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水相中无配体铃木反应合成联芳基和聚芳基化合物。

Synthesis of biaryls and polyaryls by ligand-free Suzuki reaction in aqueous phase.

作者信息

Liu Leifang, Zhang Yuhong, Xin Bingwei

机构信息

Department of Chemistry, Zhejiang University, Hangzhou 310027, People's Republic of China.

出版信息

J Org Chem. 2006 May 12;71(10):3994-7. doi: 10.1021/jo060122v.

Abstract

A highly efficient palladium acetate-catalyzed ligand-free Suzuki reaction in aqueous phase was developed in short reaction times (0.5-1 h) at 35 degrees C in air. The key for such a successful catalytic system was the use of a suitable amount of cosolvents in the aqueous phase. The method could be extended to the consecutive multi-Suzuki coupling, and polyaryls were prepared in a single one-pot step in high selectivity and excellent yield under mild reaction conditions (60 degrees C).

摘要

在空气中35℃的条件下,开发了一种高效的醋酸钯催化的水相无配体铃木反应,反应时间短(0.5 - 1小时)。这种成功的催化体系的关键在于在水相中使用适量的助溶剂。该方法可扩展至连续多步铃木偶联反应,并且在温和的反应条件(60℃)下,通过单步一锅法以高选择性和优异产率制备多芳基化合物。

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