Access to Axially Chiral Vinyl Sulfilimines via Copper‐Catalyzed Enantioselective Radical Relay Trifluoromethyl‐Sulfilimination of Terminal Alkynes
Abstract
Abstract Sulfilimines have garnered increasing attention as valuable scaffolds in drug discovery and asymmetric synthesis. Nevertheless, catalytic enantioselective construction of sulfilimines in both axial and point chirality chemical space remains a substantial challenge. Herein, we report copper‐catalyzed atroposelective sulfilimination of terminal alkynes with sulfenamides via a radical relay mechanism, enabling the direct assembly of axially chiral vinyl sulfilimines with high levels of chemo‐, regio‐, diastereo‐, and enantioselectivity. The success of this strategy hinges on the atroposelective trapping of transient high active vinyl radicals by a chiral Cu–sulfinimidoyl intermediate. Experimental and computational mechanistic studies reveal a novel asymmetric radical sulfilimination mechanism through an enantioselective reductive elimination of a Cu(III) intermediate, thereby establishing a mechanism distinct from outer‐sphere HAT‐initiated radical–radical coupling or S H 2 pathway.
Article Details
Authors (9)
Wei Wang
Qi Yang
Yunfei Yao
School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 China
Lan Hu
Mingwei Jiang
Juan Tan
Key Laboratory of Green Chemistry and Technology of Ministry of Education, College of Chemistry, Sichuan University, 29 Wangjiang Road, Chengdu 610064, P. R. China
Guangfan Zheng
Department of Chemistry Northeast Normal University Changchun China
Jichao Xiao
School of Chemistry and Chemical Engineering
Xingwei Li
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education and School of Chemistry and Chemical Engineering