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Stable Methylenequinones

Aleksandr Aleksandrovich Volod'kin 1
Aleksandr Aleksandrovich Volod'kin
, 
Vladimir Vladimirovich Ershov 1
Vladimir Vladimirovich Ershov
1 Institute of Chemical Physics of the USSR Academy of Sciences, Moscow
Published 30 November 1987
Communication , Volume 57, Issue 4, 336-349
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Volod'kin A. A., Ershov V. V. Stable Methylenequinones // Russian Chemical Reviews. 1988. Vol. 57. No. 4. pp. 336-349.
GOST all authors (up to 50)
Volod'kin A. A., Ershov V. V. Stable Methylenequinones // Russian Chemical Reviews. 1988. Vol. 57. No. 4. pp. 336-349.
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TY - JOUR
DO - 10.1070/RC1988v057n04ABEH003354
UR - https://rcr.colab.ws/publications/10.1070/RC1988v057n04ABEH003354
TI - Stable Methylenequinones
T2 - Russian Chemical Reviews
AU - Volod'kin, Aleksandr Aleksandrovich
AU - Ershov, Vladimir Vladimirovich
PY - 1988
DA - 1987/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 336-349
IS - 4
VL - 57
ER -
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@article{1988_Volod'kin,
author = {Aleksandr Aleksandrovich Volod'kin and Vladimir Vladimirovich Ershov},
title = {Stable Methylenequinones},
journal = {Russian Chemical Reviews},
year = {1988},
volume = {57},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1988v057n04ABEH003354},
number = {4},
pages = {336--349},
doi = {10.1070/RC1988v057n04ABEH003354}
}
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Volod'kin, Aleksandr Aleksandrovich, and Vladimir Vladimirovich Ershov. “Stable Methylenequinones.” Russian Chemical Reviews, vol. 57, no. 4, Nov. 1988, pp. 336-349. https://rcr.colab.ws/publications/10.1070/RC1988v057n04ABEH003354.
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Abstract

Data obtained in studies on the chemistry of a vigorously developing class of conjugated compounds (methylenequinones) are surveyed. The structure of these compounds and the influence of substituents on their properties and reactivity are discussed. Typical methods of synthesis of methylenequinones are described and the mechanism of their formation as well as the interconversions of methylenequinones and the corresponding phenols in radical and heterolytic reactions are considered.
The bibliography includes 144 references.