DIASTEREOSELECTIVE RADICAL-ADDITION TO METHYLENEOXAZOLIDINONES - AN ENANTIOSELECTIVE ROUTE TO ALPHA-AMINO-ACIDS

Citation
Jr. Axon et Alj. Beckwith, DIASTEREOSELECTIVE RADICAL-ADDITION TO METHYLENEOXAZOLIDINONES - AN ENANTIOSELECTIVE ROUTE TO ALPHA-AMINO-ACIDS, Journal of the Chemical Society, Chemical Communications, (5), 1995, pp. 549-550
Citations number
16
Categorie Soggetti
Chemistry
ISSN journal
00224936
Issue
5
Year of publication
1995
Pages
549 - 550
Database
ISI
SICI code
0022-4936(1995):5<549:DRTM-A>2.0.ZU;2-G
Abstract
The diastereoselectivity of radical addition to methyleneoxazolidinone s depends on the nature of the addend radical and of the N-protecting group; the reaction provides a convenient enantioselective route to al pha-amino acids.