AN ENANTIOSPECIFIC NITRONE CYCLOADDITION ROUTE TO 3-HYDROXY-2-AZETIDINONES

Authors
BASAK A BDOUR HMM BHATTACHARYA G
Citation
A. Basak et al., AN ENANTIOSPECIFIC NITRONE CYCLOADDITION ROUTE TO 3-HYDROXY-2-AZETIDINONES, Tetrahedron letters, 38(14), 1997, pp. 2535-2538
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
14
Year of publication
1997
Pages
2535 - 2538
Database
ISI
SICI code
0040-4039(1997)38:14<2535:AENCRT>2.0.ZU;2-O
Abstract
4-Aryl or heteroaryl 3-methylene beta-lactams 2a-2c underwenthighly st ereospecific cycloaddition with various nitrones 3a-3c. The method off ers an enantiospecific route to 3-hydroxy-beta-lactams. (C) 1997 Publi shed by Elsevier Science Ltd.