Cargando…
Verification of preparations of (1H-indol-3-yl)methyl electrophiles and development of their microflow rapid generation and substitution
Although highly reactive (1H-indol-3-yl)methyl electrophiles such as (1H-indol-3-yl)methyl halides are potential precursors for the synthesis of various indole derivatives, some researchers have reported difficulties in their preparation due to concomitant undesired dimerization/oligomerization. Nev...
Autores principales: | Masui, Hisashi, Kanda, Sena, Fuse, Shinichiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985609/ https://www.ncbi.nlm.nih.gov/pubmed/36871078 http://dx.doi.org/10.1038/s42004-023-00837-1 |
Ejemplares similares
-
Efficient Amide Bond Formation through a Rapid and Strong Activation of Carboxylic Acids in a Microflow Reactor**
por: Fuse, Shinichiro, et al.
Publicado: (2014) -
Iodine-catalyzed electrophilic substitution of indoles: Synthesis of (un)symmetrical diindolylmethanes with a quaternary carbon center
por: Pillaiyar, Thanigaimalai, et al.
Publicado: (2021) -
Regioselective Electrophilic Aromatic Bromination: Theoretical Analysis and Experimental Verification
por: Li, Hui-Jing, et al.
Publicado: (2014) -
Energetics of Electron Pairs in Electrophilic Aromatic Substitutions
por: Munárriz, Julen, et al.
Publicado: (2021) -
Microflows and Nanoflows: Fundamentals and Simulation
por: Karniadakis, George E
Publicado: (2005)