One-pot lipase-catalyzed synthesis of enantiopure secondary alcohols from carbonyl compounds: a new protocol for lipase-mediated resolution

This publication has 16 references indexed in Scilit:

• A facile preparation of (±)-β-hydroxy nitriles and their enzymatic resolution with lipases
  Tetrahedron: Asymmetry, 2001
• Chiral monoaminoalcohols and diaminoalcohols of squaric acid: new catalysts for the asymmetric reduction of ketones by borane
  Tetrahedron Letters, 2001
• Chemoenzymatic Synthesis of Pyrrolo[2,1-b]quinazolinones: Lipase-Catalyzed Resolution of Vasicinone
  The Journal of Organic Chemistry, 2001
• Highly enantioselective borohydride reductions of 2-phenacylpyridine catalyzed by optically active β-ketoiminato cobalt(II) complexes
  Tetrahedron: Asymmetry, 2000
• Mechanism for improving stereoselectivity for asymmetric reduction using acetone powder of microorganism
  Tetrahedron Letters, 2000
• Convenient Enzymatic Resolution of Alcohols Using Highly Reactive, Nonharmful Acyl Donors, 1-Ethoxyvinyl Esters
  The Journal of Organic Chemistry, 2000
• Alumina-assisted reduction of carbonyl compounds with sodium borohydride in hexane
  Canadian Journal of Chemistry, 1998
• Chiral carbamates through an enzymatic alkoxycarbonylation reaction.
  Tetrahedron, 1993
• Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp.; an attractive alternative to ester hydrolysis
  Journal of the Chemical Society, Chemical Communications, 1988
• Enzyme-catalyzed processes in organic solvents.
  Proceedings of the National Academy of Sciences, 1985