Issue 5, 2020
From the journal:

Chemical Communications

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

Junxuan Li,a   Xiang Liu,a   Jiadi Deng,a   Yingshan Huang,a   Zihao Pan,a   Yue Yu ORCID logo *a  and  Hua Cao ORCID logo *a  

* Corresponding authors

a School of Chemistry and Chemical Engineering and Guangdong Cosmetics Engineering & Technology Research Center, Guangdong Pharmaceutical University, Zhongshan 528458, China
E-mail: yuyue@gdpu.edu.cn, caohua@gdpu.edu.cn

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

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C9CC08784B
Article type
Communication
Submitted
11 Nov 2019
Accepted
06 Dec 2019
First published
06 Dec 2019

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

Permissions

Request permissions

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

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements