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The asymmetric synthesis of chiral cyclic α-hydroxy phosphonates and quaternary cyclic a-hydroxy phosphonates

机译:手性环状α-羟基膦酸酯和季环状α-羟基膦酸酯的不对称合成

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摘要

A highly practical, catalytic enantioselective cyclic phosphite addition to aldehydes and ketones was developed. The reaction rate of the asymmetric hydrophosphonylation was significantly enhanced by the addition of silver carbonate. Particularly, significant improvement has been achieved on the asymmetric hydrophosphonylation of unactivated ketones, giving quaternary a-hydroxy phosphonates with excellent enantioselectivity (up to 99% ee).
机译:开发了一种高度实用的对醛和酮的催化对映选择性环状亚磷酸酯。通过添加碳酸银,不对称羰基化反应的反应速率大大提高。特别是,未活化的酮的不对称加氢膦酰基化已经获得了显着的改进,从而得到具有优异对映选择性(高达99%ee)的季α-羟基膦酸酯。

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  • 来源
    《Organic & biomolecular chemistry》 |2012年第8期|p.1680-1685|共6页
  • 作者单位

    Current address: Institute of Energy and Fuel, Xinxiang University, Xinxiang, Henan 453003, P. R. China;

    Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei, 430079, P. R. China;

    Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei, 430079, P. R. China;

    Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei, 430079, P. R. China;

    Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan, Hubei, 430079, P. R. China;

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