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首页> 外文期刊>Transition Metal Chemistry >Catalysis of the coupling reaction of aryl chlorides with bis(pinacolato)diboron by tricyclohexylphosphine-cyclopalladated ferrocenylimine complexes
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Catalysis of the coupling reaction of aryl chlorides with bis(pinacolato)diboron by tricyclohexylphosphine-cyclopalladated ferrocenylimine complexes

机译:三环己基膦-环钯二茂铁亚胺配合物催化芳基氯与双(频哪醇)二硼的偶联反应

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摘要

Tricyclohexylphosphine-cyclopalladated ferrocenylimine complexes were found to be very efficient catalysts for the one-pot borylation/Suzuki cross-coupling reactions of aryl chlorides with bis(pinacolato)diboron.Typically,using 0.5-1.0 mol% of catalyst in the presence of 3.0 equivalents of K2CO3 as base in dioxane at 100 °C provided the corresponding symmetrical biaryls in good to excellent yields.
机译:发现三环己基膦-环钯的二茂铁基亚胺配合物是芳基氯与双(频哪醇)二硼的一锅法硼化/ Suzuki交叉偶联反应的非常有效的催化剂。通常,在3.0当量的存在下使用0.5-1.0 mol%的催化剂在100°C下于二恶烷中以K2CO3为碱提供了相应的对称联芳基,收率良好至极佳。

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