Results 61 to 70 of about 112 (84)
Some of the next articles are maybe not open access.
Journal of the Chemical Society, Perkin Transactions 2, 1982
Rate constants have been determined for the reactions at 30, 35, and 40 °C of diazodiphenylmethane with 4′-substituted biphenyl-4-carboxylic acids and 4-substituted 1-naphthoic acids in 14 alcohols. Hammett ρ values have been evaluated for the reactions in 11 of the alcohols.
P. Ananthakrishnanadar +2 more
openaire +1 more source
Rate constants have been determined for the reactions at 30, 35, and 40 °C of diazodiphenylmethane with 4′-substituted biphenyl-4-carboxylic acids and 4-substituted 1-naphthoic acids in 14 alcohols. Hammett ρ values have been evaluated for the reactions in 11 of the alcohols.
P. Ananthakrishnanadar +2 more
openaire +1 more source
2004
The rate constants for the reaction of diazodiphenylmethane with cyclohexylcarboxylic, cyclopentylcarboxylic, cyclohex-3-enylcarboxylic and cyclopent-3-enylcarboxylic acids have been determined in ten alcohols at 30degreesC using the UV-spectroscopic method.
Nikolić, Jasmina +2 more
openaire +1 more source
The rate constants for the reaction of diazodiphenylmethane with cyclohexylcarboxylic, cyclopentylcarboxylic, cyclohex-3-enylcarboxylic and cyclopent-3-enylcarboxylic acids have been determined in ten alcohols at 30degreesC using the UV-spectroscopic method.
Nikolić, Jasmina +2 more
openaire +1 more source
Canadian Journal of Chemistry, 1966
The rate coefficients for the reaction with diazodiphenylmethane, in ethanol at 30.0°, of a number of substituted indole-2-carboxylic acids, indole-3-carboxylic acids, coumarin-3-carboxylic acids, coumarilic acids, and N-phenylglycines have been determined.
Keith Bowden, D. C. Parkin
openaire +1 more source
The rate coefficients for the reaction with diazodiphenylmethane, in ethanol at 30.0°, of a number of substituted indole-2-carboxylic acids, indole-3-carboxylic acids, coumarin-3-carboxylic acids, coumarilic acids, and N-phenylglycines have been determined.
Keith Bowden, D. C. Parkin
openaire +1 more source
ChemInform, 1995
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
G. S. USCUMLIC, M. D. MUSKATIROVIC
openaire +1 more source
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
G. S. USCUMLIC, M. D. MUSKATIROVIC
openaire +1 more source
ChemInform, 1998
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
G. S. USCUMLIC, V. V. KRSTIC
openaire +1 more source
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
G. S. USCUMLIC, V. V. KRSTIC
openaire +1 more source
Chemischer Informationsdienst, 1976
AbstractDurch Oxidation der Hydrazone (I) mit Peressigsäure in Gegenwart von Tetramethylguanidin (TMG) als Base und einer Spur Jod in einem organischen Lösungsmittel (Methode A) werden die Diazomethanderivate (II) dargestellt.
J. ROBERT ADAMSON +5 more
openaire +1 more source
AbstractDurch Oxidation der Hydrazone (I) mit Peressigsäure in Gegenwart von Tetramethylguanidin (TMG) als Base und einer Spur Jod in einem organischen Lösungsmittel (Methode A) werden die Diazomethanderivate (II) dargestellt.
J. ROBERT ADAMSON +5 more
openaire +1 more source
Canadian Journal of Chemistry, 1964
Rate coefficients have been determined for the reactions in ethanol at 30° of diazodiphenylmethane with several groups of carboxylic acids. Each group included the parent acid and three nuclear substituted acids. The parent acids were: benzoic, phenylacetic, β-phenylpropionic, phenoxyacetic, and trans-cinnamic acid.
K. Bowden, N. B. Chapman, J. Shorter
openaire +1 more source
Rate coefficients have been determined for the reactions in ethanol at 30° of diazodiphenylmethane with several groups of carboxylic acids. Each group included the parent acid and three nuclear substituted acids. The parent acids were: benzoic, phenylacetic, β-phenylpropionic, phenoxyacetic, and trans-cinnamic acid.
K. Bowden, N. B. Chapman, J. Shorter
openaire +1 more source
Reaction mechanisms of peroxybenzoic acid toward diazodiphenylmethanes
The Journal of Organic Chemistry, 1971Ruggero Curci +2 more
openaire +1 more source
Chemischer Informationsdienst, 1975
AbstractZahlreiche Cärbonsäuren (I) werden mit Diphenyldiazomethan (II) umgesetzt.
openaire +1 more source
AbstractZahlreiche Cärbonsäuren (I) werden mit Diphenyldiazomethan (II) umgesetzt.
openaire +1 more source

