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首页> 外文期刊>Journal of the American Chemical Society >Intermolecular Reductive C-N Cross Coupling of Nitroarenes and Boronic Acids by P~Ⅲ/P~Ⅴ=O Catalysis
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Intermolecular Reductive C-N Cross Coupling of Nitroarenes and Boronic Acids by P~Ⅲ/P~Ⅴ=O Catalysis

机译:P〜Ⅲ/ P〜Ⅴ= O催化硝基芳烃与硼酸的分子间还原性C-N交叉偶联

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摘要

A main group-catalyzed method for the synthesis of aryl- and heteroarylamines by intermolecular C-N coupling is reported. The method employs a small ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane) and a terminal hydrosilane reductant (phenylsilane) to drive reductive intermolecular coupling of nitro(hetero)arenes with boronic acids. Applications to the construction of both C-sp2-N (from arylboronic acids) and C-sp3-N bonds (from alkylboronic acids) are demonstrated; the reaction is stereospecific with respect to C-sp3-N bond formation. The method constitutes a new route from readily available building blocks to valuable nitrogen-containing products with complementarity in both scope and chemoselectivity to existing catalytic C-N coupling methods.
机译:报道了通过分子间C-N偶联合成芳基-和杂芳基胺的主要基团催化方法。该方法采用基于有机化合物的小环催化剂(1,2,2,3,4,4-六甲基膦烷)和末端氢硅烷还原剂(苯基硅烷)来驱动硝基(杂)芳烃与硼酸的还原分子间偶联。证明了在C-sp2-N(来自芳基硼酸)和C-sp3-N键(来自烷基硼酸)的构建中的应用。该反应对于C-sp3-N键的形成是立体定向的。该方法构成了一条从容易获得的结构单元到有价值的含氮产品的新途径,该产品在范围和化学选择性方面都与现有的催化C-N偶联方法互补。

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