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Titolo:
SYNTHESIS OF QUINOLINES VIA INTRAMOLECULAR CYCLIZATION OF BENZYLACETONE OXIME DERIVATIVES CATALYZED WITH TETRABUTYLAMMONIUM PERRHENATE(VII)AND TRIFLUOROMETHANESULFONIC ACID
Autore:
KUSAMA H; YAMASHITA Y; NARASAKA K;
Indirizzi:
UNIV TOKYO,GRAD SCH SCI,DEPT CHEM,BUNKYO KU,7-3-1 HONGO TOKYO 113 JAPAN UNIV TOKYO,GRAD SCH SCI,DEPT CHEM,BUNKYO KU TOKYO 113 JAPAN
Titolo Testata:
Chemistry Letters
fascicolo: 1, , anno: 1995,
pagine: 5 - 6
SICI:
0366-7022(1995):1<5:SOQVIC>2.0.ZU;2-5
Fonte:
ISI
Lingua:
ENG
Soggetto:
BECKMANN REARRANGEMENT; SULFONATE;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
12
Recensione:
Indirizzi per estratti:
Citazione:
H. Kusama et al., "SYNTHESIS OF QUINOLINES VIA INTRAMOLECULAR CYCLIZATION OF BENZYLACETONE OXIME DERIVATIVES CATALYZED WITH TETRABUTYLAMMONIUM PERRHENATE(VII)AND TRIFLUOROMETHANESULFONIC ACID", Chemistry Letters, (1), 1995, pp. 5-6

Abstract

Intramolecular cyclization reaction on the nitrogen atom of benzylacetone oxime derivatives, which have electron donating group(s) on the phenyl group, proceeds by treatment with tetrabutylammonium perrhenate,trifluoromethanesulfonic acid, and 4-chloranil in refluxing 1,2-dichloroethane to afford quinoline derivatives in good yield.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/11/17 alle ore 05:51:51