1. 2017
  2. Primary mono- and bis-sulfonamides obtained via regiospecific sulfochlorination of N-arylpyrazoles: inhibition profile against a panel of human carbonic anhydrases

    Krasavin, M., Korsakov, M., Ronzhina, O., Tuccinardi, T., Kalinin, S., Tanç, M. & Supuran, C. T., 1 Jan 2017, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 32, 1, p. 920-934 15 p.

    Research output: Contribution to journalArticlepeer-review

  3. o-Phenylenediacetic Acid Anhydride in the Castagnoli–Cushman Reaction: Extending the Product Space to ε-Lactams

    Bakulina, O., Dar’in, D. & Krasavin, M., 2017, In: Synlett. 28, 10, p. 1165-1169

    Research output: Contribution to journalArticlepeer-review

  4. Short Approach to Pyrrolopyrazino-, Pyrrolodiazepino-Isoindoles and their Benzo Analogues via the IMDAF Reaction

    Zubkov, F. I., Orlova, D. N., Zaytsev, V. P., Voronov, A. A., Nikitina, E. V., Khrustalev, V. N., Novikov, R. A., Krasavin, M. & Varlamov, A. V., 2017, In: Current Organic Synthesis. 14, 5, p. 733-746 14 p.

    Research output: Contribution to journalArticlepeer-review

  5. Structurally Diverse Arene-Fused Ten-Membered Lactams Accessed via Hydrolytic Imidazoline Ring Expansion

    Сапегин, А. В., Осипян, А. Т. & Красавин, М. Ю., 2017, In: Organic and Biomolecular Chemistry. 15, p. 2906-2909 4 p.

    Research output: Contribution to journalArticlepeer-review

  6. Synthesis, structure and properties of N-aminosaccharin – A selective inhibitor of human carbonic anhydrase I

    Kuznetsov, M. A., Shestakov, A. N., Zibinsky, M., Krasavin, M., Supuran, C. T., Kalinin, S. & Tanç, M., 2017, In: Tetrahedron Letters. 58, 2, p. 172-174 3 p.

    Research output: Contribution to journalArticlepeer-review

  7. 2016
  8. Facile entry into structurally diverse, privileged, (hetero)arene-fused N-alkoxy 3,4-dihydrobenzo[f][1,4]oxazepin-5(2H)-ones

    Sapegin, A., Reutskaya, E., Smirnov, A., Korsakov, M. & Krasavin, M., 28 Dec 2016, In: Tetrahedron Letters. 57, 52, p. 5877-5880 4 p.

    Research output: Contribution to journalArticlepeer-review

  9. A novel, flexible strategy to construct privileged dibenzo[b,f][1,4,5] oxathiazepine 5,5-dioxides and their heterocyclic isosteres

    Sapegin, A., Panova, V., Reutskaya, E., Smirnov, A. V. & Krasavin, M., 24 Nov 2016, In: Tetrahedron. 72, 47, p. 7570-7578 9 p.

    Research output: Contribution to journalArticlepeer-review

  10. Free fatty acid receptor 1 (GPR40) agonists containing spirocyclic periphery inspired by LY2881835

    Krasavin, M., Lukin, A., Bagnyukova, D., Zhurilo, N., Zahanich, I., Zozulya, S., Ihalainen, J., Forsberg, M. M., Lehtonen, M., Rautio, J., Moore, D. & Tikhonova, I. G., 1 Nov 2016, In: Bioorganic and Medicinal Chemistry. 24, 21, p. 5481-5494 14 p.

    Research output: Contribution to journalArticlepeer-review

  11. Library of diversely substituted 2-(quinolin-4-yl)imidazolines delivers novel non-cytotoxic antitubercular leads

    Krasavin, M., Mujumdar, P., Parchinsky, V., Vinogradova, T., Manicheva, O. & Dogonadze, M., 1 Nov 2016, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 31, 6, p. 1146-1155 10 p.

    Research output: Contribution to journalArticlepeer-review

  12. Novel agonists of free fatty acid receptor 1 (GPR40) based on 3-(1,3,4-thiadiazol-2-yl)propanoic acid scaffold

    Krasavin, M., Lukin, A., Zhurilo, N., Kovalenko, A., Zahanich, I. & Zozulya, S., 1 Nov 2016, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 31, 6, p. 1404-1410 7 p.

    Research output: Contribution to journalArticlepeer-review

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