Cargando…
Expanding the scope of Metal-Free enantioselective allylic substitutions: Anthrones
The highly enantioselective asymmetric allylic alkylation of Morita–Baylis–Hillman carbonates with anthrones is presented. The reaction is simply catalyzed by cinchona alkaloid derivatives affording the final alkylated products in good yields and excellent enantioselectivities.
Autores principales: | Ceban, Victor, Tauchman, Jiří, Meazza, Marta, Gallagher, Greg, Light, Mark E., Gergelitsová, Ivana, Veselý, Jan, Rios, Ramon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655356/ https://www.ncbi.nlm.nih.gov/pubmed/26592555 http://dx.doi.org/10.1038/srep16886 |
Ejemplares similares
-
Effect of Substitution of Hydrogen Atoms in the Molecules of Anthrone and Anthraquinone
por: Szymańska, Małgorzata, et al.
Publicado: (2021) -
Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives
por: Genc, Hayriye Nevin
Publicado: (2019) -
10,10-Dimethylanthrone
por: Fun, Hoong-Kun, et al.
Publicado: (2010) -
Synergistic formal ring contraction for the enantioselective synthesis of spiropyrazolones
por: Meazza, Marta, et al.
Publicado: (2018) -
Studying the reactivity of alkyl substituted BODIPYs: first enantioselective addition of BODIPY to MBH carbonates
por: Meazza, Marta, et al.
Publicado: (2021)