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  1. 2023

  2. Phosphonium salts based on 2H-imidazole: synthesis by direct C–H functionalization of imidazole N-oxides

    Akulov, A., Pershin, A., Deleva, A., Varaksin, M., Charushin, V. & Chupakhin, O., 1 Nov 2023, In: Russian Chemical Bulletin. 72, 11, p. 2693-2697 5 p.

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

  3. Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds

    Lavrinchenko, I., Moseev, T., Varaksin, M., Seleznev, Y., Sadieva, L., Zyryanov, G., Tsmokaluk, A., Charushin, V. & Chupakhin, O., 1 Sept 2023, In: Doklady Chemistry. 512, 1, p. 232-241 10 p.

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

  4. An Effective Synthetic Approach to of 2-([5'-Aryl-2,2'-bipyridin]-6-yl)-5-aryl-1,3,4-oxadiazoles

    Valieva, M., Starnovskaya, E., Kopchuk, D., Sharafieva, E., Slovesnova, N., Kovalev, I., Nosova, E., Zyryanov, G. & Chupakhin, O., 1 Aug 2023, In: Russian Journal of Organic Chemistry. 59, 8, p. 1445-1448 4 p.

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

  5. Approbation of a New Model of Secondary Damage after Traumatic Brain Injury Based on Reprogrammed Rat Embryo Fibroblasts

    Rykunova, E. B., Mikeladze, M. A., Utepova, I. A., Chupakhin, O. N., Guzhova, I. V. & Lazarev, V. F., 1 Aug 2023, In: Doklady Biochemistry and Biophysics. 511, 1, p. 235-239 5 p.

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

  6. Highly Regioselective Synthesis of 3,6-Diaryl-2-(het)arylpyridines by aza-Diels-Alder Reactions between 6-H-1,2,4-Triazine Dienes and 2-Amino-4-aryloxazole-Based Dienophiles

    Shtaitz, Y. K., Rammohan, A., Krinochkin, A. P., Ladin, E. D., Butorin, I. I., Mochulskaya, N. N., Khalymbadzha, I. A., Slepukhin, P. A., Shevyrin, V. A., Kopchuk, D. S., Zyryanov, G. V. & Chupakhin, O. N., 14 Jul 2023, In: ChemistrySelect. 8, 26

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

  7. Direct Cross-Dehydrogenative C–N-Coupling of Phenanthridine with 1H-Benzotriazole

    Akulov, A. A., Pershin, A. A., Kopchuk, D. S., Varaksin, M. V., Zyryanov, G. V. & Chupakhin, O. N., 1 Jul 2023, In: Russian Journal of Organic Chemistry. 59, 7, p. 1255-1259 5 p.

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

  8. Transformations of 2-(1-Chloroethenyl)naphthalene in the Presence of Glass-Supported Pd(0) Nanoparticles

    Mohammed, M. S., Kovalev, I. S., Volkova, N. N., Zyryanov, G. V., Ranu, B. C. & Chupakhin, O. N., 1 Jul 2023, In: Russian Journal of Organic Chemistry. 59, 7, p. 1248-1250 3 p.

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

  9. Применение 2-(пирен-1-ил)нафто[1,2-d]оксазолил-5-сульфокислоты в качестве мономолекулярного агента для фотодинамической терапии: патент на изобретение

    Криночкин, А. П., Никонов, И. Л., Копчук, Д. С., Ковалев, И. С., Тания, О. С., Платонов, В. А., Петрова, В. Е., Зырянов, Г. В., Штайц, Я. К., Старновская, Е. С., Валиева, М. И., Рыбакова, С. С., Словеснова, Н. В., Чупахин, О. Н. & Чарушин, В. Н., 2 May 2023, IPC No. C07D 263/60, A61K 31/423, A61P 31/00, A61P 35/00, Федеральный институт промышленной собственности, Patent No. 2795221, 28 Jul 2022, Priority date 28 Jul 2022, Priority No. 2022120723

    Research output: Patent

  10. Amino Derivatives of Acridine: Synthesis and Study of Anticholinesterase and Antioxidant Activity

    Shchepochkin, A. V., Uglova, A. F., Utepova, I. A., Gradoblyanskaya, E. S., Averkov, M. A., Kovaleva, N. V., Rudakova, E. V., Boltneva, N. P., Serebryakova, O. G., Makhaeva, G. F., Charushin, V. N. & Chupakhin, O. N., 1 Apr 2023, In: Doklady Chemistry. 509, 2, p. 100-105

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

  11. Heterocycles Based on Bis(trifluoromethyl)imidazolidin-2-ones, 2-Aminoethanol, and 2-Aminophenol

    Saloutina, L., Kodess, M., Ganebnykh, I., Slepukhin, P., Saloutin, V. & Chupakhin, O., 1 Apr 2023, In: Russian Journal of Organic Chemistry. 59, 4, p. 623-630 8 p.

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

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