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Design,Synthesis of Chiral Ketone and Application in Asymmetric Epoxidation

         

摘要

A class of chiral ketone was synthesized for asymmetric epoxidation. High ee values have been obtained for a number of cis olefin and trans olefin. The epoxidation was stereospecific with no isomerizatiom observed in the epoxidation of acyclic system. Encourageingly high ee value has also been obtained for a number of terminal olefins. Mechanistic studies show that electronic interactions play an important role in the stereodifferentiation.

著录项

  • 来源
    《合成化学》 |2004年第z1期|22-22|共1页
  • 作者单位

    Department of Chemistry, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China;

    Department of Chemistry, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China;

    Department of Chemistry, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China;

  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类
  • 关键词

    Asymmetric Epoxidation; olefins;

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