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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:
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- 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