Affordable Access

Publisher Website

Position specific α-tert-alkylation of ketones

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
20
Issue
16
Identifiers
DOI: 10.1016/s0040-4039(01)86168-2

Abstract

Abstract Lewis acid mediated α-tert-alkylation of ketones via their silyl enol ethers is possible utilizing a variety of branched tertiary alkyl halides. The latter react position specifically without undesired rearrangements.

There are no comments yet on this publication. Be the first to share your thoughts.