Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1954, 19, 349-356
https://doi.org/10.1135/cccc19540349

On steroids. IX. Synthesis of 3-hydroxy-16-ketoandrostane and of 3,16-diketoandrostene-(4)

J. Fajkoš and F. Šorm

Crossref Cited-by Linking

  • Qian Mingxing, Krishnan Kathiresan, Kudova Eva, Li Ping, Manion Brad D., Taylor Amanda, Elias George, Akk Gustav, Evers Alex S., Zorumski Charles F., Mennerick Steven, Covey Douglas F.: Neurosteroid Analogues. 18. Structure–Activity Studies of ent-Steroid Potentiators of γ-Aminobutyric Acid Type A Receptors and Comparison of Their Activities with Those of Alphaxalone and Allopregnanolone. J. Med. Chem. 2014, 57, 171. <https://doi.org/10.1021/jm401577c>
  • Kane Vinayak V., Singh Vishwakarma, Martin Arnold, Doyle Donald L.: The chemistry of 1,2-carbonyl transposition. Tetrahedron 1983, 39, 345. <https://doi.org/10.1016/S0040-4020(01)88538-0>
  • Habermehl Gerhard, Haaf Arthur: Darstellung von 19β‐Nor‐Δ4‐androstendion‐(3.16). Chem. Ber. 1969, 102, 186. <https://doi.org/10.1002/cber.19691020123>
  • Oka Kitaro, Hara Shoji: The total synthesis of samanine. Tetrahedron Letters 1969, 10, 1193. <https://doi.org/10.1016/S0040-4039(01)87840-0>
  • Irmscher Klaus, Kraemer Josef M., Halpaap Herbert: Cholesterol analogues with oxa- and oxa-aza side chain A novel class of inhibitors of cholesterol biosynthesis. Steroids 1966, 7, 557. <https://doi.org/10.1016/0039-128X(66)90144-9>