Cargando…
Deazaflavin reductive photocatalysis involves excited semiquinone radicals
Flavin-mediated photocatalytic oxidations are established in synthetic chemistry. In contrast, their use in reductive chemistry is rare. Deazaflavins with a much lower reduction potential are even better suited for reductive chemistry rendering also deazaflavin semiquinones as strong reductants. How...
Autores principales: | Graml, Andreas, Neveselý, Tomáš, Jan Kutta, Roger, Cibulka, Radek, König, Burkhard |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7311442/ https://www.ncbi.nlm.nih.gov/pubmed/32576821 http://dx.doi.org/10.1038/s41467-020-16909-y |
Ejemplares similares
-
Tuning Deazaflavins Towards Highly Potent Reducing Photocatalysts Guided by Mechanistic Understanding – Enhancement of the Key Step by the Internal Heavy Atom Effect
por: Pavlovska, Tetiana, et al.
Publicado: (2022) -
Biosynthetic
Versatility and Coordinated Action of
5′-Deoxyadenosyl Radicals in Deazaflavin Biosynthesis
por: Philmus, Benjamin, et al.
Publicado: (2015) -
Artificial Metalloproteins for Binding and Stabilization
of a Semiquinone Radical
por: Ségaud, Nathalie, et al.
Publicado: (2017) -
Metal-Independent Reduction
of Hydrogen Peroxide by
Semiquinones
por: Sanchez-Cruz, Pedro, et al.
Publicado: (2014) -
Semiquinone anion radicals of catechol(amine)s, catechol estrogens, and their metal ion complexes.
por: Kalyanaraman, B, et al.
Publicado: (1985)