Cargando…
Direct allylic C–H alkylation of enol silyl ethers enabled by photoredox–Brønsted base hybrid catalysis
Strategies for altering the reaction pathway of reactive intermediates are of significant importance in diversifying organic synthesis. Enol silyl ethers, versatile enolate equivalents, are known to undergo one-electron oxidation to generate the radical cations that spontaneously form electrophilic...
Autores principales: | Ohmatsu, Kohsuke, Nakashima, Tsubasa, Sato, Makoto, Ooi, Takashi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586846/ https://www.ncbi.nlm.nih.gov/pubmed/31221955 http://dx.doi.org/10.1038/s41467-019-10641-y |
Ejemplares similares
-
Photoredox-catalyzed silyldifluoromethylation of silyl enol ethers
por: Supranovich, Vyacheslav I, et al.
Publicado: (2020) -
Catalytic asymmetric defluorinative allylation of silyl enol ethers
por: Duran, Jordi, et al.
Publicado: (2023) -
Expanding the chemical space of enol silyl ethers: catalytic dicarbofunctionalization enabled by iron catalysis
por: Sar, Dinabandhu, et al.
Publicado: (2023) -
Enantioselective α-functionalizations of ketones via allylic substitution of silyl enol ethers
por: He, Zhi-Tao, et al.
Publicado: (2018) -
Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters
por: Aikawa, Haruo, et al.
Publicado: (2011)