Issue 17, 2004
From the journal:

Chemical Communications

CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine†

Dawei Ma*a  and  Feng Liua  

* Corresponding authors

a Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China
E-mail: madw@mail.sioc.ac.cn
Fax: 86-21-64166128
Tel: 86-21-64163300

Abstract

CuI/N,N-dimethylglycine-catalyzed coupling reaction of aryl halides with terminal alkynes is carried out in DMF at 100 °C to provide the corresponding coupling products in good to excellent yields with a great diversity.

Graphical abstract: CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine

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Article information

DOI
https://doi.org/10.1039/B407090A
Article type
Communication
Submitted
13 May 2004
Accepted
07 Jun 2004
First published
28 Jul 2004

Chem. Commun., 2004, 1934-1935

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CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine

D. Ma and F. Liu, Chem. Commun., 2004, 1934 DOI: 10.1039/B407090A

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