Abstract

A facile and versatile catalyst-free method for the preparation of a wide range of pentasubstituted pyrroles has been reported using four-component reactions of arylglyoxal monohydrate, β-keto esters, amines, and various cyclic 1,3-dicarbonyls under mild reaction conditions. Employing this methodology, pseudo seven-component reactions have also been achieved in the case of <i>p</i>-phenylenediamine to provide conjugated bispyrroles with arene spacers.

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