Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1987, 52, 476-486
https://doi.org/10.1135/cccc19870476

Brassino steroids with androstane and pregnane skeleton

Ladislav Kohouta, Helena Velgováa, Miroslav Strnadb and Miroslav Kamínekc

a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6
b Institute of Experimental Botany, Czechoslovak Academy of Sciences, 722 00 Olomouc
c Institute of Experimental Botany, Czechoslovak Academy of Sciences, 160 00 Prague 6

Crossref Cited-by Linking

  • Zeferino-Diaz Reyna, Hilario-Martinez J. Ciciolil, Rodriguez-Acosta Maricela, Carrasco-Carballo Alan, Hernandez-Linares Maria Guadalupe, Sandoval-Ramirez Jesus, Fernandez-Herrera Maria A.: Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters. Steroids 2017, 125, 20. <https://doi.org/10.1016/j.steroids.2017.06.004>
  • Ferrer-Pertuz Karoll, Espinoza Luis, Mella Jaime: Insights into the Structural Requirements of Potent Brassinosteroids as Vegetable Growth Promoters Using Second-Internode Elongation as Biological Activity: CoMFA and CoMSIA Studies. IJMS 2017, 18, 2734. <https://doi.org/10.3390/ijms18122734>
  • Marek Aleš, Klepetářová Blanka, Elbert Tomáš: A Study of the Reactivity of Polyhydroxylated Sterol Derivatives. Asian J Org Chem 2015, 4, 808. <https://doi.org/10.1002/ajoc.201500138>
  • Marek Aleš, Klepetářová Blanka, Elbert Tomáš: The introduction of a double bond on the steroid skeleton – The preparation of enol silyl ether derivatives from vicinal diols. Collect. Czech. Chem. Commun. 2011, 76, 443. <https://doi.org/10.1135/cccc2010145>
  • Baranovskii A. V., Litvinovskaya R. P., Aver’kova M. A., Khripach N. B., Khripach V. A.: NMR spectra of androstane analogs of brassinosteroids. J Appl Spectrosc 2007, 74, 642. <https://doi.org/10.1007/s10812-007-0104-x>
  • Litvinovskaya R. P., Baranovsky A. V., Averkova M. A., Khripach V. A.: The synthesis of 2α,3α-isopropylidenedioxy-6,6-ethylenedioxy-5α-androst-15-en-17-one and its 2β,3β-isomer. Russ J Bioorg Chem 2007, 33, 320. <https://doi.org/10.1134/S1068162007030089>
  • Rivera Daniel G, Coll Francisco: Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds. Can. J. Chem. 2005, 83, 1084. <https://doi.org/10.1139/v05-051>
  • Rivera Daniel G., Coll Francisco, León Fredy: Synthesis of pregnane ketols as metabolic precurs ors of analogues of plant growth regulators. Journal of Chemical Research 2004, 2004, 284. <https://doi.org/10.3184/0308234041209239>
  • Gil R. Pérez, Martínez C. S. Pérez, Manchado F. Coll: Synthesis of Analogues of Brassinosteroids with 5β-Cholanic Acid Skeleton. Synth Common 1998, 28, 3387. <https://doi.org/10.1080/00397919808004446>
  • Gaudinová A., Süssenbeková H., Vojtěchová M., Kamínek M., Eder J., Kohout L.: Different effects of two brassinosteroids on growth, auxin and cytokinin content in tobacco callus tissue. Plant Growth Regul 1995, 17, 121. <https://doi.org/10.1007/BF00024171>
  • KOHOUT L., VELGOVA H., STRNAD M., KAMINEK M.: ChemInform Abstract: Steroids. Part 328. Brassino Steroids with Androstane and Pregnane Skeleton. ChemInform 1987, 18. <https://doi.org/10.1002/chin.198727289>