Affordable Access

Publisher Website

Enehydroxylamines as versatile compounds in 3,3-sigmatropic rearrangements

Authors
Journal
Tetrahedron Letters
0040-4039
Publisher
Elsevier
Publication Date
Volume
35
Issue
17
Identifiers
DOI: 10.1016/s0040-4039(00)77022-5

Abstract

Abstract Enehydroxylamines react readily, in the presence of base, with electrophiles containing unsaturation to afford intermediates that, either spontaneously or upon heating, lead via a 3,3-sigmatropic rearrangement to α-substituted products.

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