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首页> 外文期刊>Organic & biomolecular chemistry >The asymmetric Cu(Ⅱ)-indolinylmethanol complex catalyzed Diels-Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles
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The asymmetric Cu(Ⅱ)-indolinylmethanol complex catalyzed Diels-Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters: an efficient route to functionalized tetrahydrocarbazoles

机译:Cu(Ⅱ)-吲哚基甲醇络合物的不对称催化2-乙烯基吲哚与β,γ-不饱和α-酮酸酯的Diels-Alder反应:官能化四氢咔唑的有效途径

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摘要

An efficient asymmetric Diels-Alder reaction of 2-vinylindoles with β,γ-unsaturated α-ketoesters has been developed for the construction of functionalized tetrahydrocarbazoles. The products were obtained in high yields (up to 96%) with good stereoselectivities (ee up to 95%, dr up to >99 :1).
机译:已经开发了2-乙烯基吲哚与β,γ-不饱和α-酮酸酯的有效不对称Diels-Alder反应,用于构造官能化的四氢咔唑。以高产率(高达96%)和良好的立体选择性(ee高达95%,dr高达> 99∶1)获得产物。

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  • 来源
    《Organic & biomolecular chemistry》 |2014年第24期|4172-4176|共5页
  • 作者单位

    Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, P. R. China;

    Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, P. R. China;

    Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, P. R. China;

    Institute of Medicinal Chemistry, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, P. R. China,Institute of Human Virology, Sun Yat-sen University, Guangzhou 510080, P. R. China;

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