ASYMMETRIC-SYNTHESIS OF CIS-3-PHTHALIMIDO-4-STYRYL-2-AZETIDINONES - APPLICATION OF A NEW CHIRAL N-PROTECTING GROUP IN MONOBACTAM CHEMISTRY

Authors
GUNDA TE SZTARICSKAI F
Citation
Te. Gunda et F. Sztaricskai, ASYMMETRIC-SYNTHESIS OF CIS-3-PHTHALIMIDO-4-STYRYL-2-AZETIDINONES - APPLICATION OF A NEW CHIRAL N-PROTECTING GROUP IN MONOBACTAM CHEMISTRY, Bioorganic & medicinal chemistry letters, 3(11), 1993, pp. 2379-2382
Citations number
7
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
2379 - 2382
Database
ISI
SICI code
0960-894X(1993)3:11<2379:AOC-A>2.0.ZU;2-N
Abstract
-dihydroxy-2-propyl)-3-phthalimido-4-styrylazetidi n-2-ones (6a-d), ob tained in optically pure form via chiral Staudinger reactions, were tr ansformed to the N-deprotected derivatives (8a,b) by means of a two-st ep oxidative procedure.