PLE catalyzed hydrolyses of α-substituted α-hydroxy esters: The influence of the substituents.

This publication has 18 references indexed in Scilit:

• Pig-liver-esterase-catalyzed hydrolyses of racemic .alpha.-substituted .alpha.-hydroxy esters
  The Journal of Organic Chemistry, 1990
• Enzymes in organic synthesis. 47. Active-site model for interpreting and predicting the specificity of pig liver esterase
  Journal of the American Chemical Society, 1990
• Application of Pig Liver Esterases (PLE) in Asymetric Synthesis
  Tetrahedron, 1990
• Enantiotoposelective PLE-catalyzed hydrolysis of cis-5-substituted-1,3-diacyloxycyclohexanes. Preparation of some useful chiral building blocks
  Tetrahedron: Asymmetry, 1990
• Kinetic resolution of racemic β,γ-epoxy esters with pig liver esterase (PLE, e.c. 3.1.1.1.)
  Tetrahedron Letters, 1989
• Enzyme-catalyzed asymmetric synthesis. 8. Enantioselectivity of pig liver esterase catalyzed hydrolyses of 4-substituted meso cyclopentane 1,2-diesters
  The Journal of Organic Chemistry, 1989
• Structural requirements in the enzymic optical resolution of bicyclic esters using pig liver esterase
  Tetrahedron Letters, 1988
• Enzymes in organic synthesis. 39. Preparations of chiral cyclic acid-esters and bicyclic lactones via stereoselective pig liver esterase catalyzed hydrolyses of cyclic meso diesters
  The Journal of Organic Chemistry, 1987
• Enantioselective hydrolysis of 3-hydroxy-3-methylalkanoic acid esters with pig liver esterase
  The Journal of Organic Chemistry, 1983
• Quantitative analyses of biochemical kinetic resolutions of enantiomers
  Journal of the American Chemical Society, 1982