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DOI: 10.1055/s-0040-1707247
Silylboranes as Powerful Tools in Organic Synthesis: Stereo- and Regioselective Reactions with 1,n-Enynes
Publication History
Received: 08 June 2020
Accepted after revision: 13 July 2020
Publication Date:
20 August 2020 (online)
Abstract
Bismetalated alkenes, accessible by element–element addition to alkynes, are valuable building blocks in organic synthesis, providing wide opportunities for divergent synthesis. Silaboration of alkynes with a pendant olefinic group, catalyzed by group 10 metal complexes, and subsequent transformation of the silicon and boron functional groups give access to densely functionalized 1,3-dienes and 1,3,5-trienes with defined stereo- and regiochemistry, 1,2-dienes, and carbocyclic and heterocyclic products.
1 Introduction
2 Background
3 Reactions with 1,3-Enynes
4 Cyclization 1,6-Enynes
5 Cyclization 1,7-Enynes
6 Cyclization of 1,n-Enynes (n > 7)
7 Cyclization of Dienynes and Enediynes
8 Cyclization of 1,6-Diynes
9 Conclusions
-
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Recent reports suggest that some boronic acids and boronic acid derivatives are mutagenic in vitro, however not in vivo: