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- The conversion of 24-ethylidene-sterols into poriferasterol by Ochromonas malhamensis. F. F. Knapp, J. B. Greig, L. J. Goad, T. W. Goodwin
, J. Chem. Soc. D
, 1971
, 707
- Inversion of the 4β-hydrogen during the conversion of the sterol obtusifoliol into poriferasterol by Ochromonas malhamensis. Furn F. Knapp, L. John Goad, Trevor W. Goodwin
, J. Chem. Soc., Chem. Commun.
, 1973
, 149
- Mechanism of the transmethylation reaction by S-adenosylmethionine: stereochemistry of hydride migration from C-24 to C-25 in the biosynthesis of poriferasterol in the crysophyte Ochromonas malharnensis. Francesco Nicotra, Fiamma Ronchetti, Giovanni Russo, Lucio Toma, Pierluigi Gariboldi, Bianca M. Ranzi
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 521
- Biosynthesis of poriferasterol in Ochromonas malhamensis: 13C NMR assignment of the isopropyl methyl groups of 2-methylpentan-3-ol. Diego Colombo, Fiamma Ronchetti, Giovanni Russo, Lucio Toma
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 962
- Origin of the 28-pro-R and 28-pro-S hydrogens in the biosynthesis of poriferasterol in Ochromonas malhamensis. Francesco Nicotra, Bianca Maria Ranzi, Fiamma Ronchetti, Giovanni Russo, Lucio Toma
, J. Chem. Soc., Chem. Commun.
, 1980
, 752
- The sterochemistry of hydrogen elimination at C-6 and C-23 in phytosterol biosynthesis by Ochromonas malhamensis. A. R. H. Smith, L. J. Goad, T. W. Goodwin
, Chem. Commun. (London)
, 1968
, 1259
- Biosynthesis of the C29-phytosterol side-chain: evidence that the same stereochemistry at C-25 can originate from different mechanisms. Fiamma Ronchetti, Giovanni Russo, Lucio Toma
, J. Chem. Soc., Chem. Commun.
, 1988
, 1375
- The stereochemistry of hydrogen elimination at C(7) and C(22) in phytosterol biosynthesis by Ochromonas malhamensis. A. R. H. Smith, L. J. Goad, T. W. Goodwin
, Chem. Commun. (London)
, 1968
, 926
- Stereochemistry of hydride migration from C-24 to C-25 in the biosynthesis of priferasterol in Ochromonas malhamensis. Francesco Nicotra, Fiamma Ronchetti, Giovanni Russo, Lucio Toma, Pierluigi Gariboldi, Bianca M. Ranzi
, J. Chem. Soc., Chem. Commun.
, 1984
, 383
- Stereoselective synthesis of the C-24 and C-25 stereoisomeric pairs of 24-ethyl-26-hydroxy- and 24-ethyl-[26-2H]sterols and their Δ22-derivatives: reassignment of 13C n.m.r. signals of the pro-R and the pro-S methyl groups at C-25 of 24-ethylsterols. Isao Horibe, Hiroshi Nakai, Tomohiro Sato, Shujiro Seo, Ken'ichi Takeda, Suguru Takatsuto
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1957