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首页> 外文期刊>Organic letters >Ga(OTf)(3)-Catalyzed Temperature-Controlled Regioselective Friedel-Crafts Alkylation of Trifluoromethylated 3-Indolylmethanols with 2-Substituted Indoles: Divergent Synthesis of Trifluoromethylated Unsymmetrical 3,3 '-and 3,6 '-Bis(indolyl)methanes
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Ga(OTf)(3)-Catalyzed Temperature-Controlled Regioselective Friedel-Crafts Alkylation of Trifluoromethylated 3-Indolylmethanols with 2-Substituted Indoles: Divergent Synthesis of Trifluoromethylated Unsymmetrical 3,3 '-and 3,6 '-Bis(indolyl)methanes

机译:Ga(otf)(3) - 用2取代的吲哚(Trifloromethylated 3-吲哚基甲醇)的催化温度控制的催化剂烷基化:三氟甲基化的非对称3,3'-和3,6'-bis(吲哚基)甲烷的发散合成

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摘要

An unprecedented Ga(OTf)(3)-catalyzed, temperature-controlled regiodivergent alkylation of 2-substituted indoles with trifluoromethylated 3-indolylmethanols is described that provides structurally diverse unsymmetrical 3,3'-and 3,6'-bis(indolyl)methanes with a CF3-containing quaternary carbon center in good to excellent yields under mild conditions. In addition, this present protocol could be successfully extended to the synthesis of difluoromethylated 3,3'- and 3,6'-bis(indolyl)methanes with excellent efficiency.
机译:描述了前所未有的Ga(otf)(3) - 用三氟甲基化的3-吲哚基甲醇的2-取代的吲哚糖的催化,温度控制的直肠烷基化,其提供了结构不同的非对称3,3'-and 3,6'-Bis(吲哚基)甲烷 在温和条件下,含CF3的季碳中心良好至优异的产率。 此外,该本文方案可以成功地延伸到二氟甲基化的3,3'-和3,6'-双(吲哚基)甲醇的合成,具有优异的效率。

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  • 来源
    《Organic letters》 |2019年第9期|共6页
  • 作者单位

    Nanjing Forestry Univ Coll Chem Engn Jiangsu Key Lab Biomass Based Green Fuels &

    Chem Nanjing 210037 Jiangsu Peoples R China;

    Nanjing Forestry Univ Coll Chem Engn Jiangsu Key Lab Biomass Based Green Fuels &

    Chem Nanjing 210037 Jiangsu Peoples R China;

    Nanjing Forestry Univ Coll Chem Engn Jiangsu Key Lab Biomass Based Green Fuels &

    Chem Nanjing 210037 Jiangsu Peoples R China;

    Nanjing Forestry Univ Coll Chem Engn Jiangsu Key Lab Biomass Based Green Fuels &

    Chem Nanjing 210037 Jiangsu 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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