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  1. 2022

  2. Significant Broadening of the Substrate Scope for the Hydrated Imidazoline Ring Expansion (HIRE) via the Use of Lithium Hexamethyldisilazide

    Grintsevich, S., Sapegin, A. & Krasavin, M., 1 May 2022, In: Synthesis (Germany). 54, 10, p. 2494-2510 17 p., ss-2021-t0715-op.

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

  3. 2,3-Dihydro-benzo[f][1,4]oxazepines as a novel substrates for Castagnoli-Cushman reaction

    Lebedev, R. E., Bakulina, O. Y., Dar’in, D. V. & Krasavin, M., 22 Apr 2022, Материалы Международного молодежного научного форума «ЛОМОНОСОВ-2022». М: МАКС Пресс

    Research output: Chapter in Book/Report/Conference proceeding › Conference abstracts › Research

  4. Dicarboxylic Acid Monoesters in β-and δ-Lactam Synthesis

    Ananeva, A., Bakulina, O., Dar’in, D., Kantin, G. & Krasavin, M., 11 Apr 2022, In: Molecules. 27, 8, 2469.

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

  5. Heteroatom is not needed: Access to dibenzo[e,h][1,4]diazecin-9-ones from dibenzo[b,e]azepin-6-one via the hydrated imidazoline ring expansion (HIRE) approach

    Gritsevich, S., Sapegin, A. & Krasavin, M., 30 Mar 2022, In: Tetrahedron Letters. 94, 153718.

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

  6. Preparation and Synthetic Applications of Five-to-Seven-Membered Cyclic α-Diazo Monocarbonyl Compounds

    Zhukovsky, D., Dar’in, D., Bakulina, O. & Krasavin, M., 21 Mar 2022, In: Molecules. 27, 6, 47 p., 2030.

    Research output: Contribution to journal › Review article › peer-review

  7. Diversely substituted sulfamides for fragment-based drug discovery of carbonic anhydrase inhibitors: synthesis and inhibitory profile

    Sharonova, T., Zhmurov, P., Kalinin, S., Nocentini, A., Angeli, A., Ferraroni, M., Korsakov, M., Supuran, C. T. & Krasavin, M., 16 Mar 2022, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 37, 1, p. 857-865 9 p.

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

  8. Homophthalic Monoesters: A New Type of Reagents for the Castagnoli‐Cushman Reaction: A New Type of Reagents for the Castagnoli-Cushman Reaction

    Guranova, N., Bakulina, O., Dar'in, D., Kantin, G. & Krasavin, M., 7 Mar 2022, In: European Journal of Organic Chemistry. 2022, 9, e202101281.

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

  9. (E)-3-Arylidene-4-diazopyrrolidine-2,5-diones conveniently elaborated into cytotoxic compounds bearing primary sulfonamide and Michael acceptor moieties

    Paramonova, P., Sharonova, T., Kalinin, S., Chupakhin, E., Bunev, A. & Krasavin, M., 1 Mar 2022, In: Mendeleev Communications . 32, 2, p. 176-177 2 p.

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

  10. Natural compounds as inhibitors of thioredoxin reductase (TrxR1)

    Chupakhin, E. G. & Krasavin, M. Y., 1 Mar 2022, In: Russian Chemical Bulletin. 71, 3, p. 443-448 6 p.

    Research output: Contribution to journal › Review article › peer-review

  11. Synthesis, Structure, and Antiproliferative Action of 2-Pyridyl Urea-Based Cu(II) Complexes

    Geyl, K. K., Baykov, S. V., Kalinin, S. A., Bunev, A. S., Troshina, M. A., Sharonova, T. V., Skripkin, M. Y., Kasatkina, S. O., Presnukhina, S. I., Shetnev, A. A., Krasavin, M. Y. & Boyarskiy, V. P., 16 Feb 2022, In: Biomedicines. 10, 2, 18 p., 461.

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

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