首页> 外文期刊>Organic & biomolecular chemistry >Modular synthesis of bis- and tris-1,2,3-triazoles by permutable sequential azide-aryne and azide-alkyne cycloadditions
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Modular synthesis of bis- and tris-1,2,3-triazoles by permutable sequential azide-aryne and azide-alkyne cycloadditions

机译:可置换的叠氮化物-芳烃和叠氮化物-炔烃环加成的模块化合成双-和三-1,2,3-三唑

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摘要

A modular synthetic method for bis- and tris-1,2,3-triazoles that include a benzotriazole structure was developed on the basis of sequential azide-aryne and azide-alkyne cycloadditions. The key to success was efficient halogen-metal exchange reaction-mediated generation of aryne from ortho-iodoaryl triflates bearing a base-sensitive terminal alkyne moiety, which was achieved using trimethylsilylmethyl Grignard reagent.
机译:在顺序叠氮化物-芳烃和叠氮化合物-炔烃环加成反应的基础上,开发了包括苯并三唑结构的双-和三-1,2,3-三唑的模块化合成方法。成功的关键是由卤素-金属交换反应介导的从带有碱敏性末端炔基部分的邻碘芳基三氟甲磺酸酯生成芳烃,这是使用三甲基甲硅烷基甲基格氏试剂实现的。

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  • 来源
    《Organic & biomolecular chemistry》 |2014年第38期|7489-7493|共5页
  • 作者单位

    Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan;

    Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan;

    Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan;

    Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan;

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