1. 2026
  2. 2-Azadiene-Derived 2-Amino-2H-1,4-oxazines as Intermediates on the Way to 2,3-Fused Pyrrolo[3,4-d]oxazoles

    Агафонова, А. В., Куляев, П. О., Сметанин, А. В., Хлебников, А. Ф. & Новиков, М. С., 25 Jul 2026, In: Organic Letters. 28, 31, p. 9985-9990

    Research output: Contribution to journalArticlepeer-review

  3. Azirine-2-carbonyl Azides as C3-Synthons in the Reaction with Amidines toward 5‑Aminopyrimidin-4(3H)‑ones

    Ляхов, Д. Д., Занахов, Т. О., Галенко, Е. Е., Новиков, М. С. & Хлебников, А. Ф., 29 Jun 2026, In: Organic Letters. 28, p. 8730−8735 6 p.

    Research output: Contribution to journalArticlepeer-review

  4. Cascade transformation of 2-(diazoacetyl)-2H-azirines to 2-aroyl-3-hydroxy-1H-pyrroles via condensation with aromatic aldehydes

    Занахов, Т. О., Галенко, Е. Е., Новиков, М. С. & Хлебников, А. Ф., 9 Jun 2026, In: Beilstein Journal of Organic Chemistry. 22, p. 897–904 8 p.

    Research output: Contribution to journalArticlepeer-review

  5. Synthesis of 2-Aminonicotinonitriles via Photodecarboxylation of Azirine-2-Carboxylic Acids

    Павленко, Ю. И., Новиков, М. С. & Агафонова, А. В., 14 Apr 2026, In: MolBank. 2026, 2, 6 p., M2165 .

    Research output: Contribution to journalArticlepeer-review

  6. Azirine-Based Synthesis of Fully Substituted 5-Alkynyloxazoles

    Таишев, А. Э., Галенко, Е. Е., Новиков, М. С. & Хлебников, А. Ф., 1 Feb 2026, In: Russian Journal of General Chemistry. 96, 2, 3.

    Research output: Contribution to journalArticlepeer-review

  7. Azirine-Based Synthesis of Alkynylpyrroles

    Таишев, А. Э., Галенко, Е. Е., Новиков, М. С. & Хлебников, А. Ф., 9 Jan 2026, In: Journal of Organic Chemistry. 91, 1, p. 767-779 13 p.

    Research output: Contribution to journalArticlepeer-review

  8. 2025
  9. Substituent-dependent synthesis of isomeric imidazoles from azirines and amidines

    Галенко, Е. Е., Прокопьева, И. Н., Иванов, А. Ю., Занахов, Т. О., Новиков, М. С. & Хлебников, А. Ф., 1 Dec 2025, In: Tetrahedron. 188, 8 p., 134950.

    Research output: Contribution to journalArticlepeer-review

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