Liu Yufeng, Ji Peng, Zou Gongfeng, Liu Yongbing, Yang Bin-Miao, Zhao Yu
Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, 350207, Fuzhou, China.
Department of Chemistry, National University of Singapore, 3 Science Drive 3, 117543, Singapore, Republic of Singapore.
Angew Chem Int Ed Engl. 2024 Dec 2;63(49):e202410351. doi: 10.1002/anie.202410351. Epub 2024 Nov 2.
We present herein a catalytic enantioconvergent diamination of racemic allylic alcohols with the construction of two C-N bonds and 1,3-nonadjacent stereocenters. This iridium/chiral phosphoric acid cooperative catalytic system operates through an atom-economical borrowing hydrogen amination/aza-Michael cascade, and converts readily available phenylenediamines and racemic allylic alcohols to 1,5-tetrahydrobenzodiazepines in high enantioselectivity. An intriguing solvent-dependent switch of diastereoselectivity was also observed. Mechanistic studies suggested a dynamic kinetic resolution process involving racemization through a reversible Michael addition, making the last step of asymmetric imine reduction the enantiodetermining step of this cascade process.
我们在此展示了一种外消旋烯丙醇的催化对映汇聚二胺化反应,该反应构建了两个C-N键和1,3-非相邻立体中心。这种铱/手性磷酸协同催化体系通过原子经济的借氢胺化/氮杂-Michael级联反应运行,并以高对映选择性将易得的苯二胺和外消旋烯丙醇转化为1,5-四氢苯并二氮杂䓬。还观察到了一种有趣的溶剂依赖性非对映选择性开关。机理研究表明这是一个动态动力学拆分过程,涉及通过可逆Michael加成进行的外消旋化,使得不对称亚胺还原的最后一步成为该级联反应的对映体决定步骤。