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Collect. Czech. Chem. Commun. 1978, 43, 2609-2618
https://doi.org/10.1135/cccc19782609

1H-NMR investigations. Application of trichloroacetyl isocyanate to structure determination of 3-, 6-, 7-, 7a- and 17-hydroxy steroids

Bruno Schönecker, Dieter Tresselt, Gerd Schubert, Ladislav Kohout and Jan Fajkoš

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  • Vincze Irén, Somlai Csaba, Schneider Gyula: Steroids, XLIV. Neighbouring group participation, XI. Decomposition of 2‐amidomethylene‐3‐hydroxysteroids. Liebigs Ann. Chem. 1991, 1991, 1049. <https://doi.org/10.1002/jlac.1991199101181>
  • Vincze Irén, Somlai Csaba, Schneider Gyula, Dombi György: Steroids, XL. 15‐(hydroxymethyl)androstene and ‐estratriene derivatives. Liebigs Ann. Chem. 1988, 1988, 973. <https://doi.org/10.1002/jlac.198819881007>
  • Schade Wolfgang, Schubert Gerd, Schönecker Bruno: Mass spectra of dihydroxy stereoisomers of 3‐methoxy‐1,3,5(10)‐estratrienes. Org. Mass Spectrom. 1988, 23, 252. <https://doi.org/10.1002/oms.1210230406>
  • Schönecker B., Tresselt D., Schubert G., Ponsold K.: Steroide. 66. 1H‐NMR‐Untersuchungen. Konfigurationszuordnung 15, 16, 17‐trisubstituierter Steroide. J. Prakt. Chem. 1981, 323, 207. <https://doi.org/10.1002/prac.19813230205>