Journal
CHEMICAL COMMUNICATIONS
Volume 59, Issue 14, Pages 2003-2006Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc05842a
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A mild metal-free C-N bond activation strategy is introduced for the direct conversion of inert tertiary amines with acyl chlorides into tertiary amides via organic photoredox catalysis. A novel organic photocatalyst (Cz-NI-Ph) is developed, showing excellent catalytic performance in C-N bond cleavage. This reaction features green and mild conditions, broad substrate scope, and readily available raw materials.
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.
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