Gold-Catalyzed syn-1,2-Difunctionalization of Ynamides via Nitrile Activation

被引:64
|
作者
Vanjari, Rajeshwer [1 ]
Dutta, Shubham [1 ]
Gogoi, Manash P. [1 ]
Gandon, Vincent [2 ,3 ]
Sahoo, Akhila K. [1 ]
机构
[1] Univ Hyderabad, Sch Chem, Hyderabad 500046, Telangana, India
[2] Univ Paris Saclay, Univ Paris Sud, ICMMO, CNRS,UMR 8182, Batiment 420, F-91405 Orsay, France
[3] Univ Paris Saclay, Ecole Polytech, LCM, CNRS,UMR 9168, Route Saclay, F-91128 Palaiseau, France
关键词
DUAL-ACTIVATION; RAPID ACCESS; CYCLIZATION; CYCLOISOMERIZATION; ALKYNES;
D O I
10.1021/acs.orglett.8b03830
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Developed is an unprecedented Au(I)-catalyzed syn-1,2-difunctionalization of ynamides with 2-amino-benzonitriles via nitrile activation. The coupling between ynamides and 2-aminobenzonitriles is explicitly regioselective, providing a straightforward access to 2,4-diamino-substituted quinolines. Density functional theory (DFT) study provides insightful information and rationalizes the reaction pathway. It shows how the synergy between ynamide pi-activation and nitrile sigma-coordination by the Au(I) catalyst makes the cyclization viable.
引用
收藏
页码:8077 / 8081
页数:5
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