Crown Ethers as Regulators of Enzymatic Reactions: Enhanced Reaction Rate and Enantioselectivity in Lipase-Catalyzed Hydrolysis of 2-Cyano-1-methylethyl Acetate

This publication has 24 references indexed in Scilit:

• A 2-Propanol Treatment Increases the Enantioselectivity of Candida rugosa Lipase toward Esters of Chiral Carboxylic Acids
  The Journal of Organic Chemistry, 1995
• Lipases fromRhizomucor miehei andHumicola lanuginosa: Modification of the lid covering the active site alters enantioselectivity
  Protein Journal, 1993
• Control of enzyme enantioselectivity with pressure changes in supercritical fluoroform
  Journal of the American Chemical Society, 1993
• Tailoring lipase specificity by solvent and substrate chemistries
  The Journal of Organic Chemistry, 1993
• Biocatalytic synthesis of acrylates in organic solvents and supercritical fluids: I. Optimization of enzyme environment
  Biotechnology & Bioengineering, 1992
• Enhanced enantioselectivity of an enzymatic reaction by the sulfur functional group. A simple preparation of optically active .beta.-hydroxy nitriles using a lipase
  The Journal of Organic Chemistry, 1991
• Structural chemistry of crown ethers
  Published by Wiley ,1989
• The effect of crown ethers on enzyme-catalysed reactions in organic solvents
  Journal of the Chemical Society, Chemical Communications, 1989
• Rules for optimization of biocatalysis in organic solvents
  Biotechnology & Bioengineering, 1987
• Synthesis and Alkali-cation Complexing Properties of 12-Crown-4 Derivatives
  Bulletin of the Chemical Society of Japan, 1982