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Iridium-Catalyzed Reductive Alkylations of Secondary Amides

机译:铱催化的仲酰胺的还原烷基化

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摘要

Reported herein is the first direct, metal-catalyzed reductive functionalization of secondary amides to give functionalized amines and heterocycles. The method is shown to have exceptionally broad scope with respect to suitable nucleophiles, which cover both hard and soft Cnucleophiles as well as a Pnucleophile. The reaction exhibits good chemoselectivity and tolerates several sensitive functional groups.
机译:本文报道的是仲酰胺的第一种直接,金属催化的还原官能化,得到官能化胺和杂环。 该方法显示出相对于合适的亲核试剂具有特别广泛的核心,其覆盖硬质和软的核磁素以及核核试剂。 该反应表现出良好的化学选择性并耐受几种敏感官能团。

著录项

  • 来源
    《Angewandte Chemie》 |2018年第35期|共5页
  • 作者单位

    Xiamen Univ Fujian Prov Key Lab Chem Biol Dept Chem Coll Chem &

    Chem Engn Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Fujian Prov Key Lab Chem Biol Dept Chem Coll Chem &

    Chem Engn Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Fujian Prov Key Lab Chem Biol Dept Chem Coll Chem &

    Chem Engn Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Fujian Prov Key Lab Chem Biol Dept Chem Coll Chem &

    Chem Engn Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Fujian Prov Key Lab Chem Biol Dept Chem Coll Chem &

    Chem Engn Xiamen 361005 Fujian Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 应用化学;
  • 关键词

    amides; homogeneous catalysis; iridium; reductive alkylation; synthetic methods;

    机译:酰胺;均匀催化;铱;还原烷基化;合成方法;

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