Cargando…
Ruthenium(II)-enabled para-selective C–H difluoromethylation of anilides and their derivatives
Transition-metal-catalyzed direct site-selective functionalization of arene C–H bonds has emerged as an innovative approach for building the core structure of pharmaceutical agents and other versatile complex compounds. However, para-selective C–H functionalization has seldom been explored, only a f...
Autores principales: | Yuan, Chunchen, Zhu, Lei, Chen, Changpeng, Chen, Xiaolan, Yang, Yong, Lan, Yu, Zhao, Yingsheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864885/ https://www.ncbi.nlm.nih.gov/pubmed/29567953 http://dx.doi.org/10.1038/s41467-018-03341-6 |
Ejemplares similares
-
Para‐Fluorination of Anilides Using Electrochemically Generated Hypervalent Iodoarenes
por: Berger, Michael, et al.
Publicado: (2022) -
Facile Entry to Pharmaceutically Important 3-Difluoromethyl-Quinoxalin-2-Ones Enabled by Visible-Light-Driven Difluoromethylation of Quinoxalin-2-Ones
por: Fu, Kai-Zhong, et al.
Publicado: (2022) -
Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids
por: Zhu, Yan, et al.
Publicado: (2017) -
On Two Cases of Poisoning by Anilides (Exalgine and Antifebrin)
por: Bokenham, T. Jessopp, et al.
Publicado: (1890) -
Direct Addition of Grignard Reagents to Aliphatic Carboxylic Acids Enabled by Bulky turbo‐Organomagnesium Anilides
por: Colas, Kilian, et al.
Publicado: (2022)