首页> 外文期刊>Organic Chemistry Frontiers >Selective assembly of N1-and N2-alkylated 1,2,3-triazoles via copper-catalyzed decarboxylative cycloaddition of alkynyl carboxylic acids with ethers and azidotrimethylsilane
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Selective assembly of N1-and N2-alkylated 1,2,3-triazoles via copper-catalyzed decarboxylative cycloaddition of alkynyl carboxylic acids with ethers and azidotrimethylsilane

机译:通过铜催化的甲基羧酸与醚和氮丙酮甲基硅烷选择性组装N1-和N2-烷基化的1,2,3-三唑的选择性组装N1-和N2-烷基化的1,2,3-三唑

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摘要

A convenient and practical copper-catalyzed three component protocol has been developed for the selective assembly of N1- and N2-alkylated 1,2,3-triazoles from readily available alkynyl carboxylic acids, azidotrimethylsilane (TMSN3) and ethers. The present reaction can be achieved by decarboxylative cycloaddition of alkynyl carboxylic acids with TMSN3 and ethers, which is an efficient and selective approach to access a number of N1- and N2-alkylated 1,2,3-triazoles in moderate to good yields.
机译:已经开发了一种方便实用的铜催化的三种组分方案,用于从容易获得的炔基羧酸,氮杂甲基硅烷(TMSN3)和醚的N1-和N 2烷基化1,2,3-三唑的选择性组装。 通过具有TMSN3和醚的炔基羧酸的脱羧环加入可以实现本反应,这是一种有效且选择性的方法,可进入中等至良好产率的N1-和N 2烷基化的1,2,3-三唑。

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  • 来源
    《Organic Chemistry Frontiers》 |2019年第24期|共6页
  • 作者单位

    Qufu Normal Univ Sch Chem &

    Chem Engn Qufu 273165 Shandong Peoples R China;

    Qufu Normal Univ Sch Chem &

    Chem Engn Qufu 273165 Shandong Peoples R China;

    Qufu Normal Univ Sch Chem &

    Chem Engn Qufu 273165 Shandong Peoples R China;

    Chinese Acad Sci Northwest Inst Plateau Biol Qinghai Prov Key Lab Tibetan Med Res Xining 810008 Qinghai Peoples R China;

    Changsha Univ Sci &

    Technol Sch Chem &

    Food Engn Changsha 410114 Hunan Peoples R China;

    Qufu Normal Univ Sch Chem &

    Chem Engn Qufu 273165 Shandong 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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