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  1. The decisive role of mutual arrangement of hydroxy and methoxy groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8ahexahydro- 2H-chromene-4,8-diols in their Biological Activity

    Pavlova, A., Patrusheva, O., Il'ina, I., Volcho, K., Tolstikova, T. & Salakhutdinov, N., 1 May 2017, In: Letters in Drug Design and Discovery. 14, 5, p. 508-514 7 p.

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

  2. Synthesis of Sulfones and Sulfoxides Based on (+)-usnic Acid

    Sokolov, D. N., Luzina, O. A. & Salakhutdinov, N. F., 1 Jan 2018, In: Chemistry of Natural Compounds. 54, 1, p. 46-49 4 p.

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

  3. Synthesis of Secondary Amines of Bornylamine and Isobornylamine Containing a Saturated N-Heterocycle and Study of Their Antiviral Activity against Respiratory Syncytial Virus

    Tishchenko, S. A., Sokolova, A. S., Yarovaya, O. I., Krasnov, V. I., Shtro, A. A., Galochkina, A. V., Klabukov, A. M., Razgulyaeva, D. N. & Salakhutdinov, N. F., 27 Feb 2025, In: Russian Journal of General Chemistry. 95, 1, p. 79-87 9 p.

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

  4. Synthesis of Norabietyl and Nordehydroabietyl Imidazolidine-2,4,5-Triones and Their Activity against Tyrosyl-DNA Phosphodiesterase 1

    Kovaleva, K. S., Yarovaya, O. I., Chernyshova, I. A., Zakharenko, A. L., Cheresiz, S. V., Azimirad, A., Pokrovsky, A. G., Lavrik, O. I. & Salakhutdinov, N. F., Dec 2023, In: MolBank. 2023, 4, М1743.

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

  5. Synthesis of non-symmetric N-benzylbispidinol amides and study of their inhibitory activity against the main protease of the SARS-CoV-2 virus

    Dalinger, A. I., Baev, D. S., Yarovaya, O. I., Chirkova, V. Y., Sharlaeva, E. A., Belenkaya, S. V., Shcherbakov, D. N., Salakhutdinov, N. F. & Vatsadze, S. Z., 1 Jan 2023, In: Russian Chemical Bulletin. 72, 1, p. 239-247 9 p.

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

  6. Synthesis of N-heterocyclic amides based on (+)-camphoric acid and study of their antiviral activity and pharmacokinetics

    Yarovaya, O. I., Baranova, D. V., Sokolova, A. S., Nemolochnova, A. G., Sal'nikova, O. P., Fat'anova, A. V., Rogachev, A. D., Volobueva, A. S., Zarubaev, V. V., Pokrovsky, A. G. & Salakhutdinov, N. F., Mar 2023, In: Russian Chemical Bulletin. 72, 3, p. 807-818 12 p.

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

  7. Synthesis of new heterocyclic dehydroabietylamine derivatives and their biological activity

    Kovaleva, K. S., Yarovaya, O. I., Shernyukov, A. V., Zarubaev, V. V., Shtro, A. A., Orshanskaya, Y. R. & Salakhutdinov, N. F., 1 Mar 2017, In: Chemistry of Heterocyclic Compounds. 53, 3, p. 364-370 7 p.

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

  8. Synthesis of new compounds combining adamantanamine and monoterpene fragments and their antiviral activity against influenza virus A(H1N1)pdm09

    Teplov, G. V., Suslov, E. V., Zarubaev, V. V., Shtro, A. A., Karpinskaya, L. A., Rogachev, A. D., Korchagina, D. V., Volcho, K. P., Salakhutdinov, N. F. & Kiselev, O. I., Jul 2013, In: Letters in Drug Design and Discovery. 10, 6, p. 477-485 9 p.

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

  9. Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes

    Sidorenko, A. Y., Kravtsova, A. V., Mäki-Arvela, P., Aho, A., Sandberg, T., Il'ina, I. V., Li-Zhulanov, N. S., Korchagina, D. V., Volcho, K. P., Salakhutdinov, N. F., Murzin, D. Y. & Agabekov, V. E., Jul 2020, In: Molecular Catalysis. 490, 8 p., 110974.

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

  10. Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System

    Il’ina, I. V., Patrusheva, O. S., Korchagina, D. V., Volcho, K. P. & Salakhutdinov, N. F., 1 Jul 2020, In: Chemistry of Heterocyclic Compounds. 56, 7, p. 867-874 8 p.

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

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