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- Microbiological hydroxylation of steroids. Part X. 1β,11α-Dihydroxylation of 3β-hydroxy-5α-pregnan-20-one and the hydroxylation of other 20-oxo-5α-pregnanes with the fungus Aspergillus ochraceus. Andrew S. Clegg, William A. Denny, Ewart R. H. Jones, G. Denis Meakins, John T. Pinhey
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 2137
- Synthesis of ring-A and -B substituted 17α-acetoxypregnan-20-one derivatives with potential activity on the digitalis receptor in cardiac muscle. John F. Templeton, V. P. Sashi Kumar, Ryungsoon S. Kim, Frank S. LaBella
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 1361
- The preparation of 1β,11α-dihydroxy-steroids by microbiological hydroxylation. A. S. Clegg, Ewart R. H. Jones, G. D. Meakins, J. T. Pinhey
, J. Chem. Soc. D
, 1970
, 1029
- 706. Steroids. Part XVIII. The preparation of some 11-ethynyl-steroids. C. W. Shoppee, Ruth E. Lack
, J. Chem. Soc.
, 1962
, 3624
- Bishomoisomandapamate, a New Tetracyclic Diterpenoid from a New Species of the Sinularia Genus of the Indian Ocean. Ammanamanchi, S. R. Anjaneyulu, Putcha Sarada
, J. Chem. Res. (S)
, 1999
, 600
- Detection and characterization of 20-oxosteroids in rat brains using LC-electron capture APCI-MS after derivatization with 2-nitro-4-trifluoromethylphenylhydrazine. Tatsuya Higashi, Natsuko Takido, Kazutake Shimada
, Analyst
, 2003
, 128
, 130