Results 71 to 80 of about 252 (117)
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Helvetica Chimica Acta, 2008
AbstractDiazodiphenylmethane (DDM) undergoes cycloadditions to 1‐substituted buta‐1,3‐dienes exclusively at the C(3)C(4) bond. At room temperature, the N2 loss from the initially formed 4,5‐dihydro‐3H‐pyrazoles 2 is faster than the cycloaddition and furnishes the vinylcyclopropane derivatives 7 and 9 with structural retention at the C(1)C(2) bond.
Akihiro Ohta +4 more
exaly +2 more sources
AbstractDiazodiphenylmethane (DDM) undergoes cycloadditions to 1‐substituted buta‐1,3‐dienes exclusively at the C(3)C(4) bond. At room temperature, the N2 loss from the initially formed 4,5‐dihydro‐3H‐pyrazoles 2 is faster than the cycloaddition and furnishes the vinylcyclopropane derivatives 7 and 9 with structural retention at the C(1)C(2) bond.
Akihiro Ohta +4 more
exaly +2 more sources
Ring-Chain Tautomerism. Part 10. The Reaction of Oxocarboxylic Acids with Diazodiphenylmethane
Collection of Czechoslovak Chemical Communications, 1999 The rate coefficients for the esterification of a series of oxocarboxylic acids with diazodiphenylmethane have been determined in ethanol or 2-methoxyethanol at 30.0 °C. These and the rates of reaction with model compounds have been used to estimate the equilibrium constants for ring-chain tautomerism for the oxocarboxylic acids.
Keith Bowden +2 more
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Acid-catalyzed decomposition of diazodiphenylmethane in dimethylsulfoxide
Canadian Journal of Chemistry, 1999 Acid-catalyzed decomposition of diazodiphenylmethane (DDM) has been studied in DMSO containing varying amounts of water. The reaction was found to be first-order in DDM and first-order in acid. The Brønsted plot for a series of carboxylic acids is curved with the H+ point falling below the curve defined by the carboxylic acids. In near-anhydrous DMSO,
Robert Eliason
core +3 more sources
Journal of the Chemical Society Perkin Transactions 1, 1975
Diazodiphenylmethane has been prepared from benzophenone hydrazone by oxidation with peracetic acid in the presence of a base and a trace of iodine. Two variants of the process are described: (a) benzophenone hydrazone in an organic solvent is oxidised with peracetic acid in the presence of 1,1,3,3-tetramethylguanidine and a trace of iodine; (b) a ...
J. Robert Adamson +5 more
exaly +2 more sources
Diazodiphenylmethane has been prepared from benzophenone hydrazone by oxidation with peracetic acid in the presence of a base and a trace of iodine. Two variants of the process are described: (a) benzophenone hydrazone in an organic solvent is oxidised with peracetic acid in the presence of 1,1,3,3-tetramethylguanidine and a trace of iodine; (b) a ...
J. Robert Adamson +5 more
exaly +2 more sources
Carbohydrate Research, 2001
A kinetic study of the tin(II) chloride catalyzed reaction of diazodiphenylmethane with ethylene glycol in dimethoxyethane is reported. The preparation and characterization of ethylene glycol monodiphenylmethyl ether, the main product from this reaction, is also reported as well as the preparation of the two diphenylmethyl monoethers of methyl 4,6-O ...
Sigthor Petursson
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A kinetic study of the tin(II) chloride catalyzed reaction of diazodiphenylmethane with ethylene glycol in dimethoxyethane is reported. The preparation and characterization of ethylene glycol monodiphenylmethyl ether, the main product from this reaction, is also reported as well as the preparation of the two diphenylmethyl monoethers of methyl 4,6-O ...
Sigthor Petursson
exaly +3 more sources
International Journal of Chemical Kinetics, 2013
ABSTRACTThe kinetics of the reaction of benzoic, 2‐methylbenzoic, phenylacetic, cyclohex‐1‐enecarboxylic, 2‐methylcyclohex‐1‐enecarboxylic, and cyclohex‐1‐eneacetic acids with diazodiphenylmethane was studied at 30, 33, 37, 40, and 45°C in a set of 12 protic and aprotic solvents. The reactions were found to follow the second‐order kinetics.
Nikolić, Jasmina, Ušćumlić, Gordana
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ABSTRACTThe kinetics of the reaction of benzoic, 2‐methylbenzoic, phenylacetic, cyclohex‐1‐enecarboxylic, 2‐methylcyclohex‐1‐enecarboxylic, and cyclohex‐1‐eneacetic acids with diazodiphenylmethane was studied at 30, 33, 37, 40, and 45°C in a set of 12 protic and aprotic solvents. The reactions were found to follow the second‐order kinetics.
Nikolić, Jasmina, Ušćumlić, Gordana
exaly +3 more sources
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
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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
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Diazodiphenylmethane, C13H10N2.
Journal of Synthetic Organic Chemistry, Japan, 1992 Yoshihiko HIRAYAMA, Yukitomo KOUNO
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Nature of the ortho effect. XI. Reaction rates of carboxylic acids with diazodiphenylmethane
Journal of Organic Chemistry, 1975exaly +2 more sources