Collect. Czech. Chem. Commun.
1993, 58, 2505-2516
https://doi.org/10.1135/cccc19932505
Oxidation of 3β,28-Diacetoxy-18-lupen-21-one with Peroxy Acids: A Way to Des-E-lupane Derivatives
Eva Klinotováa, Martin Rejzeka, Hana Zůnováa, Jan Sejbala, Jiří Klinota and Jiří Urbanb
a Department of Organic Chemistry, Charles University, 128 40 Prague 2, Czech Republic
b J. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, 182 23 Prague 8, Czech Republic
Crossref Cited-by Linking
- Kvasnica Miroslav, Sarek Jan, Vlk Martin, Budesinsky Milos, Stepanek Ondrej, Kubelka Tomas, Plutnarova Iva: Study of stereoselectivity of reduction of 18-oxo des-E triterpenoids by sodium borohydride in the presence of cerium chloride. Tetrahedron: Asymmetry 2011, 22, 1011. <https://doi.org/10.1016/j.tetasy.2011.05.017>
- Kvasnica Miroslav, Tišlerová Iva, Šarek Jan, Sejbal Jan, Císařová Ivana: Preparation of New Oxidized 18-α-Oleanane Derivatives. Collect. Czech. Chem. Commun. 2005, 70, 1447. <https://doi.org/10.1135/cccc20051447>
- Tišlerová Iva, Klinotová Eva, Klinot Jiří, Sejbal Jan, Rejzek Martin, Hilgard Stanislav: Preparation of E-Secolupane Acids and Lactones. Collect. Czech. Chem. Commun. 2003, 68, 751. <https://doi.org/10.1135/cccc20030751>
- KLINOTOVA E., REJZEK M., ZUNOVA H., SEJBAL J., KLINOT J., URBAN J.: ChemInform Abstract: Triterpenes. Part 101. Oxidation of 3β,28‐Diacetoxy‐18‐lupen‐21‐ one with Peroxy Acids: A Way to Des‐E‐lupane Derivatives. ChemInform 1994, 25. <https://doi.org/10.1002/chin.199407245>
