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- Amino-steroids. Part 6. Stereospecific syntheses of eight, isomeric, steroidal vicinal 2,3-amino-alcohols. Malcolm M. Campbell, Raymond C. Craig, Andrew C. Boyd, Iain M. Gilbert, Robert T. Logan, James Redpath, Robert G. Roy, David S. Savage, Thomas Sleigh
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 2235
- Microbiological transformations. Part 4. Microbiological transformations of 5α-androstan-17-ones and of 17a-aza-D-homo-5α-androstan-17-ones with the fungus Cunninghamella elegans. Trevor A. Crabb, John A. Saul, Roger O. Williams
, J. Chem. Soc., Perkin Trans. 1
, 1981
, 1041
- Microbiological transformations of 3α-acetoxy-17a-aza-D-homo-5α-androstan-17-one and of 3α-acetoxy-5α-androstan-17-one with the fungus Cunninghamella elegans. Trevor A. Crabb, John A. Saul, Roger O. Williams
, J. Chem. Soc., Perkin Trans. 1
, 1977
, 2599
- Amino-steroids. Part III. 2- and 3-Amino-5α-androstanes. C. L. Hewett, D. S. Savage
, J. Chem. Soc. C
, 1968
, 1134
- Microbiological hydroxylation of steroids. Part XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5α-androstanes and to 5α-androstan-11-one. Alan M. Bell, Virginia E. M. Chambers, Sir Ewart, R. H. Jones, G. Denis Meakins, Wilhelm E. Müller, John Pragnell
, J. Chem. Soc., Perkin Trans. 1
, 1974
, 312
- The solvolysis of 4β-hydroxy-3β-p-tolylsulphonyloxyandrost-5-enes. James R. Hanson, Harry J. Wadsworth
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 933
- 619. Steroids and walden inversion. Part XL. The configurations of the bromination products of androstan-17-one. C. W. Shoppee, R. H. Jenkins, G. H. R. Summers
, J. Chem. Soc.
, 1958
, 3048
- 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
- 798. Steroids. Part XLIII. Comparison of the 16-bromo-17-ketones and 16-bromo-17-alcohols in the 3-unsubstituted and 3β-oxygenated 5α-androstone series. J. Fajkoš
, J. Chem. Soc.
, 1959
, 3966
- Microbiological hydroxylation. Part XXI. Hydroxylations of 3-halogeno-17-oxo-, 3-halogeno-7-oxo-, and 17-halogeno-3-oxo-androstanes by the fungi Calonectria decora, Rhizopus nigricans, and Aspergillus ochraceus. Ewart R. H. Jones, G. Denis Meakins, John O. Miners, Alistair L. Wilkins
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 2308