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 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
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. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d3cc03532h |