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A new synthetic approach to 6-unsubstituted phenanthridine and phenanthridine-like compounds under mild and metal-free conditions

机译:温和无金属条件下6-未取代菲啶类和菲啶类化合物的新合成方法

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摘要

A new and mild synthetic approach for the synthesis of 6-unsubstituted phenanthridine and phenanthridine-like compounds under metal-free conditions at room temperature has been developed. The strategy involved a tandem azide rearrangement/intramolecular annulation and oxidation reactions of biarylmethyl azide precursors to obtain the desired products in up to 99% yields with high regioselectivity.
机译:开发了一种新的温和的合成方法,用于在室温下在无金属条件下合成6-未取代的菲啶和菲啶类化合物。该策略涉及联芳基叠氮化物前体的串联叠氮化物重排/分子内环化和氧化反应,以高的区域选择性以高达99%的产率获得所需的产物。

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  • 来源
    《Organic & biomolecular chemistry》 |2014年第28期|5077-5081|共5页
  • 作者单位

    Chulabhom Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand;

    Chulabhom Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand;

    Chulabhom Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand;

    Chulabhom Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand,Program on Chemical Biology, Chulabhom Graduate Institute, Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand;

    Chulabhom Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand,Program on Chemical Biology, Chulabhom Graduate Institute, Center of Excellence on Environmental Health and Toxicology, CHE, Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand;

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