Enhanced reactivity and enantioselectivity in lipase-catalysed hydrolysis of 12-crown-4 ester via crown ether–metal complexation

This publication has 15 references indexed in Scilit:

• 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
• Asymmetric transformations catalyzed by enzymes in organic solvents
  Accounts of Chemical Research, 1990
• Enhancing the enantioselectivity of Candida lipase-catalyzed ester hydrolysis via noncovalent enzyme modification
  Journal of the American Chemical Society, 1990
• General Aspects and Optimization of Enantioselective Biocatalysis in Organic Solvents: The Use of Lipases [New Synthetic Methods (76)]
  Angewandte Chemie International Edition in English, 1989
• The effect of crown ethers on enzyme-catalysed reactions in organic solvents
  Journal of the Chemical Society, Chemical Communications, 1989
• Tetrahedron report number 203
  Tetrahedron, 1986
• Enzymes as Catalysts in Synthetic Organic Chemistry [New Synthetic Methods (53)]
  Angewandte Chemie International Edition in English, 1985
• Dissolution of proteins in organic solvents using macrocyclic polyethers: association constants of a cytochrome c–[1,2-¹⁴C₂]-18-crown-6 complex in methanol
  Journal of the Chemical Society, Chemical Communications, 1985
• Quantitative analyses of biochemical kinetic resolutions of enantiomers
  Journal of the American Chemical Society, 1982
• Synthesis and Alkali-cation Complexing Properties of 12-Crown-4 Derivatives
  Bulletin of the Chemical Society of Japan, 1982