Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 2002, 67, 91-102
https://doi.org/10.1135/cccc20020091

Synthesis of 2,24-Diepicastasterone and 3,24-Diepicastasterone as Potential Brassinosteroid Metabolites of the Cockroach Periplaneta americana

Brunhilde Voigta,*, Andrea Porzela, Günter Adama, Dieter Golschb, Waldemar Adamb, Christoph Wagnerc and Kurt Merzweilerc

a Abteilung für Naturstoffchemie, Leibniz-Institut für Pflanzenbiochemie, Weinberg 3, 06120 Halle/S., Germany
b Institut für Organische Chemie, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany
c Fachbereich Chemie, Martin-Luther-Universität, Kurt-Mothes-Str. 2, 06120 Halle/S., Germany

Crossref Cited-by Linking

  • Zhabinskii Vladimir N, Osiyuk Darya A, Ermolovich Yuri V, Chaschina Natalia M, Dalidovich Tatsiana S, Strnad Miroslav, Khripach Vladimir A: Synthesis of ergostane-type brassinosteroids with modifications in ring A. Beilstein J. Org. Chem. 2017, 13, 2326. <https://doi.org/10.3762/bjoc.13.229>
  • 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>
  • Tossi Vanesa E., Acebedo Sofía L., Cassia Raúl O., Lamattina Lorenzo, Galagovsky Lydia R., Ramírez Javier A.: A bioassay for brassinosteroid activity based on the in vitro fluorimetric detection of nitric oxide production. Steroids 2015, 102, 46. <https://doi.org/10.1016/j.steroids.2015.07.003>
  • Sepe Valentina, Ummarino Raffaella, D'Auria Maria Valeria, Renga Barbara, Fiorucci Stefano, Zampella Angela: The First Total Synthesis of Solomonsterol B, a Marine Pregnane X Receptor Agonist. Eur J Org Chem 2012, 2012, 5187. <https://doi.org/10.1002/ejoc.201200619>
  • Sepe Valentina, Ummarino Raffaella, D’Auria Maria Valeria, Mencarelli Andrea, D’Amore Claudio, Renga Barbara, Zampella Angela, Fiorucci Stefano: Total Synthesis and Pharmacological Characterization of Solomonsterol A, a Potent Marine Pregnane-X-Receptor Agonist Endowed with Anti-Inflammatory Activity. J. Med. Chem. 2011, 54, 4590. <https://doi.org/10.1021/jm200241s>
  • 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>
  • Khripach Vladimir A., Zhabinskii Vladimir N., Zhiburtovich Yuliya Y., Ivanova Galina V., Konstantinova Olga V., Tsavlovskii Dmitrii V., Lorenz Sybille, Schneider Bernd: Preparation and synthetic application of partially protected brassinosteroids. Steroid 2010, 75, 27. <https://doi.org/10.1016/j.steroids.2009.09.010>
  • Cong Rigang, Zhang Yihua, Tian Weisheng: A concise synthesis of the steroidal core of clathsterol. Tetrahetron Lett 2010, 51, 3890. <https://doi.org/10.1016/j.tetlet.2010.05.072>
  • Zhu Chunsheng, Tang Pingping, Yu Biao: Total Synthesis of Lobatoside E, A Potent Antitumor Cyclic Triterpene Saponin. J. Am. Chem. Soc. 2008, 130, 5872. <https://doi.org/10.1021/ja801669r>
  • Rivera Daniel G., León Fredy, Coll Francisco, Davison Gema P.: Novel 5β-hydroxyspirostan-6-ones ecdysteroid antagonists: Synthesis and biological testing. Steroid 2006, 71, 1. <https://doi.org/10.1016/j.steroids.2005.02.024>
  • Voigt Brunhilde, Porzel Andrea, Adam Guenter, Golsch Dieter, Adam Waldemar, Wagner Christoph, Merzweiler Kurt: ChemInform Abstract: Synthesis of 2,24‐Diepicastasterone (I) and 3,24‐Diepicastasterone (II) as Potential Brassinosteroid Metabolites of the Cockroach Periplaneta americana. ChemInform 2002, 33. <https://doi.org/10.1002/chin.200237196>