Cargando…
Conjugate Addition of Indoles to α,β-Unsaturated Ketones Using a Brønsted Acid Ionic Liquid as an Efficient Catalyst
The Brønsted acid ionic liquid [PyN(CH(2))(4)SO(3)H][p-CH(3)PhSO(3)] has been reported as an efficient catalyst for the Michael addition reaction of indoles to α,β-unsaturated ketones. Satisfactory results were obtained, with excellent yields and a simple experimental procedure. The catalyst could b...
Autores principales: | Yu, Chuan-Ji, Liu, Chen-Jiang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254839/ https://www.ncbi.nlm.nih.gov/pubmed/19783920 http://dx.doi.org/10.3390/molecules14093222 |
Ejemplares similares
-
Enantioselective conjugate hydrosilylation of α,β-unsaturated ketones
por: Yang, Huan, et al.
Publicado: (2019) -
Efficient synthesis of β’-amino-α,β-unsaturated ketones
por: Abrunhosa-Thomas, Isabelle, et al.
Publicado: (2013) -
Addition of dithi(ol)anylium tetrafluoroborates to α,β-unsaturated ketones
por: Huang, Yu-Chieh, et al.
Publicado: (2018) -
Geminal Brønsted Acid Ionic Liquids as Catalysts for the Mannich Reaction in Water
por: He, Leqin, et al.
Publicado: (2014) -
Brønsted acid catalyzed remote C6 functionalization of 2,3-disubstituted indoles with β,γ-unsaturated α-ketoester
por: Zhang, You-Ya, et al.
Publicado: (2022)