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Collect. Czech. Chem. Commun. 1986, 51, 687-697
https://doi.org/10.1135/cccc19860687

Preparation of 2α,3α-dihydroxy-7-oxa-6-oxo-23,24-dinor-B-homo-5α-cholanic acid, its esters and amides as brassinolide analogues

Václav Černýa, Miroslav Strnadb and Miroslav Kamínekb

a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Praha 6
b Institute of Experimental Botany, Czechoslovak Academy of Sciences, 160 00 Praha 6

Crossref Cited-by Linking

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  • Aitken Vanessa, Diaz Katy, Soto Mauricio, Olea Andrés F., Cuellar Mauricio A., Nuñez Maria, Espinoza-Catalán Luis: New Brassinosteroid Analogs with 23,24-Dinorcholan Side Chain, and Benzoate Function at C-22: Synthesis, Assessment of Bioactivity on Plant Growth, and Molecular Docking Study. IJMS 2023, 25, 419. <https://doi.org/10.3390/ijms25010419>
  • Soto Nitza, González César, Mellado Marco, Olea Andrés F., Coll Yamilet, Díaz Katy, Espinoza Luis: Epimeric Mixtures of Brassinosteroid Analogs: Synthesis, Plant Growth, and Germination Effects in Tomato (Lycopersicum esculentum Mill.). Agronomy 2020, 10, 808. <https://doi.org/10.3390/agronomy10060808>
  • Díaz Katy, Espinoza Luis, Carvajal Rodrigo, Conde-González Marcos, Niebla Vladimir, Olea Andrés F., Coll Yamilet: Biological Activities and Molecular Docking of Brassinosteroids 24-Norcholane Type Analogs. IJMS 2020, 21, 1832. <https://doi.org/10.3390/ijms21051832>
  • Oyarce Jocelyn, Aitken Vanessa, González César, Ferrer Karoll, Olea Andrés F., Parella Teodor, Espinoza Catalán Luis: Synthesis and Structural Determination of New Brassinosteroid 24-Nor-5α-Cholane Type Analogs. Molecules 2019, 24, 4612. <https://doi.org/10.3390/molecules24244612>
  • Kvasnica Miroslav, Oklestkova Jana, Bazgier Vaclav, Rarova Lucie, Berka Karel, Strnad Miroslav: Biological activities of new monohydroxylated brassinosteroid analogues with a carboxylic group in the side chain. Steroids 2014, 85, 58. <https://doi.org/10.1016/j.steroids.2014.04.007>
  • Antonchick Andrey P., Schneider Bernd, Zhabinskii Vladimir N., Khripach Vladimir A.: Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester. Steroid 2004, 69, 617. <https://doi.org/10.1016/j.steroids.2004.05.014>
  • Kohout Ladislav, Chodounská Hana, Macek Tomáš, Strnad Miroslav: Synthesis of (20S)-2α,3α-Dihydroxy-6-oxo-7-oxa-7a-homo-5α-pregnane-20-carboxylic Acid as a Brassinosteroid Part of Ligands for Binding to Affinity Chromatography Carriers. Collect. Czech. Chem. Commun. 2000, 65, 1754. <https://doi.org/10.1135/cccc20001754>
  • Wei-Shan Zhou, Li-Zhong Jiang, Wei-Sheng Tian, Xu-Yang Zhao, Xu Zheng: Studies on steroidal plant-growth regulator: VII. Synthesis of 2α, 3α-dihydroxy-7-oxa-6-oxo-23, 24-dinor-B-homo-5α-cholanic acid and 2α, 3α-dihydroxy-7-oxa-6-oxo-24-nor-B-homo-5α-cholanic acid. Acta Chim. Sin. 1988, 6, 332. <https://doi.org/10.1002/cjoc.19880060409>
  • Adam Günter, Marquardt Volker: Synthese von Brassinosteroiden. Zeitschrift fuer Chemie 1987, 27, 41. <https://doi.org/10.1002/zfch.19870270202>
  • CERNY V., STRNAD M., KAMINEK M.: ChemInform Abstract: Steroids. Part 322. Preparation of 2α,3α‐Dihydroxy‐7‐oxa‐6‐oxo‐23,24‐dinor‐B‐homo‐5α‐cholanic Acid, its Esters and Amides as Brassinolide Analogues. Chemischer Informationsdienst 1986, 17. <https://doi.org/10.1002/chin.198629298>