Intermolecular Amidation of Unactivated sp 2 and sp 3 C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion
State Key Laboratory of Synthetic Chemistry · University of Hong Kong
Abstract
This communication describes the Pd(OAc)2-catalyzed intermolecular amidation reactions of unactivated sp2 and sp3 C-H bonds using primary amides and potassium persulfate. The substrates containing a pendent oxime or pyridine group were amidated with excellent chemo- and regioselectivities. It is noteworthy that reactive C-X bonds were well-tolerated and a variety of primary amides can be effective nucleophiles for the Pd-catalyzed C-H amidation reactions. For the reaction of unactivated sp3 C-H bonds, beta-amidation of 1 degrees sp3 C-H bonds versus 2 degrees C-H bonds is preferred. The catalytic reaction is initiated by chelation-assisted cyclopalladation involving C-H bond activation. Preliminary mechanistic…
Citation impact
- FWCI
- 20.03
- Percentile
- 100%
- References
- 28
Authors
3Topics & keywords
- Chemistry
- Nitrene
- Catalysis
- Medicinal chemistry
- Nucleophile
- Palladium
- Pyridine
- Amination