Abstract

A novel approach for the synthesis of pyrrole derivatives has been reported. The reactions starting from terminal alkynes, carbodiimides, and malononitrile using CuI, DBU, and TBPAc in anhydrous MeCN afforded the functionalized pyrroles in acceptable yields. Alkyl‐, aryl‐, and heteroaromatic terminal alkynes were tolerated. Carbodiimides could be symmetrical and unsymmetrical substrates with aryl or alkyl substituents. The reaction exhibited a good regioselectivity when unsymmetrical carbodiimides were employed.

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