Palladium??Free Copper??Catalyzed Coupling Reaction of Aryl Iodides and Terminal Acetylenes in Water
G Chen, X Zhu, J Cai, Y Wan
Index: Chen, Gong; Zhu, Xinhai; Cai, Jiwen; Wan, Yiqian Synthetic Communications, 2007 , vol. 37, # 8 p. 1355 - 1361
Full Text: HTML
Citation Number: 42
Abstract
Abstract An efficient and general method has been developed for palladium??free copper?? catalyzed cross??coupling reactions of aryl iodides and terminal acetylenes under microwave irradiation in water, producing various alkynes in excellent yields. This process can also be successfully carried out under reflux in an oil bath.
Related Articles:
[Li, Tingyi; Sun, Peng; Yang, Hailong; Zhu, Yan; Yan, Hong; Lu, Linhua; Mao, Jincheng Tetrahedron, 2012 , vol. 68, # 32 p. 6413 - 6419]
Cross-coupling of alkynylsilanols with aryl halides promoted by potassium trimethylsilanolate
[Denmark, Scott E.; Tymonko, Steven A. Journal of Organic Chemistry, 2003 , vol. 68, # 23 p. 9151 - 9154]
[Yang, Fan; Wu, Yangjie European Journal of Organic Chemistry, 2007 , # 21 p. 3476 - 3479]
Palladium-catalyzed decarboxylative coupling of alkynyl carboxylic acids and aryl halides
[Moon, Jeongju; Jang, Mihee; Lee, Sunwoo Journal of Organic Chemistry, 2009 , vol. 74, # 3 p. 1403 - 1406]
[Okuro, Kazumi; Furuune, Makoto; Enna, Masahiro; Miura, Masahiro; Nomura, Masakatsu Journal of Organic Chemistry, 1993 , vol. 58, # 17 p. 4716 - 4721]