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PUBMED FOR HANDHELDS

Journal Abstract Search


119 related items for PubMed ID: 1239450

  • 1.
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  • 2. Microbiological hydroxylation. Part XVI. Incubation of derivatives (mainly acetals) of 5alpha-androstane ketones with the fungi Calonectria decora, Aspergillus ochraceus, and Rhizopus nigricans.
    Evans JM, Jones ER, Meakins GD, Miners JO, Pendlebury A, Wilkins AL.
    J Chem Soc Perkin 1; 1975; (14):1356-9. PubMed ID: 1172504
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  • 6. Microbiological hydroxylation of steroids. XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5 alpha-androstanes and to 5 alpha-androstan-11-one.
    Bell AM, Chambers VE, Jones ER, Meakins GD, Müller WE, Pragnell J.
    J Chem Soc Perkin 1; 1974; 2():312-7. PubMed ID: 4593349
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  • 7. Microbiological hydroxylation of steroids. VII. The pattern of dihydroxylation of mono-oxo-5 alpha-androstanes and 5 alpha-estranes with the fungus Rhizopus nigricans.
    Browne JW, Denny WA, Jones ER, Meakins GD, Morisawa Y, Pendlebury A, Pragnell J.
    J Chem Soc Perkin 1; 1973; 14():1493-9. PubMed ID: 4739028
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  • 8. Microbiological hydroxylation of steroids. IX. Hydroxylation of diketones and keto-alcohols derived from 5 alpha-androstane with the fungi Rhizopus arrhizus and Rhizopus circinnans. Steroidal 18- and 19-proton magnetic resonance signals.
    Bell AM, Clark IM, Denny WA, Jones ER, Meakins GD, Müller WE.
    J Chem Soc Perkin 1; 1973; 19():2131-6. PubMed ID: 4796662
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  • 9. Microbiological hydroxylation of steroids. VI. Hydroxylation of simple mono- and di-oxygenated 5 -androstanes and of 3-oxoestranes with the fungus Aspergillus ochraceus.
    Bell AM, Browne JW, Denny WA, Jones ER, Kasal JA, Meakins GD.
    J Chem Soc Perkin 1; 1972; 23():2930-6. PubMed ID: 4675916
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  • 10. Microbiological hydroxylation of steroids. X. 1 beta, 11 alpha-dihydroxylation of 3 beta-hydroxy-5 alpha-prepnan-20-one and the hydroxylation of other 20-oxo-5 alpha-pregnanes with the fungus Aspergillys ochraceus.
    Clegg AS, Denny WA, Jones ER, Meakins GD, Pinhey JT.
    J Chem Soc Perkin 1; 1973; 19():2137-41. PubMed ID: 4796663
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  • 11. Microbiological hydroxylation. XII. Comparative behaviour of D-homogonane (perhydrochrysene) ketones and steroids.
    Ashton MJ, Bailey AS, Jones ER.
    J Chem Soc Perkin 1; 1974; 0(14):1658-65. PubMed ID: 4472200
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  • 12. [7alpha-hydroxylation of steroid 5-olefins by mold fungi].
    Andriushina VG, Druzhinina AV, Iaderets VV, Stytsenko TS, Voĭshvillo NE.
    Prikl Biokhim Mikrobiol; 2010; 46(1):78-83. PubMed ID: 20198922
    [Abstract] [Full Text] [Related]

  • 13. Hydroxylations of carbaryl by soil fungi.
    Bollag JM, Liu SY.
    Nature; 1972 Mar 24; 236(5343):177-8. PubMed ID: 4623228
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  • 14. The alkaoids of fungi. I. The formation of ergoline alkaloids by representative mold fungi.
    el-Refai AM, Sallam LA, Naim N.
    Jpn J Microbiol; 1970 Mar 24; 14(2):91-7. PubMed ID: 5309855
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  • 15. Hydroxylation of steroids with nonpolar side chains with 11 alpha-hydroxylase of Rhizopus nigricans.
    Zakelj-Mavric M, Kastelic-Suhadolc T, Gottlieb HE, Belic I.
    J Steroid Biochem; 1989 Aug 24; 33(2):287-8. PubMed ID: 2788778
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  • 16. Microbiological hydroxylation. XIV. Hydroxylation in the terminal rings of dioxygenated 5alpha-androstanes with the fungi Wojnowicia graminis and Ophiobolus herpotrichus.
    Chambers VE, Jones ER, Meakins GD, Miners JO, Wilkins AL.
    J Chem Soc Perkin 1; 1975 Aug 24; (1):55-8. PubMed ID: 1169239
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  • 18. Novel metabolite structures from biotransformation of a sesquiterpenoid ketone by selected fungal strains.
    Hebda C, Szykula J, Orpiszewski J, Fischer P.
    Biol Chem Hoppe Seyler; 1991 May 24; 372(5):337-44. PubMed ID: 1872996
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  • 19. Microbial hydroxylations. II. Oxidative cleavage of the 17-beta-acetyl side-chain of progesterone by Aspergillus ochraceus.
    Tan L, Smith LL.
    Biochim Biophys Acta; 1968 Jul 01; 152(4):758-69. PubMed ID: 5660090
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