Cargando…
Introduction of a 7-aza-6-MeO-indoline auxiliary in Lewis-acid/photoredox cooperative catalysis: highly enantioselective aminomethylation of α,β-unsaturated amides
An efficient cooperative chiral Lewis acid/photoredox catalytic system for engaging highly reactive radicals in highly enantioselective conjugate addition to α,β-unsaturated carbonyls is highly desirable. Direct photoexcitation of unbound substrates typically induces undesired background pathways fo...
Autores principales: | Pagire, Santosh K., Kumagai, Naoya, Shibasaki, Masakatsu |
---|---|
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/PMC8159422/ https://www.ncbi.nlm.nih.gov/pubmed/34122973 http://dx.doi.org/10.1039/d0sc01890b |
Ejemplares similares
-
Reductive annulations of arylidene malonates with unsaturated electrophiles using photoredox/Lewis acid cooperative catalysis
por: Betori, Rick C., et al.
Publicado: (2019) -
Correction: Reductive annulations of arylidene malonates with unsaturated electrophiles using photoredox/Lewis acid cooperative catalysis
por: Betori, Rick C., et al.
Publicado: (2021) -
Divergent regioselectivity in photoredox-catalyzed hydrofunctionalization reactions of unsaturated amides and thioamides
por: Morse, Peter D., et al.
Publicado: (2015) -
Enantioselective photoredox dehalogenative protonation
por: Hou, Meimei, et al.
Publicado: (2019) -
Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki–Miyaura cross-coupling
por: Hoang, Gia L., et al.
Publicado: (2017)