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Direct enantioselective vinylogous aldol-cyclization cascade reaction of allyl pyrazoleamides with isatins: asymmetric construction of spirocyclic oxindole-dihydropyranones

机译:烯丙基吡唑酰胺与靛红的直接对映选择性乙烯基醛醇醛化环化级联反应:螺环式羟吲哚-二氢吡喃酮的不对称结构

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摘要

The first enantioselective vinylogous aldol-cyclization cascade reaction of allyl pyrazoleamides with isatins is reported. With 1 mol% of Takemoto catalyst, optically active spirocyclic oxindole-dihydropyranones were obtained in excellent yields (93-99%) and good-to-excellent enantioselectivities (82-97% ee).
机译:报道了烯丙基吡唑酰胺与靛红的第一对映选择性乙烯基醛醇醛化环化级联反应。用1 mol%的Takemoto催化剂,可以以优异的收率(93-99%)和良好至优异的对映选择性(82-7%ee)获得旋光性螺环肟基-二氢吡喃酮。

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  • 来源
    《Chemical Communications》 |2014年第74期|10790-10792|共3页
  • 作者单位

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China;

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  • 入库时间 2022-08-17 13:16:20

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