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Metal-free, highly efficient organocatalytic amination of benzylic C-H bondst

机译:苄基C-H键的无金属高效有机催化胺化

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摘要

A new synthetic approach toward direct C-N bond formation through sp~3 C-H activation has been developed under metal-free conditions. Both primary and secondary benzylic C-H substrates could react smoothly with various amines to give only mono-amination products with good to excellent yields.
机译:在无金属条件下,开发了一种通过sp〜3 C-H活化直接形成C-N键的合成方法。伯和仲苄基C-H底物均可以与各种胺顺利反应,仅以良好或优异的收率得到单胺化产物。

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  • 来源
    《Chemical Communications》 |2013年第35期|3700-3702|共3页
  • 作者单位

    State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093,People's Republic of China;

    State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093,People's Republic of China;

    State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093,People's Republic of China;

    State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093,People's Republic of China;

    State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093,People's Republic of China State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai 200032, People's Republic of China;

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