Cargando…
Stereochemical Control of Enzymatic Carbon–Carbon Bond‐Forming Michael‐Type Additions by “Substrate Engineering”
The enzyme 4‐oxalocrotonate tautomerase (4‐OT) promiscuously catalyzes the Michael‐type addition of acetaldehyde to β‐nitrostyrene derivatives to yield chiral γ‐nitroaldehydes, which are important precursors for pharmaceutically active γ‐aminobutyric acids. In this study, we investigated the effect...
Autores principales: | Miao, Yufeng, Tepper, Pieter G., Geertsema, Edzard M., Poelarends, Gerrit J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113669/ https://www.ncbi.nlm.nih.gov/pubmed/27917069 http://dx.doi.org/10.1002/ejoc.201601126 |
Ejemplares similares
-
Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective
por: Boyko, Yaroslav Dmitrievich, et al.
Publicado: (2017) -
Enantiocomplementary Michael Additions of Acetaldehyde to Aliphatic Nitroalkenes Catalyzed by Proline‐Based Carboligases
por: Kunzendorf, Andreas, et al.
Publicado: (2022) -
Structural Basis for the Catalytic Mechanism of Ethylenediamine-N,N′-disuccinic Acid Lyase,
a Carbon–Nitrogen Bond-Forming Enzyme with a Broad Substrate
Scope
por: Poddar, Harshwardhan, et al.
Publicado: (2018) -
Engineering a Promiscuous Tautomerase into a More Efficient Aldolase for Self‐Condensations of Linear Aliphatic Aldehydes
por: Rahimi, Mehran, et al.
Publicado: (2017) -
Modular Enzymatic Cascade Synthesis of Vitamin B(5) and Its Derivatives
por: Abidin, Mohammad Z., et al.
Publicado: (2018)