Influence of a 9-double bond on stereospecific microbial 4,5-reductions

This publication has 12 references indexed in Scilit:

• Microbial transformation of 17α-cyanomethyl-17-hydroxy-4,9-estradien-3-one (STS 557) and 17α-cyanomethyl-19-nortestosterone by Mycobacterium smegmatis
  Steroids, 1982
• Influence of the substituents at C11 on hydroxylation at C6, of C21-steroids by Syncephalastrum racemosum
  The Journal of Steroid Biochemistry and Molecular Biology, 1981
• Steroid flexibility and receptor specificity
  Journal of Steroid Biochemistry, 1980
• STS 557, a new orally active progestin with antiprogestational and contragestational properties in rabbits
  Contraception, 1980
• Competitive Progesterone Antagonists: Receptor Binding and Biologic Activity of Testosterone and 19-Nortestosterone Derivatives
  Fertility and Sterility, 1979
• In vitro inhibition of rat uterine contractility induced by 5α and 5β progestins
  Steroids, 1979
• The regulation of haemoglobin synthesis in cultured chick blastoderms by steroids related to 5β-androstane
  Biochemical Journal, 1976
• Comparison of the Metabolites Formed in Rat Prostate Following thein VivoAdministration of Seven Natural Androgens*
  Endocrinology, 1971
• Stoffwechsel von steroidpharmaka: VI. Metaboliten von 4-chlor-17α-methyl-17β-hydroxy-1,4-androstadien-3-on durch mikrobielle hydrierung
  Journal of Steroid Biochemistry, 1970
• Notes - The Direct Conversion of Steroidal Δ⁵-3β-Alcohols to Δ⁵- and Δ⁴-3-Ketones
  The Journal of Organic Chemistry, 1956