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Enantioselective Synthesis of Highly Substituted Furans by a Copper(Ⅱ)-Catalyzed Cycloisomerization-lndole Addition Reaction

机译:铜(Ⅱ)催化的环异构化-吲哚加成反应对映选择性合成高取代度的呋喃

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摘要

A catalytic enantioselective reaction based on a copper(Ⅱ) catalyst strictly containing chiral anionic ligands is described. In the present work, copper(Ⅱ)-phosphate catalyst promotes the intramolecular heterocyclization of 2-(l-alkynyl)-2-alkene-l-ones and facilitates high levels of enantioselectivity in the subsequent nucleophile attack. Mechanistic studies suggest that formation of a copper(Ⅱ) -indole species is important for catalysis.
机译:描述了一种基于严格含有手性阴离子配体的铜(Ⅱ)催化剂的催化对映选择性反应。在目前的工作中,磷酸铜(Ⅱ)催化剂促进了2-(1-炔基)-2-烯烃-1-酮的分子内杂环化,并在随后的亲核试剂攻击中促进了高水平的对映选择性。机理研究表明,铜(Ⅱ)-吲哚物种的形成对于催化很重要。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第22期|p.8486-8489|共4页
  • 作者单位

    Department of Chemistry, University of California, Berkeley, California 94720, United States;

    Department of Chemistry, University of California, Berkeley, California 94720, United States;

    Department of Chemistry, University of California, Berkeley, California 94720, United States;

    Department of Chemistry, University of California, Berkeley, California 94720, United States;

  • 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);
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  • 正文语种 eng
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