Cargando…
Asymmetric Chemoenzymatic One-Pot Synthesis of α-Hydroxy Half-Esters
[Image: see text] A new chemoenzymatic one-pot strategy has been developed for the synthesis of α-hydroxy half-esters containing consecutive quaternary and tertiary stereocenters using asymmetric cascade catalysis. In this study, an asymmetric Ca(2+)-catalyzed [2,3]-Wittig rearrangement reaction was...
Autores principales: | Murre, Aleksandra, Erkman, Kristin, Järving, Ivar, Kanger, Tõnis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359131/ https://www.ncbi.nlm.nih.gov/pubmed/34396014 http://dx.doi.org/10.1021/acsomega.1c02973 |
Ejemplares similares
-
Asymmetric organocatalytic Michael addition of cyclopentane-1,2-dione to alkylidene oxindole
por: Silm, Estelle, et al.
Publicado: (2022) -
Enantioselective Michael addition to vinyl phosphonates via hydrogen bond-enhanced halogen bond catalysis
por: Kaasik, Mikk, et al.
Publicado: (2021) -
Primary amines as heterogeneous catalysts in an enantioselective [2,3]-Wittig rearrangement reaction
por: Murre, Aleksandra, et al.
Publicado: (2023) -
Organocatalytic asymmetric addition of malonates to unsaturated 1,4-diketones
por: Žari, Sergei, et al.
Publicado: (2012) -
An Enantio‐ and Diastereoselective Chemoenzymatic Synthesis of α‐Fluoro β‐Hydroxy Carboxylic Esters
por: Howard, James K., et al.
Publicado: (2016)