| 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, 
											