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首页> 外文期刊>Organic & biomolecular chemistry >In situ activation of benzyl alcohols with XtalFluor-E: formation of 1,1-diarylmethanes and 1,1,1-triarylmethanes through Friedel-Crafts benzylation
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In situ activation of benzyl alcohols with XtalFluor-E: formation of 1,1-diarylmethanes and 1,1,1-triarylmethanes through Friedel-Crafts benzylation

机译:用XtalFluor-E原位活化苄醇:通过Friedel-Crafts苄基化反应形成1,1-二芳基甲烷和1,1,1-三芳基甲烷

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摘要

The Friedel-Crafts benzylation of arenes using benzyl alcohols activated in situ with XtalFluor-E is described. A wide range of 1,1-diarylmethanes and 1,1,1-triarylmethanes were prepared under experimentally simple and mild conditions, without the need for a transition metal or a strong Lewis acid. Notably, the reactivity observed demonstrates the potential of XtalFluor-E to induce C-OH bond ionization and S_N1 reactivity of benzylic alcohols.
机译:描述了使用用XtalFluor-E原位活化的苄醇对芳烃的Friedel-Crafts苄基化。在实验上简单温和的条件下,无需过渡金属或强路易斯酸即可制备各种1,1,1-二芳基甲烷和1,1,1-三芳基甲烷。值得注意的是,观察到的反应性证明XtalFluor-E可能诱导C-OH键电离和苄醇的S_N1反应性。

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  • 来源
    《Organic & biomolecular chemistry》 |2015年第8期|2243-2246|共4页
  • 作者单位

    Canada Research in Organic and Medicinal Chemistry, CGCC, PROTEO, Departement de chimie, Universite Laval, 1045 Avenue de la Medecine, Pavilion Alexandre-Vachon, Quebec, Quebec G1V 0A6, Canada;

    Canada Research in Organic and Medicinal Chemistry, CGCC, PROTEO, Departement de chimie, Universite Laval, 1045 Avenue de la Medecine, Pavilion Alexandre-Vachon, Quebec, Quebec G1V 0A6, Canada;

    Canada Research in Organic and Medicinal Chemistry, CGCC, PROTEO, Departement de chimie, Universite Laval, 1045 Avenue de la Medecine, Pavilion Alexandre-Vachon, Quebec, Quebec G1V 0A6, Canada;

    Canada Research in Organic and Medicinal Chemistry, CGCC, PROTEO, Departement de chimie, Universite Laval, 1045 Avenue de la Medecine, Pavilion Alexandre-Vachon, Quebec, Quebec G1V 0A6, Canada;

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