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Collect. Czech. Chem. Commun. 1980, 45, 3008-3022
https://doi.org/10.1135/cccc19803008

Synthesis of 3,4-, 4,5- and 5,6-unsaturated 19-substituted cholestane derivatives and related epoxides

Pavel Kočovský

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

Crossref Cited-by Linking

  • Numazawa Mitsuteru, Yamada Keiko: Synthesis of 19-oxygenated derivatives of the competitive inhibitor of aromatase, 5-androstene-4,17-dione. Steroids 1999, 64, 320. <https://doi.org/10.1016/S0039-128X(98)00113-5>
  • Numazawa Mitsuteru, Yamada Keiko: Reaction of androst-5-en-17-one with hypobromous acid and its use for synthesis of 19-oxygenated 5-ene and 4-en-6-one steroids. Steroids 1998, 63, 62. <https://doi.org/10.1016/S0039-128X(97)00136-0>
  • Jankowski Paweł, Marczak Stanisław, Wicha Jerzy: Methods for the construction of trans-hydrindane rings and their origins in steroid chemistry. Vitamin D total synthesis. Tetrahedron 1998, 54, 12071. <https://doi.org/10.1016/S0040-4020(98)00570-5>
  • M. Libu[sbreve]e, Arno[sbreve]tová, Pouzar Vladimír, Dra[sbreve]ar Pavel: Preparation of Steroid Hydroxy Sulfates. Synthetic Communications 1990, 20, 1521. <https://doi.org/10.1080/00397919008052869>
  • Kočovský Pavel, Tureček František: Mechanism and structural effects in bromolactonization. Tetrahedron 1983, 39, 3621. <https://doi.org/10.1016/S0040-4020(01)88674-9>
  • KOCOVSKY P.: ChemInform Abstract: STEROIDS. CCXXXVIII. SYNTHESIS OF 3,4‐, 4,5‐AND 5,6‐UNSATURATED 19‐SUBSTITUTED CHOLESTANE DERIVATIVES AND RELATED EPOXIDES. Chemischer Informationsdienst 1981, 12. <https://doi.org/10.1002/chin.198108302>
  • Kočovsky Pavel, Tureček František: Neighboring group participation and rearrangement in hypobromous acid addition to 10β-vinyl-cholestanes. Tetrahedron Letters 1981, 22, 2699. <https://doi.org/10.1016/S0040-4039(01)92974-0>