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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 39, 2009 - Issue 17
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Original Articles

Polyaniline-Anchored Metal Salts for Michael Reaction of α,β-Unsaturated Ketones

, , &
Pages 3016-3023 | Received 23 Oct 2008, Published online: 03 Aug 2009
 

Abstract

A catalyst consisting of polyaniline-anchored metal salts is used as a Lewis acid to promote the Michael reaction of α,β-unsaturated ketones. The reaction is performed efficiently with imidazole, acetyl acetone, and ethyl acetate as Michel donors and chalcones as the acceptors under ultrasound irradiation.

ACKNOWLEDGMENTS

We thank Prof. S. Devi and Prof. B. V. Kamath for providing laboratory facilities and for suggestions and encouragement.

Notes

Note. All the reactions were run in an ultrasonic bath for 2 h in 1,2-dichloroethane.

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