Cargando…
Origin of enantioselectivity reversal in Lewis acid-catalysed Michael additions relying on the same chiral source
Enantiodivergence is an important concept in asymmetric catalysis that enables access to both enantiomers of a product relying on the same chiral source as reagent. This strategy is particularly appealing as an alternate approach when only one enantiomer of the required chiral ligand is readily acce...
Autores principales: | Riehl, Paul S., Richardson, Alistair D., Sakamoto, Tatsuhiro, Reid, Jolene P., Schindler, Corinna S. |
---|---|
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/PMC8565382/ https://www.ncbi.nlm.nih.gov/pubmed/34760198 http://dx.doi.org/10.1039/d1sc03741b |
Ejemplares similares
-
Bifunctional iminophosphorane catalysed enantioselective sulfa-Michael addition of alkyl thiols to alkenyl benzimidazoles
por: Formica, Michele, et al.
Publicado: (2018) -
Enantioselective isothiourea-catalysed reversible Michael addition of aryl esters to 2-benzylidene malononitriles
por: Nimmo, Alastair J., et al.
Publicado: (2023) -
Enantioselective Michael Addition of Water
por: Chen, Bi-Shuang, et al.
Publicado: (2015) -
Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters
por: Shu, Chang, et al.
Publicado: (2019) -
Enantioselective Michael Addition of Aldehydes to Maleimides Organocatalyzed by a Chiral Primary Amine-Salicylamide
por: Torregrosa-Chinillach, Alejandro, et al.
Publicado: (2018)