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作 者:付兴丽[1]
出 处:《企业科技与发展》2012年第6期26-28,共3页Sci-Tech & Development of Enterprise
基 金:2012年广西教育厅科研处课题"水相中钯催化吡啶硼酸的Suzuki反应研究"阶段性成果
摘 要:将双齿膦配体P-Phos应用于钯催化的3-吡啶硼酸的Suzuki反应中,通过对溶剂和碱等反应条件的考察,确定了最佳的催化条件,并对一系列底物进行了普适性拓展。实验表明,该催化剂对大多数卤代芳烃底物起到了良好的催化效果,并且可以实现惰性底物氯代芳烃与吡啶硼酸的高效偶联,产率高达99%。A highly active catalyst system derived from PdC12 and 2 2',6,6'-tetramethoxy-4,4'-bis(diphenylphosphanyl) -3,3'-bipyridine(P-Phos) has been developed for the Suzuki cross-coupling reaction of pyridylboronic acid with a variety of arylhalides in good to excellent yields,even in the presence of hindered and functional groups.In addition,P-Phos also exhibites high activity in the palladium-catalyzed Suzuki reaction of 2,6-dimethoxypyridylboronic acid in excellent yields wita fast rate.The steric and electronic effects of the P-Phos-palladium complex to this cross-coupling reaction were also discussed.
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