Synthesis of chiral sulfilimines by organocatalytic enantioselective sulfur alkylation of sulfenamides

被引:5
|
作者
Wang, Fucheng
Xiang, Wanxing
Xie, Yiting
Huai, Linge
Zhang, Luoqiang [1 ]
Zhang, Xin [1 ]
机构
[1] Sichuan Univ, West China Sch Publ Hlth, Chengdu 610041, Peoples R China
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 37期
关键词
SULFINIMIDATE ESTERS; DESIGN; SULFOXIMINES; INHIBITOR; SCAFFOLDS; DISCOVERY; CATALYSIS;
D O I
10.1126/sciadv.adq2768
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sulfilimines are versatile synthetic intermediates and important moieties in bioactive molecules. However, their applications in drug discovery are underexplored, and efficient asymmetric synthetic methods are highly desirable. Here, we report a transition metal-free pentanidium-catalyzed sulfur alkylation of sulfenamides with exclusive chemoselectivity over nitrogen and high enantioselectivity. The reaction conditions were mild, and a wide range of enantioenriched aryl and alkyl sulfilimines were obtained. The synthetic utility and practicability of this robust protocol were further demonstrated through gram-scale reactions and late-stage functionalization of drugs.
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页数:8
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