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Oxidative dimerization of 2,6-Di-tert-butyl-4-(2-hydroxyethyl)phenol Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2014, Volume: 50, Number: 3, Pages: 367-370 Pages count : 4 DOI: 10.1134/S1070428014030117
Authors Krysin A.P. 1 , Genaev A.M. 1 , Pokrovskii L.M. 1 , Shakirov M.M. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: 2,6-Di-tert-butyl-4-(2-hydroxyethyl)phenol undergoes oxidative self-coupling by the action of K3Fe(CN)(6) in alkaline medium at room temperature to give 7,9-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxyphenyl)-1-hydroxymethyl-2-oxaspiro[4.5]deca-6,9-dien-8-one. The composition of the reaction products has been determined, and the mechanism of their formation is discussed.
Cite: Krysin A.P. , Genaev A.M. , Pokrovskii L.M. , Shakirov M.M.
Oxidative dimerization of 2,6-Di-tert-butyl-4-(2-hydroxyethyl)phenol
Russian Journal of Organic Chemistry. 2014. V.50. N3. P.367-370. DOI: 10.1134/S1070428014030117 WOS Scopus РИНЦ OpenAlex
Original: Крысин А.П. , Генаев А.М. , Покровский Л.М. , Шакиров М.М.
Окислительное сдваивание 4-(2-гидроксиэтил)-2,6-ди- трет-бутилфенола
Журнал органической химии (RUSS J ORG CHEM+). 2014. Т.50. №3. С.378-381. РИНЦ
Dates:
Published print: Mar 1, 2014
Published online: Apr 23, 2014
Identifiers:
Web of science: WOS:000334998300011
Scopus: 2-s2.0-84900827710
Elibrary: 21878076
OpenAlex: W2008277769
Citing:
DB Citing
Web of science 1
Scopus 2
Elibrary 2
OpenAlex 3
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