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Intensification of Pd-catalyzed Suzuki cross-coupling: influence of second metal addition, reactor type and visible light irradiation

机译:PD催化铃木交叉耦合的强化:第二金属添加,反应器型和可见光照射的影响

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Suzuki cross-coupling is an important reaction of C-C bond formation that uses arylhalides and arylboronic acids as starting compounds. Suzuki reaction is often used in the synthesis of APIsand new functional materials[1]. Homogeneous Pd complexesare traditionallyused as catalysts for the Suzuki reaction with high yields of desired products [2]. Last decades the development of new ligandless palladium catalysts is of high importance, since they can be easily separated from the reaction mixture and reused [3]. In order to improve the efficiency of cross-coupling processes, bimetallic ligandless catalysts can be used since they allow: increasing the lifetime of catalysts due to the decrease of palladium leaching; carrying out cross-coupling at milder reaction conditions; increasing activity and selectivity in comparison with monometallic analogues.
机译:Suzuki交叉偶联是C-C键形成的重要反应,其使用芳基烷基酯和芳基硼酸作为起始化合物。铃木反应通常用于合成APISAND新功能材料[1]。均相PD复合体传统地用作铃木反应的催化剂,其具有高收率的所需产物[2]。去年几十年来,新型配棒钯催化剂的开发具有很高的重要性,因为它们可以容易地与反应混合物分离并重复使用[3]。为了提高交叉偶联方法的效率,可以使用双金属配棒催化剂,因为它们允许:由于钯浸出的降低,增加催化剂的寿命;在Milder反应条件下进行交叉偶联;与单仪类似物相比,增加活性和选择性。

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