Issue 46, 2006

The use of calcium carbide in one-pot synthesis of symmetric diaryl ethynes

Abstract

An efficient Pd-catalyzed copper and amine free coupling reaction of acetylene and aryl bromides was achieved with calcium carbide as an acetylene source, using inorganic base and easily prepared, air-stable aminophosphine ligand in common organic solvents, providing symmetric diaryl ethynes in one-pot with yields ranged from moderate to excellent.

Graphical abstract: The use of calcium carbide in one-pot synthesis of symmetric diaryl ethynes

Supplementary files

Article information

Article type
Communication
Submitted
02 Jun 2006
Accepted
13 Sep 2006
First published
02 Oct 2006

Chem. Commun., 2006, 4826-4828

The use of calcium carbide in one-pot synthesis of symmetric diaryl ethynes

W. Zhang, H. Wu, Z. Liu, P. Zhong, L. Zhang, X. Huang and J. Cheng, Chem. Commun., 2006, 4826 DOI: 10.1039/B607809E

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