Issue 5, 2020

Electrochemical diselenylation of indolizines via intermolecular C–Se formation with 2-methylpyridines, α-bromoketones and diselenides

Abstract

An efficient electrochemical system for the construction of diselenytlated indolizines from available pyridines, ketones and diselenides under undivided electrolytic conditions was developed. No external oxidants and transition-metal catalysts are needed for achieving this three-component tandem reaction realizing C–C, C–N and C–Se bond formations.

Graphical abstract: Electrochemical diselenylation of indolizines via intermolecular C–Se formation with 2-methylpyridines, α-bromoketones and diselenides

Supplementary files

Article information

Article type
Communication
Submitted
11 Nov 2019
Accepted
06 Dec 2019
First published
06 Dec 2019

Chem. Commun., 2020,56, 735-738

Electrochemical diselenylation of indolizines via intermolecular C–Se formation with 2-methylpyridines, α-bromoketones and diselenides

J. Li, X. Liu, J. Deng, Y. Huang, Z. Pan, Y. Yu and H. Cao, Chem. Commun., 2020, 56, 735 DOI: 10.1039/C9CC08784B

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