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首页> 外文期刊>Organic letters >Radical Hydroboration and Hydrosilylation of gem-Difluoroalkenes: Synthesis of alpha-Difluorinated Alkylborons and Alkylsilanes
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Radical Hydroboration and Hydrosilylation of gem-Difluoroalkenes: Synthesis of alpha-Difluorinated Alkylborons and Alkylsilanes

机译:纯粹的硫代芳烃和氢化硅烷化的自由基水合液:α-二氟化烷基硼和烷基硅烷的合成

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摘要

A first example of radical hydroboration and hydrosilylation of gem-difluoroalkenes using ABIN as the radical initiator is described. This protocol features good functional group tolerance, operational simplicity, high atom economy, and easy scale-up, enabling efficient assembly of a wide range of alpha-difluorinated alkylborons and alkylsilanes in moderate to excellent yields. The synthetic utility of these products is demonstrated by further transformation of the C-B bond and C-Si bond into valuable CF2-containing molecules.
机译:描述了使用Abin作为自由基引发剂的初始氟烷基的自由基水合和氢化硅烷化的第一例。 该方案具有良好的官能团耐受性,操作简单性,高原子经济,并且易于扩大,使得有效地组装各种α-二氟化烷基硼和中等至优异产率的烷基硅烷。 通过进一步将C-B键和C-Si键转变为有价值的CF 2分子,通过进一步转化来证明这些产品的合成效用。

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  • 来源
    《Organic letters 》 |2019年第20期| 共5页
  • 作者单位

    Zunyi Med Univ Sch Pharm Gener Drug Res Ctr Guizhou Prov Key Lab Biocatalysis &

    Chiral Drug Synth Guizhou Zunyi 563006 Guizhou Peoples R China;

    Sun Yat Sen Univ Sch Pharmaceut Sci Guangzhou 510006 Guangdong Peoples R China;

    Zunyi Med Univ Sch Pharm Gener Drug Res Ctr Guizhou Prov Key Lab Biocatalysis &

    Chiral Drug Synth Guizhou Zunyi 563006 Guizhou Peoples R China;

    Sun Yat Sen Univ Sch Pharmaceut Sci Guangzhou 510006 Guangdong Peoples R China;

    Zunyi Med Univ Sch Pharm Gener Drug Res Ctr Guizhou Prov Key Lab Biocatalysis &

    Chiral Drug Synth Guizhou Zunyi 563006 Guizhou Peoples R China;

    Sun Yat Sen Univ Sch Pharmaceut Sci Guangzhou 510006 Guangdong 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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