Catalytic asymmetric 1,6-type Friedel–Crafts (hetero)arylations of δ-Cyano substituted para-quinone methides with 5-aminopyrazoles

Abstract

Triarylmethanes is a privileged motif in numerous biologically significant natural molecules and materials. Herein, we achieved a highly efficient enantioselective 1,6-type Friedel–Crafts (hetero)arylations of δ-Cyano substituted para-quinone methides with 5-aminopyrazoles. This method enabled the precise synthesis of chiral triarylmethanes with a cyanide-substituted all-carbon quaternary center, with high yields and exceptional enantioselectivities (up to 92% ee) for the majority of substrates.

Supplementary files

Article information

Article type
Communication
Submitted
05 Nov 2025
Accepted
09 Dec 2025
First published
22 Dec 2025

Org. Biomol. Chem., 2025, Accepted Manuscript

Catalytic asymmetric 1,6-type Friedel–Crafts (hetero)arylations of δ-Cyano substituted para-quinone methides with 5-aminopyrazoles

S. Zhao, H. Song, Y. Hu, F. Gao, Y. He and X. Zhao, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB01738F

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