Regioselective Diels-Alder Reactions of 3-Vinylindoles with Quinones

Miguel A. Alonso; Pilar Lopez-Alvarado; Carmen Avendano; J. Carlos Menendez

doi:10.2174/1570178043488635

ISSN: 1570-1786
E-ISSN: 1875-6255

Regioselective Diels-Alder Reactions of 3-Vinylindoles with Quinones
Authors: Miguel A. Alonso¹, Pilar Lopez-Alvarado², Carmen Avendano³ and J. Carlos Menendez⁴
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¹ Departamento de Quimica Organica y Farmaceutica, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain. ² Departamento de Quimica Organica y Farmaceutica, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain. ³ Departamento de Quimica Organica y Farmaceutica, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain. ⁴ Departamento de Quimica Organica y Farmaceutica, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain.
Source: Letters in Organic Chemistry, Volume 1, Issue 1, Jan 2004, p. 20 - 22
DOI: https://doi.org/10.2174/1570178043488635
- Available online: 01 Jan 2004

Abstract

The Diels-Alder reactions of in situ generated vinylindoles and several non-symmetrical quinones, such as 2,5,8(1H)-quinolinetriones and 6-bromoquinolinequinones, were found to be regioselective.

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2004-01-01

2025-10-04

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Article Type: Review Article

Keyword(s): diels-alder reactions; quinolinones; quinones; vinylindoles

Regioselective Diels-Alder Reactions of 3-Vinylindoles with Quinones

Abstract

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