THE RING-CLOSURE OF SUBSTITUTED AZETIDINONES - A NEW ROUTE TO [4.2.0]FUSED BETA-LACTAMS

Authors
TERNANSKY RJ JORDAN CL
Citation
Rj. Ternansky et Cl. Jordan, THE RING-CLOSURE OF SUBSTITUTED AZETIDINONES - A NEW ROUTE TO [4.2.0]FUSED BETA-LACTAMS, Bioorganic & medicinal chemistry letters, 3(11), 1993, pp. 2443-2446
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Medicinal
Journal title
Bioorganic & medicinal chemistry letters → ACNP
ISSN journal
0960894X
Volume
3
Issue
11
Year of publication
1993
Pages
2443 - 2446
Database
ISI
SICI code
0960-894X(1993)3:11<2443:TROSA->2.0.ZU;2-8
Abstract
The synthesis of 1-carba-1-dethiacephalosporin nuclei is described. Th e new route utilizes a readily-available penicillin derivative as star ting material and features an intramolecular ring closure to form the six-membered ring.