Cargando…
A third generation of radical fluorinating agents based on N-fluoro-N-arylsulfonamides
Radical fluorination has been known for a long time, but synthetic applications were severely limited by the hazardous nature of the first generation of reagents such as F(2) and the strongly electrophilic nature of the second generation of reagents such as N-fluorobenzenesulfonimide (NFSI) and Sele...
Autores principales: | Meyer, Daniel, Jangra, Harish, Walther, Fabian, Zipse, Hendrik, Renaud, Philippe |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244228/ https://www.ncbi.nlm.nih.gov/pubmed/30459353 http://dx.doi.org/10.1038/s41467-018-07196-9 |
Ejemplares similares
-
Radical chain monoalkylation of pyridines
por: Rieder, Samuel, et al.
Publicado: (2021) -
Molecule‐Induced Radical Formation (MIRF) Reactions—A Reappraisal
por: Sandhiya, Lakshmanan, et al.
Publicado: (2020) -
Development of N-F fluorinating agents and their fluorinations: Historical perspective
por: Umemoto, Teruo, et al.
Publicado: (2021) -
Inhibition of Insulin-Regulated Aminopeptidase (IRAP) by Arylsulfonamides
por: Borhade, Sanjay R, et al.
Publicado: (2014) -
Exosite inhibition of ADAMTS-5 by a glycoconjugated arylsulfonamide
por: Santamaria, Salvatore, et al.
Publicado: (2021)