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Photoredox-Mediated Direct Cross-Dehydrogenative Coupling of Heteroarenes and Amines

机译:摄影氧介导的杂种和胺的直接交叉脱氢偶联

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摘要

A photoredox-mediated direct cross-dehydrogenative coupling reaction to accomplish alpha-aminoalkylation of N-hetero-arenes is reported. This mild reaction has a broad substrate scope, offers the first general method for synthesis of aminoalkylated N-heteroarenes without the need for substrate prefunctionalization, and is scalable to the gram level. Furthermore, the reaction was found to be applicable to other hydrogen donors besides amines (i.e., ethers, an aldehyde, a formamide, p-xylene, and alkanes), thus enabling the preparation of N-heteroarenes bearing various types of substituents.
机译:据报道了一种光毒氧介导的直接交叉脱氢偶联反应,以实现N-杂芳烃的α-氨基烷基化。 这种温和的反应具有宽的基材范围,提供了第一一般方法,用于合成氨基烷基化的N-杂烷,而不需要底物预官能化,并且可扩展到克克水平。 此外,发现反应可应用于除胺(即醚,醛,甲酰胺,对二甲苯和烷烃)之外的其它氢供体,从而使得制备含有各种类型取代基的N-杂种。

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  • 来源
    《Organic letters》 |2018年第18期|共5页
  • 作者单位

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

    Nankai Univ Coll Chem Res Inst Elementoorgan Chem State Key Lab Elementoorgan Chem Tianjin 300071 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
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