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首页> 外文期刊>Tetrahedron >Efficient 2-aryl benzothiazole formation from acetophenones, anilines, and elemental sulfur by iodine-catalyzed oxidative C(CO)-C(alkyl) bond cleavage
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Efficient 2-aryl benzothiazole formation from acetophenones, anilines, and elemental sulfur by iodine-catalyzed oxidative C(CO)-C(alkyl) bond cleavage

机译:通过碘催化氧化C(CO)-C(烷基)粘合裂解从苯乙酮,苯胺和元素硫形成的高效2-芳基苯并噻唑形成

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摘要

A novel and efficient iodine-catalyzed one-pot reaction of aromatic amines, acetophenones, and elemental sulfur for the synthesis of 2-aryl benzothiazoles is described. The process involves sequential C-S and C-N bond formation followed by C(CO)-C bond cleavage from readily accessible starting materials. A wide range of functional groups is tolerated under oxidant and metal-free condition and moderate to good product yields are obtained. (C) 2018 Elsevier Ltd. All rights reserved.
机译:描述了一种新颖而有效的碘胺催化的芳族胺,苯乙烯和元素硫的合成的2-芳基苯并噻唑的含量的单罐反应。 该方法涉及顺序C-S和C-N键形成,然后是C(CO)-C粘合从易于可接近的原料切割。 在氧化剂和无金属条件下耐受各种官能团,得到中等至良好的产量。 (c)2018年elestvier有限公司保留所有权利。

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  • 来源
    《Tetrahedron 》 |2018年第41期| 共6页
  • 作者单位

    Lanzhou Univ Dept Chem Key Lab Nonferrous Met Chem &

    Resources Utilizat State Key Lab Appl Organ Chem Lanzhou Gansu Peoples R China;

    Lanzhou Univ Dept Chem Key Lab Nonferrous Met Chem &

    Resources Utilizat State Key Lab Appl Organ Chem Lanzhou Gansu Peoples R China;

    Lanzhou Univ Dept Chem Key Lab Nonferrous Met Chem &

    Resources Utilizat State Key Lab Appl Organ Chem Lanzhou Gansu Peoples R China;

    Lanzhou Univ Dept Chem Key Lab Nonferrous Met Chem &

    Resources Utilizat State Key Lab Appl Organ Chem Lanzhou Gansu Peoples R China;

    Lanzhou Univ Dept Chem Key Lab Nonferrous Met Chem &

    Resources Utilizat State Key Lab Appl Organ Chem Lanzhou Gansu 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

    Benzothiazoles; Acetophenones; Anilines; Elemental sulfur; C-C bond cleavage;

    机译:苯并噻唑;紫酮;苯胺;元素硫;C-C键分裂;

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