BECKMANN REARRANGEMENT OF O-4-PENTENYL OXIME THROUGH N-BROMOSUCCINIMIDE-MEDIATED ACTIVATING PROCESS

Authors
KITAGAWA O FUJITA M OKADA M TAGUCHI T
Citation
O. Kitagawa et al., BECKMANN REARRANGEMENT OF O-4-PENTENYL OXIME THROUGH N-BROMOSUCCINIMIDE-MEDIATED ACTIVATING PROCESS, Chemical and Pharmaceutical Bulletin, 45(1), 1997, pp. 32-35
Citations number
20
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
Chemical and Pharmaceutical Bulletin → ACNP
ISSN journal
00092363
Volume
45
Issue
1
Year of publication
1997
Pages
32 - 35
Database
ISI
SICI code
0009-2363(1997)45:1<32:BROOOT>2.0.ZU;2-K
Abstract
Beckmann rearrangement of O-4-pentenyl oxime derivatives proceeds in g ood yield under mild conditions through the formation of a cationic te trahydrofuranium intermediate in the halocyclization reaction with N-b romosuccinimide.