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Collect. Czech. Chem. Commun. 1991, 56, 1512-1524
https://doi.org/10.1135/cccc19911512

Revision of the structure of 3-methoxy-14α-hydroxy-D-homo-1,3,5-(10)-estratrien-17a-one. A simple 1H NMR method for the determination of configuration of hydroxy group in position 5 and/or 14 of the D-homo-steroid skeleton

Miloš Buděšínský, Alexander Kasal, Želimír Procházka, Huynh Kim Thoa, Soňa Vašíčková and Pavel Kočovský

Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6

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  • BUDESINSKY M., KASAL A., PROCHAZKA Z., HUYNH KIM THOA HUYNH KIM THOA, VASICKOVA S., KOCOVSKY P.: ChemInform Abstract: Steroids. Part 358. Revision of the Structure of 3-Methoxy-14α- hydroxy-D-homo-1,3,5(10)-estratrien-17a-one. A Simple 1H NMR Method for the Determination of Configuration of Hydroxy Group in Position 5 and/or 14 of the D-Homo-steroid. ChemInform 2010, 22, no. <https://doi.org/10.1002/chin.199141228>
  • Wölfling János, Mernyák Erzsébet, Frank Éva, Falkay George, Márki Árpád, Minorics Renáta, Schneider Gyula: Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers. Steroids 2003, 68, 277. <https://doi.org/10.1016/S0039-128X(02)00181-2>
  • Haddad M, Blazejewski JC, Wakselman C, Dorai V, Duc I: The angular trifluoromethyl group. V. Total synthesis and biological properties of 14-dehydro-18,18,18-trifluoro-19-nortestosterone. European Journal of Medicinal Chemistry 1994, 29, 627. <https://doi.org/10.1016/0223-5234(94)90154-6>