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首页> 外文期刊>The Journal of Organic Chemistry >Photoredox-Catalyzed Intermolecular Radical Arylthiocyanation/Arylselenocyanation of Alkenes: Access to Aryl-Substituted Alkylthiocyanates/Alkylselenocyanates
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Photoredox-Catalyzed Intermolecular Radical Arylthiocyanation/Arylselenocyanation of Alkenes: Access to Aryl-Substituted Alkylthiocyanates/Alkylselenocyanates

机译:光致毒催化的分子间自由基芳基氰基氰酸化/烯烃烷烃:获得芳基取代的烷基硫氰酸酯/烷基硒菁酸酯

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摘要

An efficient and highly selective approach for intermolecular arylthiocyanation/arylselenocyanation of alkenes has been reported under mild conditions. Using diazonium salts as the arylating agent and ammonium thiocyanate as the thiocyanate source, chemoselective difunctionalization of alkenes has been done under irradiation of visible light. Both styrenes and acrylates work well to deliver various aryl-substituted alkylthiocyanates in good to excellent yields. In addition, hitherto unknown beta-aryl alkylselenocyanates were also synthesized using the developed protocol with potassium selenocyanate.
机译:在温和条件下,报道了在温和条件下报道了对分子间氧化苯氰化/芳基苯胺硅烷化的高效且高度选择的含量。 使用重氮盐作为芳基氰酸酯作为硫氰酸盐源的芳酸酯源,在可见光的照射下已经进行了烯烃的化学选择性偏移。 苯乙烯和丙烯酸酯都是良好的,以良好地提供各种芳基取代的烷基硫氰酸酯,优异的产率。 此外,还使用与硒氰酸氢钾的发育方案合成,合成迄今为止未知的β-芳基烷基硒酸酯。

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