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Russian Chemical Reviews, 1995, Volume 64, Issue 1, Pages 25–46
DOI: https://doi.org/10.1070/RC1995v064n01ABEH000135
(Mi rcr1211)
 

This article is cited in 5 scientific papers (total in 5 papers)

Silicon-containing alka-1,3-dienes and their functional derivatives in organic synthesis

M. D. Stadnichuk, T. I. Voropaeva

State Technological Institute of St. Petersburg
English full-text Citations (5)
Abstract: Data on the synthesis and chemical reactions of silicon-containing 1,3-dienes are surveyed for the first time in the present review. It is shown that the addition reactions of 1- and 2-triorganosilylalka-1,3-dienes and their derivatives are the most interesting and promising in fine organic synthesis. The application of the trialkylsilyl group as a protecting group and as a new reaction centre, which makes it possible to obtain carbon–carbon or carbon–heteroatom bonds, is examined. It has been found that the double bonds remote from the silicon atom are the most reactive in addition reactions and that regardless of the nature of the reagent the attacking species always binds to the terminal carbon atom of the buta-1,3-diene fragment. The bibliography includes 329 references.
Received: 18.03.1994
Russian version:
Uspekhi Khimii, 1995, Volume 64, Issue 1, Pages 28–50
DOI: https://doi.org/10.1070/RC1995v064n01ABEH000135
Bibliographic databases:
Document Type: Article
UDC: 547.345
Language: English
Original paper language: Russian


Citation: M. D. Stadnichuk, T. I. Voropaeva, “Silicon-containing alka-1,3-dienes and their functional derivatives in organic synthesis”, Usp. Khim., 64:1 (1995), 28–50; Russian Chem. Reviews, 64:1 (1995), 25–46
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