Optical Resolution of a d-Biotin Chiral Intermediate by Use of Lipoprotein Lipase

This publication has 12 references indexed in Scilit:

• A simple and enantioselective synthesis of (+)-biotin
  Published by Elsevier ,2001
• The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks
  Chemical Reviews, 1992
• Enzyme reactions in apolar solvent. 5. The effect of adjacent unsaturation on the porcine pancreatic lipase catalyzed kinetic resolution of secondary alcohols
  The Journal of Organic Chemistry, 1992
• Chemical Inactivation of Lipase in Organic Solvent: A Lipase fromPseudomonas aeruginosaTE3285 is More Like a Typical Serine Enzyme in an Organic Solvent than in Aqueous Media
  Bioscience, Biotechnology, and Biochemistry, 1992
• How can the solvent affect enzyme enantioselectivity?
  Journal of the American Chemical Society, 1991
• Asymmetric transformations catalyzed by enzymes in organic solvents
  Accounts of Chemical Research, 1990
• Highly effective resolution of 1,3-dibenzyl-6-hydroxy-3,3a,6,6a-tetrahydro-1H-furo(3,4-d)imidazole-2,4-dione, an intermediate for biotin, with optically active amines and reutilization of the unwanted epimer.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1990
• Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcohols
  The Journal of Organic Chemistry, 1988
• Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallics
  Journal of the American Chemical Society, 1988
• Nucleophilic displacements on an .alpha.-chloro thioether by organocuprates: a novel synthesis of desoxybiotin
  The Journal of Organic Chemistry, 1986