INTRAMOLECULAR NITRONE CYCLOADDITION - STEREOSELECTIVE SYNTHESIS OF PIPERIDINE SYSTEMS

Authors
CHIACCHIO U RESCIFINA A CASUSCELLI F PIPERNO A PISANI V ROMEO R
Citation
U. Chiacchio et al., INTRAMOLECULAR NITRONE CYCLOADDITION - STEREOSELECTIVE SYNTHESIS OF PIPERIDINE SYSTEMS, Tetrahedron, 52(45), 1996, pp. 14311-14322
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
45
Year of publication
1996
Pages
14311 - 14322
Database
ISI
SICI code
0040-4020(1996)52:45<14311:INC-SS>2.0.ZU;2-5
Abstract
A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting f rom beta-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused delta-lactams. Copyright (C) 1996 Published by Els evier Science Ltd