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Catalytic Asymmetric Umpolung Allylation of Imines

机译:亚胺的催化不对称Uppolung烯丙基化

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摘要

Here we report an iridium-catalyzed asymmetric umpolung allylation of imines as a general approach to prepare 1,4-disubstituted homoallylic amines, a fundamental class of compounds that are hitherto not straightforward to obtain. This transformation proceeds by a cascade involving an intermolecular regioselective allylation of 2-azaallyl anions and a following 2-aza-Cope rearrangement, utilizes easily available reagents and catalysts, tolerates a substantial scope of substrates, and readily leads to various enantipenriched, 1,4-disubstituted homoallylic primary amines.
机译:在这里,我们报告铱的亚胺催化的不对称聚烯丙基烯丙基化作为制备1,4-二取代的均烯丙基胺的通用方法,这是迄今为止尚不容易获得的一类基本化合物。这种转化是通过级联反应进行的,该级联反应涉及2-氮杂烯丙基阴离子的分子间区域选择性烯丙基化和随后的2-氮杂-Cope重排,利用容易获得的试剂和催化剂,可耐受较大范围的底物,并容易导致各种对映体富集,1,4 -二取代的均烯丙基伯胺。

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  • 来源
    《Journal of the American Chemical Society》 |2016年第40期|13103-13106|共4页
  • 作者单位

    Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China;

    Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China;

    Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China;

    Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China;

    Department of Emergency, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, 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);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:08:58

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