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  1. 2022

  2. Design, Synthesis, and Biological Evaluation of (+)-Camphor- and (−)-Fenchone-Based Derivatives as Potent Orthopoxvirus Inhibitors

    Sokolova, A. S., Kovaleva, K. S., Kuranov, S. O., Bormotov, N. I., Borisevich, S. S., Zhukovets, A. A., Yarovaya, O. I., Serova, O. A., Nawrozkij, M. B., Vernigora, A. A., Davidenko, A. V., Khamitov, E. M., Peshkov, R. Y., Shishkina, L. N., Maksuytov, R. A. & Salakhutdinov, N. F., 20 Jun 2022, In: ChemMedChem. 17, 12, p. e202100771 26 p., e202100771.

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

  3. Symmetric Spirenes: Promising Building Blocks for New Generation Opto-Electronic Materials

    Шеповалов, К. М., Пешков, Р. Ю., Бенасси, Э. & Мостович, Е. А., 20 Jun 2022, In: Physical Chemistry Chemical Physics. 24, 27, p. 16836-16851 16 p.

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

  4. P2O5-Promoted Cyclization of Di[aryl(hetaryl)methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]nonane-1,6-Diones

    Ivanov, K. S., Riesebeck, T., Skolyapova, A., Liakisheva, I., Kazantsev, M. S., Sonina, A. A., Peshkov, R. Y. & Mostovich, E. A., 4 Mar 2022, In: Journal of Organic Chemistry. 87, 5, p. 2456-2469 14 p.

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

  5. Aryldifluoroboranes: Lewis acidity and catalytic activity in the alkylation of phenols

    Shmakov, M. M., Prikhod'ko, S. A., Peshkov, R. Y., Bardin, V. V. & Adonin, N. Y., Mar 2022, In: Molecular Catalysis. 521, 112202.

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

  6. 2021

  7. New class of hantaan virus inhibitors based on conjugation of the isoindole fragment to (+)-camphor or (−)-fenchone hydrazonesv

    Yarovaya, O. I., Kovaleva, K. S., Zaykovskaya, A. A., Yashina, L. N., Scherbakova, N. S., Scherbakov, D. N., Borisevich, S. S., Zubkov, F. I., Antonova, A. S., Peshkov, R. Y., Eltsov, I. V., Pyankov, O. V., Maksyutov, R. A. & Salakhutdinov, N. F., 15 May 2021, In: Bioorganic and Medicinal Chemistry Letters. 40, 127926.

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

  8. Unexpected Ring Opening During the Imination of Camphor-Type Bicyclic Ketones

    Chernyshov, V. V., Yarovaya, O. I., Vatsadze, S. Z., Borisevich, S. S., Trukhan, S. N., Gatilov, Y. V., Peshkov, R. Y., Eltsov, I. V., Martyanov, O. N. & Salakhutdinov, N. F., 22 Jan 2021, In: European Journal of Organic Chemistry. 2021, 3, p. 452-463 12 p.

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

  9. 2020

  10. Synthesis of cyclic D-(+)-camphoric acid imides and study of their antiviral activity

    Chernyshov, V. V., Yarovaya, O. I., Peshkov, R. Y. & Salakhutdinov, N. F., 1 Jun 2020, In: Chemistry of Heterocyclic Compounds. 56, 6, p. 763-768 6 p.

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

  11. Design, Synthesis and Molecular Modeling Study of Conjugates of ADP and Morpholino Nucleosides as A Novel Class of Inhibitors of PARP-1, PARP-2 and PARP-3

    Sherstyuk, Y. V., Ivanisenko, N. V., Zakharenko, A. L., Sukhanova, M. V., Peshkov, R. Y., Eltsov, I. V., Kutuzov, M. M., Kurgina, T. A., Belousova, E. A., Ivanisenko, V. A., Lavrik, O. I., Silnikov, V. N. & Abramova, T. V., 1 Jan 2020, In: International Journal of Molecular Sciences. 21, 1, 25 p., 214.

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

  12. 2019

  13. Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles

    Peshkov, R. Y., Wang, C., Panteleeva, E. V., Rybalova, T. V. & Tretyakov, E. V., 18 Jan 2019, In: Journal of Organic Chemistry. 84, 2, p. 963-972 10 p.

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

  14. 2018

  15. Synthesis of 4'-alkyl-[1,1'-biphenyl]-2,3'-dicarbonitriles via dimerisation of phthalonitrile radical anion in liquid ammonia

    Peshkov, R. Y., Wang, C., Panteleeva, E. V. & Tretyakov, E. V., 25 Nov 2018, In: Arkivoc. 2018, 7, p. 349-356 8 p.

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

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