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  1. 2019

  2. Synthesis and optical properties of new 2-(5-arylpyridine-2-yl)-6-(het)arylquinoline-based “push-pull” fluorophores

    Kopchuk, D. S., Chepchugov, N. V., Starnovskaya, E. S., Khasanov, A. F., Krinochkin, A. P., Santra, S., Zyryanov, G. V., Das, P., Majee, A., Rusinov, V. L. & Charushin, V. N., 1 Aug 2019, In: Dyes and Pigments. 167, p. 151-156 6 p.

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

  3. 2017

  4. 3,4,5,6-Tetrafluoro-1,2-dehydrobenzene in reactions with 1,2,4-triazines

    Kopchuk, D. S., Chepchugov, N. V., Gorbunov, E. B., Zyryanov, G. V., Kovalev, I. S., Nosova, E. V., Slepukhin, P. A., Rusinov, V. L. & Chupakhin, O. N., 1 Jul 2017, In: Journal of the Iranian Chemical Society. 14, 7, p. 1507-1512 6 p.

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

  5. Effect of substituent in pyridine-2-carbaldehydes on their heterocyclization to 1,2,4-triazines and 1,2,4-triazine 4-oxides

    Krinochkin, A. P., Kopchuk, D. S., Chepchugov, N. V., Kovalev, I. S., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 1 Jul 2017, In: Russian Journal of Organic Chemistry. 53, 7, p. 963-970 8 p.

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

  6. An efficient synthetic approach towards new 5,5’-diaryl-2,2’-bipyridine-based fluorophores

    Krinochkin, A. P., Kopchuk, D. S., Chepchugov, N. V., Kim, G. A., Kovalev, I. S., Rahman, M., Zyryanov, G. V., Majee, A., Rusinov, V. L. & Chupakhin, O. N., 1 May 2017, In: Chinese Chemical Letters. 28, 5, p. 1099-1103 5 p.

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

  7. Solvent-free reaction of 1,2,4-triazine-5-carbonitriles with 4-(cyclohex-1-en-1-yl)morpholine. Unexpected decyanation in addition to classical aza-Diels–Alder reaction

    Kopchuk, D. S., Khasanov, A. F., Chepchugov, N. V., Kovalev, I. S., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 1 Jan 2017, In: Russian Journal of Organic Chemistry. 53, 1, p. 99-102 4 p.

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

  8. Solvent-free synthesis of 5-(aryl/alkyl)amino-1,2,4-triazines and alpha-arylamino-2,2 '-bipyridines with greener prospects

    Kopchuk, D. S., Chepchugov, N. V., Kovalev, I. S., Santra, S., Rahman, M., Giri, K., Zyryanov, G. V., Majee, A., Charushin, V. N. & Chupakhin, O. N., 2017, In: RSC Advances. 7, 16, p. 9610-9619 10 p.

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

  9. Unsymmetrically functionalized 5,5″-diaryl-and 5,6,5″-triaryl-2,2′:6′,2″-terpyridines: An efficient synthetic route and photophysical properties

    Krinochkin, A. P., Kopchuk, D. S., Khasanov, A. F., Chepchugov, N. V., Kovalev, I. S., Santra, S., Zyryanov, G. V., Majee, A., Rusinov, V. L. & Chupakhin, O. N., 2017, In: Canadian Journal of Chemistry. 95, 8, p. 851-857 7 p.

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

  10. Взаимодействие 1,2,4-триазин-5 -карбонитрилов с 4-(циклогекс-1-ен-1-ил)мор- К фолином в отсутствие растворителя. Неожиданное децианирование наряду с протеканием классической реакции аза- Дильса-Альдера

    Копчук, Д. С., Хасанов, А. Ф., Чепчугов, Н. В., Ковалев, И. С., Зырянов, Г. В., Русинов, В. Л. & Чупахин, О. Н., 2017, In: Журнал органической химии. 53, 1, p. 103-106 4 p.

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

  11. ВЛИЯНИЕ ЗАМЕСТИТЕЛЯ В ПИРИДИН-2-КАРБАЛЬДЕГИДАХ НА ВОЗМОЖНОСТИ ИХ ГЕТЕРОЦИКЛИЗАЦИИ В 1,2,4-ТРИАЗИНЫ И 1,2,4-ТРИАЗИН-4-ОКСИДЫ

    Криночкин, А. П., Копчук, Д. С., Чепчугов, Н. В., Ковалев, И. С., Зырянов, Г. В., Русинов, В. Л. & Чупахин, О. Н., 2017, In: Журнал органической химии. 53, 7, p. 951-958 8 p.

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

  12. 2016

  13. A one-pot approach to 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles via aryne-mediated transformations of 3-(pyrimidin-2-yl)-1,2,4-triazines

    Kopchuk, D. S., Chepchugov, N. V., Khasanov, A. F., Kovalev, I. S., Santra, S., Nosova, E. V., Zyryanov, G. V., Majee, A., Rusinov, V. L. & Chupakhin, O. N., 24 Aug 2016, In: Tetrahedron Letters. 57, 34, p. 3862-3865 4 p.

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

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