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作 者:WU Xiang-mei WANG Yan GUO Sheng-rong
机构地区:[1]College of Chemistry and Life Science, Lishui University, Lishui 323000, P. R. China
出 处:《Chemical Research in Chinese Universities》2010年第2期331-334,共4页高等学校化学研究(英文版)
基 金:Supported by the Zhejiang Province Natural Science Foundation,China(No.Y407240)
摘 要:1 Introduction The Suzuki cross-coupling reaction is a powerful and versatile method for the generation of unsymmetrical biaryls from arylboronic acids and aryl halides in a single step. However, the reaction is usually performed in the presence of Pd catalyst along with phosphine ligand, which sometimes creates practical problems because organophosphines tend to be expensive, poisonous, and air sensitive. Recently, phos-phine-free ligands,1 Introduction The Suzuki cross-coupling reaction is a powerful and versatile method for the generation of unsymmetrical biaryls from arylboronic acids and aryl halides in a single step. However, the reaction is usually performed in the presence of Pd catalyst along with phosphine ligand, which sometimes creates practical problems because organophosphines tend to be expensive, poisonous, and air sensitive. Recently, phos-phine-free ligands,
关 键 词:Suzuki reaction Phosphine-free ligand PALLADIUM 4-Amino-1 2 4-triazole resin
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