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  1. 2019

  2. Synthesis of novel racemic 3,4-dihydroferroceno[c]pyridines via the Ritter reaction

    Rozhkova, Y. S., Plekhanova, I. V., Gorbunov, A. A., Stryapunina, O. G., Chulakov, E. N., Krasnov, V. P., Ezhikova, M. A., Kodess, M. I., Slepukhin, P. A. & Shklyaev, Y. V., 14 Mar 2019, In: Tetrahedron Letters. 60, 11, p. 768-772 5 p.

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

  3. Lithium benzenechromiumtricarbonyl as C-nucleophile in the cross-dehydrogenative coupling reactions of azaaromatics

    Nemytov, A. I., Utepova, I. A., Chupakhin, O. N., Slepukhin, P. A. & Charushin, V. N., 1 Mar 2019, In: Inorganica Chimica Acta. 487, p. 339-344 6 p.

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

  4. Synthesis of Fluorine-Containing 2-Pyrrolyl- and 2-Indolyl-Substituted 1,3-Benzothiazin-4-ones

    Nosova, E. V., Poteeva, A. D., Lipunova, G. N., Slepukhin, P. A. & Charushin, V. N., 1 Mar 2019, In: Russian Journal of Organic Chemistry. 55, 3, p. 384-387 4 p.

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

  5. Complex of Cadmium(II) Iodide with 3,4-Diphenyl-1-(Pyridin-2-yl)-6,7-Dihydro-5H-Cyclopenta[c]pyridine: Synthesis and X-ray Diffraction Study

    Khasanov, A. F., Slepukhin, P. A., Kopchuk, D. S., Krinochkin, A. P., Kovalev, I. S., Zyryanov, G. V., Kim, G. A., Rusinov, V. L. & Chupakhin, O. N., 1 Feb 2019, In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 45, 2, p. 92-96 5 p.

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

  6. Synthesis, characterization, DFT calculations, and biological activity of copper(II) complexes with 1,1,1-trifluoro-4-(2-methoxyphenyl)butan-2,4-dione

    Khamidullina, L. A., Puzyrev, I. S., Glukhareva, T. V., Shatunova, S. A., Slepukhin, P. A., Dorovatovskii, P. V., Zubavichus, Y., Khrustalev, V. N., Fan, Z., Kalinina, T. A. & Pestov, A. V., 15 Jan 2019, In: Journal of Molecular Structure. 1176, p. 515-528 14 p.

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

  7. Reaction of sodium 4-acetyl-1-phenyl-1 H -1,2,3-triazol-5-olate with 1,2,3-thiadiazole-4-carboxylic acid hydrazide

    Tokareva, M. A., Obydennov, K. L., Slepukhin, P. A., Vysokova, O. A. & Glukhareva, T. V., 11 Jan 2019, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2018: Proceedings of the II International. Santra, S., Zyryanov, G. V. & Sadieva, L. K. (eds.). American Institute of Physics Inc., Vol. 2063. 5 p. 040060. (AIP Conference Proceedings; vol. 2063).

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

  8. 1-Nicotinoylbenzotriazole: A Convenient Tool for Site-Selective Protection of 5,7-Dihydroxycoumarins

    Fatykhov, R. F., Khalymbadzha, I. A., Chupakhin, O. N., Charushin, V. N., Inyutina, A. K., Slepukhin, P. A. & Kartsev, V. G., 1 Jan 2019, In: Synthesis (Germany). 51, 19, p. 3617-3624 8 p.

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

  9. Cationic—Anionic Pd(II) Complexes with Adamantylimidazolium Cation: Synthesis, Structural Study, and MAO-Inhibiting Activity

    Dmitriev, M. V., Slepukhin, P. A., Glushkov, V. A., Eroshenko, D. V., Shavkunov, S. P. & Denisov, M. S., 1 Jan 2019, In: Russian Journal of Inorganic Chemistry. 64, 1, p. 56-67 12 p.

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

  10. Convenient Synthesis of Fluorine-Containing 2-Aryl-5H-[1,3,4]thiadiazolo[3,2-a]quinazolin-5-ones

    Nosova, E. V., Poteeva, A. D. & Slepukhin, P. A., 1 Jan 2019, In: Russian Journal of Organic Chemistry. 55, 1, p. 83-86 4 p.

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

  11. Dinuclear lanthanide-lithium complexes based on fluorinated β-diketonate with acetal group: Magnetism and effect of crystal packing on mechanoluminescence

    Bazhin, D. N., Kudyakova, Y. S., Bogomyakov, A. S., Slepukhin, P. A., Kim, G. A., Burgart, Y. V. & Saloutin, V. I., 1 Jan 2019, In: Inorganic Chemistry Frontiers. 6, 1, p. 40-49 10 p.

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

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