Enantioselective Reductive (Hetero)Arylation of Cyclic <i>N</i>‐Sulfonyl Imines by Cobalt Catalysis
Jieshuai Xiao, Minyan Wang, Xuwen Yin, Shuo Yang, Pei Gu, Xueli Lv, Yue Zhao, Zhuangzhi Shi
Abstract
Transition-metal-catalyzed enantioselective addition of aryl organometallic reagents to imines has emerged as one of the most powerful tools for the formation of optically active diarylmethylamines. Here, we report the first asymmetric reductive (hetero)arylations of imines using aryl and heteroaryl halides enabled by a chiral cobalt-bisphosphine catalyst. This approach shows good functional group compatibility and complements the reported strategy without use of organometallic reagents. Mechanistic investigations supported that aryl-cobalt, instead of an arylzinc reagent, was formed in situ in this reductive aryl-addition event.
Topics & Concepts
Enantioselective synthesisArylReagentCobaltCatalysisCombinatorial chemistryChemistrySulfonylHalideOrganic chemistryTransition metalAlkylCatalytic C–H Functionalization MethodsAsymmetric Hydrogenation and CatalysisAdvanced Synthetic Organic Chemistry