Collect. Czech. Chem. Commun.
1998, 63, 1528-1542
https://doi.org/10.1135/cccc19981528
Long-Range Effect of 17-Substituents in 3-Oxo Steroids on 4,5-Double Bond Hydrogenation
Romana Šídová, Karel Stránský, Alexander Kasal, Barbora Slavíková and Ladislav Kohout
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic
Crossref Cited-by Linking
- Szánti-Pintér Eszter, Jirkalová Lada, Pohl Radek, Bednárová Lucie, Kudova Eva: Stereoselective Reduction of Steroidal 4-Ene-3-ketones in the Presence of Biomass-Derived Ionic Liquids Leading to Biologically Important 5β-Steroids. ACS Omega 2024, 9, 7043. <https://doi.org/10.1021/acsomega.3c08963>
- Kapras Vojtech, Slavickova Alena, Stastna Eva, Vyklicky Ladislav, Vales Karel, Chodounska Hana: Synthesis of deuterium labeled NMDA receptor inhibitor – 20-Oxo-5β-[9,12,12-2H3]pregnan-3α-yl-l-glutamyl 1-ester. Steroids 2012, 77, 282. <https://doi.org/10.1016/j.steroids.2011.12.019>
- Chodounská Hana, Buděšínský Miloš, Šídová Romana, Šíša Miroslav, Kasal Alexander, Kohout Ladislav: Simple NMR Determination of 5α/5β Configuration of 3-Oxosteroids. Collect. Czech. Chem. Commun. 2001, 66, 1529. <https://doi.org/10.1135/cccc20011529>
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