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  1. 2015

  2. Pd-catalyzed amination of imidazolin-1-yl azines: toward a new kinase-inhibitory chemotype.

    Красавин, М. Ю., 2015, In: Tetrahedron Letters. 56, p. 2827-2831

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

  3. Phenoxymethyl 1,3-oxazoles and 1,2,4-oxadiazoles as potent and selective agonists of free fatty acid receptor 1 (GPR40)

    Zahanich, I., Kondratov, I., Naumchyk, V., Kheylik, Y., Platonov, M., Zozulya, S. & Krasavin, M., 2015, In: Bioorganic and Medicinal Chemistry Letters. p. 3105-3111

    Research output: Contribution to journal › Article

  4. Probing the ‘bipolar’ nature of the carbonic anhydrase active site: aromatic sulfonamides containing 1,3-oxazol-5-yl moiety as picomolar inhibitors of cytosolic CA I and CA II isoforms

    Krasavin, M., Korsakov, M., Dorogov, M., Tuccinardi, T., Dedeoglu, N. & Supuran, C. T., 2015, In: European Journal of Medicinal Chemistry. p. 334-347

    Research output: Contribution to journal › Article

  5. Reactions of CF3-enones with arenes under superelectrophilic activation: a pathway to trans-1,3-diaryl-1-CF3-indanes, new cannabinoid receptor ligands

    Iakovenko, R. O., Kazakova, A. N., Muzalevskiy, V. M., Ivanov, A. Y., Boyarskaya, I. A., Chicca, A., Petrucci, V., Gertsch, J., Krasavin, M., Starova, G. L., Zolotarev, A. A., Avdontceva, M. S., Nenajdenko, V. G. & Vasilyev, A. V., 2015, In: Organic and Biomolecular Chemistry. 13, 33, p. 8827-8842 16 p.

    Research output: Contribution to journal › Article

  6. Reactions of CF3-enones with arenes under super-lectrophilic activation: a pathway to trans-1,3-diaryl-1-CF3-indanes, new cannabinoid receptor ligands.

    Iakovenko, R. O., Kazakova, A. N., Muzalevskiy, V. M., Ivanov, A. Y., Boyarkaya, I. A., Chicca, A., Petrucci, V., Gertsch, J., Krasavin, M., Starova, G. L., Zolotarev, A. A., Avdontceva, M. S., Nenajdenko, V. G. & Vasilyev., A. V., 2015, In: Organic and Biomolecular Chemistry. 13, p. 8827-8842

    Research output: Contribution to journal › Article

  7. 2014

  8. Convenient access to novel functionalized pyrazino[1,2-b]isoquinolin-6-one and diazepino[1,2-b]isoquinolin-7-one scaffolds via the Cushman multicomponent reaction followed by post-condensation

    Sarnpitak, P. & Krasavin, M., 2 Apr 2014, In: Tetrahedron Letters. 55, 14, p. 2299-2303 5 p.

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

  9. An expeditious and atom-economic synthesis of lead-like, medicinally important 4,5-dihydropyrazolo[1,5-a]pyrazin-6-ones

    Mujumdar, P., Sapegin, A., Dorogov, M. & Krasavin, M., 2014, In: Tetrahedron Letters. 55, 42, 4 p.

    Research output: Contribution to journal › Article

  10. Antiproliferative 4-(1,2,4-oxadiazol-5-yl)piperidine-1-carboxamides, a new tubulin inhibitor chemotype.

    Krasavin, M., Sosnov, A. V., Karapetian, R., Konstantinov, I., Soldatkina, O., Godovykh, E., Zubkov, F., Bai, R., Hamel, E. & Gakh, A. A., 2014, In: Bioorganic and Medicinal Chemistry Letters. 24, 18, p. 4477-4481

    Research output: Contribution to journal › Article

  11. Atom-economical construction of a rare 6,7-dihydropyrido[3',2':4,5]imidazo[1,2-d][1,4]benzodiazepine scaffold.

    Mujumdar, P., Korsakov, M., Dorogov, M. & Krasavin, M., 2014, In: Synlett. 25, 16, p. 2323-2326

    Research output: Contribution to journal › Article

  12. Naturally occurring scaffolds for compound library design: convenient access to bis-aryl 1-azaadamantanes carrying a vicinal amino alcohol motif

    Taheri, A., Quinn, R. J. & Krasavin, M., 2014, In: Tetrahedron Letters. 55, 39, p. 5390-5393

    Research output: Contribution to journal › Article

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