Structures and stereochemical assignments of some novel chiral synthons derived from the biotransformation of 2,3-dihydrobenzofuran and benzofuran by Pseudomonas putida

This publication has 14 references indexed in Scilit:

• A 1h-nmr method for the determination of enantiomeric excess and absolute configuration of cis-dihydrodiol metabolites of polycyclic arenes and heteroarenes
  Tetrahedron Letters, 1992
• Absolute configurations of the arene oxide, trans-dihydrodiol and cis-dihydeodiol products resulting from metabolism of quinoline at the 5,6-bond
  Tetrahedron Letters, 1991
• Microbiological transformation of flavone and isoflavone
  Xenobiotica, 1990
• Preparation of the 8,9-epoxide of the mycotoxin aflatoxin B1: the ultimate carcinogenic species
  Journal of the American Chemical Society, 1988
• Benzylic monooxygenation catalyzed by toluene dioxygenase from Pseudomonas putida
  Biochemistry, 1988
• The role of 5,8-dihydroxypsoralen in the biosynthesis of isopimpinellin
  Phytochemistry, 1983
• Initial reactions in the oxidation of naphthalene by Pseudomonas putida
  Biochemistry, 1975
• Biosynthesis of aromatic isoprenoids. Part III. Mechanism of formation of the furan ring and origin of the 4-methoxy-group in the biosynthesis of furoquinoline alkaloids
  Journal of the Chemical Society, Perkin Transactions 1, 1975
• Flavan derivatives. XVI. Acid-catalysed reactions of secondary benzyl alcohols and 1-tetralols in methanol
  Australian Journal of Chemistry, 1967
• Reaction of ortho-hydroxyaldehydes with dimethylsulphoxonium methylide
  Tetrahedron Letters, 1966