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首页> 外文期刊>Organic Chemistry Frontiers >Efficient and practical synthesis of unsymmetrical disulfides via base-catalyzed aerobic oxidative dehydrogenative coupling of thiols
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Efficient and practical synthesis of unsymmetrical disulfides via base-catalyzed aerobic oxidative dehydrogenative coupling of thiols

机译:通过碱催化的硫醇碱催化的有氧氧化脱氢偶联的不对称二硫化的高效和实际合成

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摘要

An efficient M2CO3-catalyzed (M = K or Cs) aerobic cross dehydrogenative coupling reaction of thiols was described. This reaction provided an efficient approach to unsymmetrical disulfides which are ubiquitous structures of pharmaceuticals and pesticides. This is the first aerobic oxidative CDC of thiols to unsymmetrical disulfides. The high atom-economy, easy accessibility of catalyst, O-2 as the ideal green oxidant, mild reaction conditions, and broad substrate scope demonstrate that the present methodology provides a green, attractive, and practical approach to disulfides.
机译:描述了硫醇的有效的M 2 CO 3催化(M = K或CS)有氧交叉脱氢偶联反应。 该反应提供了一种有效的方法,即非对称二硫化物,这是药物和农药的无处不在的结构。 这是第一种至非对称二硫化硫醇的有氧氧化镉。 高原子经济性,易于催化剂的可易于使用,O-2作为理想的绿色氧化剂,温和的反应条件和宽底物范围证明了本方法提供了一种绿色,有吸引力和实用的二硫化方法。

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  • 来源
    《Organic Chemistry Frontiers》 |2019年第13期|共6页
  • 作者单位

    Peking Univ Sch Pharmaceut Sci State Key Lab Nat &

    Biomimet Drugs Xue Yuan Rd 38 Beijing 100191 Peoples R China;

    Peking Univ Sch Pharmaceut Sci State Key Lab Nat &

    Biomimet Drugs Xue Yuan Rd 38 Beijing 100191 Peoples R China;

    Peking Univ Sch Pharmaceut Sci State Key Lab Nat &

    Biomimet Drugs Xue Yuan Rd 38 Beijing 100191 Peoples R China;

    Peking Univ Sch Pharmaceut Sci State Key Lab Nat &

    Biomimet Drugs Xue Yuan Rd 38 Beijing 100191 Peoples R China;

    Peking Univ Sch Pharmaceut Sci State Key Lab Nat &

    Biomimet Drugs Xue Yuan Rd 38 Beijing 100191 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;
  • 关键词

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