1. 2023
  2. First Examples of Phosphoric Anhydride-Promoted O- and N-Acylation

    Shafran, Y. & Pospelova, T., 2023, In: Russian Journal of General Chemistry. 93, 12, p. 3021-3033 13 p.

    Research output: Contribution to journalArticlepeer-review

  3. O- И N-АЦИЛИРОВАНИЕ ПРИ СОДЕЙСТВИИ ФОСФОРНОГО АНГИДРИДА. ПЕРВЫЕ ПРИМЕРЫ

    Шафран, Ю. М. & Поспелова, Т. А., 2023, In: Журнал общей химии. 93, 12, p. 1807-1821 5 p.

    Research output: Contribution to journalArticlepeer-review

  4. Solvent-Free Reaction of 3,6-Diaryl-1,2,4-triazine-5-carbonitriles with 2-Amino-4-aryloxazoles

    Rammohan, A., Shtaitz, Y. K., Ladin, E. D., Krinochkin, A. P., Slepukhin, P. A., Sharutin, V. V., Sharafieva, E. R., Pospelova, T. A., Kopchuk, D. S. & Zyryanov, G. V., 2023, In: Russian Journal of General Chemistry. 93, 2, p. 263-267 5 p.

    Research output: Contribution to journalArticlepeer-review

  5. СИНТЕЗ ПРОИЗВОДНЫХ N-(5-(МЕТИЛСУЛЬФАНИЛ)- 4H-1,2,4-ТРИАЗОЛ-3-ИЛ)ПИРИДИН-2-АМИНА И ИХ 1,2,4-ТРИАЗИНОВЫХ ПРЕДШЕСТВЕННИКОВ

    Штайц, Я. К., Ладин, Е. Д., Шарутин, В. В., Копчук, Д. С., Рыбакова, А. В., Шарафиева, Э. Р., Криночкин, А. П., Зырянов, Г. В., Поспелова, Т. А. & Матерн, А. И., 2023, In: Вестник Южно-Уральского государственного университета. Серия: Химия. 15, 2, p. 82-89 8 p.

    Research output: Contribution to journalArticlepeer-review

  6. 2022
  7. 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 proceedingConference contributionpeer-review

  8. 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 journalArticlepeer-review

  9. 2021
  10. 2020
  11. 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 journalArticlepeer-review

  12. 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 journalArticlepeer-review

  13. 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 proceedingConference contributionpeer-review

  14. New pathways for the synthesis of indolyl-containing quinazoline trifluoroacetohydrazides

    Azev, Y. A., Koptyaeva, O. S., Eltsov, O. S., Yakovleva, Y. A. & Pospelova, T. A., 2020, In: Chimica Techno Acta. 7, 3, p. 109-115 7 p.

    Research output: Contribution to journalArticlepeer-review

  15. 2019
  16. Synthesis of Stable σ-Adducts by Arylation of Quinazoline

    Azev, Y. A., Koptyaeva, O. S., Seliverstova, E. A., Ivoilova, A. V. & Pospelova, T. A., 1 Dec 2019, In: Russian Journal of General Chemistry. 89, 12, p. 2374-2377 4 p.

    Research output: Contribution to journalArticlepeer-review

  17. Efficient one-step synthesis of 3-aryl-2-pyridones from 6-aryl-1,2,4-triazin-5-ones

    Savchuk, M. I., Shtaitz, Y. K., Kopchuk, D. S., Zyryanov, G. V., Eltsov, O. S., Pospelova, T., Rusinov, V. L. & Chupakhin, O. N., 1 Oct 2019, In: Chemistry of Heterocyclic Compounds. 55, 10, p. 985-988 4 p.

    Research output: Contribution to journalArticlepeer-review

  18. Design and synthesis of disubstituted and trisubstituted thiazoles as multifunctional fluorophores with large Stokes shifts

    Suntsova, P. O., Eltyshev, A. K., Pospelova, T. A., Slepukhin, P. A., Benassi, E. & Belskaya, N. P., 1 Jul 2019, In: Dyes and Pigments. 166, p. 60-71 12 p.

    Research output: Contribution to journalArticlepeer-review

  19. Reactions of N-sulfonyl-1,2,3-thiadiazole-4-carbimidamides with sulfonyl: regiospecific synthesis and structure of 2-sulfonyl-1,2,3-triazoleschlorides

    Beryozkina, T. V., Filimonov, V. O., Dianova, L. N., Slepukhin, P., Mazur, D. M., Pospelova, T. & Bakulev, V., 15 Jun 2019, In: Chemistry of Heterocyclic Compounds. 55, 6, p. 547-553 7 p.

    Research output: Contribution to journalArticlepeer-review

  20. СН functionalization of (hetero)arenes with ethyne and ethene moieties

    Kopchuk, D. S., Taniya, O. S., Khasanov, A. F., Krinochkin, A. P., Kovalev, I. S., Pospelova, T. A., Zyryanov, G. V., Rusinov, V. L. & Chupakhin, O. N., 15 Jun 2019, In: Chemistry of Heterocyclic Compounds. 55, 6, p. 490-504 15 p.

    Research output: Contribution to journalArticlepeer-review

  21. A Convenient Synthetic Approach to Phenazone Derivatives Containing a 1,2,4-Triazine or Pyridine Fragment

    Kovalev, I. S., Savchuk, M. I., Kopchuk, D. S., Zyryanov, G. V., Pospelova, T. A., Rusinov, V. L. & Chupakhin, O. N., 1 Jun 2019, In: Russian Journal of Organic Chemistry. 55, 6, p. 886-889 4 p.

    Research output: Contribution to journalArticlepeer-review

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