Enzyme catalysed irreversible transesterifications with vinyl acetate. Are they really irreversible?

This publication has 17 references indexed in Scilit:

• Biocatalysis as a useful tool in pheromone synthesis. Enantiomerically pure building blocks from baker's yeast reductions and enzyme catalysed resoluti
  Catalysis Today, 1994
• A biocatalytic approach to nonracemic 2-methyl-3-(2-thiophene)-1-propanols as chiral building blocks for the synthesis of pyridine alkaloids
  Tetrahedron: Asymmetry, 1994
• Enantioselective transesterifications of 2-methyl-1-alcohols catalysed by lipases from Pseudomonas
  Tetrahedron: Asymmetry, 1994
• Lipase-catalyzed transesterification in organic solvents: Applications to the preparation of enantiomerically pure compounds
  Enzyme and Microbial Technology, 1993
• S-ethyl thiooctanoate as acyl donor in lipase catalysed resolution of secondary alcohols
  Tetrahedron Letters, 1993
• Kinetic Resolution of Racemic GlycerolDerivatives with Lipase and Quinohemoprotein Alcohol Dehydrogenase
  Annals of the New York Academy of Sciences, 1992
• Displacement of the equilibrium in lipase catalysed transesterification in ethyl octanoate by continous evaporation of ethanol
  Biotechnology Letters, 1992
• Bakers' yeast reduction of thiophenepropaenals. Enantioselective synthesis of (S)-2-methyl-1-alkanols via bakers' yeast mediated reduction of 2-methyl-3-(2-thiophene)propenals
  The Journal of Organic Chemistry, 1992
• Quantitative analyses of biochemical kinetic resolutions of enantiomers
  Journal of the American Chemical Society, 1982
• Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?
  Journal of the American Chemical Society, 1981