Issue 21, 2014

Synthesis of multi-substituted pyrroles using enamides and alkynes catalyzed by Pd(OAc)2 with molecular oxygen as an oxidant

Abstract

A cyclization reaction between enamides and alkynes catalyzed by palladium(II) acetate is described. In this method, the molecular oxygen serves as an efficient oxidant for the Pd(II)/Pd(0) catalytic cycle. The simple reaction conditions permit this methodology to be used as a general tool for the preparation of multi-substituted pyrroles.

Graphical abstract: Synthesis of multi-substituted pyrroles using enamides and alkynes catalyzed by Pd(OAc)2 with molecular oxygen as an oxidant

Supplementary files

Article information

Article type
Communication
Submitted
21 Dec 2013
Accepted
23 Jan 2014
First published
23 Jan 2014

Chem. Commun., 2014,50, 2784-2786

Author version available

Synthesis of multi-substituted pyrroles using enamides and alkynes catalyzed by Pd(OAc)2 with molecular oxygen as an oxidant

Y. Xu, T. He, Q. Zhang and T. Loh, Chem. Commun., 2014, 50, 2784 DOI: 10.1039/C3CC49683J

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