Studies on enzymic oxidation of sulfides. V. Switching of the direction of enzyme-mediated oxidation and reduction of sulfur-substituted 2-propanols and 2-propanones

This publication has 9 references indexed in Scilit:

• Microbial Oxidation of Alkyl Aryl Sulfides to the Corresponding Optically Active Sulfoxides
  Agricultural and Biological Chemistry, 1985
• Oxidation ofsec-Alcohols to the Corresponding Ketones byCorynebacterium equi
  Agricultural and Biological Chemistry, 1984
• Asymmetric synthesis of five- and six-membered lactones from chiral sulfoxides: application to the asymmetric synthesis of insect pheromones, (R)-(+)-.delta.-n-hexadecanolactone and (R)-(+)-.gamma.-n-dodecanolactone
  The Journal of Organic Chemistry, 1982
• Enzymes in organic synthesis. 16. Heterocyclic ketones as substrates of horse liver alcohol dehydrogenase. Stereospecific reductions of 2-substituted tetrahydrothiopyran-4-ones
  Journal of the American Chemical Society, 1979
• TAXONOMIC SIGNIFICANCE OF CELL-WALL ACYL TYPE IN CORYNEBACTERIUM-MYCOBACTERIUM-NOCARDIA GROUP BY A GLYCOLATE TEST
  The Journal of General and Applied Microbiology, 1979
• Comparative Asymmetric Reduction of Phenylthioacetone, (±)-Phenylsulfinylacetone and Phenylsulfonylacetone with Fermenting Bakers’ Yeast
  Agricultural and Biological Chemistry, 1978
• Regiospecific horse liver alcohol dehydrogenase-catalyzed oxidations of some bishydroxycyclohexanes
  Canadian Journal of Chemistry, 1977
• The Actinomycete-genus Rhodococcus: A Home for the 'rhodochrous' Complex
  Journal of General Microbiology, 1977
• Stereoselective horse liver alcohol dehydrogenase catalyzed oxidoreductions of some bicyclic [2.2.1] and [3.2.1] ketones and alcohols
  Journal of the American Chemical Society, 1976