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Diphenylprolinol silyl ether as a catalyst in an asymmetric,catalytic and direct α-benzoyloxylation of aldehydesf

机译:二苯基脯氨醇甲硅烷基醚作为醛的不对称,催化和直接α-苯甲酰氧基化的催化剂

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摘要

Diphenylprolinol silyl ether was found to promote asymmetric, catalytic and direct a-benzoyloxylation of aldehydes with benzoyl peroxide to afford oxidized products in good yields with excellent enantioselectivity.rnOptically active α-acyloxy- or α-hydroxy-aldehydes are important intermediates in organic synthesis. α-Oxygenation of aldehydes is one of the direct and straightforward methods for their synthesis, and there are several enantioselective and catalytic methods. For instance, the nitroso aldol reaction of aldehyde and nitrosobenzene catalyzed by proline, which has been developed independently by three groups including our group, is one of the powerful methods for the formation of α-aminoxy aldehydes, which are easily transformed into α-hydroxy aldehydes.
机译:发现二苯基脯氨醇甲硅烷基醚可促进醛与过氧化苯甲酰的不对称,催化和直接的α-苯甲酰氧基化反应,以良好的收率和良好的对映选择性提供氧化产物。光学活性的α-酰氧基-或α-羟基-醛是有机合成中的重要中间体。醛的α-氧合反应是直接合成醛的方法之一,并且有几种对映选择性和催化方法。例如,脯氨酸催化的醛和亚硝基苯的亚硝基羟醛反应(包括我们的研究小组在内)是由三个小组独立开发的,是形成α-氨基醛的有效方法之一,易于转化为α-羟基醛。

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  • 来源
    《Chemical Communications》 |2009年第21期|3083-3085|共3页
  • 作者

    Hiroaki Gotoh; Yujiro Hayashi;

  • 作者单位

    Department of Industrial Chemistry, Faculty of Engineering,Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo,162-8601, Japan;

    Department of Industrial Chemistry, Faculty of Engineering,Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo,162-8601, Japan Research Institute for Science and Technology, Tokyo University of Science, Kagurazaka, Shinjuku-ku, Tokyo, 162-8601, Japan;

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  • 入库时间 2022-08-17 13:25:42

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