Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5224690 | Tetrahedron | 2009 | 6 Pages |
Abstract
Allylic ethers undergo insertions of silylenes into C-O bonds to form allylic silanes. Silylene insertion into C-O acetal bonds was also observed. Formation of silylene ylide intermediates led to [1,2]-Stevens rearrangement products as well as [2,3]-sigmatropic products depending upon the steric environment of the starting allylic ether.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Laura E. Bourque, Pamela A. Haile, Janice M.N. Loy, K.A. Woerpel,