1. 2019
  2. Continued exploration of 1,2,4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: Discovery of subnanomolar inhibitors of membrane-bound hCA IX isoform that selectively kill cancer cells in hypoxic environment

    Krasavin, M., Shetnev, A., Sharonova, T., Baykov, S., Kalinin, S., Nocentini, A., Sharoyko, V., Poli, G., Tuccinardi, T., Presnukhina, S., Tennikova, T. B. & Supuran, C. T., 15 Feb 2019, In: European Journal of Medicinal Chemistry. 164, p. 92-105

    Research output: Contribution to journalArticlepeer-review

  3. Novel monoamine oxidase inhibitors based on the privileged 2-imidazoline molecular framework

    Shetnev, A., Osipyan, A., Baykov, S., Sapegin, A., Chirkova, Z., Korsakov, M., Petzer, A., Engelbrecht, I. & Petzer, J. P., 1 Jan 2019, In: Bioorganic and Medicinal Chemistry Letters. 29, 1, p. 40-46 7 p.

    Research output: Contribution to journalArticlepeer-review

  4. 2018
  5. An efficient synthesis and antimicrobial evaluation of 5-alkenyl- and 5-styryl-1,2,4-oxadiazoles

    Tarasenko, M., Sidneva, V., Belova, A., Romanycheva, A., Шаронова, Т. В., Байков, С. В., Shetnev, A., Kofanov, E. & Кузнецов, М. А., Dec 2018, In: Arkivoc. 2018, 7, p. 458-470 13 p.

    Research output: Contribution to journalArticlepeer-review

  6. Pt/Pd and I/Br Isostructural Exchange Provides Formation of C-I···Pd, C-Br···Pt, and C-Br···Pd Metal-Involving Halogen Bonding

    Baykov, S. V., Dabranskaya, U., Ivanov, D. M., Novikov, A. S. & Boyarskiy, V. P., Oct 2018, In: Crystal Growth and Design. 18, 10, p. 5973-5980 8 p.

    Research output: Contribution to journalArticlepeer-review

  7. One-Pot Synthesis of 3,5-Disubstituted 1,2,4-Oxadiazoles Using Catalytic System NaOH‒DMSO

    Pankrat’eva, V. E., Sharonova, T. V., Tarasenko, M. V., Baikov, S. V. & Kofanov, E. R., 1 Aug 2018, In: Russian Journal of Organic Chemistry. 54, 8, p. 1250-1255 6 p.

    Research output: Contribution to journalArticlepeer-review

  8. Facile room-temperature assembly of the 1,2,4-oxadiazole core from readily available amidoximes and carboxylic acids

    Шаронова, Т., Панкратьева, В., Савко, П., Байков, С. В. & Шетнев, А., 18 Jul 2018, In: Tetrahedron Letters. 59, 29, p. 2824-2827 4 p.

    Research output: Contribution to journalArticlepeer-review

  9. Heterocyclic periphery in the design of carbonic anhydrase inhibitors: 1,2,4-Oxadiazol-5-yl benzenesulfonamides as potent and selective inhibitors of cytosolic hCA II and membrane-bound hCA IX isoforms

    Krasavin, M., Shetnev, A., Sharonova, T., Baykov, S., Tuccinardi, T., Kalinin, S., Angeli, A. & Supuran, C. T., 1 Feb 2018, In: Bioorganic Chemistry. 76, p. 88-97 10 p.

    Research output: Contribution to journalArticlepeer-review

  10. 2017
  11. Room-temperature synthesis of pharmaceutically important carboxylic acids bearing the 1,2,4-oxadiazole moiety

    Tarasenko, M., Duderin, N., Sharonova, T., Baykov, S., Shetnev, A. & Smirnov, A. V., 13 Sep 2017, In: Tetrahedron Letters. 58, 37, p. 3672-3677 6 p.

    Research output: Contribution to journalArticlepeer-review

  12. 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 journalArticlepeer-review

  13. 2016
  14. A convenient and mild method for 1,2,4-oxadiazole preparation: Cyclodehydration of O-acylamidoximes in the superbase system MOH/DMSO

    Baykov, S., Sharonova, T., Osipyan, A., Rozhkov, S., Shetnev, A. & Smirnov, A. V., 29 Jun 2016, In: Tetrahedron Letters. 57, 26, p. 2898-2900 3 p.

    Research output: Contribution to journalArticlepeer-review

Previous 1...7 8 9 10 11 Next

ID: 7797029