Enantioselective reductions of ethyl 2-oxo-4-phenylbutyrate by Saccharomyces cerevisiae dehydrogenases

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 acids
  Tetrahedron: 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 ester
  Chemical Communications, 2000
• Asymmetric Nucleophilic Acylation of Aldehydes via 1,1-Heterodisubstituted Alkenes
  Chemistry – A European Journal, 1999
• Highly Enantioselective Heterogeneously Catalyzed Hydrogenation of α-Ketoesters under Mild Conditions
  Journal 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 conditions
  Tetrahedron Letters, 1997
• A new process for the enantioselective synthesis of chiral α-aryloxy- and α-hydroxy acids
  Tetrahedron Letters, 1992
• A novel synthesis of both enantiomers of α-hydroxycarboxylic esters amides from (−)-1-chlorobutyl p-tolyl sulfoxide
  Tetrahedron Letters, 1990
• Asymmetric Hydrocyanation of Aldehydes Using Chiral Titanium Reagents
  Bulletin of the Chemical Society of Japan, 1988
• Composing as a Woman
  College Composition and Communication, 1988
• NAD(P)+–NAD(P)H Models. 59. 1,2- Versus 1,4-Reduction of β,γ-Unsaturated α-Keto Ester
  Bulletin of the Chemical Society of Japan, 1986