AN ASYMMETRIC APPROACH TO PYRROLIDINONE AND PYRROLIZIDINONE SYSTEMS BY INTRAMOLECULAR OXIME-OLEFIN CYCLOADDITION

Authors
CHIACCHIO U CORSARO A PISTARA V RESCIFINA A ROMEO G ROMEO R
Citation
U. Chiacchio et al., AN ASYMMETRIC APPROACH TO PYRROLIDINONE AND PYRROLIZIDINONE SYSTEMS BY INTRAMOLECULAR OXIME-OLEFIN CYCLOADDITION, Tetrahedron, 52(23), 1996, pp. 7875-7884
Citations number
42
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
23
Year of publication
1996
Pages
7875 - 7884
Database
ISI
SICI code
0040-4020(1996)52:23<7875:AAATPA>2.0.ZU;2-7
Abstract
Homochiral functionalized pyrrolidinone and pyrrolizidinone systems ha ve been achieved by stereoselective intramolecular oxime-olefin cycloa ddition starting from homochiral amino acids, and by subsequent reduct ion of the obtained fused isoxazolidines. Copyright (C) 1996 Elsevier Science Ltd