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Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

PdCl2 Immobilized in Ionic Liquids: A Novel and Efficient Catalytic System for Michael Additions of Indoles to ,α,β-Unsaturated Ketones

Author(s): Xufeng Lin, Sunliang Cui and Yanguang Wang

Volume 3, Issue 5, 2006

Page: [414 - 418] Pages: 5

DOI: 10.2174/157017806776611881

Price: $65

Abstract

Palladium(II) chloride immobilized in ionic liquid [bmim][BF4] catalyzes the Michael reaction of indoles with α,β-unsaturated ketones to afford the corresponding β-indolylketones in excellent yields. The reaction proceeds at 0.1 mol% of Pd loading with high efficiency and great selectivity. The possible mechanism of the reaction was suggested.

Keywords: Palladium(II) chloride, Michael-addition, ionic liquid, indole, α,β-unsaturated ketones

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