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Amide as an efficient ligand in the palladium-catalyzed Suzuki coupling reaction in water/ethanol under aerobic conditions
Authors:Hai Yang Liu  Kun Wang  Hai Yan Fu  Mao Lin Yuan  Hua Chen  Rui Xiang Li Key Lab of Green Chemistry  Technology  Ministry of Education  the Institute of Homogeneous Catalysis  College of Chemistry  Sichuan University  Chengdu  China
Institution:Key Lab of Green Chemistry and Technology, Ministry of Education, the Institute of Homogeneous Catalysis, College of Chemistry, Sichuan University, Chengdu 610064, China
Abstract:Amide,which is derived from proline and is inexpensive and air-stable,has been synthesized and characterized by ~1H NMR,~(13)C NMR,and MS.It was found to be an efficient ligand in the palladium-catalyzed Suzuki cross-coupling reaction.In the Pd/amide catalytic system,aryl bromides can be coupled with phenylboronic acid in ethanol/water(1:2;v/v) in excellent yields even with a low Pd loading of 0.01 mol%.Moreover,the scope of the reaction is broad,and a wide variety of functional groups are tolerant.
Keywords:Suzuki cross-coupling  Palladium catalyst  Aryl bromides  Amide  Water  
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