Issue 9, 2017

Electrochemical intramolecular dehydrogenative C–S bond formation for the synthesis of benzothiazoles

Abstract

An external oxidant-free intramolecular dehydrogenative C–S cross-coupling has been developed under undivided electrolytic conditions. Various 2-aminobenzothiazoles could be synthesized with up to 99% yield from the direct combination of aryl isothiocyanates with amines. In the presence of a base, this reaction protocol is also applicable for the synthesis of benzothiazoles from N-aryl thioamides.

Graphical abstract: Electrochemical intramolecular dehydrogenative C–S bond formation for the synthesis of benzothiazoles

Supplementary files

Article information

Article type
Communication
Submitted
13 Feb 2017
Accepted
21 Mar 2017
First published
21 Mar 2017

Green Chem., 2017,19, 2092-2095

Electrochemical intramolecular dehydrogenative C–S bond formation for the synthesis of benzothiazoles

P. Wang, S. Tang and A. Lei, Green Chem., 2017, 19, 2092 DOI: 10.1039/C7GC00468K

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