Issue 3, 2018

A thiol-free synthesis of alkynyl chalcogenides by the copper-catalyzed C–X (X = S, Se) cross-coupling of alkynyl carboxylic acids with Bunte salts

Abstract

An efficient copper-catalyzed C–X (X = S, Se) decarboxylative coupling of alkynyl carboxylic acids with Bunte salts has been developed. The process is amenable to various alkynyl carboxylic acids and Bunte salts and is compatible with a wide range of functional groups. In addition, this catalytic reaction could also be performed with seleno Bunte salts and alkynyl carboxylic acids under the same conditions, giving the alkynyl selenosulfides in good yields. Importantly, this route avoids the use of odorous thiol or selenol starting materials.

Graphical abstract: A thiol-free synthesis of alkynyl chalcogenides by the copper-catalyzed C–X (X = S, Se) cross-coupling of alkynyl carboxylic acids with Bunte salts

Supplementary files

Article information

Article type
Research Article
Submitted
15 Aug 2017
Accepted
03 Oct 2017
First published
11 Oct 2017

Org. Chem. Front., 2018,5, 428-433

A thiol-free synthesis of alkynyl chalcogenides by the copper-catalyzed C–X (X = S, Se) cross-coupling of alkynyl carboxylic acids with Bunte salts

F. Liu and W. Yi, Org. Chem. Front., 2018, 5, 428 DOI: 10.1039/C7QO00724H

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