Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5277868 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
A diverse array of nitrosoalkenes derived from both acyclic and cyclic ketones, as well as aldehydes, via the Denmark protocol using α-chloro-O-TBS-oximes can be trapped efficiently in situ by a wide variety of potassium ester enolates to afford conjugate addition products in good yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Puhui Li, Max M. Majireck, Jason A. Witek, Steven M. Weinreb,