首页> 外文期刊>Beilstein journal of organic chemistry. >One-pot gold-catalyzed synthesis of 3-silylethynyl indoles from unprotected o-alkynylanilines
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One-pot gold-catalyzed synthesis of 3-silylethynyl indoles from unprotected o-alkynylanilines

机译:一锅金催化从未保护的邻炔基苯胺合成3-甲硅烷基乙炔基吲哚

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The Au(III)-catalyzed cyclization of 2-alkynylanilines was combined in a one-pot procedure with the Au(I)-catalyzed C3-selective direct alkynylation of indoles using the benziodoxolone reagent TIPS-EBX to give a mild, easy and straightforward entry to 2-substituted-3-alkynylindoles. The reaction can be applied to unprotected anilines, was tolerant to functional groups and easy to carry out (RT, and requires neither an inert atmosphere nor special solvents).
机译:一锅法将Au(III)催化的2-炔基苯胺的环化与Au(I)催化的吲哚的C3选择性直接烷基化的吲哚结合使用苯齐多唑酮试剂TIPS-EBX进行合成,可得到温和,简便和直接的反应进入2-取代的3-炔基吲哚。该反应可用于未保护的苯胺,对官能团具有耐受性且易于进行(RT,既不需要惰性气氛也不需要特殊的溶剂)。

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