Substrate modification to increase the enantioselectivity of hydrolases. A route to optically-active cyclic allylic alcohols.

This publication has 30 references indexed in Scilit:

• Lipase-catalyzed enantioselective transesterification of O-trityl 1,2-diols. Practical synthesis of (R)-tritylglycidol
  The Journal of Organic Chemistry, 1992
• Resolution of secondary alcohols by enzyme-catalyzed transesterification in alkyl carboxylates as the solvent.
  Tetrahedron, 1991
• Enantioselective esterifications of unsaturated alcohols mediated by a lipase prepared from Pseudomonas sp
  Journal of the American Chemical Society, 1991
• 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
• Stereochemical observation on the enantioselective hydrolysis using Pseudomonas fluorescens lipase
  Tetrahedron: Asymmetry, 1990
• Use of enzymes as catalysts to promote key transformations in organic synthesis
  Philosophical Transactions of the Royal Society of London. B, Biological Sciences, 1989
• Biocatalytic resolution of (±)-hydroxyalkanoic esters. A strategy for enhancing the enantiomeric specificity of lipase-catalyzed ester hydrolysis.
  Tetrahedron Letters, 1988
• Lipase-catalyzed hydrolysis as a route to esters of chiral epoxy alcohols
  Journal of the American Chemical Society, 1984
• Microbially mediated enantioselective ester hydrolyses utilizing Rhizopus nigricans. A new method of assigning the absolute stereochemistry of acyclic 1-arylalkanols
  The Journal of Organic Chemistry, 1983
• Structural and optical selectivity of hydroxy ester hydrolysis by α-chymotrypsin
  Tetrahedron Letters, 1975