Cargando…
Metal and Activating Group Free C-4 Alkylation of Isoquinolines via a Temporary Dearomatization Strategy
[Image: see text] A simple method for the C-4 alkylation of isoquinolines is described using benzoic acid as a nucleophilic reagent and vinyl ketones as an electrophile. The reaction shows tolerance for substitution at C-3, and C-5–C-8 positions as well as allowing some variation of the vinyl ketone...
Autores principales: | Day, Aaron J., Jenkins, Timothy C., Kischkewitz, Marvin, Christensen, Kirsten E., Poole, Darren L., Donohoe, Timothy J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903316/ https://www.ncbi.nlm.nih.gov/pubmed/36688518 http://dx.doi.org/10.1021/acs.orglett.2c04149 |
Ejemplares similares
-
Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope
por: Kischkewitz, Marvin, et al.
Publicado: (2022) -
Transition‐Metal‐Free Reductive Hydroxymethylation of Isoquinolines
por: Reeves, Benjamin M., et al.
Publicado: (2019) -
Tandem
Dearomatization/Enantioselective Allylic Alkylation
of Pyridines
por: Greßies, Steffen, et al.
Publicado: (2023) -
Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization
por: Dai, Chunhui, et al.
Publicado: (2012) -
Enantioselective dearomatization of isoquinolines by anion-binding catalysis en route to cyclic α-aminophosphonates
por: Ray Choudhury, Abhijnan, et al.
Publicado: (2016)