Center for Metareceptome Research, College of Pharmacy, Chung-Ang University , 84 Heukseok-ro, Dongjak, Seoul 06974, Republic of Korea.
Org Lett. 2017 Oct 6;19(19):5264-5267. doi: 10.1021/acs.orglett.7b02532. Epub 2017 Sep 12.
A palladium-catalyzed intermolecular hydroamination of vinylarene derivatives using anilines has been developed for the first time under aerobic conditions, where the regioselective formation of N-arylketimines is accomplished. The current aerobic oxidative hydroamination pathway of anilines is distinct from that of palladium-catalyzed hydroamination reactions that proceed to give sec-arylethylamine and arylethylamine derivatives, identifying a longstanding missing reaction pathway, Wacker-type amination, to N-arylketimines using anilines. The ready availability of both starting materials, vinylarenes and anilines, offers an attractive and facile synthetic route to N-arylketimines in good to excellent yields.
首次在有氧条件下发展了钯催化的乙烯基芳基衍生物与苯胺的分子间氢胺化反应,其中完成了 N-芳基酮亚胺的区域选择性形成。目前苯胺的有氧氧化氢胺化途径与钯催化氢胺化反应途径不同,后者进行得到仲-乙胺和芳基乙胺衍生物,确定了使用苯胺向 N-芳基酮亚胺的长期缺失反应途径,即 Wacker 型胺化。两种起始原料乙烯基芳烃和苯胺的易得性为 N-芳基酮亚胺提供了一种有吸引力且简便的合成途径,产率良好至优秀。