37056-34-1Relevant articles and documents
Transformations of peroxide products of oleic acid ozonolysis at treatment with hydroxylamine and semicarbazide hydrochlorides
Ishmuratov, G. Yu.,Yakovleva,Botsman,Legostaeva, Yu. V.,Nazarov,Baidimirov
, p. 610 - 614 (2015/07/02)
Peroxide products of oleic acid ozonolysis treated with semicarbazide and hydroxylamine hydrochlorides in methanol are predominantly converted into methyl nonanoate and dimethyl nonanedioate, in 2-propanol, into isopropyl nonanoate and monoisopropyl ester of nonanedioic acid, and also into nonanenitrile, in tetrahydrofuran and in a mixture of acetic acid with dichloromethane, into nonanoic and nonanedioc acids, and also in nonanal oxime and 9-(hydroxyimino)nonanoic acid.
Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid
Ishmuratov,Legostaeva,Garifullina,Botsman,Muslukhov,Tolstikov
, p. 1075 - 1081 (2015/02/02)
Hydrochlorides of hydroxylamine and semicarbazide efficiently reduce peroxide products of olefin ozonolysis in a system CH2Cl2-AcOH leading to the formation of carboxylic acids and their derivatives. The application of water as the solvent component favors the increase in the fraction of nitrogen-containing organic compounds (semicarbazones, keto- and aldoximes, nitriles) and reduction in the yield of carboxylic acids.
Polar Effects in Free-radical Reactions; Reductive Alkylation of Olefins Conjugated with Electron-withdrawing Groups: Kinetics and Mechanism
Citterio, Attilio,Minisci, Francesco,Serravalle, Marco
, p. 2174 - 2189 (2007/10/02)
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