Zhai Rong L, Xue Yun S, Liang Ting, Mi Jia J, Xu Zhou
Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, School of Pharmacy , Xuzhou Medical University , Tongshan Road 209 , Xuzhou , 221004 , People's Republic of China.
J Org Chem. 2018 Sep 7;83(17):10051-10059. doi: 10.1021/acs.joc.8b01388. Epub 2018 Jul 30.
A direct regioselective functionalization of arenes and heteroarenes using N-alkenoxypyridinium salts as electrophilic alkylating agents for the synthesis of α-aryl/heteroaryl ketones has been developed. The method generates alkylating agents from alkynes and N-pyridine oxide followed by site-selective electrophilic substitution with a broad range of arenes and heteroarenes including benzene derivates, phenols, ethers, indoles, pyrroles, furans, and thiophenes in one pot. Kinetic isotope effect measurements and DFT studies reveal that this reaction likely proceeds through a carbon-cation intermediate.
已开发出一种使用N-烯氧基吡啶鎓盐作为亲电烷基化剂对芳烃和杂芳烃进行直接区域选择性官能化的方法,用于合成α-芳基/杂芳基酮。该方法由炔烃和N-吡啶氧化物生成烷基化剂,然后与包括苯衍生物、酚类、醚类、吲哚、吡咯、呋喃和噻吩在内的多种芳烃和杂芳烃进行位点选择性亲电取代,一步完成。动力学同位素效应测量和密度泛函理论研究表明,该反应可能通过碳阳离子中间体进行。