Biocatalytic synthesis of some chiral drug intermediates by oxidoreductases

This publication has 42 references indexed in Scilit:

• Electrophysiological effects of selective ?-receptor agonists, antagonists, and the selective phencyclidine receptor agonist MK-801 on midbrain dopamine neurons
  Neuropsychopharmacology, 1989
• Chirospecific synthesis of .beta.-hydroxy .alpha.-amino acids
  The Journal of Organic Chemistry, 1989
• Chiral Compounds Synthesized by Biocatalytic Reductions [New Synthetic Methods (51)]
  Angewandte Chemie International Edition in English, 1985
• O-Sulfated .beta.-lactam hydroxamic acids (monosulfactams). Novel monocyclic .beta.-lactam antibiotics of synthetic origin
  Journal of the American Chemical Society, 1982
• Asymmetric Syntheses via Heterocyclic Intermediates; XV¹. Enantioselective Synthesis of (R)-(-)-β-Hydroxyvaline using L,-Valine or (S)-O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents
  Synthesis, 1982
• A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
  Analytical Biochemistry, 1976
• L-aminoacide oxydases des enveloppes de Proteus mirabilis : propriétés générales
  Biochimie, 1972
• A Novel Synthesis of β-Hydroxyvaline
  Canadian Journal of Chemistry, 1971
• The absolute configuration of β‐hydroxyvaline
  Recueil des Travaux Chimiques des Pays-Bas, 1967
• A New Bio-isostere : Alkylsulphonamidophenethanolamines
  Nature, 1964