Cargando…
Site-selective redox isomerizations of furanosides using a combined arylboronic acid/photoredox catalyst system
In the presence of an arylboronic acid and a hydrogen atom transfer mediator under photoredox conditions, furanoside derivatives undergo site-selective redox isomerizations to 2-keto-3-deoxyfuranosides. Experimental evidence and computational modeling suggest that the transformation takes place by a...
Autores principales: | Dimakos, Victoria, Gorelik, Daniel, Su, Hsin Y., Garrett, Graham E., Hughes, Gregory, Shibayama, Hiromitsu, Taylor, Mark S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8148048/ https://www.ncbi.nlm.nih.gov/pubmed/34084383 http://dx.doi.org/10.1039/c9sc05173b |
Ejemplares similares
-
Autocatalytic photoredox Chan-Lam coupling of free diaryl sulfoximines with arylboronic acids
por: Wang, Cong, et al.
Publicado: (2021) -
Investigation of acetyl migrations in furanosides
por: Chevallier, O P, et al.
Publicado: (2006) -
Driving Force of the Pyranoside-into-Furanoside Rearrangement
por: Gerbst, Alexey G., et al.
Publicado: (2019) -
Twenty Years
of Mycobacterial Glycans: Furanosides
and Beyond
por: Lowary, Todd L.
Publicado: (2016) -
Catalyst- and solvent-free ipso-hydroxylation of arylboronic acids to phenols
por: Yang, Xiufang, et al.
Publicado: (2019)