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Russian Chemical Reviews, 1987, Volume 56, Issue 2, Pages 152–162
DOI: https://doi.org/10.1070/RC1987v056n02ABEH003263
(Mi rcr3780)
 

This article is cited in 6 scientific papers (total in 6 papers)

The 1,3-Anionic Cycloaddition Reactions of αβ-Unsaturated Thiolates and Their Analogues

M. L. Petrov, A. A. Petrov

Leningrad Technological Institute
English full-text Citations (6)
Abstract: The reactions of αβ-unsaturated alkali metal thiolates and the analogous salts of selenols and tellurols involving the 1,3-anionic cycloaddition mechanism are examined. The principal factors determining the capacity of the unsaturated triad anions for 1,3-anionic cycloaddition are identified and surveyed, which makes it possible to predict the mode of the reactions of these compounds.
The bibliography includes 93 references.
Russian version:
Uspekhi Khimii, 1987, Volume 56, Issue 2, Pages 267–286
DOI: https://doi.org/10.1070/RC1987v056n02ABEH003263
Bibliographic databases:
Document Type: Article
UDC: 547.367
Language: English
Original paper language: Russian


Citation: M. L. Petrov, A. A. Petrov, “The 1,3-Anionic Cycloaddition Reactions of αβ-Unsaturated Thiolates and Their Analogues”, Usp. Khim., 56:2 (1987), 267–286; Russian Chem. Reviews, 56:2 (1987), 152–162
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  • https://www.mathnet.ru/eng/rcr/v56/i2/p267
  • This publication is cited in the following 6 articles:
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