Molecular recognition of sec-alcohol enantiomers by Candida antarctica lipase B

This publication has 10 references indexed in Scilit:

• Molecular Modeling of the Enantioselectivity in Lipase-Catalyzed Transesterification Reactions
  Biophysical Journal, 1998
• Chiral Recognition Of Alcohol Enantiomers In Acyl Transfer Reactions Catalysed ByCandida AntarcticaLipase B
  Biocatalysis and Biotransformation, 1998
• Enantiomerically enriched bifunctional sec-alcohols prepared by Candida antarctica lipase B catalysis. Evidence of non-steric interactions
  Tetrahedron: Asymmetry, 1997
• Efficient Synthesis of Optically Pure 1,1,1-Trifluoro-2-alkanols through Lipase-Catalyzed Acylation in Organic Media
  The Journal of Organic Chemistry, 1996
• A Structural Basis for the Chiral Preferences of Lipases
  Journal of the American Chemical Society, 1994
• A simple method to determine the enantiomeric ratio in enantioselective biocatalysis
  Enzyme and Microbial Technology, 1993
• The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks
  Chemical Reviews, 1992
• Surface electrostatic potentials of halogenated methanes as indicators of directional intermolecular interactions
  International Journal of Quantum Chemistry, 1992
• A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa
  The Journal of Organic Chemistry, 1991
• A serine protease triad forms the catalytic centre of a triacylglycerol lipase
  Nature, 1990