Abstract
Transition-metal-catalyzed oxidative C-H/N-H coupling reaction is an important method to construct C-N bonds. However, stoichiometric oxidants were usually necessary. Here, we report a palladium-catalyzed electro-oxidative intramolecular C-H/N-H annulation reaction without an external oxidant or additive. A variety of pyrido[1,2-a]benzimidazoles were constructed by a simple, green, and mild path. Experimental results suggested that Pd(0) could be oxidized on the anode to be recycled.
| Original language | English |
|---|---|
| Pages (from-to) | 3828-3831 |
| Number of pages | 4 |
| Journal | ACS Catalysis |
| Volume | 10 |
| Issue number | 6 |
| DOIs | |
| State | Published - 20 Mar 2020 |
| Externally published | Yes |
Keywords
- C-H amination
- cyclization
- electro-oxidization
- hydrogen evolution
- palladium catalysis
Fingerprint
Dive into the research topics of 'Palladium-Catalyzed Electro-oxidative C-H Amination toward the Synthesis of Pyrido[1,2- a]benzimidazoles with Hydrogen Evolution'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver