absolute configuration of the k-region 4,5-dihydrodiols and 4,5-oxide of benzo[a]pyrene

This publication has 12 references indexed in Scilit:

• Fungal oxidation of benzo[a]pyrene: Formation of (−)-trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene by Cunninghamella elegans
  Biochemical and Biophysical Research Communications, 1980
• Absolute stereochemistry of the trans-dihydrodiols formed from benzo[a]anthracene by liver microsomes
  Chemico-Biological Interactions, 1979
• Synthesis of (+)- and (–)-naphthalene and anthracene 1,2-oxides
  Journal of the Chemical Society, Perkin Transactions 1, 1979
• Enzymic mechanism of benzo[a]pyrene conversion to phenols and diols and an improved high-pressure liquid chromatographic separation of benzo[a]pyrene derivatives
  Biochemistry, 1977
• Absolute stereochemistry of the highly mutagenic 7,8-diol 9,10-epoxides derived from the potent carcinogen trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene
  Journal of the American Chemical Society, 1977
• Metabolism of benzo[a]pyrene VI. Stereoselective metabolism of benzo[a]pyrene and benzo[a]pyrene 7,8-dihydrodiol to diol epoxides
  Chemico-Biological Interactions, 1977
• Absolute configuration of a ribonucleic acid adduct formed in vivo by metabolism of benzo[a]pyrene
  Journal of the American Chemical Society, 1977
• (+/-)-trans-7,8-dihydroxy-7,8-dihydrobenzo (a)pyrene: a potent skin carcinogen when applied topically to mice.
  Proceedings of the National Academy of Sciences, 1976
• Exciton chirality method and its application to configurational and conformational studies of natural products
  Accounts of Chemical Research, 1972
• The absolute configurations of the metabolites of naphthalene and phenanthrene in mammalian systems.
  Tetrahedron Letters, 1968