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Enantioselective Formal Aza-Diels-Alder Reactions of Enones with Cyclic Imines Catalyzed by Primary Aminothioureas

机译:初级氨基硫脲催化的烯酮与环状亚胺的对映选择性形式氮杂-Diels-Alder反应

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摘要

A highly enantio- and diastereoselective synthesis of indolo- and benzoquinolizidine compounds has been , developed through the formal aza-Diels-Alder reaction of enones with cyclic imines. This transformation is catalyzed by a new bifunctional primary aminothiourea that achieves simultaneous activation of both the enone and imine reaction components.
机译:通过烯酮与环状亚胺的正式氮杂-狄尔斯-阿尔德反应,已开发出吲哚-和苯并喹oli嗪化合物的高度对映体和非对映体选择性。这种转化被新型双功能伯氨基硫脲催化,该双官能伯氨基硫脲可同时激活烯酮和亚胺反应组分。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2013年第5期|1891-1894|共4页
  • 作者单位

    Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States;

    Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 03:12:25

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