Cargando…
Efficient biocatalytic stereoselective reduction of methyl acetoacetate catalyzed by whole cells of engineered E. coli
Asymmetric synthesis of chiral β-hydroxy esters, the key building blocks for many functional materials, is currently of great interest. In this study, the biocatalytic anti-Prelog reduction of methyl acetoacetate (MAA) to methyl-(R)-3-hydroxybutyrate ((R)-HBME) was successfully carried out with high...
Autores principales: | Cui, Y. H., Wei, P., Peng, F., Zong, M. H., Lou, W. Y. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078740/ https://www.ncbi.nlm.nih.gov/pubmed/35540821 http://dx.doi.org/10.1039/c8ra00883c |
Ejemplares similares
-
Whole cells in enantioselective reduction of benzyl acetoacetate
por: Ribeiro, Joyce Benzaquem, et al.
Publicado: (2014) -
Regiodivergent and stereoselective hydroxyazidation of alkenes by biocatalytic cascades
por: Wu, Jing-Fei, et al.
Publicado: (2021) -
Lithium and Not Acetoacetate Influences the Growth of Cells Treated with Lithium Acetoacetate
por: Vidali, Silvia, et al.
Publicado: (2019) -
Biocatalytic anti-Prelog reduction of prochiral ketones with whole cells of Acetobacter pasteurianus GIM1.158
por: Du, Peng-Xuan, et al.
Publicado: (2014) -
Biocatalytic C3‐Indole Methylation—A Useful Tool for the Natural‐Product‐Inspired Stereoselective Synthesis of Pyrroloindoles
por: Schneider, Pascal, et al.
Publicado: (2021)