Cargando…
Peculiarities of promiscuous l-threonine transaldolases for enantioselective synthesis of β-hydroxy-α-amino acids
ABSTRACT: The introduction of β-hydroxy-α-amino acids (βHAAs) into organic molecules has received considerable attention as these molecules have often found widespread applications in bioorganic chemistry, medicinal chemistry and biomaterial science. Despite innovation of asymmetric synthesis of βHA...
Autores principales: | Wang, Shan, Deng, Hai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8072733/ https://www.ncbi.nlm.nih.gov/pubmed/33900425 http://dx.doi.org/10.1007/s00253-021-11288-w |
Ejemplares similares
-
An L-threonine transaldolase is required for L-threo-β-hydroxy-α-amino acid assembly during obafluorin biosynthesis
por: Scott, Thomas A., et al.
Publicado: (2017) -
Discovery of l-threonine transaldolases for enhanced biosynthesis of beta-hydroxylated amino acids
por: Jones, Michaela A., et al.
Publicado: (2023) -
An unusual metal-bound 4-fluorothreonine transaldolase from Streptomyces sp. MA37 catalyses promiscuous transaldol reactions
por: Wu, Linrui, et al.
Publicado: (2020) -
Development
of ProPhenol Ligands for the Diastereo-
and Enantioselective Synthesis of β-Hydroxy-α-amino
Esters
por: Trost, Barry M., et al.
Publicado: (2014) -
Biomimetic enantioselective synthesis of β,β-difluoro-α-amino acid derivatives
por: Peng, Qiupeng, et al.
Publicado: (2021)