Cargando…
A Sterically Tuned Directing Auxiliary Promotes Catalytic 1,2‐Carbofluorination of Alkenyl Carbonyl Compounds
The site‐selective palladium‐catalyzed three‐component coupling of unactivated alkenyl carbonyl compounds, aryl‐ or alkenylboronic acids, and N‐fluorobenzenesulfonimide is described herein. Tuning of the steric environment on the bidentate directing auxiliary enhances regioselectivity and facilitate...
Autores principales: | Liu, Zhonglin, Oxtoby, Lucas J., Sun, Juntao, Li, Zi‐Qi, Kim, Nana, Davies, Geraint H. M., Engle, Keary M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851970/ https://www.ncbi.nlm.nih.gov/pubmed/36221812 http://dx.doi.org/10.1002/anie.202214153 |
Ejemplares similares
-
Directed, nickel-catalyzed 1,2-alkylsulfenylation of alkenyl carbonyl compounds
por: Li, Zi-Qi, et al.
Publicado: (2022) -
Directed nickel-catalyzed 1,2-dialkylation of alkenyl carbonyl compounds
por: Derosa, Joseph, et al.
Publicado: (2018) -
Palladium(ii)-catalyzed γ-selective hydroarylation of alkenyl carbonyl compounds with arylboronic acids
por: Matsuura, Rei, et al.
Publicado: (2018) -
Catalytic Intramolecular Aminofluorination, Oxyfluorination, and Carbofluorination with a Stable and Versatile Hypervalent Fluoroiodine Reagent**
por: Yuan, Weiming, et al.
Publicado: (2015) -
Pd(II)‐Catalyzed C(alkenyl)−H Activation Facilitated by a Transient Directing Group
por: Liu, Mingyu, et al.
Publicado: (2022)