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.
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
Linking options:
https://www.mathnet.ru/eng/rcr3780
https://doi.org/10.1070/RC1987v056n02ABEH003263
https://www.mathnet.ru/eng/rcr/v56/i2/p267
This publication is cited in the following 6 articles:
R. Maadadi, L. M. Pevzner, M. L. Petrov, Russ J Gen Chem, 87:2 (2017), 259
Anna G. Lyapunova, Mikhail L. Petrov, Dmitry A. Androsov, Org. Lett., 15:7 (2013), 1744
M. L. Petrov, A. V. Belyakov, Russ J Gen Chem, 75:7 (2005), 1142
V. P. Litvinov, V. D. Dyachenko, Russian Chem. Reviews, 66:11 (1997), 923–951
Boris A. Trofimov, Bagrat A. Shainyan, PATAI'S Chemistry of Functional Groups, Sulphur‐Containing Functional Groups (1993), 1993, 659
Annual Reports in Organic Synthesis–1987, 1988, 427
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