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- 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
- Neighbouring group participation in the allylic oxidation of a Δ5-steroid. James R. Hanson, Paul B. Reese
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 647
- Allylic acetoxylation of Δ5-steroids at C-4. James R. Hanson, Paul B. Reese, Harry J. Wadsworth
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 2941
- 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
- Preparation of androsta-2,5-dien-4-ones. James R. Hanson, David Raines, Harry Wadsworth
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 499
- The mechanism of a steroidal aromatization reaction. J. R. Hanson, T. D. Organ
, J. Chem. Soc. D
, 1970
, 1052
- Synthetic steroids. Part II. The deconjugation of Δ4-3-oxo-steroids. An improved method for the preparation of 3β-hydroxyandrost-5-ene-11,17-dione. R. W. Kelly, I. McClenaghan, P. J. Sykes
, J. Chem. Soc. C
, 1967
, 2375
- Synthesis of 21-hydroxycholesterol and 25-hydroxycholesterol from 3β-hydroxyandrost-5-en-17-one. A method for the stereospecific construction of sterol side-chains. Jerzy Wicha, Karol Bal
, J. Chem. Soc., Perkin Trans. 1
, 1978
, 1282
- Inhibition of aromatase by steroids substituted at C-19 with halogen, sulphur, and nitrogen. J. Neville Wright, Phillip T. van Leersum, Stephen G. Chamberlin, Muhammad Akhtar
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1647
- Some new steroid colour reactions. J. D. Few
, Analyst
, 1965
, 90
, 134