53111060A
Peptides of the formula:  
JPS53105436A
PURPOSE: To prepare the title cpd. in high yield by oxidation (the half amt. of palkylaniline) of p-alkylaniline, followed by condensation with the residual half of p-alkylaniline and oxidation. The first oxidation is stopped by lowering...  
JPS5353617A
PURPOSE: α-Isocyano fatty acid amide derivatives I (one of R1 and R2 is H, and the other is alkyl, cycloalkyl, etc.; R1 and R2 together with N or O at the terminal position or together with the adjacent N form a heterocyclic ring), e.g....  
JPS5315345A  
JPS5311999A  
JPS5246935B1  
JPS52139011A
PURPOSE: Novel method of preparing linear unsatd. alcohols, such as geraniol and nerol, from hydroxylamine derivatives by effecting selective hydrogenative fission of the - O - N - bond in the presence of a specific catalyst.  
JPS52133087A  
JPS52100459A
Novel steroids having the structure and the 1,2-dehydro derivatives thereof, wherein R1 is hydrogen, hydroxy, alkanoyloxy, fluorine, chlorine, or bromine; R2 is alkyl or aryl; R3 is alkyl, aryl, alkanoyl, aroyl, alkoxycarbonyl, or cyano;...  
JPS5228791B2  
JPS5227150B2  
JPS5273853A
PURPOSE: 9,10-Dihydro-9,10-methanoanthracene,N-oxide derivatives expressed by the formula I: (A is a straight or branched chain 1W6C alkylene; R1 and R2 are 1W4C alkyl, phenyl-1W4C alkyl, etc.). For example, 9-(3dimethylaminopropyl) -9,1...  
JPS5271444A
PURPOSE: Title compounds of formula I (X1 is halogen on 0-or m-position; X2 is H, halogen, lower alkyl); for example, m-carboxyphenyl-ONN-azoxycyanide.  
JPS5231008A
PURPOSE: Geraniol and nerol, useful as raw materials of perfumery components or pharmaceuticals, are prepared in high yield with a few-stages process from isoprene and sec-amines as starting materials.  
JPS5231007A
PURPOSE: 3,7-Dimethyl-2-octene-1,7-diol,useful as perfumery, is synthesized in high yield from N,N-dialkyl(3,3-dimethyl-2,6-octadienyl)-amine as a starting ma material.  
JPS5219612A
PURPOSE: Linalool is prepared in high yield with a few-stages by alcoholating after reacting isoprene with N, N-dialkylamine, and then with a peroxide.  
JPS5219613A
PURPOSE: The high purity title compound, useful as perfumery or its raw material, is prepared in high yield from N, N-dialkyl[3,7-dimethyl-2,6-octadienyl]-amine.  
JPS5212986A
The complex (I) consists of factors A, B, C and D, and the tetra (2-4C) acyl esters of factor A. The individual factors are also claimed. Factor A and its esters are of formula (II) (R, all the same, are H, a acetyl, propionyl or butyryl...  
JPS5145588B2  
JPS51124698A  
JPS51121523A  
JPS51118735A
PURPOSE: Optical active p-β-methylbutyl-p'-vinyloxyazobenzene or p- -methylbutyl-p-vinyloxyazobenzene of fromula I where X is -N=N-, -N ( O) =N-,-N= N ( O)-.  
JPS5137838B1  
JPS5136257B1  
JPS5133103B1  
JPS5186438A
The composition contains, as active ingredient, a novel compound of the formula (I) in which X represents a halogen atom and n an integer from 1 to 5, Y represents an optionally substituted aryl group, R represents an azido group or a gr...  
JPS5124504B2  
JPS5180831A  
JPS5134123A
1520441 Di-(substituted alkyl)amino-benzenes CHEM PHARMAZ FABRIK DR HERMANN THIEMANN GmbH 11 July 1975 [16 July 1974] 29218/75 Heading C3H [Also in Division C2] Novel compounds I in which R1 is Y is N or N#O, each of X1 and X2 is H or C1...  

Matches 1,001 - 1,050 out of 1,113