Abstract
A copper-catalyzed aerobic oxidative coupling of aryl methyl ketones with <i>N</i>,<i>N</i>-dimethylformamide was developed, which afforded α-ketoamides by a sequence of dioxygen activation, C–H bond functionalization, and amide formation with <i>N</i>,<i>N</i>-dimethylformamide as the nitrogen source. Molecular oxygen was found to play a crucial role in this transformation.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
