Chiral Phosphoric Acid Catalyzed Asymmetric Desymmetrization of para-Quinamines with Isocyanates: Access to Functionalized Imidazolidin-2-one Derivatives

被引:10
|
作者
Hu, Kai-Wen [1 ,2 ]
You, Xiao [1 ,2 ]
Wang, Jin-Zheng [1 ,2 ]
Wen, Xiaoan [1 ,2 ]
Sun, Hongbin [1 ,2 ]
Xu, Qing-Long [1 ,2 ]
Lai, Zengwei [3 ]
机构
[1] China Pharmaceut Univ, Jiangsu Key Lab Drug Discovery Metab Dis, Nanjing 210000, Peoples R China
[2] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210000, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
ENANTIOSELECTIVE DESYMMETRIZATION; ALKENYL ISOCYANATES; 2+2+2 CYCLOADDITION; MICHAEL REACTION; CONSTRUCT; LACTONES; ALKYNES;
D O I
10.1021/acs.orglett.1c02889
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The development of enantioselective desymmetrization of para-quinamines with isocyanates catalyzed by chiral phosphoric acid is reported. The strategy provides concise access to functionalized imidazolidin-2-one derivatives in high yields and enantioselectivities under mild reaction conditions. Remarkably, this reaction could be performed on a gram scale using 5 mol % catalyst loading and the chiral imidazolidin-2-one derivatives could be easily transformed into valuable scaffolds without disturbing the enantiopurity, demonstrating the synthetic utility of this protocol.
引用
收藏
页码:7873 / 7877
页数:5
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