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  1. 2022

  2. Рентгеноструктурное исследование 8-(пиридин-2-ил)- и 8-([1,2,4]триазин-5-ил)замещенных кумаринов

    Слепухин, П. А., Фатыхов, Р. Ф., Шарапов, А. Д., Валиева, М. И., Старновская, Е. С., Халымбаджа, И. А., Копчук, Д. С., Зырянов, Г. В. & Чупахин, О. Н., 2022, In: Журнал общей химии. 92, 7, p. 1125-1130 6 p.

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

  3. РЕНТГЕНОСТРУКТУРНЫЕ ИССЛЕДОВАНИЯ МОНОКРИСТАЛЛОВ 2,2´-БИПИРИДИНОВ, СОДЕРЖАЩИХ ОСТАТКИ АРИЛАМИНОВ

    Слепухин, П. А., Криночкин, А. П., Старновская, Е. С., Штайц, Я. К., Савчук, М. И., Копчук, Д. С., Егоров, И. Н., Сантра, С., Зырянов, Г. В. & Чупахин, О. Н., 2022, In: Известия Академии наук. Серия химическая. 7, p. 1533-1543 11 p.

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

  4. 2021

  5. Photophysics, photochemistry and bioimaging application of 8-azapurine derivatives

    Eltyshev, A. K., Agafonova, I. A., Minin, A. S., Pozdina, V. A., Shevirin, V. A., Slepukhin, P. A., Benassi, E. & Belskaya, N. P., 25 Nov 2021, In: Organic and Biomolecular Chemistry. 19, 45, p. 9880-9896 17 p.

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

  6. Unsymmetrical trifluoromethyl methoxyphenyl β-diketones: Effect of the position of methoxy group and coordination at cu(ii) on biological activity

    Khamidullina, L. A., Puzyrev, I. S., Burygin, G. L., Dorovatovskii, P. V., Zubavichus, Y. V., Mitrofanova, A. V., Khrustalev, V. N., Timofeeva, T. V., Slepukhin, P. A., Tobysheva, P. D., Pestov, A. V., Solari, E., Tskhovrebov, A. G. & Nenajdenko, V. G., 1 Nov 2021, In: Molecules. 26, 21, 20 p., 6466.

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

  7. Influence of Trifluoromethyl Groups on the Crystal Packing of the Binuclear Copper(II) Complex Based on N2O3-Pentadentate (Hydroxy)bis(СF3-Enaminoketone)

    Edilova, Y. O., Kudyakova, Y. S., Slepukhin, P. A., Burgart, Y. V., Saloutin, V. I. & Bazhin, D. N., Sept 2021, In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 47, 9, p. 631-637 7 p.

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

  8. 2-Aminooxazoles as novel dienophiles in the inverse demand Diels–Alder reaction with 1,2,4-triazines

    Krinochkin, A. P., Mallikarjuna Reddy, G., Kopchuk, D. S., Slepukhin, P. A., Shtaitz, Y. K., Khalymbadzha, I. A., Kovalev, I. S., Kim, G. A., Ganebnykh, I. N., Zyryanov, G. V., Chupakhin, O. N. & Charushin, V. N., 1 Jul 2021, In: Mendeleev Communications. 31, 4, p. 542-544 3 p.

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

  9. The Rh(iii)-catalysed C-H/N-H annulation of 2-thienyl- And 2-phenyl-quinazolin-4(3:H)-ones with diphenylacetylene

    Moshkina, T. N., Nosova, E. V., Lipunova, G. N., Zhilina, E. F., Slepukhin, P. A., Nikonov, I. L. & Charushin, V. N., 21 May 2021, In: New Journal of Chemistry. 45, 19, p. 8456-8466 11 p.

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

  10. Synthesis and structure of homoleptic copper complexes based on fluorinated functionalized 1,3-diketones

    Saloutin, V. I., Burgart, Y. V., Edilova, Y. O., Slepukhin, P. A., Kudyakova, Y. S. & Bazhin, D. N., May 2021, In: Russian Chemical Bulletin. 70, 5, p. 839-846 8 p.

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

  11. Design, synthesis, and photophysics of bi- and tricyclic fused pyrazolines dagger

    Popova, A. V., Kanaa, A., Vavilova, V. S., Mironova, M. A., Slepukhin, P. A., Benassi, E. & Belskaya, N. P., 14 Apr 2021, In: New Journal of Chemistry. 45, 14, p. 6315-6326 12 p.

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

  12. Methods of Synthesis and Antiviral Activity of New 4-Alkyl-3-Nitro-1,4-Dihydroazolo[5,1-c][1,2,4]Triazin-4-ols

    Drokin, R. A., Tiufiakov, D. V., Voinkov, E. K., Slepukhin, P. A., Ulomsky, E. N., Esaulkova, Y. L., Volobueva, A. S., Lantseva, K. S., Misyurina, M. A., Zarubaev, V. V. & Rusinov, V. L., Apr 2021, In: Chemistry of Heterocyclic Compounds. 57, 4, p. 473-478 6 p.

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

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