METALLOPORPHYRIN-CATALYZED REARRANGEMENT OF OXAZIRIDINES - AN EFFICIENT AND REGIOSELECTIVE SYNTHESIS OF LACTAMS USING RING-ENLARGEMENT OF N-PHENYL-SPIROOXAZIRIDINES

Authors
SUDA K SASHIMA M IZUTSU M HINO F
Citation
K. Suda et al., METALLOPORPHYRIN-CATALYZED REARRANGEMENT OF OXAZIRIDINES - AN EFFICIENT AND REGIOSELECTIVE SYNTHESIS OF LACTAMS USING RING-ENLARGEMENT OF N-PHENYL-SPIROOXAZIRIDINES, Journal of the Chemical Society, Chemical Communications, (8), 1994, pp. 949-950
Citations number
21
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
8
Year of publication
1994
Pages
949 - 950
Database
ISI
SICI code
0022-4936(1994):8<949:MROO-A>2.0.ZU;2-2
Abstract
Manganese(iii) tetraphenylporphyrin, Mn(tpp)Cl, is a new and specific catalyst for stereo- and regio-selective rearrangement of N-phenyl-spi rooxaziridines into lactams.