Photocatalysed C–H amidation of indoles enabled by tert -butyl alkyl((perfluoropyridin-4-yl)oxy)carbamate

Development of a new catalytic and straightforward strategy to construct C–N bonds is playing a pivotal role in synthetic chemistry. Here, we report a photocatalysed protocol to access direct C–H amidation of indoles, enabled by a rationally designed tert -butyl alkyl((perfluoropyridin-4-yl)oxy)carb...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2023-09, Vol.59 (76), p.11401-11404
Hauptverfasser: Deng, Ke-yi, Wang, Zhi-wei, Xie, Zhen-zhen, He, Jun-tao, Guan, Jian-ping, Chen, Kai, Xiang, Hao-yue, Yang, Hua
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Sprache:eng
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Zusammenfassung:Development of a new catalytic and straightforward strategy to construct C–N bonds is playing a pivotal role in synthetic chemistry. Here, we report a photocatalysed protocol to access direct C–H amidation of indoles, enabled by a rationally designed tert -butyl alkyl((perfluoropyridin-4-yl)oxy)carbamate. A series of biologically important aminoindoles were prepared under mild conditions with excellent regioselectivity and broad substrate scope.
ISSN:1359-7345
1364-548X
DOI:10.1039/d3cc03532h