Palladium‐Catalyzed Suzuki‐Miyaura Type Coupling Reaction of Aryl Halides with Triphenylborane‐Pyridine |
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Authors: | Minghua Yang Yongbing Gu Yan Wang Xiyu Zhao Guobing Yan |
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Affiliation: | Department of Chemistry, Lishui University, Lishui, Zhejiang 323000, China |
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Abstract: | The Suzuki‐Miyaura type coupling reaction of aryl halides with triphenylborane‐pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in presence of Cs2CO3 at 50°C or 80°C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups. |
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Keywords: | triphenylbroane‐pyridine Suzuki‐Miyaura coupling aryl halides palladium catalysts |
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