Abstract
Oxidative palladium couplings allow the preparation in high yields of different azepinoindole moieties. The use of CuCl2 as reoxidant leads to the formation of chloro derivatives instead of alkenes.
Keywords: Indole, palladium, oxidative cyclisation, oxidant
Letters in Organic Chemistry
Title: Preparation of Azepinoindole Derivatives via Oxidative Palladium Couplings
Volume: 2 Issue: 8
Author(s): Lionel Joucla, Cyril Montagne, Guy Fournet and Benoit Joseph
Affiliation:
Keywords: Indole, palladium, oxidative cyclisation, oxidant
Abstract: Oxidative palladium couplings allow the preparation in high yields of different azepinoindole moieties. The use of CuCl2 as reoxidant leads to the formation of chloro derivatives instead of alkenes.
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Cite this article as:
Joucla Lionel, Montagne Cyril, Fournet Guy and Joseph Benoit, Preparation of Azepinoindole Derivatives via Oxidative Palladium Couplings, Letters in Organic Chemistry 2005; 2 (8) . https://dx.doi.org/10.2174/157017805774717490
DOI https://dx.doi.org/10.2174/157017805774717490 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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