Cargando…
Kinetic resolution of substituted amido[2.2]paracyclophanes via asymmetric electrophilic amination
Planar chiral [2.2]paracyclophane derivatives are a type of structurally intriguing and practically useful chiral molecules, which have found a range of important applications in the field of asymmetric catalysis and material science. However, access to enantioenriched [2.2]paracyclophanes represent...
Autores principales: | Yu, Shaoze, Bao, Hanyang, Zhang, Dekun, Yang, Xiaoyu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10462673/ https://www.ncbi.nlm.nih.gov/pubmed/37640717 http://dx.doi.org/10.1038/s41467-023-40718-8 |
Ejemplares similares
-
Chiral isothiourea-catalyzed kinetic resolution of 4-hydroxy[2.2]paracyclophane
por: Weinzierl, David, et al.
Publicado: (2021) -
Intraannular photoreactions in pseudo-geminally substituted [2.2]paracyclophanes
por: Hopf, Henning, et al.
Publicado: (2011) -
Chiral 2-Aminobenzimidazole as Bifunctional Catalyst in the Asymmetric Electrophilic Amination of Unprotected 3-Substituted Oxindoles
por: Benavent, Llorenç, et al.
Publicado: (2018) -
Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench
por: Carter, Nicholas, et al.
Publicado: (2017) -
Substitution
Pattern Controlled Quantum Interference
in [2.2]Paracyclophane-Based Single-Molecule Junctions
por: Reznikova, Ksenia, et al.
Publicado: (2021)