Cargando…
Nitrile as Activating Group in the Asymmetric Bioreduction of β-Cyanoacrylic Acids Catalyzed by Ene-Reductases
Asymmetric bioreduction of an (E)-β-cyano-2,4-dienoic acid derivative by ene-reductases allowed a shortened access to a precursor of pregabalin [(S)-3-(aminomethyl)-5-methylhexanoic acid] possessing the desired configuration in up to 94% conversion and >99% ee. Deuterium labelling studies showed...
Autores principales: | Winkler, Christoph K, Clay, Dorina, Turrini, Nikolaus G, Lechner, Horst, Kroutil, Wolfgang, Davies, Simon, Debarge, Sebastien, O'Neill, Pat, Steflik, Jeremy, Karmilowicz, Mike, Wong, John W, Faber, Kurt |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498475/ https://www.ncbi.nlm.nih.gov/pubmed/26190962 http://dx.doi.org/10.1002/adsc.201301055 |
Ejemplares similares
-
Chemoenzymatic Asymmetric
Synthesis of Pregabalin
Precursors via Asymmetric Bioreduction of β-Cyanoacrylate
Esters Using Ene-Reductases
por: Winkler, Christoph K., et al.
Publicado: (2013) -
Overcoming co-product inhibition in the nicotinamide independent asymmetric bioreduction of activated C=C-bonds using flavin-dependent ene-reductases
por: Winkler, Christoph K, et al.
Publicado: (2013) -
Metagenomic ene-reductases for the bioreduction of sterically challenging enones
por: Dobrijevic, Dragana, et al.
Publicado: (2019) -
Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds
por: Winkler, Christoph K., et al.
Publicado: (2012) -
NAD(P)H-Independent Asymmetric C=C Bond Reduction Catalyzed by Ene Reductases by Using Artificial Co-substrates as the Hydrogen Donor
por: Winkler, Christoph K, et al.
Publicado: (2014)