Search Results - "Savchenko, Vyacheslav G."

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  1. 1
    Reactivity of alicyclic 1,5,9-triketones toward five-, six-, and seven-membered rings in acidic medium. Stereochemistry of intramolecular cyclization products

    Reactivity of alicyclic 1,5,9-triketones toward five-, six-, and seven-membered rings in acidic medium. Stereochemistry of intramolecular cyclization products by Akimova, Taisia I., Soldatkina, Olga A., Gerasimenko, Andrey V., Savchenko, Vyacheslav G., Kapustina, Alevtina A.

    “…Among nine alicyclic 1,5,9-triketones with differently fused 5-, 6-, and 7-membered rings in the molecule, existing as mixtures of 3–6 diastereomers, only…”
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    Stereoisomerism in the representative tetracyclic dispiro ozonide derived from (methylene)dicyclohexanone with the 1,5-diketo arrangement

    Stereoisomerism in the representative tetracyclic dispiro ozonide derived from (methylene)dicyclohexanone with the 1,5-diketo arrangement by Akimova, Taisia I., Soldatkina, Olga A., Savchenko, Vyacheslav G., Pilipenko, Anna V., Kapustina, Alevtina A.

    Published in Mendeleev communications (01-03-2022)
    “…[Display omitted] The conditions and reasons for the stereoselective transformation of the rac form of 2,2′-(methylene)-dicyclohexanone into the meso- or…”
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