1. 2024
  2. Cyclocondensation of 2-(α-Diazoacyl)-2H-azirines with Amidines in Diazo Synthesis of Functionalized Naphtho[1,2-d]imidazoles

    Zanakhov, T. O., Galenko, E. E., Novikov, M. S. & Khlebnikov, A. F., 7 Jun 2024, (E-pub ahead of print) In: The Journal of organic chemistry.

    Research output: Contribution to journalArticlepeer-review

  3. 2023
  4. Divergent Diazo Approach toward Alkyl 5/4- Hydroxy‑3H‑benzo[e]indole-4/5-carboxylates.

    Занахов, Т. О., Галенко, Е. Е., Новиков, М. С. & Хлебников, А. Ф., 6 Sep 2023, In: Journal of Organic Chemistry. 88, 18, p. 13191–13204 14 p.

    Research output: Contribution to journalArticlepeer-review

  5. Metal carbonyl mediated rearrangement of 5-(2-oxoalkyl)-1,2,4-oxadiazoles: Synthesis of fully substituted pyrimidines.

    Galenko, E. E., Zanakhov, T. O., Novikov, M. S. & Khlebnikov, A. F., 2023, In: Organic & Biomolecular Chemistry. 21, 14, p. 2990-3001

    Research output: Contribution to journalArticlepeer-review

  6. Pd-Catalyzed Heteroannulation of Isoxazoles: Convergent Synthesis of Isoxazolo[5,4-c]quinolines

    Galenko, E. E., Zanakhov, T. O., Novikov, M. S. & Khlebnikov, A. F., 2023, In: Tetrahedron Letters. 114, 154270.

    Research output: Contribution to journalArticlepeer-review

  7. 2022
  8. An isoxazole strategy for the synthesis of 4-oxo-1,4-dihydropyridine-3-carboxylates

    Галенко, Е. Е., Хлебников, А. Ф., Новиков, М. С. & Занахов, Т. О., 23 Jun 2022, In: Beilstein Journal of Organic Chemistry. 18, p. 738-745 8 p.

    Research output: Contribution to journalArticlepeer-review

  9. 2021
  10. Isomerization of 5-(2H-azirin-2-yl)oxazoles: An atom-economic approach to 4H-pyrrolo[2,3-d]oxazoles

    Zanakhov, T. O., Galenko, E. E., Kryukova, M. A., Novikov, M. S. & Khlebnikov, A. A., 26 Mar 2021, In: Molecules. 26, 7, 15 p., 1881.

    Research output: Contribution to journalArticlepeer-review

  11. ATOM-ECONOMIC METHOD FOR THE SYNTHESIS OF PYRROLO[2,3-d]OXAZOLES

    Zanakhov, T. O., Galenko, E. E. & Khlebnikov, A. F., 2021, p. 685. 1 p.

    Research output: Contribution to conferencePaper

ID: 45562718