Issue 56, 2015
From the journal:

RSC Advances

(2-Chlorobenzoyloxy)copper(i) catalyzed C–S cross-coupling of di(hetero)aryl disulfides with aryl boronic acids under base-free conditions†

Yan Guo,a   Zheng-Jun Quan,*a   Yu-Xia Da,a   Zhang Zhanga  and  Xi-Cun Wang*a  

* Corresponding authors

a Laboratory of Eco-Environment-Related Polymer Materials, Ministry of Education, China, Gansu Key Laboratory of Polymer Materials, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China

Abstract

(2-Chlorobenzoyloxy)copper(I) exhibited high activity towards the challenging C–S cross-coupling of di(hetero)aryl disulfides with aryl boronic acids. Herein, diheteroaryl as well as diaryl thioethers were produced with good to excellent yields under base-free conditions.

Graphical abstract: (2-Chlorobenzoyloxy)copper(i) catalyzed C–S cross-coupling of di(hetero)aryl disulfides with aryl boronic acids under base-free conditions

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5RA05594F
Article type
Communication
Submitted
30 Mar 2015
Accepted
14 May 2015
First published
14 May 2015

RSC Adv., 2015,5, 45479-45483

Author version available

Download author version (PDF)

Permissions

Request permissions

(2-Chlorobenzoyloxy)copper(I) catalyzed C–S cross-coupling of di(hetero)aryl disulfides with aryl boronic acids under base-free conditions

Y. Guo, Z. Quan, Y. Da, Z. Zhang and X. Wang, RSC Adv., 2015, 5, 45479 DOI: 10.1039/C5RA05594F

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