THE ASYMMETRIC-SYNTHESIS OF 2,3-BENZOCARBAPENEMS BY INTRAMOLECULAR ARYL RADICAL CYCLIZATIONS

Authors
ALCAIDE B MORENO AM RODRIGUEZVICENTE A SIERRA MA
Citation
B. Alcaide et al., THE ASYMMETRIC-SYNTHESIS OF 2,3-BENZOCARBAPENEMS BY INTRAMOLECULAR ARYL RADICAL CYCLIZATIONS, Tetrahedron : asymmetry, 7(8), 1996, pp. 2203-2206
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
7
Issue
8
Year of publication
1996
Pages
2203 - 2206
Database
ISI
SICI code
0957-4166(1996)7:8<2203:TAO2BI>2.0.ZU;2-2
Abstract
Racemic and enantiomerically pure 2,3-benzocarbapenems 1 are obtained in good yields by the tin-mediated, intramolecular aryl radical cycliz ations of the readily available 4-alkenyl-N-(2-halogenophenyl)-beta-la ctams 2. Copyright (C) 1996 Elsevier Science Ltd