Issue 19, 2025

Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles

Abstract

Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(II)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.

Graphical abstract: Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles

Supplementary files

Article information

Article type
Communication
Submitted
30 Nov 2024
Accepted
22 Jan 2025
First published
23 Jan 2025

Chem. Commun., 2025,61, 3872-3875

Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles

K. Pal, O. P. Dash and C. M. R. Volla, Chem. Commun., 2025, 61, 3872 DOI: 10.1039/D4CC06346E

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