Cargando…
Electron-Transfer-Enabled Concerted Nucleophilic Fluorination of Azaarenes: Selective C–H Fluorination of Quinolines
[Image: see text] Direct C–H fluorination is an efficient strategy to construct aromatic C–F bonds, but the cleavage of specific C–H bonds in the presence of other functional groups and the high barrier of C–F bond formation make the transformation challenging. Progress for the electrophilic fluorin...
Autores principales: | Zhang, Li, Yan, Jiyao, Ahmadli, Dilgam, Wang, Zikuan, Ritter, Tobias |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515641/ https://www.ncbi.nlm.nih.gov/pubmed/37695320 http://dx.doi.org/10.1021/jacs.3c07119 |
Ejemplares similares
-
Ring-opening fluorination of bicyclic azaarenes
por: Komatsuda, Masaaki, et al.
Publicado: (2021) -
Renewable Reagent for
Nucleophilic Fluorination
por: Alič, Blaž, et al.
Publicado: (2022) -
Pd-Catalyzed
Nucleophilic Fluorination of Aryl Bromides
por: Lee, Hong Geun, et al.
Publicado: (2014) -
Nucleophilic fluoroalkylation/cyclization route to fluorinated phthalides
por: Inaba, Masanori, et al.
Publicado: (2018) -
Developing organoboranes as phase transfer catalysts for nucleophilic fluorination using CsF
por: Kirschner, Sven, et al.
Publicado: (2022)