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  1. 5-acyl- and 5-nitroso-6-aminouraciles as starting reagents in the synthesis of 1,3,7,9-tetramethylpyrimidopteridine-2,4,6,8-tetraone

    Azev, Y. A., Koptyaeva, O. S., Pospelova, T. A. & Bakulev, V. A., 4 Feb 2022, Actual Problems of Organic Chemistry and Biotechnology, OCBT 2020: Proceedings of the International Scientific Conference. Bakulev, V., Kovaleva, E., Glukhareva, T., Beryozkina, T., Schafran, Y., Lyubyakina, P. & Koptyaeva, O. (eds.). American Institute of Physics Inc., 020004. (AIP Conference Proceedings; vol. 2390).

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

  2. 8-Hydroxy-5-nitroquinoline as a C-nucleophilic reagent in the reaction of C, C-coupling with quinazoline

    Azev, Y. A., Koptyaeva, O. S., Eltsov, O. S., Tsmokalyuk, A. N. & Pospelova, T. A., 30 Dec 2020, In: Chimica Techno Acta. 7, 4, p. 237-241 5 p.

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

  3. A simple means of preparing quinoxaline derivatives: direct introduction of C-nucleophiles into the quinoxaline nucleus by substituting a hydrogen atom

    Azev, Y. A., Oparina, E. D., Golomolzin, B. V., Ermakova, O. S. & Bakulev, V. S., Jun 2013, In: Pharmaceutical Chemistry Journal. 47, 3, p. 172-175 4 p.

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

  4. Accuracy of the First Stage of Hepatotoxicity Testing with the Use of Drosophila melanogaster Test System

    Gorskaya, A. V., Antosyuk, O. N., Ermakova, O. S., Mukhametzyanova, A. S. H. & Kochkina, K. N., 1 Dec 2018, In: Bulletin of Experimental Biology and Medicine. 166, 2, p. 233-236 4 p.

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

  5. Benzaldehyde phenylhydrazones as c-nucleophiles for functionalization of quinoxaline-2-one. Unusual transformations of indole-3-carbaldehyde phenylhydrazones

    Azev, Y. A., Koptyaeva, O. S., Eltsov, O. S., Yakovleva, Y. A., Pospelova, T. A. & Bakulev, V. A., 2020, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2019: Proceedings of the III International Conference. Zyryanov, G. V., Santra, S. & Sadieva, L. K. (eds.). American Institute of Physics Inc., 4 p. 0018799. (AIP Conference Proceedings; vol. 2280).

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

  6. Features of -C-C- coupling of quinoxaline-2-one with ethyl acetoacetate under acid catalysis

    Azev, Y. A., Koptyaeva, O. S., Mkrtchyan, A. A. & Pospelova, T. A., 2022, In: Chimica Techno Acta. 9, 1, 20229103.

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

  7. Features of quinoxaline reactions with C-nucleophiles: Examples of dimerization of heterocycle in course of hydrogen substitution

    Azev, Y. A., Ermakova, O. S., Bakulev, V. A., Kovalev, I. S., Tsmokalyuk, A. N., Kozitsina, A. N., Pervova, M. G. & Filyakova, V. I., Jul 2015, In: Russian Journal of General Chemistry. 85, 7, p. 1635-1638 4 p.

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

  8. Indole-3-carbaldehydes Arylhydrazones as Multisite C-Nucleophiles in the Reactions with Quinazoline

    Azev, Y. A., Koptyaeva, O. S., Eltsov, O. S., Yakovleva, Y. A., Tsmokalyuk, A. N., Ivoilova, A. V., Seliverstova, E. A., Pospelova, T. A. & Bakulev, V. A., 1 Sept 2020, In: Russian Journal of General Chemistry. 90, 9, p. 1601-1610 10 p.

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

  9. New opportunities for the synthesis of quinoxaline derivatives

    Koptyaeva, O. S., Azev, Y. A., Shafran, Y. M., Pospelova, T. A. & Chupakhin, O. N., 29 Mar 2019, In: Chimica Techno Acta. 6, 1, p. 12-23 12 p.

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

  10. New Opportunities for the Synthesis of Quinoxaline-Substituted Heterocyclic and Aryl Moieties

    Azev, Y. A., Kodess, M. I., Ezhikova, M. A., Gibor, A. M., Baranov, V. I., Ermakova, O. S. & Bakulev, V. A., Dec 2013, In: Pharmaceutical Chemistry Journal. 47, 9, p. 498-502 5 p.

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

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