Sciact
  • EN
  • RU

Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2013, Volume: 49, Number: 10, Pages: 1409-1414 Pages count : 6 DOI: 10.1134/S1070428013100011
Authors Ishmuratov G.Yu. 1 , Legostaeva Yu.V. 1 , Garifullina L.R. 1 , Botsman L.P. 1 , Idrisova Z.I. 1 , Muslukhov R.R. 1 , Ishmuratova N.M. 1 , Tolstikov G.A. 2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Ufa Res Ctr, Inst Organ Chem, Ufa 450054, Bashkortostan, Russia
2 (Данные Web of science) Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: Hydroxylamine and semicarbazide hydrochlorides were shown to be efficient as reducing agents toward peroxide products of ozonolysis of various olefins with different degrees of substitution. The rate of the transformations aldehyde -> aldehyde oxime -> nitrile -> ester upon treatment of peroxides with hydroxylamine hydrochloride in isopropyl alcohol was lower than in methanol.
Cite: Ishmuratov G.Y. , Legostaeva Y.V. , Garifullina L.R. , Botsman L.P. , Idrisova Z.I. , Muslukhov R.R. , Ishmuratova N.M. , Tolstikov G.A.
Transformations of peroxide olefin ozonolysis products under the action of hydroxylamine and semicarbazide hydrochlorides in isopropyl alcohol
Russian Journal of Organic Chemistry. 2013. V.49. N10. P.1409-1414. DOI: 10.1134/S1070428013100011 WOS Scopus РИНЦ OpenAlex
Original: Ишмуратов Г.Ю. , Мясоедова Ю.В. , Гарифуллина Л.Р. , Боцман Л.П. , Идрисова З.И. , Муслухов Р.Р. , Ишмуратова Н.М. , Толстиков Г.А.
Превращения перекисных продуктов озонолиза олефинов при действии гидрохлоридов гидроксиламина и семикарбазида в изопропиловом спирте
Журнал органической химии (RUSS J ORG CHEM+). 2013. Т.49. №10. С.1433-1438. РИНЦ
Dates:
Published print: Oct 1, 2013
Published online: Nov 8, 2013
Identifiers:
Web of science: WOS:000326813100001
Scopus: 2-s2.0-84889057077
Elibrary: 21897041
OpenAlex: W2091081586
Citing:
DB Citing
Web of science 10
Scopus 9
Elibrary 9
OpenAlex 10
Altmetrics: