Cargando…
An Enantioselective Suzuki–Miyaura Coupling To Form Axially Chiral Biphenols
[Image: see text] Axial chirality features prominently in molecules of biological interest as well as chiral catalyst designs, and atropisomeric 2,2′-biphenols are particularly prevalent. Atroposelective metal-catalyzed cross-coupling is an attractive and modular approach to access enantioenriched b...
Autores principales: | Pearce-Higgins, Robert, Hogenhout, Larissa N., Docherty, Philip J., Whalley, David M., Chuentragool, Padon, Lee, Najung, Lam, Nelson Y. S., McGuire, Thomas M., Valette, Damien, Phipps, Robert J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434994/ https://www.ncbi.nlm.nih.gov/pubmed/35969692 http://dx.doi.org/10.1021/jacs.2c06529 |
Ejemplares similares
-
Recent Developments in Enantioselective Transition
Metal Catalysis Featuring Attractive Noncovalent Interactions between Ligand and Substrate
por: Fanourakis, Alexander, et al.
Publicado: (2020) -
Hydrogen
Atom Transfer-Driven Enantioselective Minisci
Reaction of Amides
por: Proctor, Rupert S. J., et al.
Publicado: (2021) -
Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki–Miyaura cross-coupling
por: Hoang, Gia L., et al.
Publicado: (2017) -
Hydrogen Atom Transfer Driven Enantioselective Minisci Reaction of Alcohols
por: Colgan, Avene C., et al.
Publicado: (2022) -
Application of the Suzuki-Miyaura Reaction in the Synthesis of Flavonoids
por: Selepe, Mamoalosi A., et al.
Publicado: (2013)