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- Synthesis of C-19-chiral steroids. Preparation of (19R); (19S) and (19RS)-3β-hydroxy[19-2H1,19-3H1] androst-5-en-17-ones. Thangavel Arunachalam, Enzo Santaniello, Kundan Patel, Eliahu Caspi
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 61
- Backbone rearrangements of steroidal 5-enes. David N. Kirk, Philip M. Shaw
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 2284
- 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
- 18-Substituted steroids. Part 11. Synthesis of 3β,16α,18-trihydroxyandrost-5-en-17-one, a neonatal urinary metabolite, and the 3,16,18-triacetate of its 16β-epimer. Rabeya Das, David N. Kirk
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1821
- Synthetic steroids. Part VIII. The preparation of 3β,18-dihydroxy-androst-5-en-17-one and its conversion into 3β-hydroxy-18-nor-13α-androst-5-en-17-one. P. J. Sykes, R. W. Kelly
, J. Chem. Soc. C
, 1968
, 2913
- Microbiological transformations. Part 3. The oxidation of androstene derivatives with the fungus Cunninghamella elegans. Trevor A. Crabb, Philip J. Dawson, Roger O. Williams
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 2535
- 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
- Steroidal allylic and homoallylic rearrangements during halogenation with triphenylphosphine and carbon tetrachloride. James R. Hanson, Peter B. Hitchcock, Paul B. Reese, Almaz Truneh
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1469
- Epoxidation of 3α,5-cyclo-5α-androst-6-en-17-one. Richard C. Cambie, Peter W. Thomas, James R. Hanson
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 323
- 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