A NOVEL FRAGMENTATION OF THE BETA-LACTAM RING - STEREOSELECTIVE ENTRYTO VINYL ETHERS BY REACTION OF N-(ARYLIDENE(OR N-ALKYLIDENE)AMINO)-2-AZETIDINONES WITH OZONE

Authors
ALCAIDE B MIRANDA M PEREZCASTELLS J POLANCO C SIERRA MA
Citation
B. Alcaide et al., A NOVEL FRAGMENTATION OF THE BETA-LACTAM RING - STEREOSELECTIVE ENTRYTO VINYL ETHERS BY REACTION OF N-(ARYLIDENE(OR N-ALKYLIDENE)AMINO)-2-AZETIDINONES WITH OZONE, Anales de quimica, 89(1), 1993, pp. 139-140
Citations number
7
Categorie Soggetti
Chemistry
Journal title
Anales de quimica → ACNP
ISSN journal
11302283
Volume
89
Issue
1
Year of publication
1993
Pages
139 - 140
Database
ISI
SICI code
1130-2283(1993)89:1<139:ANFOTB>2.0.ZU;2-T
Abstract
Title compounds undergo a novel 2-azetidinone ring fragmentation by re action with ozone followed by NaBH4 workup to stereoselectively yield vinyl ethers in fairly good yields.