对映选择合成
化学
激进的
轴手性
手性(物理)
组合化学
催化作用
立体化学
继电器
联轴节(管道)
计算化学
机制(生物学)
分子内力
基质(水族馆)
立体异构
反应机理
终端(电信)
药物发现
作者
Wei Wang,Qi Yang,Yunfei Yao,Lan Hu,Mingwei Jiang,Juan Tan,Guangfan Zheng,Jichao Xiao,Xingwei Li
标识
DOI:10.1002/anie.202523530
摘要
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.
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