1. 2023
  2. Synthesis and Antibacterial Evaluation of Ciprofloxacin Congeners with Spirocyclic Amine Periphery

    Lukin, A., Komarova, K., Vinogradova, L., Rogacheva, E., Kraeva, L. & Krasavin, M., 4 Jan 2023, In: International Journal of Molecular Sciences. 24, 2, 954.

    Research output: Contribution to journalArticlepeer-review

  3. Second All-Russian School on Medicinal Chemistry for Young Scientists

    Bakulina, O. Y., Sapegin, A. V. & Yarovaya, O. I., 2023, In: Russ. J. Org. Chem.. 59, 12, p. 2038-2062 25 p.

    Research output: Contribution to journalArticlepeer-review

  4. 2022
  5. A novel bis-triazole scaffold accessed via two tandem [3 + 2] cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction

    Malkova, K., Bubyrev, A., Krivovicheva, V., Dar’in, D., Bunev, A. & Krasavin, M., Dec 2022, In: Beilstein Journal of Organic Chemistry. 18, p. 1636-1641

    Research output: Contribution to journalArticlepeer-review

  6. Metal-free synthetic approaches to 1,5-disubstituted 1,2,3-triazoles

    Malkova, K., Bubyrev, A., Balalaie, S., Dar'in, D. & Krasavin, M., Dec 2022, In: Tetrahedron Letters. 112, p. 154228

    Research output: Contribution to journalArticlepeer-review

  7. Synthetic Exploration of Novel Sulfamoyl Cyanide N-Oxides in Heterocycle Synthesis

    Krivovicheva, V., Bubyrev, A., Kalinin, S., Dar'in, D. & Krasavin, M., Dec 2022, In: European Journal of Organic Chemistry. 46, e202201162.

    Research output: Contribution to journalArticlepeer-review

  8. Application of a TEMPO-Polypyrrole Polymer for NOx-Mediated Oxygen Electroreduction

    Lukyanov, D. A., Kalnin, A. Y., Rubicheva, L. G., Potapenkov, V. V., Bakulina, O. Y. & Levin, O. V., 18 Nov 2022, In: Catalysts. 12, 11, p. 1466

    Research output: Contribution to journalArticlepeer-review

  9. New reagent space and new scope for the Castagnoli-Cushman reaction of oximes and 3-arylglutaconic anhydrides

    Банных, А. В., Левашова, Е. Ю., Бакулина, О. Ю. & Красавин, М. Ю., 16 Nov 2022, In: Organic and Biomolecular Chemistry. 86, 44, p. 8643-8648 6 p.

    Research output: Contribution to journalArticlepeer-review

ID: 95488030