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  1. 2024

  2. One-pot Synthesis and Photophysical Studies of Α-cycloamino-substituted 5-aryl-2,2'-bipyridines

    Guda, M., Valieva, M., Kopchuk, D., Aluru, R., Khasanov, A., Taniya, O., Novikov, A., Zyryanov, G. & Ranu, B., 1 Mar 2024, In: Journal of Fluorescence. 34, 2, p. 579-586 8 p.

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

  3. Studying the effectiveness of various chromophores of the 5-aryl-2,2ʹ-bipyridine series for the sensitization of lanthanide(III) cations

    Majee, A., Krinochkin, A. P., Valieva, M. I., Starnovskaya, E. S., Shtaitz, Y. K., Kopchuk, D. S., Santra, S., Liu, Y., Zyryanov, G. V. & Chupakhin, O. N., 1 Mar 2024, In: Journal of the Iranian Chemical Society. 21, 3, p. 731-740 10 p.

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

  4. Fluorinated derivatives of 2-azinyl-4-(4-aminophenyl)quinazolines: Synthesis and photophysical properties

    Kopotilova, A., Valieva, M., Starnovskaya, E., Moshkina, T., Nosova, E., Taniya, O., Kalinichev, A., Kopchuk, D., Slepukhin, P., Gaviko, V., Kim, G. & Charushin, V., 1 Feb 2024, In: Journal of Photochemistry and Photobiology A: Chemistry. 448, 115350.

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

  5. Synthesis of (3‐Thienyl)‐Substituted 2,2’‐Bipyridines and Their Application as Activators of Platinum Electrode Catalytic Activity Towards Cholesterol Electrooxidation

    Okhokhonin., A., Stepanova, M., Tsmokaluk, A., Mazur, A., Valieva, M., Starnovskaya, E., Gorbunov, E., Gaviko, V., Krinochkin, A., Kopchuk, D., Zyryanov, G., Kozitsina, A. & Rusinov, V., 2024, In: ChemistrySelect. 9, 10, e202304520.

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

  6. 2023

  7. Co(II), Cu(II), and Mn(II) complexes based on 2,2’-bipyridine and 3-(2-pyridyl)-1,2,4-triazine ligands containing organofluorine species

    Moseev, T. D., Nikiforov, E. A., Varaksin, M. V., Valieva, M. I., Kopchuk, D. S., Litvinov, I. A., Gaviko, V. S., Slepukhin, P. A., Zyryanov, G. V., Charushin, V. N. & Chupakhin, O. N., 1 Dec 2023, In: Inorganica Chimica Acta. 558, 121727.

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

  8. Efficient synthetic approach to 1-aza- and 1,2,4-triazatriptycenes

    Rybakova, S., Valieva, M., Kudryashova, E., Kopchuk, D., Taniya, O., Egorov, I., Zyryanov, G. & Chupakhin, O., 1 Dec 2023, In: Russian Chemical Bulletin. 72, 12, p. 3032-3036 4 p.

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

  9. Solvent-free reaction of 4-amino-1,2,4-triazole-3-thioles with 1,2,4-triazine-5-carbonitriles

    Shtaitz, Y., Ladin, E., Il’inykh, E., Starnovskaya, E., Kopchuk, D., Zyryanov, G. & Rusinov, V., 1 Dec 2023, In: Russian Chemical Bulletin. 72, 12, p. 2948-2952 5 p.

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

  10. Transformations of 6-[4-(methylthio)phenyl]-3-(2-pyridyl)-1,2,4-triazines in the reaction with an aryne intermediate

    Moseev, T., Idrisov, T., Lavrinchenko, I., Krinochkin, A., Kudryashova, E., Kopchuk, D., Varaksin, M., Zyryanov, G., Charushin, V. & Chupakhin, O., 1 Dec 2023, In: Russian Chemical Bulletin. 72, 12, p. 2922-2926 5 p.

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

  11. Reaction of 1,2,4-Triazine-5-carbonitriles with 5-[(2-Hydroxyethyl)sulfanyl]- and 5-{[2-(2-Hydroxyethoxy)-ethyl]sulfanyl}-3-amino-1,2,4-triazoles1

    Krinochkin, A. P., Ladin, E. D., Shtaitz, Y. K., Kudryashova, E. A., Kopchuk, D. S., Gorbunov, E. B., Shafran, Y. M., Zyryanov, G. V. & Rusinov, V. L., 1 Nov 2023, In: Russian Journal of Organic Chemistry. 59, 11, p. 1998-2002 5 p.

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

  12. 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

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