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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.
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页码:8077 / 8081
页数:5
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