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2000
Volume 3, Issue 5
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

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.

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/content/journals/loc/10.2174/157017806776611881
2006-05-01
2025-09-16
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