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The Reactivity of Epithio-compounds

Alexandr Vasil'evich Fokin 1
Alexandr Vasil'evich Fokin
, 
Aleksei Filippovich Kolomiets 1
Aleksei Filippovich Kolomiets
1 A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
10.1070/RC1976v045n01ABEH002590
Published 30 November 1975
Communication , Volume 45, Issue 1, 25-42
21
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Fokin A. V., Kolomiets A. F. The Reactivity of Epithio-compounds // Russian Chemical Reviews. 1976. Vol. 45. No. 1. pp. 25-42.
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Fokin A. V., Kolomiets A. F. The Reactivity of Epithio-compounds // Russian Chemical Reviews. 1976. Vol. 45. No. 1. pp. 25-42.
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TY - JOUR
DO - 10.1070/RC1976v045n01ABEH002590
UR - https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002590
TI - The Reactivity of Epithio-compounds
T2 - Russian Chemical Reviews
AU - Fokin, Alexandr Vasil'evich
AU - Kolomiets, Aleksei Filippovich
PY - 1976
DA - 1975/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 25-42
IS - 1
VL - 45
ER -
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@article{1976_Fokin,
author = {Alexandr Vasil'evich Fokin and Aleksei Filippovich Kolomiets},
title = {The Reactivity of Epithio-compounds},
journal = {Russian Chemical Reviews},
year = {1976},
volume = {45},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002590},
number = {1},
pages = {25--42},
doi = {10.1070/RC1976v045n01ABEH002590}
}
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Fokin, Alexandr Vasil'evich, and Aleksei Filippovich Kolomiets. “The Reactivity of Epithio-compounds.” Russian Chemical Reviews, vol. 45, no. 1, Nov. 1976, pp. 25-42. https://rcr.colab.ws/publications/10.1070/RC1976v045n01ABEH002590.
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Abstract

The available information about the reactions of epithio-compounds with nucleophilic and electrophilic agents, about the homolytic reactions of alkene sulphides, and about reactions leading to the elimination of sulphur with formation of alkenes is examined, the mechanisms of the opening of thiiran rings are discussed, and the comparative characteristics of the reactivities of O- and S-heteroanalogues of cyclopropane compounds are given.
The bibliography includes 276 references.