Electrochemical Synthesis of 5-Selenylbenzo[a]carbazoles via Cascade Cyclization of Indoles with Diselenides

Abstract

The substituted benzo[a]carbazoles have attracted significant attention for their applications in advanced materials and as core frameworks in biologically active alkaloids. Herein, we developed a sustainable electrochemical oxidative cyclization method using diselenides to convert 2-arylethynylaryl indoles into 5-selenylbenzo[a]carbazoles. Notably, the reaction produces the desired products in good to exceptional yields under mild, environmentally benign conditions, without the use of metals, oxidants, or bases.

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2026
Accepted
16 Mar 2026
First published
18 Mar 2026

Chem. Commun., 2026, Accepted Manuscript

Electrochemical Synthesis of 5-Selenylbenzo[a]carbazoles via Cascade Cyclization of Indoles with Diselenides

D. Shree V and S. Gedu, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC00594B

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