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  1. N-ЭТИЛПИПЕРАЗИЛАМИД БЕТУЛОНОВОЙ КИСЛОТЫ КАК ПРОТИВООПУХОЛЕВОЕ СРЕДСТВО ТРИТЕРПЕНОВОЙ ПРИРОДЫ

    Покровский, А. Г., Покровский, М. А., Салахутдинов, Н. Ф., Толстиков, Г. А. & Майнагашев, И. Я., 20 Mar 2012, IPC No. C07J53/00, C07J43/00, A61P35/00, Роспатент - Федеральная служба по интеллектуальной собственности, Patent No. 2445317, Priority date 28 Oct 2010, Priority No. 2010144219

    Research output: Patent › Patent for invention

  2. One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure

    Demidova, Y. S., Suslov, E. V., Simakova, I. L., Mozhajcev, E. S., Korchagina, D. V., Volcho, K. P., Salakhutdinov, N. F., Simakov, A. & Murzin, D. Y., 1 Apr 2018, In: Journal of Catalysis. 360, p. 127-134 8 p.

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

  3. One-Pot Myrtenol Amination over Au, Au–Pd and Pd Nanoparticles Supported on Alumina

    Demidova, Y. S., Simakova, I. L., Estrada, M., Beloshapkin, S., Suslov, E. V., Volcho, K. P., Salakhutdinov, N. F., Simakov, A. & Murzin, D. Y., 1 Dec 2019, In: Catalysis Letters. 149, 12, p. 3454-3464 11 p.

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

  4. One-pot synthesis of 1,5,3-oxathiazepanes via the three-component condensation of primary amines, formaldehyde and 2-mercaptoethanol

    Kovaleva, K. S., Yarovaya, O. I., Fadeev, D. S. & Salakhutdinov, N. F., 10 May 2017, In: Tetrahedron Letters. 58, 19, p. 1868-1870 3 p.

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

  5. Optimization of the Synthesis of 2-Adamantanecarboxylic Acid

    MUNKUEV, A. A., SHESHKOVAS, A. ZH., SUSLOV, E. V., VOLCHO, K. P. & SALAKHUTDINOV, N. F., 2022, In: Chemistry for Sustainable Development. 30, 6, p. 612-616 5 p.

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

  6. Pharmacokinetics and Dose Proportionality Study of a Novel Antiparkinsonian Agent, a 1H-1,2,4-Triazol-3-ylthio-conjugate of Prottremine

    Gorina, D. S., Lastovka, A. V., Rogachev, A. D., Podturkina, A. V., Pavlova, A. V., Ardashov, O. V., Li-Zhulanov, N. S., Tolstikova, T. G., Volcho, K. P. & Salakhutdinov, N. F., Sept 2024, In: Molecules. 29, 18, 4498.

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

  7. Pharmacokinetic study of Tdp1 inhibitor resulted in a significant increase in antitumor effect in the treatment of Lewis lung carcinoma in mice by its combination with topotecan

    Okhina, A. A., Kornienko, T. E., Rogachev, A. D., Luzina, O. A., Popova, N. A., Nikolin, V. P., Zakharenko, A. L., Dyrkheeva, N. S., Pokrovsky, A. G., Salakhutdinov, N. F. & Lavrik, O. I., 30 Nov 2023, In: Journal of Pharmaceutical and Biomedical Analysis. 236, 9 p., 115731.

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

  8. Preparation of chiral isobenzofurans from 3-carene in the presence of modified clays

    Sidorenko, A. Y., Il'ina, I. V., Kravtsova, A. V., Aho, A., Ardashov, O. V., Li-Zhulanov, N. S., Volcho, K. P., Salakhutdinov, N. F., Murzin, D. Y. & Agabekov, V. E., 1 Nov 2018, In: Molecular Catalysis. 459, p. 38-45 8 p.

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

  9. Preparation of octahydro-2H-chromen-4-ol with analgesic activity from isopulegol and thiophene-2-carbaldehyde in the presence of acid-modified clays

    Sidorenko, A. Y., Kravtsova, A. V., Wärnå, J., Aho, A., Heinmaa, I., Il'ina, I. V., Ardashov, O. V., Volcho, K. P., Salakhutdinov, N. F., Murzin, D. Y. & Agabekov, V. E., 1 Jul 2018, In: Molecular Catalysis. 453, p. 139-148 10 p.

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

  10. Prins cyclization of (-)-isopulegol with benzaldehyde for production of chromenols over organosulfonic clays

    Li-Zhulanov, N., Mäki-Arvela, P., Laluc, M., Peixoto, A. F., Kholkina, E., Sandberg, T., Aho, A., Volcho, K., Salakhutdinov, N., Freire, C., Sidorenko, A. Y. & Murzin, D. Y., 1 Nov 2019, In: Molecular Catalysis. 478, 12 p., 110569.

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

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