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Recent advances in radical-based C-N bond formation via photo-/electrochemistry

机译:通过光照/电化学的基于基于基于基于基于基于C-N键的研究进展

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摘要

The employment of nitrogen sources with free N-H bonds for amination is considered to be most straightforward and desirable, especially when the C-N bonds are prepared from N-H bonds and non-functionalized carbon sources, such as C-H bonds and C-C double/triple bonds, since this obviates the needs for the pre-installation of reactive groups in the starting materials and leads to a high atom and step economy. Recently, radical chemistry has been resuscitated owing to its great value in organic synthesis, and notable advances have been made in the direct use of N-H bonds for radical-based C-N bond formation with photo-/electrotechniques. Apart from the well-studied N-radical species addition pathway, radical-mediated aminations also proceed through N-atom nucleophilic addition, C-/N-radical cross-coupling, and a hydrogen-atom transfer (HAT) process. This review highlights the recent advances in this area with emphasis on the related reaction mechanisms.
机译:用于胺化的游离NH键的氮源的就业被认为是最直接的和理想的,特别是当Cn键由NH键和非官能化碳源如CH键和CC双/三键制备时,因此 消除了起始材料中反应基团预先安装的需要,并导致高原子和阶跃经济性。 最近,由于其在有机合成中具有很大的有机合成价值,因此重新刺除了激进的化学,并且在直接使用N-H键的基于基于基于光电的C-N键形成的N-H键的显着进展。 除了学习的N自由基物种附加途径之外,自由基介导的amination还通过N-原子亲核添加,C-/ N-自由基交叉偶联和氢原子转移(帽子)过程。 本综述突出了该领域最近的进展,重点是相关的反应机制。

著录项

  • 来源
    《Chemical Society Reviews》 |2018年第8期|共18页
  • 作者

    Zhao Yating; Xia Wujiong;

  • 作者单位

    Harbin Inst Technol Shenzhen State Key Lab Urban Water Resource &

    Environm Shenzhen 518055 Peoples R China;

    Harbin Inst Technol Shenzhen State Key Lab Urban Water Resource &

    Environm Shenzhen 518055 Peoples R China;

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

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