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Stereodivergent Synthesis of α/α-Disubstituted α-Amino Acids via Synergistic Cu/Ir Catalysis

机译:协同Cu / Ir催化立体异构合成α/α-二取代α-氨基酸

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摘要

Cu/Ir dual catalysis has been developed for the stereodivergent α-allylation of aldimine esters. The method enables the preparation of a series of nonproteinogenic α-amino acids (α-AAs) bearing two contiguous stereogenic centers in high yield with excellent stereoselectivity. All four product stereoisomers could be obtained from the same set of starting materials via pairwise combination of two chiral catalysts. Notably, one-pot protocol could be successfully applied for the preparation of the bimetallic Cu/Ir complexes to simplify the manipulation of Cu/Ir dual catalysis. This method could be further utilized for the construction of the key intermediate of a bioactive pyrrolidine derivative and the concise synthesis of a plant growth regulator (2 S ,3 S )-2-amino-3-cyclopropylbutanoic acid.
机译:已经开发了Cu / Ir双重催化用于醛亚胺酯的立体发散性α-烯丙基化。该方法能够以优异的立体选择性高产率制备一系列带有两个连续的立体中心的非蛋白原性α-氨基酸(α-AAs)。通过两种手性催化剂的成对组合,可以从同一组起始原料获得所有四种产物立体异构体。值得注意的是,一锅法可以成功地用于双金属Cu / Ir配合物的制备,以简化Cu / Ir双重催化的操作。该方法可进一步用于构建生物活性吡咯烷衍生物的关键中间体和植物生长调节剂(2 S,3 S)-2-氨基-3-环丙基丁酸的简明合成。

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  • 来源
    《Journal of the American Chemical Society》 |2018年第4期|1508-1513|共6页
  • 作者单位

    College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China;

    College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China,State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin 300071, 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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  • 入库时间 2022-08-18 03:07:17

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