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Collect. Czech. Chem. Commun. 1990, 55, 2738-2755
https://doi.org/10.1135/cccc19902738

A route to 24-epibrassinolide from ergosterol avoiding the use of osmium tetroxide

Václav Černý and Miloš Buděšínský

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

Crossref Cited-by Linking

  • Wendeborn Sebastian, Lachia Mathilde, Jung Pierre M. J., Leipner Jörg, Brocklehurst David, De Mesmaeker Alain, Gaus Katharina, Mondière Régis: Biological Activity of Brassinosteroids – Direct Comparison of Known and New Analogs in planta. Helvetica Chimica Acta 2017, 100. <https://doi.org/10.1002/hlca.201600305>
  • Porzel Andrea, Marquardt Volker, Adam Günter, Massiot Georges, Zeigan Dieter: 1H and 13C NMR analysis of brassinosteroids. Magnetic Reson in Chemistry 1992, 30, 651. <https://doi.org/10.1002/mrc.1260300714>
  • CERNY V., BUDESINSKY M.: ChemInform Abstract: Steroids. Part 354. A Route to 24‐epiBrassinolide (VII) from Ergosterol Avoiding the Use of Osmium Tetroxide. ChemInform 1991, 22. <https://doi.org/10.1002/chin.199110291>