Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271502 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
The allylation of various aldehydes with α-substituted allylsilanes in the presence of TiCl4 has been investigated. It has been shown that these reagents readily allow for good yields and high to excellent diastereoselectivities (up to >20:1) for a series of aldehydes, thereby providing a means of preparing non-conjugated (E)-homoallylic alcohols in a single step.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Aymara M.M. Albury, Michael P. Jennings,