首页> 外文期刊>The Journal of Organic Chemistry >Aqueous Reaction of Alcohols, Organohalides, and Odorless Sodium Thiosulfate under Transition-Metal-Free Conditions: Synthesis of Unsymmetrical Aryl Sulfides via Dual C-S Bond Formation
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Aqueous Reaction of Alcohols, Organohalides, and Odorless Sodium Thiosulfate under Transition-Metal-Free Conditions: Synthesis of Unsymmetrical Aryl Sulfides via Dual C-S Bond Formation

机译:过渡金属条件下醇,有机卤化物和无味硫代硫酸钠的水性反应:通过双C-S键形成合成非对称芳基硫化物

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摘要

A transition-metal-free process for the synthesis of unsymmetrical aryl sulfides via dual C-S bond formation by a one-pot three-component reaction of alcohols, organohalides, and odorless sodium thiosulfate in water has been developed. In addition, the aryl sulfides could also be prepared by the reaction of the corresponding alcohols and Bunte salts under the identical conditions. This protocol provides a green and efficient manner for the construction of various unsymmetrical aryl sulfides.
机译:已经开发出通过双泊醇,有机卤化物和无味硫代硫酸钠的单罐三组分反应通过双C-S键形成通过双C-C-C键形成的不对称芳基硫化物的过渡 - 金属化方法。 另外,芳基硫化物也可以通过相应的醇和Bunte盐的反应来制备相同的条件。 该方案为构建各种非对称芳基硫化物提供绿色和有效的方式。

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  • 来源
    《The Journal of Organic Chemistry》 |2017年第19期|共7页
  • 作者单位

    Soochow Univ Key Lab Organ Synth Jiangsu Prov Coll Chem Chem Engn &

    Mat Sci Suzhou 215123 Peoples R China;

    Soochow Univ Key Lab Organ Synth Jiangsu Prov Coll Chem Chem Engn &

    Mat Sci Suzhou 215123 Peoples R China;

    Soochow Univ Key Lab Organ Synth Jiangsu Prov Coll Chem Chem Engn &

    Mat Sci Suzhou 215123 Peoples R China;

    Jining Univ Dept Chem &

    Chem Engn Qufu 273155 Peoples R China;

    Soochow Univ Key Lab Organ Synth Jiangsu Prov Coll Chem Chem Engn &

    Mat Sci Suzhou 215123 Peoples R China;

    Soochow Univ Key Lab Organ Synth Jiangsu Prov Coll Chem Chem Engn &

    Mat Sci Suzhou 215123 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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