Direct Functionalization of Nitrogen Heterocycles via Rh-Catalyzed C−H Bond Activation
California Institute of Technology · Lawrence Berkeley National Laboratory
Abstract
[Reaction: see text]. Nitrogen heterocycles are present in many compounds of enormous practical importance, ranging from pharmaceutical agents and biological probes to electroactive materials. Direct functionalization of nitrogen heterocycles through C-H bond activation constitutes a powerful means of regioselectively introducing a variety of substituents with diverse functional groups onto the heterocycle scaffold. Working together, our two groups have developed a family of Rh-catalyzed heterocycle alkylation and arylation reactions that are notable for their high level of functional-group compatibility. This Account describes our work in this area, emphasizing the relevant mechanistic insights that enabled…
Citation impact
- FWCI
- 53.80
- Percentile
- 100%
- References
- 63
Authors
3Topics & keywords
- Carbene
- Chemistry
- Intramolecular force
- Catalysis
- Alkylation
- Combinatorial chemistry
- Functional group
- Azole