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  1. Novel Copper(II) Complexes with BIAN Ligands: Synthesis, Structure and Catalytic Properties of the Oxidation of Isopropylbenzene

    Fomenko, I. S., Koshcheeva, O. S., Kuznetsova, N. I., Larina, T. V., Gongola, M. I., Afewerki, M., Abramov, P. A., Novikov, A. S. & Gushchin, A. L., May 2023, In: Catalysts. 13, 5, 849.

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

  2. Novel Copper(II) Complexes with Dipinodiazafluorene Ligands: Synthesis, Structure, Magnetic and Catalytic Properties

    Fomenko, I. S., Afewerki, M., Gongola, M. I., Vasilyev, E. S., Shul’pina, L. S., Ikonnikov, N. S., Shul’pin, G. B., Samsonenko, D. G., Yanshole, V. V., Nadolinny, V. A., Lavrov, A. N., Tkachev, A. V. & Gushchin, A. L., 1 Jul 2022, In: Molecules. 27, 13, 4072.

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

  3. Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: Synthesis and evaluation of anti-proliferative activity

    Popadyuk, I. I., Markov, A. V., Babich, V. O., Salomatina, O. V., Logashenko, E. B., Zenkova, M. A. & Salakhutdinov, N. F., 15 Aug 2017, In: Bioorganic and Medicinal Chemistry Letters. 27, 16, p. 3755-3759 5 p.

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

  4. Novel derivatives of deoxycholic acid bearing linear aliphatic diamine and aminoalcohol moieties and their cyclic analogs at the C3 position: Synthesis and evaluation of their in vitro antitumor potential

    Markov, A. V., Babich, V. O., Popadyuk, I. I., Salomatina, O. V., Logashenko, E. B., Salakhutdinov, N. F. & Zenkova, M. A., 21 Jul 2019, In: Molecules. 24, 14, 19 p., 2644;.

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

  5. Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo

    Salomatina, O. V., Sen’kova, A. V., Moralev, A. D., Savin, I. A., Komarova, N. I., Salakhutdinov, N. F., Zenkova, M. A. & Markov, A. V., 1 Jun 2022, In: International Journal of Molecular Sciences. 23, 11, 6214.

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

  6. Novel long-lived π-heterocyclic radical anion: A hybrid of 1,2,5-thiadiazo- and 1,2,3-dithiazolidyls

    Chulanova, E. A., Irtegova, I. G., Vasilieva, N. V., Bagryanskaya, I. Y., Gritsan, N. P. & Zibarev, A. V., 1 Sept 2015, In: Mendeleev Communications. 25, 5, p. 336-338 3 p.

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

  7. Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: Synthesis, complexation with Zn(II) and photophysical properties in comparison with related compounds

    Sukhikh, T. S., Bashirov, D. A., Ogienko, D. S., Kuratieva, N. V., Sherin, P. S., Rakhmanova, M. I., Chulanova, E. A., Gritsan, N. P., Konchenko, S. N. & Zibarev, A. V., 2016, In: RSC Advances. 6, 50, p. 43901-43910 10 p.

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

  8. Novel multitarget LAMP and PCR assays for the detection of Bordetella species

    Koryukov, M. A., Oscorbin, I. P., Gordukova, M. A., Turina, I. E., Aminova, A. I. & Filipenko, M. L., Aug 2025, In: Methods. 240, p. 63-72 10 p.

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

  9. Novel ni/ce(ti)zro2catalysts for methane dry reforming prepared in supercritical alcohol media

    Bespalko, Y., Smal, E., Simonov, M., Valeev, K., Fedorova, V., Krieger, T., Cherepanova, S., Ishchenko, A., Rogov, V. & Sadykov, V., 1 Jul 2020, In: Energies. 13, 13, 24 p., 3365.

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

  10. Novel peptide conjugates of modified oligonucleotides for inhibition of bacterial RNase P

    Novopashina, D., Vorobyeva, M., Nazarov, A., Davydova, A., Danilin, N., Koroleva, L., Matveev, A., Bardasheva, A., Tikunova, N., Kupryushkin, M., Pyshnyi, D., Altman, S. & Venyaminova, A., 19 Jul 2019, In: Frontiers in Pharmacology. 10, 8 p., 813.

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

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