Jump to main content
Jump to site search

Issue 5, 2020
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Article information


Submitted
11 Nov 2019
Accepted
06 Dec 2019
First published
06 Dec 2019

Chem. Commun., 2020,56, 735-738
Article type
Communication

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

Social activity

Search articles by author

Spotlight

Advertisements