Synthesis 2012; 44(10): 1507-1510
DOI: 10.1055/s-0031-1290813
special topic
© Georg Thieme Verlag Stuttgart · New York

Microwave-Assisted Copper-Catalyzed Cross-Coupling Reaction of Alkynes with Aryl Iodides and Vinyl Halides

Wen-Ting Tsai
Department of Chemistry, National Chung Hsing University, Taichung, Taiwan 402, ROC, Fax: +886(4)22862547   Email: cfalee@dragon.nchu.edu.tw
,
Yun-Yung Lin
Department of Chemistry, National Chung Hsing University, Taichung, Taiwan 402, ROC, Fax: +886(4)22862547   Email: cfalee@dragon.nchu.edu.tw
,
Yu-Jen Wang
Department of Chemistry, National Chung Hsing University, Taichung, Taiwan 402, ROC, Fax: +886(4)22862547   Email: cfalee@dragon.nchu.edu.tw
,
Chin-Fa Lee*
Department of Chemistry, National Chung Hsing University, Taichung, Taiwan 402, ROC, Fax: +886(4)22862547   Email: cfalee@dragon.nchu.edu.tw
› Author Affiliations
Further Information

Publication History

Received: 20 February 2012

Accepted: 05 March 2012

Publication Date:
02 April 2012 (online)


Abstract

The microwave-assisted, copper-catalyzed coupling of terminal alkynes with aryl iodides and vinyl halides is reported. In general, the reactions are completed in 10–30 min using 2–5 mol% [CuI(xantphos)] as a catalyst to provide the corresponding alkynes and enynes in good to excellent yields. A broad spectrum of aryl iodides­, vinyl iodides, and bromides are coupled with aryl- and alkyl­ alkynes.

Supporting Information