Department of Chemistry , Massachusetts Institute of Technology , Cambridge , Massachusetts 02139 , United States.
Chemical and Synthetic Development , Bristol-Myers Squibb Company , One Squibb Drive , New Brunswick , New Jersey 08903 , United States.
J Am Chem Soc. 2018 Nov 14;140(45):15200-15205. doi: 10.1021/jacs.8b10769. Epub 2018 Nov 2.
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-N (from arylboronic acids) and C-N bonds (from alkylboronic acids) are demonstrated; the reaction is stereospecific with respect to C-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.
报道了一种通过分子间 C-N 偶联合成芳基和杂芳基胺的主族催化方法。该方法采用小环有机磷基催化剂(1,2,2,3,4,4-六甲基膦杂环戊烷)和末端硅烷还原剂(苯基硅烷),驱动硝基(杂)芳基与硼酸的还原分子间偶联。该方法应用于构建 C-N(来自芳基硼酸)和 C-N 键(来自烷基硼酸),对于 C-N 键形成具有立体特异性。该方法为从易得的构建块到具有互补性的有价值的含氮产物提供了一种新途径,在适用范围和化学选择性方面都优于现有的催化 C-N 偶联方法。