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Rhodium-catalyzed direct coupling of biaryl pyridine derivatives with internal a Iky nes

机译:铑催化的联芳基吡啶衍生物与内部烷基的直接偶联

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摘要

Axially chiral biaryls were synthesized by an isoquinoline or 2-pyridine-directed Rh(m)-catalyzed dual C-H cleavage and coupling with internal alkynes in good to excellent yields. Oxidation of isoquinoline derivatives with m-CPBA furnished their corresponding N-oxides, which could be utilized as Lewis base catalysts in asymmetric reactions.
机译:轴向手性联芳基是通过异喹啉或2-吡啶定向的Rh(m)催化的双C-H裂解并与内部炔烃偶联而合成的,合成的产率高至优异。用m-CPBA氧化异喹啉衍生物可得到其相应的N-氧化物,可用作不对称反应中的Lewis碱催化剂。

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  • 来源
    《Chemical Communications》 |2014年第60期|8204-8207|共4页
  • 作者

    Jun Zheng; Shu-Li You;

  • 作者单位

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

    State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China;

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