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首页> 外文期刊>Journal of the American Chemical Society >Synthesis of Adjacent Quaternary Stereocenters by Catalytic Asymmetric Allylboration
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Synthesis of Adjacent Quaternary Stereocenters by Catalytic Asymmetric Allylboration

机译:催化不对称烯丙基硼酸酯合成相邻的季立体中心。

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摘要

Allylboration of ketones with γ-disubsti-tuted allylboronic acids is performed in the presence of chiral BINOL derivatives. The reaction is suitable for single-step creation of adjacent quaternary stereocenters with high selectivity. We show that, with an appropriate choice of the chiral catalyst and the stereoisomeric prenyl substrate, full control of the stereo- and enantioselectivity is possible in the reaction.
机译:在手性BINOL衍生物存在下,用γ-二取代的烯丙基硼酸对酮进行烯丙基硼化。该反应适合以高选择性单步生成相邻的四元立体中心。我们表明,通过适当选择手性催化剂和立体异构异戊二烯基底物,可以在反应中完全控制立体和对映选择性。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2015年第35期|11262-11265|共4页
  • 作者单位

    Department of Organic Chemistry Stockholm University, SE-106 91 Stockholm, Sweden;

    Department of Organic Chemistry Stockholm University, SE-106 91 Stockholm, Sweden;

    Department of Materials and Environmental Chemistry, Stockholm University, SE-106 91 Stockholm, Sweden;

    Department of Organic Chemistry Stockholm University, SE-106 91 Stockholm, Sweden;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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