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- An environmentally benign catalytic oxidation of cholesteryl acetate with molecular oxygen by using
N-hydroxyphthalimide. Zhen Yao, Xingbang Hu, Jianyong Mao, Haoran Li
, Green Chem.
, 2009
, 11
, 2013
- 360. Studies in the sterol group. Part XLVII. A new route to 7-dehydrocholesterol (provitamin D3) and its derivatives. A. E. Bide, H. B. Henbest, E. R. H. Jones, R. W. Peevers, P. A. Wilkinson
, J. Chem. Soc.
, 1948
, 1783
- 1117. A convenient synthesis of [9,19-3H2]cholecalciferol 3,5-dinitrobenzoate and the mechanism of the precholecalciferol ⇌ calciferol reaction. M. Akhtar, C. J. Gibbons
, J. Chem. Soc.
, 1965
, 5964
- Steroids: reactions and partial syntheses. V. Cerny
, Nat. Prod. Rep.
, 1994
, 11
, 419
- 464. cis-Elimination in thermal decompositions. D. H. R. Barton
, J. Chem. Soc.
, 1949
, 2174
- The isomerisation of unsaturated steroids in liquid sulphur dioxide. A. W. D. Hudgell, J. H. Turnbull, Walter Wilson
, J. Chem. Soc.
, 1954
, 814
- 873. Steroids and Walden inversion. Part XXXVIII. The deamination of epimeric cholestan-2-, -4-, and -7-ylamines. C. W. Shoppee, R. J. W. Cremlyn, D. E. Evans, G. H. R. Summers
, J. Chem. Soc.
, 1957
, 4364
- Catalytic β-stereospecific epoxidation of unsaturated steroids by trans-dioxoruthenium(VI)tetramesitylporphyrin. Stereochemical grounds for the β-diastereofacial selection. Manuella Tavarès, René Ramasseul, Jean-Claude Marchon, Bernard Bachet, Claude Brassy, Jean-Paul Mornon
, J. Chem. Soc., Perkin Trans. 2
, 1992
, 1321
- Steroids: reactions and partial synthesis. James R. Hanson
, Nat. Prod. Rep.
, 1996
, 13
, 227
- 566. Steroids of unnatural configuration. Part VIII. Isomerisation of lumisterol and its derivatives with acids. A new method for locating double bonds in steroids. J. Castells, G. D. Meakins, R. Swindells
, J. Chem. Soc.
, 1962
, 2917