Recyclable Catalysts for Suzuki-Miyaura Cross-Coupling Reactions at Ambient Temperature Based on a Simple Merrifield Resin Supported Phenanthroline-Palladium(II) Complex
Jin Yang, Pinhua Li, Lei Wang*
*Department of Chemistry, Huaibei Normal University, Huaibei,
Anhui 235000, P. R. of China, Email: leiwang
chnu.edu.cn
J. Yang, P. Li, L. Wang, Synthesis, 2011, 1295-1301.
Abstract
A Merrifield resin immobilized phenanthroline-palladium(II) complex is an efficient catalyst for Suzuki-Miyaura cross-coupling reaction between arylboronic acids and a range of aryl halides under mild reaction conditions. The catalyst exhibited both high catalytic activity and stability for Suzuki-Miyaura reaction and could be recycled at least 10 times without a significant loss of activity.
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Key Words
immobilized catalyst, phenanthroline-palladium(II) complex, Suzuki coupling, biaryls, recyclability, green chemistry
ID: J66-Y2011-1190
