A simple catalyst system for the palladium-catalyzed coupling of aryl halides with terminal alkynes |
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| Authors: | Eiji Shirakawa Takaaki Kitabata Teruhisa Tsuchimoto |
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| Institution: | a Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan
b Graduate School of Materials Science, Japan Advanced Institute of Science and Technology, Asahidai, Nomi, Ishikawa 923-1292, Japan |
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| Abstract: | A convenient catalyst system consisting of Pd(OAc)2, PPh3, K3PO4 and DMSO was found to be effective for the coupling reaction of aryl halides with terminal alkynes as well as the deacetonative coupling reaction using a 4-aryl-2-methylbut-3-yn-2-ol as a terminal alkyne precursor. An iminophosphine as a ligand worked more effectively for some combination of substrates than triphenylphosphine. |
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| Keywords: | Alkynes Aryl halides Coupling reactions Palladium and compounds |
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