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- Amino-steroids. Part 7. The synthesis of 3α-amino-2β-hydroxy- and 2β-amino-3α-hydroxy-androst-5-en-17-one. Malcolm M. Campbell, Raymond C. Craig, James Redpath, David S. Savage, Thomas Sleigh
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 3042
- Aromatization of some steroidal enediols. Derek Baldwin, James R. Hanson, Ann M. Holtom
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 1704
- A nuclear magnetic resonance study of the conversion of 4β-acetoxy-3β-hydroxy-Δ5-steroids into 3β,6β-diacetoxy-Δ4-steroids. James R. Hanson, Paul B. Reese
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 331
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Synthesis of 19-hydroxy-1β,19-cyclosteroids
. John F. Templeton, Weiyang Lin, Yangzhi Ling, Helena Majgier-Baranowska, Kirk Marat
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 2037
- 969. Modified steroid hormones. Part XXIX. Some 17α-chloroethynyl-17β-hydroxy-derivatives. C. Burgess, D. Burn, J. W. Ducker, B. Ellis, P. Feather, A. K. Hiscock, A. P. Leftwick, J. S. Mills, V. Petrow
, J. Chem. Soc.
, 1962
, 4995
- 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
- Preparation of androsta-2,5-dien-4-ones. James R. Hanson, David Raines, Harry Wadsworth
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 499
- Steroids. Part LII. Synthesis of steroidal hormone analogues hydroxylated at C(6). C. Amendolla, G. Rosenkranz, Franz Sondheimer
, J. Chem. Soc.
, 1954
, 1226
- Microbiological hydroxylation of steroids. Part I. Proton magnetic resonance spectra of ketones, alcohols, and acetates in the androstane, pregnane, and œstrane series. J. E. Bridgeman, P. C. Cherry, A. S. Clegg, J. M. Evans, Ewart R. H. Jones, A. Kasal, V. Kumar, G. D. Meakins, Y. Morisawa, E. E. Richards, P. D. Woodgate
, J. Chem. Soc. C
, 1970
, 250
- 155. Modified steroid hormones. Part VIII. Some 16-bromo- and 16-chloro-derivatives of testosterone. B. Ellis, D. Patel, V. Petrow
, J. Chem. Soc.
, 1958
, 800