Diastereoselectivity in Michael additions to a pyrrolidinyl enone

Citation
Rw. Bates et P. Kongsaeree, Diastereoselectivity in Michael additions to a pyrrolidinyl enone, SYNLETT, (8), 1999, pp. 1307-1309
Citations number
24
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
8
Year of publication
1999
Pages
1307 - 1309
Database
ISI
SICI code
0936-5214(199908):8<1307:DIMATA>2.0.ZU;2-3
Abstract
Michael additions of stabilized carabanions to an alpha-pyrrolidinylenone a re highly diastereoselective. Epoxidation is similarly selective.