Cargando…
Stereodivergent entry to β-branched β-trifluoromethyl α-amino acid derivatives by sequential catalytic asymmetric reactions
Currently, conventional reductive catalytic methodologies do not guarantee general access to enantioenriched β-branched β-trifluoromethyl α-amino acid derivatives. Herein, a one-pot approach to these important α-amino acids, grounded on the reduction – ring opening of Erlenmeyer–Plöchl azlactones, i...
Autores principales: | Corti, Vasco, Riccioli, Riccardo, Martinelli, Ada, Sandri, Sofia, Fochi, Mariafrancesca, Bernardi, Luca |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336586/ https://www.ncbi.nlm.nih.gov/pubmed/34447530 http://dx.doi.org/10.1039/d1sc01442k |
Ejemplares similares
-
A General Catalytic Enantioselective Transfer Hydrogenation Reaction of β,β-Disubstituted Nitroalkenes Promoted by a Simple Organocatalyst
por: Bernardi, Luca, et al.
Publicado: (2016) -
Catalytic Asymmetric Reactions of 4‐Substituted Indoles with Nitroethene: A Direct Entry to Ergot Alkaloid Structures
por: Romanini, Simone, et al.
Publicado: (2015) -
The Emergence of Quinone Methides in Asymmetric Organocatalysis
por: Caruana, Lorenzo, et al.
Publicado: (2015) -
Protocol for stereodivergent asymmetric hydrogenation of quinoxalines
por: Wang, Mingyang, et al.
Publicado: (2023) -
Stereodivergent assembly of tetrahydro-γ-carbolines via synergistic catalytic asymmetric cascade reaction
por: Xu, Shi-Ming, et al.
Publicado: (2019)