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An Expeditious Synthesis of the MDM2-p53 Inhibitor AM-8553

机译:MDM2-p53抑制剂AM-8553的快速合成

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摘要

The development of the structurally complex MDM2/p53 inhibitor AM-8553 was impeded by the low yield of the initial synthesis. A second generation synthesis is described that features a Noyori dynamic kinetic resolution, a highly diastereoselective allylation, and a novel oxazoline-assisted piperidinone forming reaction to provide AM-8553 in 35.6% yield and 11 steps.
机译:结构复杂的MDM2 / p53抑制剂AM-8553的开发受到初始合成产量低的阻碍。描述了具有Noyori动态动力学分辨率,高度非对映选择性烯丙基化和新型恶唑啉辅助哌啶酮形成反应的第二代合成方法,以35.6%的产率和11个步骤提供AM-8553。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2012年第30期|p.12855-12860|共6页
  • 作者单位

    Department of Medicinal Chemistry, Amgen, Inc., 1120 Veterans Boulevard, S. San Francisco, California 94080, United States;

    Department of Medicinal Chemistry, Amgen, Inc., 1120 Veterans Boulevard, S. San Francisco, California 94080, United States;

    Department of Medicinal Chemistry, Amgen, Inc., 1120 Veterans Boulevard, S. San Francisco, California 94080, United States;

    Department of Medicinal Chemistry, Amgen, Inc., 1120 Veterans Boulevard, S. San Francisco, California 94080, United States;

    Department of Medicinal Chemistry, Amgen, Inc., 1120 Veterans Boulevard, S. San Francisco, California 94080, United States;

    Department of Pharmaceutics, Amgen, Inc., 360 Binney Street, Cambridge, Massachusetts 02142, 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
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  • 入库时间 2022-08-18 03:13:35

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