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  1. 2021

  2. 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

  3. Synthesis of 5-[(Thiophen-3-yl)amino]-1,2,4-triazines

    Krinochkin, A. P., Guda, M. R., Kopchuk, D. S., Shtaitz, Y. K., Starnovskaya, E. S., Savchuk, M. I., Rybakova, S. S., Zyryanov, G. V. & Chupakhin, O. N., Apr 2021, In: Russian Journal of Organic Chemistry. 57, 4, p. 675-677 3 p.

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

  4. Synthesis of Novel 3-(Pyridin-4-yl)-1,2,4-Triazines, their Analogs and Study of the Activity Against Vaccinia Virus

    Shabunina, O. V., Shtaitz, Y. K., Kopchuk, D. S., Krinochkin, A. P., Santra, S., Zyryanov, G. V., Wang, Z., Rusinov, V. L. & Chupakhin, O. N., Apr 2021, In: Chemistry of Heterocyclic Compounds. 57, 4, p. 462-466 5 p.

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

  5. Asymmetrically substituted 5,5′′-diaryl-2,2′:6′,2′′-terpyridines as efficient fluorescence “turn-on” probes for Zn2+ in food/cosmetic samples and human urine

    Shabunina, O. V., Starnovskaya, E. S., Shaitz, Y. K., Kopchuk, D. S., Sadieva, L. K., Kim, G. A., Taniya, O. S., Nikonov, I. L., Santra, S., Zyryanov, G. V. & Charushin, V. N., 1 Mar 2021, In: Journal of Photochemistry and Photobiology A: Chemistry. 408, 12 p., 113101.

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

  6. A facile synthesis of triazine integrated antipyrine derivatives through ecofriendly approach

    Rammohan, A., Reddy, G. M., Krinochkin, A. P., Kopchuk, D. S., Savchuk, M. I., Shtaitz, Y. K., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 2021, In: Synthetic Communications. 51, 2, p. 256-262 7 p.

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

  7. МЕТОД СИНТЕЗА 1,2,4-ТРИАЗИНОВ, ИМЕЮЩИХ В ПОЛОЖЕНИИ С5 ОСТАТКИ 3-АМИНОТИОФЕНА

    Криночкин, А. П., Гуда, М. Р., Копчук, Д. С., Штайц, Я. К., Старновская, Е. С., Савчук, М. И., Рыбакова, С. С., Зырянов, Г. В. & Чупахин, О. Н., 2021, In: Журнал органической химии. 57, 4, p. 597-600 4 p.

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

  8. ЭФФЕКТИВНЫЙ СИНТЕТИЧЕСКИЙ ПОДХОД К 1,2,4-ТРИАЗИНАМ, ИМЕЮЩИМ В ПОЛОЖЕНИИ С5 ОСТАТКИ 2-(АМИНОФЕНИЛ)-1,3,4-ОКСАДИАЗОЛОВ

    Криночкин, А. П., Гуда, М. Р., Копчук, Д. С., Словеснова, Н. В., Ковалев, И. С., Савчук, М. И., Штайц, Я. К., Старновская, Е. С., Зырянов, Г. В. & Чупахин, О. Н., 2021, In: Журнал органической химии. 57, 10, p. 1496-1500 5 p.

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

  9. 2020

  10. New monomers for (bi)pyridine-containing polymers

    Krinochkin, A. P., Savchuk, M. I., Starnovskaya, E. S., Shtaitz, Y. K., Kopchuk, D. S., Nikonov, I. L., Kovalev, I. S., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 30 Dec 2020, In: Chimica Techno Acta. 7, 4, p. 209-214 6 p.

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

  11. 5-Aryl-2,2′-bipyridines bearing fluorinated anilines residues at C6 position: synthesis and photophysical properties

    Kopchuk, D. S., Starnovskaya, E. S., Shtaitz, Y. K., Khasanov, A. F., Kim, G. A., Nosova, E. V., Krinochkin, A. P., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 1 Aug 2020, In: Research on Chemical Intermediates. 46, 8, p. 3929-3944 16 p.

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

  12. Polynuclear Aromatic Amines as N-Nucleophiles in the ipso-Substitution of the Cyano Group in 1,2,4-Triazines

    Starnovskaya, E. S., Savchuk, M. I., Shtaitz, Y. K., Kopchuk, D. S., Kovalev, I. S., Pavlyuk, D. E., Khasanov, A. F., Zyryanov, G. V. & Chupakhin, O. N., 1 Apr 2020, In: Russian Journal of Organic Chemistry. 56, 2, p. 335-338 4 p.

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

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