Issue 3, 2017

A practical synthesis of benzothiophenes via visible-light-promoted cyclization of disulfides and alkynes

Abstract

Visible-light-promoted intermolecular radical cyclization of disulfides and alkynes has been developed. Benzothiophenes bearing ester, ketone, aldehyde and aryl substituents were synthesized in good yields. The reaction was carried out in the absence of transition-metal catalysts and extra additives. Oxygen was used as the sole oxidant. In addition, the irradiation of sunlight could also promote the reaction efficiently.

Graphical abstract: A practical synthesis of benzothiophenes via visible-light-promoted cyclization of disulfides and alkynes

Supplementary files

Article information

Article type
Communication
Submitted
11 Nov 2016
Accepted
02 Dec 2016
First published
02 Dec 2016

Org. Biomol. Chem., 2017,15, 550-554

A practical synthesis of benzothiophenes via visible-light-promoted cyclization of disulfides and alkynes

L. Ye, L. Qian, Y. Chen, X. Zhang and M. Yan, Org. Biomol. Chem., 2017, 15, 550 DOI: 10.1039/C6OB02461K

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