Pyrroles are important building blocks in natural products and medicinal chemistry; they can be linked together in various ways to make a multitude of functional oligomers and macrocycles. One simple way in which pyrroles have not previously been linked together, is through the beta-positions of two pyrroles to make a chalcone. To address this knowledge gap, we report herein an efficient method for synthesising beta,betaʹ-linked bispyrrolyl chalcones, proceeding via a Knoevenagel-type reaction of a pyrrolyl aldehyde, followed by a late-stage Friedel-Crafts reaction to attach the second pyrrole. We envisage that the obtained structures may be elaborated in the future within medicinal chemistry programs.
Zhang et al. (Tue,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: