Issue 22, 2025

Organocatalytic asymmetric synthesis of axially and centrally chiral heterotriarylmethanes by a Friedel–Crafts reaction

Abstract

A highly enantioselective Friedel–Crafts reaction between C2-unsubstituted naphthyl-indoles and racemic 3-methylated-3H-pyrrolides catalyzed by chiral phosphoric acids has been developed. This reaction provides an efficient and facile route to a series of heterotricyclic triarylmethanes containing axially chiral naphthyl-indole and centrally chiral pyrrole moieties under mild conditions. Moreover, biological evaluation discovered one of these products with promising antitumor activity, and demonstrates its potential application in medicinal chemistry.

Graphical abstract: Organocatalytic asymmetric synthesis of axially and centrally chiral heterotriarylmethanes by a Friedel–Crafts reaction

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2025
Accepted
01 May 2025
First published
01 May 2025

Org. Biomol. Chem., 2025,23, 5359-5372

Organocatalytic asymmetric synthesis of axially and centrally chiral heterotriarylmethanes by a Friedel–Crafts reaction

Y. Min, H. Shen, S. Huang, H. Gu and X. Lin, Org. Biomol. Chem., 2025, 23, 5359 DOI: 10.1039/D5OB00532A

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