Cargando…
Enantioselective, Visible Light Mediated Aza Paternò–Büchi Reactions of Quinoxalinones
3‐Substituted quinoxalin‐2(1H)‐ones and various aryl‐substituted or tethered olefins underwent an enantioselective, inter‐ or intramolecular aza Paternò–Büchi reaction upon irradiation at λ=420 nm in the presence of a chiral sensitizer (10 mol %). For the intermolecular reaction with 1‐arylethenes a...
Autores principales: | Li, Xinyao, Großkopf, Johannes, Jandl, Christian, Bach, Thorsten |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898282/ https://www.ncbi.nlm.nih.gov/pubmed/33084097 http://dx.doi.org/10.1002/anie.202013276 |
Ejemplares similares
-
Functionalized azetidines via visible light-enabled aza Paternò-Büchi reactions
por: Becker, Marc R., et al.
Publicado: (2019) -
Synthesis of azetidines by aza Paternò–Büchi reactions
por: Richardson, Alistair D., et al.
Publicado: (2020) -
Oxetane Synthesis through the Paternò-Büchi Reaction
por: D’Auria, Maurizio, et al.
Publicado: (2013) -
Formation of macrocyclic lactones in the Paternò–Büchi dimerization reaction
por: Arimura, Junya, et al.
Publicado: (2011) -
A visible-light Paternò–Büchi dearomatisation process towards the construction of oxeto-indolinic polycycles
por: Mateos, Javier, et al.
Publicado: (2020)