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Side-Arm-Promoted Highly Enantioselective Ring-Opening Reactions and Kinetic Resolution of Donor-Acceptor Cyclopropanes with Amines

机译:侧臂促进的高对映选择性开环反应和胺给体-受体环丙烷的动力学拆分

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摘要

A Ni-catalyzed asymmetric ring-opening reaction of 2-substituted cyclopropane-1,1-dicarboxylates with aliphatic amines has been accomplished using the chiral indane-trisoxazoline (In-TOX) ligand. This highly enantioselective reaction provides an efficient approach to a variety of chiral γ-substituted γ-amino acid derivatives, which are readily transformed into multifunctionalized piperidines and γ-lactams. The single-crystal X-ray structure of the TOX-Ni complex is provided, and the role of the side arm in the chiral ligand is discussed.
机译:使用手性茚满-三恶唑啉(In-TOX)配体已经完成了Ni催化的2-取代的环丙烷-1,1-二羧酸酯与脂肪族胺的不对称开环反应。这种高度对映选择性的反应为各种手性γ-取代的γ-氨基酸衍生物提供了一种有效的方法,这些衍生物很容易转化为多官能化的哌啶和γ-内酰胺。提供了TOX-Ni络合物的单晶X射线结构,并讨论了侧臂在手性配体中的作用。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第22期|p.9066-9069|共4页
  • 作者单位

    The State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345Lingling Lu, Shanghai 200032, P. R. China;

    The State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345Lingling Lu, Shanghai 200032, P. R. China;

    The State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345Lingling Lu, Shanghai 200032, P. R. China;

    The State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345Lingling Lu, Shanghai 200032, P. R. China;

    The State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345Lingling Lu, Shanghai 200032, P. R. 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
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