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Asymmetric Suzuki-Miyaura Cross-Coupling for the Synthesis of Chiral Biaryl Compounds as Potential Monophosphine Ligands

机译:不对称的Suzuki-Miyaura交叉偶联用于合成潜在的单膦配体的手性联芳基化合物

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摘要

Efficient asymmetric Suzuki-Miyaura coupling reactions have been employed for the first time to synthesize chiral biaryl compounds with phosphinate groups as chiral auxiliaries. A series of functionalized chiral biaryls are thereby synthesized in excellent yields and good diastereoselectivities (up to > 95: 5 d.r.) and axially chiral monophosphorus ligands are obtained through further functionalizations.
机译:高效的不对称Suzuki-Miyaura偶联反应已首次用于合成具有次膦酸酯基团的手性联芳基化合物作为手性助剂。由此以优异的产率和良好的非对映选择性(高达> 95∶5 d.r.)合成了一系列官能化的手性联芳基,并且通过进一步的官能化获得了轴向手性的单磷配体。

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