Diels–Alder Reactions of 2-Vinylindoles with Cyclic Dienophiles: Synthesis of [c]-Annulated Tetrahydrocarbazoles
Articolo
Data di Pubblicazione:
2012
Citazione:
Diels–Alder Reactions of 2-Vinylindoles with Cyclic Dienophiles: Synthesis of
[c]-Annulated Tetrahydrocarbazoles / V. Pirovano, G. Abbiati, M. Dell'Acqua, D. Facoetti, M. Giordano, E. Rossi. - In: SYNLETT. - ISSN 0936-5214. - 23:20(2012), pp. 2913-2918.
Abstract:
Diels–Alder reactions of 2-vinylindoles with cyclic carbo-
and heterodienophiles, in the presence of suitable Lewis acids,
led to uncommon [c]-carbo- and furoannulated tetrahydrocarbazoles.
The obtained compounds encompass a carbonyl group in an
angular position, suitable for further transformations, and represent
useful intermediates for the synthesis of more complex structures.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Diels-Alder reaction; heterocycles; indoles; Lewis acids; polycycles
Elenco autori:
V. Pirovano, G. Abbiati, M. Dell'Acqua, D. Facoetti, M. Giordano, E. Rossi
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