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A Stereoselective Hydroamination Transform To Access Polysubstituted Indolizidines

机译:立体选择性加氢胺化反应可访问多取代的吲哚并咪唑

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摘要

Stereoselective, intramolecular, formal hydroamination of dienamines via directed hydroboration is reported. Four stereocenters are set in the process. Natural and unnatural indolizidine alkaloids can be synthesized from simple unsaturated amines using the title process.
机译:据报道,通过定向的硼氢化作用,对二烯胺进行了立体选择性的,分子内的,正式的氢化胺化反应。在此过程中设置了四个立体中心。天然和非天然的吲哚并立定生物碱可以使用标题方法由简单的不饱和胺合成。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第4期|p.2012-2015|共4页
  • 作者单位

    Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, Lajolla, California 92037, United States;

    Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, Lajolla, California 92037, United States;

    Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, Lajolla, California 92037, United States;

    Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, Lajolla, California 92037, 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 03:13:21

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