Biotransformation of organic sulfides. Part 12. Conversion of heterocyclic sulfides to chiral sulfoxides by Helminthosporium sp. NRRL 4671 and Mortierella isabellina ATCC 42613

This publication has 24 references indexed in Scilit:

• Enantioselective synthesis and pharmacological evaluation of a new type of verapamil analog with hypotensive and calcium antagonist activities.
  Pharmaceutical Research, 1999
• Biocatalytic and chemical preparation of all four diastereomers of methionine sulfoxide
  Tetrahedron: Asymmetry, 1998
• Remote Asymmetric Induction Using Chiral Sulfoxides.
  Journal of Synthetic Organic Chemistry, Japan, 1998
• Side chain oxidation of aromatic compounds by fungi. 7. A rationale for sulfoxidation, benzylic hydroxylation, and olefin oxidation by Mortierella isabellina
  Journal of Molecular Catalysis B: Enzymatic, 1997
• Biotransformation of organic sulfides—VII. A predictive model for sulfoxidation by Helminthosporium species NRRL 4671
  Tetrahedron: Asymmetry, 1997
• Bakers' yeast oxidation of methyl para-tolylsuifide: Synthesis of a chiral intermediate in the preparation of the mevinic acid-type hypocholestemic agents
  Tetrahedron, 1995
• Applications of Sulfoxides to Asymmetric Synthesis of Biologically Active Compounds
  Chemical Reviews, 1995
• Oxidation of methyl p-tolyl sulfide with bakers' yeast: preparation of a synthon of the mevinic acid-type hypocholestemic agents
  Journal of the Chemical Society, Perkin Transactions 1, 1995
• Chiral sulfoxidation by biotransformation of organic sulfides
  Chemical Reviews, 1988
• The oxidation of organic sulphides by Mortierellaisabellina. 2. Effects of substituents on the stereochemistry of sulphoxide formation
  Canadian Journal of Chemistry, 1985