RING-OPENING OF CARBOXY-SUBSTITUTED ISOXAZOLIDINES - SYNTHESIS OF LACTONES AND ALPHA-HYDROXY-GAMMA-LACTAMS

Authors
CASUSCELLI F DIBELLA MR FICARRA R MELARDI S ROMEO G CHIACCHIO U RESCIFINA A
Citation
F. Casuscelli et al., RING-OPENING OF CARBOXY-SUBSTITUTED ISOXAZOLIDINES - SYNTHESIS OF LACTONES AND ALPHA-HYDROXY-GAMMA-LACTAMS, Gazzetta chimica italiana, 127(7), 1997, pp. 367-371
Citations number
17
Categorie Soggetti
Chemistry
Journal title
Gazzetta chimica italiana → ACNP
ISSN journal
00165603
Volume
127
Issue
7
Year of publication
1997
Pages
367 - 371
Database
ISI
SICI code
0016-5603(1997)127:7<367:ROCI-S>2.0.ZU;2-G
Abstract
The synthetic possibilities offered by isoxazolidines containing a car boxy group at various position of the N,O-ring have been exploited. A new easy entry towards substituted delta-lactones is described.