Organic photoredox catalyzed dealkylation/acylation of tertiary amines to access amides

A mild metal-free C-N bond activation strategy for the direct conversion of inert tertiary amines with acyl chlorides into tertiary amides via organic photoredox catalysis is presented. In this protocol, a novel organic photocatalyst (Cz-NI-Ph) that showed excellent catalytic performance during C-N...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2023-02, Vol.59 (14), p.23-26
Hauptverfasser: Liu, Chen, Chen, Han-Nan, Xiao, Teng-Fei, Hu, Xiu-Qin, Xu, Peng-Fei, Xu, Guo-Qiang
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Sprache:eng
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Zusammenfassung:A mild metal-free C-N bond activation strategy for the direct conversion of inert tertiary amines with acyl chlorides into tertiary amides via organic photoredox catalysis is presented. In this protocol, a novel organic photocatalyst (Cz-NI-Ph) that showed excellent catalytic performance during C-N bond cleavage is developed. Moreover, this reaction features green and mild conditions, broad substrate scope, and readily available raw materials. A novel C-N bond activation strategy was established by developing new organic photoredox catalyst (Cz-NI-Ph), which provides a concise approach for the synthesis of amides from tertiary amines.
ISSN:1359-7345
1364-548X
DOI:10.1039/d2cc05842a