Enantioselective reductions of ethyl 2-oxo-4-phenylbutyrate by Saccharomyces cerevisiae dehydrogenases
- 1 April 2002
- journal article
- other
- Published by Elsevier in Journal of Molecular Catalysis B: Enzymatic
- Vol. 17 (2), 101-105
- https://doi.org/10.1016/s1381-1177(02)00006-1
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Stereoselective cyanation of chiral α-amino aldehydes by reaction with Nagata's reagent: a route to enantiopure β-amino-α-hydroxy acidsTetrahedron: Asymmetry, 2001
- Enantio- and chemoselective reduction of 2,4-diketo acid derivatives with cinchona modified Pt-catalyst—Synthesis of (R)-2-hydroxy-4-phenylbutyric acid ethyl esterChemical Communications, 2000
- Asymmetric Nucleophilic Acylation of Aldehydes via 1,1-Heterodisubstituted AlkenesChemistry – A European Journal, 1999
- Highly Enantioselective Heterogeneously Catalyzed Hydrogenation of α-Ketoesters under Mild ConditionsJournal of the American Chemical Society, 1999
- Facile synthesis of (S)-β-hydroxy-β-trichloromethylated aromatic ketones by the regioselective ring cleavage of chiral β-trichloromethyl-β-propiolactone under the Friedel-Crafts conditionsTetrahedron Letters, 1997
- A new process for the enantioselective synthesis of chiral α-aryloxy- and α-hydroxy acidsTetrahedron Letters, 1992
- A novel synthesis of both enantiomers of α-hydroxycarboxylic esters amides from (−)-1-chlorobutyl p-tolyl sulfoxideTetrahedron Letters, 1990
- Asymmetric Hydrocyanation of Aldehydes Using Chiral Titanium ReagentsBulletin of the Chemical Society of Japan, 1988
- Composing as a WomanCollege Composition and Communication, 1988
- NAD(P)+–NAD(P)H Models. 59. 1,2- Versus 1,4-Reduction of β,γ-Unsaturated α-Keto EsterBulletin of the Chemical Society of Japan, 1986