Issue 1, 2001

Conjugate additions of heteronucleophiles to enones and alkynoates. A ‘benign by design’ functionalization of heteroaromatics

Abstract

A simple and convenient functionalization of pyrrole and thiophene nuclei has been accomplished by one-step clay-catalyzed conjugate addition reactions of these heteroaromatics with some enones and alkynoates under very mild conditions. The experimental protocol can be easily modified to accommodate one or two alkyl groups.

Article information

Article type
Paper
Submitted
01 Nov 2000
First published
17 Jan 2001

Green Chem., 2001,3, 26-29

Conjugate additions of heteronucleophiles to enones and alkynoates. A ‘benign by design’ functionalization of heteroaromatics

M. Avalos, R. Babiano, J. L. Bravo, P. Cintas, J. L. Jiménez, J. C. Palacios and M. A. Silva, Green Chem., 2001, 3, 26 DOI: 10.1039/B008795P

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