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Collect. Czech. Chem. Commun. 1994, 59, 435-443
https://doi.org/10.1135/cccc19940435

Synthesis of Some Epitestosterone Analogues

Hana Chodounská, Barbora Slavíková and Alexander Kasal

Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic

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  • Cabaj John E., Kairys David, Benson Thomas R.: Development of a Commercial Process to Produce Oxandrolone. Org. Process Res. Dev. 2007, 11, 378. <https://doi.org/10.1021/op060231b>
  • Ciuffreda P., Casati S., Manzocchi A.: Complete 1H and 13C NMR spectral assignment of 17‐hydroxy epimeric sterols with planar A or A and B rings. Magnetic Reson in Chemistry 2004, 42, 360. <https://doi.org/10.1002/mrc.1342>
  • Chodounská Hana, Šaman David, Ubik Karel, Kasal Alexander: An expedient synthesis of [16,16,17-2H3)-epitestosterone via a one pot deuteration and reduction of the 17-ketone followed by epimerization of a deuterated alcohol. Tetrahedron Letters 1995, 36, 7769. <https://doi.org/10.1016/0040-4039(95)01623-P>
  • CHODOUNSKA H., SLAVIKOVA B., KASAL A.: ChemInform Abstract: On Steroids. Part 372. Synthesis of Some Epitestosterone Analogues. ChemInform 1994, 25. <https://doi.org/10.1002/chin.199428249>