Organic Chemistry Section - Research output

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Synthesis of unsaturated precursors for parahydrogen-induced polarization and molecular imaging of 1-¹³C-Acetates and 1-¹³C-pyruvates via side arm hydrogenation
Chukanov, N. V., Salnikov, O. G., Shchepin, R. V., Kovtunov, K. V., Koptyug, I. V. & Chekmenev, E. Y., 30 Jun 2018, In: ACS Omega. 3, 6, p. 6673-6682 10 p.
Research output: Contribution to journal › Article › peer-review
Synthesis, structure and biological properties of the zinc(II) complexes with 5-(4-chlorophenyl)-1H-tetrazole and oligopyridine derivatives
Ermakova, E. A., Golubeva, Y. A., Smirnova, K. S., Klyushova, L. S., Eltsov, I. V., Sheven’, D. G., Fetisov, L. N., Svyatogorova, A. E., Zubenko, A. A. & Lider, E. V., 1 Oct 2024, In: Inorganica Chimica Acta. 571, 122217.
Research output: Contribution to journal › Article › peer-review
Synthesis, structure, and cytotoxicity of complexes of zinc(II), palladium(II), and copper(I) chlorides with (−)-camphor thiosemicarbazone
Kokina, T. E., Glinskaya, L. A., Sheludyakova, L. A., Eremina, Y. A., Klyushova, L. S., Komarov, V. Y., Piryazev, D. A., Tkachev, A. V. & Larionov, S. V., 1 May 2019, In: Polyhedron. 163, p. 121-130 10 p.
Research output: Contribution to journal › Article › peer-review
Synthesis, Structure, and Cytotoxicity of Pd(II) and Cu(II) Complexes with 1-Terpenyl-3-Thiosemicarbazides of Pinane and para-Menthane Series
Kokina, T. E., Komarov, V. Y., Glinskaya, L. A., Bizyaev, S. N., Sheludyakova, L. A., Eremina, Y. A., Klyushova, L. S. & Tkachev, A. V., 1 Jan 2020, In: Journal of Structural Chemistry. 61, 1, p. 44-56 13 p.
Research output: Contribution to journal › Article › peer-review
Synthesis, structure and study of the biological activity of Co(II), Ni(II), and Cu(II) complexes with an enaminedione derivative
Eremina, Y. A., Ermakova, E. A., Sukhikh, T. S., Klyushova, L. S., El’tsov, I. V., Samsonenko, D. G., Dotsenko, V. V., Zubenko, A. A., Fetisov, L. N., Kononenko, K. N. & Lider, E. V., Feb 2021, In: Journal of Structural Chemistry. 62, 2, p. 309-320 12 p.
Research output: Contribution to journal › Article › peer-review
Synthesis, Structure, and Study of the Cytotoxic Activity of Zinc(II) Complex with 5-Benzyltetrazole and 1,10-Phenanthroline
Ermakova, E. A., Golubeva, Y. A., Smirnova, K. S., Klyushova, L. S., El’tsov, I. V. & Lider, E. V., Sept 2023, In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 49, 9, p. 593-600 8 p.
Research output: Contribution to journal › Article › peer-review
Synthesis, Structure, Magnetic and Photoluminescent Properties of Lanthanide(III) Complexes with a Ligand Based on 1,10-Phenanthroline and (+)−3-Carene
Bryleva, Y. A., Glinskaya, L. A., Agafontsev, A. M., Rakhmanova, M. I., Bogomyakov, A. S., Sukhikh, T. S., Gorbunova, E. A., Tkachev, A. V. & Larionov, S. V., 1 Aug 2019, In: Journal of Structural Chemistry. 60, 8, p. 1314-1326 13 p.
Research output: Contribution to journal › Article › peer-review
Synthetic Approaches for ¹⁵N-Labeled Hyperpolarized Heterocyclic Molecular Imaging Agents for ¹⁵N NMR Signal Amplification by Reversible Exchange in Microtesla Magnetic Fields
Chukanov, N. V., Shchepin, R. V., Joshi, S. M., Kabir, M. S. H., Salnikov, O. G., Svyatova, A., Koptyug, I. V., Gelovani, J. G. & Chekmenev, E. Y., 7 Jul 2021, In: Chemistry - A European Journal. 27, 38, p. 9727-9736 10 p.
Research output: Contribution to journal › Review article › peer-review
Synthetic Transformations of Sesquiterpene Lactones. 11.* Conjugates Based on Caffeine and Eudesmanolides with N-Containing Linkers
Reshetnikov, D. V., Patrushev, S. S. & Shults, E. E., 1 Sept 2020, In: Chemistry of Natural Compounds. 56, 5, p. 855-860 6 p.
Research output: Contribution to journal › Article › peer-review
Synthetic transformations of sesquiterpene lactones. Controllable synthesis of 11,13-dihydroisoalantolactone azides and 13-(1,2,3-triazolyl)eudesmanolides based on sesquiterpene lactones
Patrushev, S. S., Rybalova, T. V. & Shults, E. E., Nov 2021, In: Chemistry of Heterocyclic Compounds. 57, 11, p. 1116-1129 14 p.
Research output: Contribution to journal › Article › peer-review

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