THE ASYMMETRIC-SYNTHESIS OF NOVEL TIN-FUNCTIONALIZED CARBAPENAM SYSTEMS THROUGH RADICAL CYCLIZATION OF ENYNE BETA-LACTAMS

Authors
ALCAIDE B BENITO JL RODRIGUEZCAMPOS IM RODRIGUEZLOPEZ J RODRIGUEZVICENTE A SIERRA MA GARCIAGRANDA S GUTIERREZRODRIGUEZ A
Citation
B. Alcaide et al., THE ASYMMETRIC-SYNTHESIS OF NOVEL TIN-FUNCTIONALIZED CARBAPENAM SYSTEMS THROUGH RADICAL CYCLIZATION OF ENYNE BETA-LACTAMS, Tetrahedron : asymmetry, 6(5), 1995, pp. 1055-1058
Citations number
31
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
5
Year of publication
1995
Pages
1055 - 1058
Database
ISI
SICI code
0957-4166(1995)6:5<1055:TAONTC>2.0.ZU;2-G
Abstract
New chiral, non-racemic, vinylstannyl carbapenams 2 are easily-accessi ble by the regio- and stereocontrolled tin-mediated, vinyl radical int ramolecular cyclization of enyne beta-lactams 1.