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Collect. Czech. Chem. Commun. 1992, 57, 1731-1738

Brassinosteroids with Ester Function with Five Carbon Atoms at the 20 Position

Ladislav Kohouta and Miroslav Strnadb

a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10, Prague 6
b Institute of Experimental Botany, Czechoslovak Academy of Sciences, 772 00 Olomouc

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  • Marek Aleš, Klepetářová Blanka, Elbert Tomáš: A Study of the Reactivity of Polyhydroxylated Sterol Derivatives. Asian J Org Chem 2015, 4, 808. <>
  • Marek Aleš, Klepetářová Blanka, Elbert Tomáš: A facile method for steroid labeling by heavy isotopes of hydrogen. Tetrahedron 2015, 71, 4874. <>
  • Rivera Daniel G, Coll Francisco: Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds. Can. J. Chem. 2005, 83, 1084. <>
  • 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. <>
  • Gil R. Pérez, Martínez C. S. Pérez, Manchado F. Coll: Synthesis of Analogues of Brassinosteroids with 5β-Cholanic Acid Skeleton. Synthetic Communications 1998, 28, 3387. <>
  • Kovganko N. V., Ananich S. K.: Advances in the chemical synthesis of brassinosteroids. Chem Nat Compd 1997, 33, 389. <>
  • KOHOUT L., STRNAD M.: ChemInform Abstract: Steroids. Part 363. Brassinosteroids with Ester Function with Five Carbon Atoms at the 20 Position. ChemInform 1992, 23. <>