Issue 7, 2017

Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions

Abstract

A simple and efficient strategy for the synthesis of 3-sulfenyl and 3-selenyl indoles via a visible light-induced tandem cyclization of 2-alkynylanilines with disulfides (diselenides) was developed. The reaction generated the corresponding products in good yields at room temperature under transition metal-free and photocatalyst-free conditions.

Graphical abstract: Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions

Supplementary files

Article information

Article type
Research Article
Submitted
23 Feb 2017
Accepted
25 Mar 2017
First published
28 Mar 2017

Org. Chem. Front., 2017,4, 1322-1330

Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions

Q. Shi, P. Li, Y. Zhang and L. Wang, Org. Chem. Front., 2017, 4, 1322 DOI: 10.1039/C7QO00152E

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