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The asymmetric synthesis of 2,3-benzocarbapenems by intramolecular aryl radical cyclizations

Authors
Journal
Tetrahedron Asymmetry
0957-4166
Publisher
Elsevier
Publication Date
Volume
7
Issue
8
Identifiers
DOI: 10.1016/0957-4166(96)00271-6

Abstract

Abstract Racemic and enantiomerically pure 2,3-benzocarbapenems 1 are obtained in good yields by the tin-mediated, intramolecular aryl radical cyclizations of the readily available 4-alkenyl- N-(2-halogenophenyl)-β-lactams 2.

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