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Asymmetric Fluorination of α-Branched Aldehydes by Chiral Primary Amine Catalysis: Reagent-Controlled Enantioselectivity Switch

机译:手性伯胺催化作用的α-支链醛的不对称氟化:试剂控制的倾向性开关

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摘要

Asymmetric fluorination of α-branched aldehydes catalyzed by chiral primary amines under mild conditions has been developed. Both enantiomers could be obtained with good yields (up to 96%) and a high enantioselectivity (up to 90% ee) by a simple swap of the fluorination reagents.
机译:开发了在温和条件下由手性伯胺催化的α-支链醛的不对称氟化。 通过简单的氟化试剂,可以通过良好的产率(高达96%)和高映选择性(高达90%ee)获得的映异构体。

著录项

  • 来源
    《The Journal of Organic Chemistry》 |2018年第7期|共7页
  • 作者单位

    College of Chemistry Beijing Normal University Xinjiekouwai Street 19 Beijing 100875 China;

    Key Laboratory for Molecular Recognition and Function Institute of Chemistry The Chinese Academy of Sciences Beijing 100190 China;

    College of Chemistry Beijing Normal University Xinjiekouwai Street 19 Beijing 100875 China;

    Key Laboratory for Molecular Recognition and Function Institute of Chemistry The Chinese Academy of Sciences Beijing 100190 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

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