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Russian Chemical Reviews, 1963, Volume 32, Issue 2, Pages 75–93
DOI: https://doi.org/10.1070/RC1963v032n02ABEH001294
(Mi rcr1749)
 

This article is cited in 30 scientific papers (total in 30 papers)

Phenol–dienone rearrangement in the reactions of phenols

V. V. Ershov, A. A. Volod'kin, G. N. Bogdanov

Institute of Chemical Physics of the USSR Academy of Sciences, Moscow
Abstract: CONTENTS
I. Introduction 75
II. Effect of structure of phenol on ease of formation of dienone compounds 75
III. Halogenation of phenol. Tribromophenol bromide 78
IV. Halogenation of alkylphenols 79
V. Reactivity of quinohalide compounds. Problem of methylenequinone 82
VI. Nitration of phenols 84
VII. Alkylation of phenols 85
VIII. Formation of dienones in radical reactions of phenols 87
Document Type: Article
Language: English
Original paper language: Russian


Citation: V. V. Ershov, A. A. Volod'kin, G. N. Bogdanov, “Phenol–dienone rearrangement in the reactions of phenols”, Usp. Khim., 32:2 (1963), 154–194; Russian Chem. Reviews, 32:2 (1963), 75–93
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  • https://doi.org/10.1070/RC1963v032n02ABEH001294
  • https://www.mathnet.ru/eng/rcr/v32/i2/p154
  • This publication is cited in the following 30 articles:
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