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- Residues and metabolism of 19-nortestosterone laurate in steers†. M. J. Sauer, L. G. Howells, S. J. Bellworthy, S. Anderson, N. G. Coldham, T. P. W. Samuels, M. A. Seymour, A. Nedderman, E. Houghton
, Analyst
, 1998
, 123
, 2653
- Application of the exciton chirality method for the stereochemical assignment of remote groups. Determination of the α- or β-configuration of a 2-hydroxy-substituent in 2,17- and 2,16-dihydroxy-A-nor-5α-androstane and -estrane derivatives. Josette Canceill, André Collet, Jean Jacques
, J. Chem. Soc., Perkin Trans. 2
, 1982
, 83
- Microbiological hydroxylation. Part XVII. C-19 hydroxylation of 17-oxo-5α-androstanes and 17-oxo-3α,5-cyclo-5α-androstanes by the fungus Calonectria decora. Virginia E. M. Chambers, William A. Denny, Ewart R. H. Jones, G. Denis Meakins, John O. Miners, John T. Pinhey, Alistair L. Wilkins
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 1359
- Chiral construction of the estrane ring system by an intramolecular double Michael reaction. Masataka Ihara, Takako Takahashi, Noriko Shimizu, Yohhei Ishida, Izumi Sudow, Keiichiro Fukumoto, Tetsuji Kametani
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 529
- Microbiological hydroxylation of steroids. Part VII. The pattern of dihydroxylation of mono-oxo-5α-androstanes and -5α-estranes with the fungus Rhizopus nigricans. John W. Browne, William A. Denny, Ewart R. H. Jones, G. Denis Meakins, Yasu Morisawa, Anthony Pendlebury, John Pragnell
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1493
- Photoinduced molecular transformations. Part 112. Transformation of steroids into ring-A-aromatized steroids and 19-norsteroids involving a regioselective β-scission of alkoxyl radicals; synthesis of two marine natural products, 19-nor-5α-cholestan-3β-ol and 19-norcholest-4-en-3-one, and new synthesis of estrone and 19-nortestosterone. Hiroshi Suginome, Hisanori Senboku, Shinji Yamada
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 2199
- In vitro liver models are important tools to monitor the abuse of anabolic steroids in cattle†. M. Van Puymbroeck, L. Leyssens, J. Raus, M. Van Puymbroeck, D. Vanderzande, J. Gelan, J. Raus, M. E. M. Kuilman, R. F. M. Maas, R. F. Witkamp, R. F. Witkamp
, Analyst
, 1998
, 123
, 2453
- Microbiological hydroxylation of steroids. Part VI. Hydroxylation of simple mono- and di-oxygenated 5α-androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceus. A. M. Bell, J. W. Browne, W. A. Denny, Ewart R. H. Jones, A. Kasal, G. D. Meakins
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2930
- Index pages
, J. Chem. Soc., Perkin Trans. 2
, 1982
, A001
- The use of symmetry in enantioselective synthesis: Four pairs of chrysene enantiomers prepared from 19-nortestosterone. Eva Stastna, Nigam P. Rath, Douglas F. Covey
, Org. Biomol. Chem.
, 2011
, 9
, 4685