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首页> 外文期刊>Organic & biomolecular chemistry >Chiral phosphine-catalyzed asymmetric allylic alkylation of 3-substituted benzofuran-2(3H)-ones or oxindoles with Morita-Baylis-Hillman carbonates
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Chiral phosphine-catalyzed asymmetric allylic alkylation of 3-substituted benzofuran-2(3H)-ones or oxindoles with Morita-Baylis-Hillman carbonates

机译:森田-贝利斯-希尔曼碳酸盐的3-取代苯并呋喃-2(3H)-一或羟吲哚的手性膦催化不对称烯丙基烷基化

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摘要

An efficient chiral phosphine-catalyzed asymmetric substitution reaction of MBH carbonates with 3-substituted benzofiiran-2(3H)-ones or 3-substituted oxindoles has been described in this context, giving the corresponding allylic alkylation products bearing adjacent quaternary and tertiary stereogenic centers in high yields, moderate diastereoselectivities and high enantioselectivities under mild conditions.
机译:在此背景下,已经描述了MBH碳酸酯与3-取代的苯并呋喃-2(3H)-一或3-取代的羟吲哚的有效手性膦催化的不对称取代反应,得到了相应的烯丙基烷基化产物,该产物带有相邻的季铵和叔立体异构中心。在温和条件下具有高收率,中等非对映选择性和高对映选择性。

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  • 来源
    《Organic & biomolecular chemistry》 |2012年第35期|p.7158-7166|共9页
  • 作者单位

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China;

    Key Laboratory for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China,State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Lu, Shanghai 200032, China;

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