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Direct Asymmetric Reductive Amination

机译:直接不对称还原胺化

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摘要

β-Amino acid derivatives are valuable chiral building blocks in the synthesis of Pharmaceuticals.' Asymmetric hydrogenation of protected dehydroamino acid derivatives such as N-acyl enamines, along with other methods for chiral amine synthesis, has proven to be a valuable methodology for the preparation of these targets. However, from an efficiency standpoint, all of these methods require additional steps involving manipulation of the N-protecting group.
机译:β-氨基酸衍生物是药物合成中有价值的手性结构单元。被保护的脱氢氨基酸衍生物(例如N-酰基烯胺)的不对称氢化,以及用于手性胺合成的其他方法,已被证明是制备这些靶标的一种有价值的方法。然而,从效率的观点来看,所有这些方法都需要涉及操纵N-保护基团的额外步骤。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2009年第32期|11316-11317|共2页
  • 作者单位

    Department of Process Research, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065;

    Department of Process Research, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065;

    Corporate Research & Development Division, Takasago International Corporation, 1-4-11 Nishi-yawata, Hiratsuka City,Kanagawa 254-0073, Japan;

    Corporate Research & Development Division, Takasago International Corporation, 1-4-11 Nishi-yawata, Hiratsuka City,Kanagawa 254-0073, Japan;

    Corporate Research & Development Division, Takasago International Corporation, 1-4-11 Nishi-yawata, Hiratsuka City,Kanagawa 254-0073, Japan;

  • 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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  • 入库时间 2022-08-18 03:17:12

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