Issue 94, 2014

Selective sulfonylation and diazotization of indoles

Abstract

A metal-free synthesis of bifunctionalized indole derivatives was developed through a novel TBHP/TBAI-mediated oxidative coupling of C2,C3-unsubstituted indoles with arylsulfonyl hydrazide. Under the same conditions C3-methyl substituted indoles underwent a diazotization process, affording 2-sulfonyldiazenyl-1H-indoles. The former reaction simultaneously established C–S and C–N bonds through selective sulfonylation and diazotization of the indole framework, enabling a mild and practical access to polyfunctionalized indoles with good to excellent yields.

Graphical abstract: Selective sulfonylation and diazotization of indoles

Supplementary files

Article information

Article type
Communication
Submitted
28 Aug 2014
Accepted
01 Oct 2014
First published
06 Oct 2014

Chem. Commun., 2014,50, 14782-14785

Selective sulfonylation and diazotization of indoles

J. Qiu, W. Hao, D. Wang, P. Wei, J. Sun, B. Jiang and S. Tu, Chem. Commun., 2014, 50, 14782 DOI: 10.1039/C4CC06795A

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