首页> 外文期刊>Journal of the American Chemical Society >The Michael Addition-Elimination of Ylides to alpha,beta-Unsaturated (mines.Highly Stereoselective Synthesis of Vinylcyclopropanecarbaldehydes and Vinylcyclopropylaziridines
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The Michael Addition-Elimination of Ylides to alpha,beta-Unsaturated (mines.Highly Stereoselective Synthesis of Vinylcyclopropanecarbaldehydes and Vinylcyclopropylaziridines

机译:内酯的迈克尔加成反应消除为α,β-不饱和键(胺。乙烯基环丙烷甲醛和乙烯基环丙基氮丙啶的高度立体选择性合成

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摘要

Much attention has been paid to the construction of multisub-stituted cyclopropanes,the basic structural elements in a wide range of biologically active compounds as well as important intermediates in organic synthesis.The tandem Michael addition-elimination of ylides to electron-deficient alkenes provides easy access to functionalized cyclopropanes.
机译:多元取代的环丙烷的构建,广泛的生物活性化合物的基本结构要素以及有机合成中的重要中间体已经引起了人们的广泛关注。串联的迈克尔加成-消除电子不足的烯烃可轻松实现获得功能化的环丙烷。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2005年第35期|p.12222-12223|共2页
  • 作者单位

    State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China;

    State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China;

    State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China;

    State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China;

    State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,354 Fenglin Lu,Shanghai 200032,China;

  • 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 化学;
  • 关键词

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