Enzymatic kinetic separation of stereoisomeric macrocyclic lactone derivatives, 7α,β-O-acyl trans-zearalenols and 7α,β-O-acyl zearanols

This publication has 31 references indexed in Scilit:

• Preparation of optically active secondary alcohols by combination of enzymatic hydrolysis and chemical transformation
  Tetrahedron, 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
• Lipase-catalyzed resolution of acyclic amino alcohol precursors
  The Journal of Organic Chemistry, 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
• Contributions of steric, electrical, and polarizability effects in enantioselective hydrolyses with Rhizopus nigricans: a quantitative analysis
  The Journal of Organic Chemistry, 1987
• Preparation of chiral allylic alcohols using Rhizopusnigricans. Use of the Harada–Nakanishi exciton chirality method for verifying configurational assignments of allylic alcohols
  Canadian Journal of Chemistry, 1987
• Lipase-catalyzed ester formation in organic solvents an easy preparative resolution α-substituted cyclohexanols
  Tetrahedron Letters, 1985
• Resolution of racemic mixtures via lipase catalysis in organic solvents
  Journal of the American Chemical Society, 1985
• Enantioselective ester hydrolyses employing Rhizopus nigricans. A method of preparing and assigning the absolute stereochemistry of cyclic alcohols
  The Journal of Organic Chemistry, 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