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Titolo:
ELECTRON TRANSFER-CATALYZED DIELS-ALDER REACTIONS WITH 2-VINYLINDOLES
Autore:
WIEST O; STECKHAN E;
Indirizzi:
UNIV BONN,INST ORGAN CHEM & BIOCHEM,GERHARD DOMAGKSTR 1 W-5300 BONN 1GERMANY UNIV BONN,INST ORGAN CHEM & BIOCHEM,GERHARD DOMAGKSTR 1 W-5300 BONN 1GERMANY
Titolo Testata:
Angewandte Chemie, International Edition in English
fascicolo: 6, volume: 32, anno: 1993,
pagine: 901 - 903
SICI:
0570-0833(1993)32:6<901:ETDRW2>2.0.ZU;2-D
Fonte:
ISI
Lingua:
ENG
Soggetto:
HETERO-COPE REARRANGEMENTS; ORGANIC-SYNTHESIS; INDOLE; VINYLINDOLES; DERIVATIVES; ADDITIONS; ACCESS; IONS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
33
Recensione:
Indirizzi per estratti:
Citazione:
O. Wiest e E. Steckhan, "ELECTRON TRANSFER-CATALYZED DIELS-ALDER REACTIONS WITH 2-VINYLINDOLES", Angewandte Chemie, International Edition in English, 32(6), 1993, pp. 901-903

Abstract

A Diels-Alder reaction between two electron-rich components is possible with electron transfer catalysis. 2-vinylindole radical cations generated in this way react with 1,3-cyclohexadienes to yield highly substituted carbazole derivatives such as 1. This reaction is interesting above all for the synthesis of indole alkaloids. R1-R3 are, are for example, H, Me, iPr, Ph.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/12/20 alle ore 16:33:18