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- Conformational studies. Part 2. Synthesis of 17β-hydroxy-4,4-dimethyl-5α-androstan-3-one, and of the 19-nor-analogue. John M. Midgley, W. Basil Whalley, Patricia A. Dodson, Gerald F. Katekar, Bruce A. Lodge
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 823
- Microbial transformation of mestanolone by Macrophomina phaseolina and Cunninghamella blakesleeana and anticancer activities of the transformed products. Rabia Farooq, Nusrat Hussain, Sammer Yousuf, Atia-tul-Wahab, Malik Shoaib Ahmad, Atta-ur-Rahman, M. Iqbal Choudhary
, RSC Adv.
, 2018
, 8
, 21985
- 709. Aza-steroids. Part II. 3-Aza- and 4-aza-A-homo-5α- and -5β-androstane, and the structure of neosaman. C. W. Shoppee, G. Krueger
, J. Chem. Soc.
, 1961
, 3641
- Seven new metabolites of drostanolone heptanoate by using Beauveria bassiana, and Macrophomina phaseolina cell suspension cultures. Zahid Hussain, Atia-tul-Wahab, Nusrat Hussain, Shabbir Hussain, Atta-ur-Rahman, M. Iqbal Choudhary
, RSC Adv.
, 2020
, 10
, 451
- Microbiological hydroxylation of steroids. Part VIII. The pattern of monohydroxylation of diketones and keto-alcohols derived from 5α-androstane with cultures of the fungus, Rhizopus nigricans. Virginia E. M. Chambers, William A. Denny, John M. Evans, Ewart R. H. Jones, Alexander Kasal, G. Denis Meakins, John Pragnell
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1500
- Conformational studies. Part 12. The crystal and molecular structure of 17β-iodoacetoxy-4,4-dimethyl-19-nor-5α-androstan-3-one and of 17β-iodoacetoxy-4,4-dimethyl-5α-androstan-3-one. George Ferguson, Ernest W. Macaulay, J. Monteath Robertson, John M. Midgley, W. Basil Whalley, Bruce A. Lodge
, J. Chem. Soc., Perkin Trans. 2
, 1980
, 1170
- Conformational studies. Part 9. Some exceptions to the axial halogeno-ketone rule. John S. E. Holker, W. Reginald Jones, Michael G. R. Leeming, Gerald M. Holder, John M. Midgley, John E. Parkin, W. Basil Whalley
, J. Chem. Soc., Perkin Trans. 1
, 1978
, 253
- Efficient approach to novel 1α-triazolyl-5α-androstane derivatives as potent antiproliferative agents. Zalán Kádár, Ádám Baji, István Zupkó, Tibor Bartók, János Wölfling, Éva Frank
, Org. Biomol. Chem.
, 2011
, 9
, 8051
- 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
- Microbiological hydroxylation of steroids. Part IV. The pattern of dihydroxylation of mono-oxygenated 5α-androstanes with cultures of the fungus Calonectria decora. A. M. Bell, P. C. Cherry, I. M. Clark, W. A. Denny, Ewart R. H. Jones, G. D. Meakins, P. D. Woodgate
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2081