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Amine-N-heterocyclic carbene cascade catalysis for the asymmetric synthesis of fused indane derivatives with multiple chiral centres

机译:胺-N-杂环卡宾级联催化不对称合成具有多个手性中心的稠合茚满衍生物

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摘要

An aminocatalytic asymmetric Diels-Alder reaction of 2/4-dienals and labile 1-indenones in situ generated from 3-bromo-1-indanones was developed, producing highly fused indane products with multiple chiral centres followed by a cascade N-heterocyclic carbene-mediated benzoin condensation.
机译:开发了由3-溴-1-茚满酮生成的2 / 4-二烯醛和不稳定的1-茚满的氨基催化不对称Diels-Alder反应,产生具有多个手性中心的高度稠合的茚满产物,随后是级联的N-杂环卡宾介导的安息香缩合。

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  • 来源
    《Chemical Communications》 |2013年第52期|5892-5894|共3页
  • 作者单位

    Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China;

    College of Pharmacy, Third Military Medical University, Chongqing 400038, China;

    Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China;

    Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China;

    Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China;

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