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 |
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Output data | Year: 2014, Volume: 50, Number: 3, Pages: 367-370 Pages count : 4 DOI: 10.1134/S1070428014030117 | ||
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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
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
ArticleLinkType.TRANSLATED_TO_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
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 |