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Titolo:
BECKMANN REARRANGEMENT OF O-4-PENTENYL OXIME THROUGH N-BROMOSUCCINIMIDE-MEDIATED ACTIVATING PROCESS
Autore:
KITAGAWA O; FUJITA M; OKADA M; TAGUCHI T;
Indirizzi:
TOKYO COLL PHARM,1432-1 HORINOUCHI HACHIOJI TOKYO 19203 JAPAN TOKYO COLL PHARM HACHIOJI TOKYO 19203 JAPAN TOKYO WOMENS MED COLL,SHINJUKU KU TOKYO 162 JAPAN
Titolo Testata:
Chemical and Pharmaceutical Bulletin
fascicolo: 1, volume: 45, anno: 1997,
pagine: 32 - 35
SICI:
0009-2363(1997)45:1<32:BROOOT>2.0.ZU;2-K
Fonte:
ISI
Lingua:
ENG
Soggetto:
ALPHA-IODINATION; TETRABUTYLAMMONIUM PERRHENATE(VII); TRIFLUOROMETHANESULFONIC ACID; CARBOXAMIDES; DERIVATIVES;
Keywords:
BECKMANN REARRANGEMENT; HALOCYCLIZATION; TETRAHYDROFURANIUM; N-BROMOSUCCINIMIDE; O-4-PENTENYL OXIME;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Science Citation Index Expanded
Citazioni:
20
Recensione:
Indirizzi per estratti:
Citazione:
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

Abstract

Beckmann rearrangement of O-4-pentenyl oxime derivatives proceeds in good yield under mild conditions through the formation of a cationic tetrahydrofuranium intermediate in the halocyclization reaction with N-bromosuccinimide.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/11/17 alle ore 05:48:12