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  1. 2017

  2. Lucky Switcheroo: Dramatic Potency and Selectivity Improvement of Imidazoline Inhibitors of Human Carbonic Anhydrase VII

    Kalinin, S., Kopylov, S., Tuccinardi, T., Sapegin, A., Dar'In, D., Angeli, A., Supuran, C. T. & Krasavin, M., 12 Oct 2017, In: ACS Medicinal Chemistry Letters. 8, 10, p. 1105-1109 5 p.

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

  3. Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3- and 4-(hetero)arylisoxazol-5-amine scaffolds

    Krasavin, M., Korsakov, M., Zvonaryova, Z., Semyonychev, E., Tuccinardi, T., Kalinin, S., Tanç, M. & Supuran, C. T., 1 Jan 2017, In: Bioorganic and Medicinal Chemistry. 25, 6, p. 1914-1925 12 p.

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

  4. 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 journal › Article › peer-review

  5. The first one-pot ambient-temperature synthesis of 1,2,4-oxadiazoles from amidoximes and carboxylic acid esters

    Baykov, S., Sharonova, T., Shetnev, A., Rozhkov, S., Kalinin, S. & Smirnov, A. V., 1 Jan 2017, In: Tetrahedron. 73, 7, p. 945-951 7 p.

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

  6. 2016

  7. Isoform-selective inhibitory profile of 2-imidazoline-substituted benzenesulfonamides against a panel of human carbonic anhydrases.

    Supuran, C. T., Kalinin, S., Tanç, M., Sarnpitak, P., Mujumdar, P., Poulsen, SA. & Krasavin, M., 2016, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 31 (Suppl. 1), p. 197-202

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

  8. Multicomponent chemistry in the synthesis of carbonic anhydrase inhibitors

    Kalinin, S., Supuran, C. T. & Krasavin, M., 2016, In: Journal of Enzyme Inhibition and Medicinal Chemistry. 31 , Sup4, p. 185-199

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

  9. 2015

  10. Efficient Use of 1,2-Dihaloazine Synthons in Transition-Metal-Free Preparation of Doverse Heterocycle-Fused 1,4-Oxazepines

    Sapegin, A. V., Kalinin, S. A., Smirnov, A. V., Dorogov, M. V. & Krasavin, M., 2015, In: European Journal of Organic Chemistry. 2015, 6, p. 1333-1340

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

  11. 2014

  12. New tetracyclic 1,4-oxazepines constructed via practically simple tandem condensation strategy from readily available synthons

    Sapegin, A. V., Kalinin, S. A., Smirnov, A. V., Dorogov, M. V. & Krasavin, M., 2014, In: Tetrahedron. 70, 5, p. 1077-1083 7 p.

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

  13. 2012

  14. Dibenzo[b,f]pyrazolo[1,5-d][1,4]oxazepines: Facile Construction of a Rare Heterocyclic System via Tandem Aromatic Nucleophilic Substitution–Smiles Rearrangement–Denitrocyclization

    Sapegin, A. V., Kalinin, S. A., Smirnov, A. V., Dorogov, M. V. & Krasavin, M., 2012, In: Synthesis. 44, p. 2401-2407

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

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