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Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst

机译:手性铱单膦催化剂促进的氧杂苯并降冰片二烯与胺的不对称开环

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摘要

A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).
机译:发现一种新型铱单膦催化剂可有效地使苯并降冰片二烯与胺类不对称开环,从而以高收率(高达98%)和出色的对映选择性(> 99%)提供一系列手性取代的二氢萘。

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  • 来源
    《Chemical Communications》 |2013年第85期|9959-9961|共3页
  • 作者单位

    State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Ling Ling Road, Shanghai, 200032, China,School of Pharmaceutical Sciences, Gannon Medical University, 1 Yixueyuan Road, Ganzhou, Jiangxi, 341000, China;

    School of Pharmaceutical Sciences, Gannon Medical University, 1 Yixueyuan Road, Ganzhou, Jiangxi, 341000, China;

    School of Pharmaceutical Sciences, Gannon Medical University, 1 Yixueyuan Road, Ganzhou, Jiangxi, 341000, China;

    State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Ling Ling Road, Shanghai, 200032, China;

    Institute of Creativity, Hong Kong Baptist University, Hong Kong, China;

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  • 入库时间 2022-08-17 13:18:44

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