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.