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- 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
- Microbiological hydroxylation of steroids. Part II. Structural information and infrared spectrometry: carbonyl, perturbed methylene, and hydroxy-vibrations of steroidal ketones and alcohols. A. D. Boul, J. W. Blunt, J. W. Browne, V. Kumar, G. D. Meakins, J. T. Pinhey, V. E. M. Thomas
, J. Chem. Soc. C
, 1971
, 1130
- Microbiological hydroxylation of steroids. Part IX. Hydroxylation of diketones and keto-alcohols derived from 5α-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals. Alan M. Bell, Ian M. Clark, William A. Denny, Ewart R. H. Jones, G. Denis Meakins, Wilhelm E. Müller, Eva E. Richards
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 2131
- Proton chemical shifts in NMR. Part 13.1 Proton chemical shifts in ketones and the magnetic anisotropy and electric field effect of the carbonyl group. Raymond J. Abraham, Nick J. Ainger
, J. Chem. Soc., Perkin Trans. 2
, 1999
, 441
- Boar taint steroid derivatives for immunological studies. Synthesis of 11 α-hydroxy-5α-androst-16-en-3-one and its hemisuccinate. Alan B. Turner, Philip T. van Leersum
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1653
- Steroids and Walden inversion. Part LXIX. Substitution reactions of the 5α-androstan-11-ols. C. W. Shoppee, J. Nemorin
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 542
- A broad-selective enzyme immunoassay for non-invasive stress assessment in African penguins (Spheniscus demersus) held in captivity. L. Anfossi, L. Ozella, F. Di Nardo, C. Giovannoli, C. Passini, L. Favaro, D. Pessani, E. Mostl, C. Baggiani
, Anal. Methods
, 2014
, 6
, 8222
- 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
- A study of the Henbest reduction: the preparation of 3α-hydroxy-5α- and 3β-hydroxy-5β-steroids. P. A. Browne, D. N. Kirk
, J. Chem. Soc. C
, 1969
, 1653
- 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