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  1. 2023

  2. Synthesis and transformations of 2,4-dioxa- and 2,4-diazaspiro[5.5]undecanones equipped with a diterpenoid substituent

    Mironov, M. E. & Shults, E. E., Oct 2023, In: Russian Chemical Bulletin. 72, 10, p. 2453-2465 13 p.

    Research output: Contribution to journal › Article › peer-review

  3. Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents

    Mironov, M. E., Rybalova, T. V., Pokrovskii, M. A., Emaminia, F., Gandalipov, E. R., Pokrovskii, A. G. & Shults, E. E., Feb 2023, In: Steroids. 190, 13 p., 109133.

    Research output: Contribution to journal › Article › peer-review

  4. Mannich Reaction of Solasodine with Acetylenes and Formaldehyde. Cytotoxicity of N-Propargyl-Substituted Alkaloid Derivatives

    Finke, A. O., Mironov, M. E., Pokrovskii, M. A. & Shults, E. E., Jan 2023, In: Chemistry of Natural Compounds. 59, 1, p. 87-93 7 p.

    Research output: Contribution to journal › Article › peer-review

  5. 2022

  6. Synthesis of anti-inflammatory spirostene-pyrazole conjugates by a consecutive multicomponent reaction of diosgenin with oxalyl chloride, arylalkynes and hydrazines or hydrazones

    Mironov, M. E., Borisov, S. A., Rybalova, T. V., Baev, D. S., Tolstikova, T. G. & Shults, E. E., 1 Jan 2022, In: Molecules. 27, 1, 162.

    Research output: Contribution to journal › Article › peer-review

  7. 2020

  8. Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety

    Mironov, M. E., Poltanovich, A. I., Rybalova, T. V., Dolgikh, M. P., Tolstikova, T. G. & Shults, E. E., Mar 2020, In: Russian Chemical Bulletin. 69, 3, p. 537-546 10 p.

    Research output: Contribution to journal › Article › peer-review

  9. 2019

  10. 6-(4′-Aryl-1′,2′,3′-triazolyl)-spirostan-3,5-diols and 6-(4′-Aryl-1′,2′,3′-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity

    Mironov, M. E., Oleshko, O. S., Pokrovskii, M. A., Rybalova, T. V., Pechurov, V. K., Pokrovskii, A. G., Cheresis, S. V., Mishinov, S. V., Stupak, V. V. & Shults, E. E., 1 Nov 2019, In: Steroids. 151, p. 108460 10 p., 108460.

    Research output: Contribution to journal › Article › peer-review

  11. 2018

  12. Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid

    Finke, A. O., Mironov, M. E., Skorova, A. B. & Shults, E. E., Apr 2018, In: Chemistry of Heterocyclic Compounds. 54, 4, p. 411-416 6 p.

    Research output: Contribution to journal › Article › peer-review

  13. 2013

  14. 6-ГИДРОКСИНАФТОХИНОНЫ ЛАБДАНОВОГО ТИПА, ОБЛАДАЮЩИЕ ЦИТОТОКСИЧЕСКОЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К ОПУХОЛЕВЫМ КЛЕТКАМ ЧЕЛОВЕКА

    Шульц, Э. Э., Миронов, М. Е., Покровский, М. А., Шерман, К. М., Покровский, А. Г. & Толстиков, Г. А., 20 Apr 2013, IPC No. C07D307/40, A61K31/341, A61P35/00, Роспатент - Федеральная служба по интеллектуальной собственности, Patent No. 2479582, Priority date 19 Apr 2012, Priority No. 2012115828

    Research output: Patent › Patent for invention

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