Демидов Олег Петрович

1994 – 1999 гг. – обучение на специальности «Химия» в Ставропольском государственном университете, квалификацией «Учитель Химии по специальности «Химия».

1999 – 2002 гг. – обучение в аспирантуре Ставропольского государственного университета по специальности 02.00.03 «Органическая химия». В 2002 г. защитил диссертацию на соискание ученой степени кандидата химических наук на тему «1,3-Диазапирены: синтез и некоторые свойства».

В 2006 г. – присвоено звание доцента по кафедре химии гетероциклических соединений.

С 2014 года старший научный сотрудник кафедры химии. В настоящее время главный научный сотрудник.

В 2017 году защитил докторскую диссертацию – «Реакции 1,3,7-триазапирена и его производных с нуклеофильными реагентами и применение найденных методов на 3-нитропиридине и акридине» по специальности 02.00.03 «Органическая химия»

• Исполнитель в научных грантах при финансовой поддержке Минобрнауки РФ: проект № 4.141.2014/K и № 4.6306.2017/8.9). Руководитель проекта научных групп и отдельных ученых Северо-Кавказского федерального университета, №121110800217-0

• физические методы исследования
• планирование синтеза

• Химия гетероциклов.
• Реакционная способность.
• Физические методы исследования

1. Demidov O.P., Pobedinskaya D.Y., Avakyan E.K., Amangasieva G.A., Borovlev I.V. SNH Arylamination of Nitroquinolines: Access to Nitro and Nitroso Derivatives of Arylaminoquinolines // Chemistry of Heterocyclic Compounds. – 2018. - 54 (9). - P. 875- 886. https://doi.org/10.1007/s10593-018-2368-x

   2. Borovlev I.V., Demidov O.P., Amangasieva G.A., Avakyan E.K., Borovleva A.A., Pobedinskaya D.Y. SNH Arylamination of 3-Nitropyridine: A Competitive Formation of 2-Arylamino-5-nitropyridines and 2-Arylamino-5-nitrosopyridines // Synthesis (Germany). 2018. - 50 (17). - P. 3520-3530. DOI: 10.1055/s-0037-1610173

   3. Amangasieva G.A., Borovlev I.V., Demidov O.P., Avakyan E.K., Borovleva A.A. Synthesis of Amides by Nucleophilic Substitution of Hydrogen in 3-Nitropyridine // Russian Journal of Organic Chemistry. – 2018. - 54 (6). - P. 867-872. https://doi.org/10.1134/S1070428018060076

   4. Avakyan E.K., Amangasieva G.А., Demidov O.P., Borovleva A.A., Beketova E.S. Nechaeva O.А., Borovlev I.V. Nucleophilic addition of amide anions to 1-methyl- 5(6,7,8)-nitroquinolinium salts // Chemistry of Heterocyclic Compounds – 2019. – Т. 55. – № 8. – P. 739-747. https://doi.org/10.1007/s10593-019-02529-y

   5. Pobedinskaya D.Y., Demidov O.P., Borovlev I.V., Avakyan E.K., Amangasieva G.А. Synthesis of pyrido[2,3-a]phenazines by intramolecular cyclization of 7-arylamino-8- nitrosoquinolines // Chemistry of Heterocyclic Compounds –2019. – Т. 55. – № 7. – P. 684-687. https://doi.org/10.1007/s10593-019-02518-1

   6. Amangasieva G.А., Avakyan E.K., Demidov O.P., Borovleva A.A., Pobedinskaya D.Y., Borovlev I.V. SNH Amidation of nitroquinolines: synthesis of amides on the basis of nitro- and nitrosoquinolines // Chemistry of Heterocyclic Compounds. – 2019. – Т. 55. – № 7. – P. 623-631 https://doi.org/10.1007/s10593-019-02508-3

   7. Gutnov A.V., Abaev V.T., Demidov O.P. Betti reaction of 2-naphthol, furfural, and acetamide: an unexpected case of secondary carbo-piancatelli rearrangement // Chemistry of Heterocyclic Compounds. - 2019. - Т. 55. № 3. - P. 280-282. 8. Pugachev A.D., Kozlenko A.S., Luk’yanova M.B., Luk’yanov B.S., Tkachev V.V., Shilov G.V., Demidov O.P., Minkin V.I., Aldoshin S.M. One-Pot Synthesis and Structure Study of a New Indoline Spiropyran with Cationic Substituent // Doklady Chemistry. – 2019. - 488(2). - P. 252-256. DOI 10.1134/S0012500819100021

   9. Vetrova E.V., Tupaeva I.O., Sayapin Y.A., Gusakov E.A., Nikolaevskii S.A., Demidov O.P., Minkin V.I., Metelitsa A.V. Chromogenic properties of 2-(2-carbomethoxy-3,4- dichloro-6-hydroxyphenyl)benzoxazole and its zn(II) and cd(II) complexes // Dyes. Pigm. – 2020. – 180. –P. 108417. https://doi.org/10.1016/j.dyepig.2020.108417 10. Plieva A.T., Chalikidi P.N., Gutnov A.V., Turiev A.M., Demidov O.P., Aksenov N.A., Magkoev T.T., Abaev V.T. Novel synthetic approach to pyrrolo[1,2-b]cinnolines // Chem. Heterocycl. Compd. – 2020. –56(8). –P.1030-1041. https://doi.org/10.1007/s10593-020-02770-w

   11. Gromachevskava E.V., Kaigorogova E.A., Bespalov A.V., Demidov O.P., Krapivin G.D. Investigation in the field of quinazolines. 8*. New reaction of N-alkylation of 4,4- diphenyl-3,4-dihydroquinazolines // Chemistry of Heterocyclic Compounds. – 2020. - 56(12). - P. 1548-1553. DOI 10.1007/s10593-020-02848-5

   12. Osyanin V.A., Osipov D.V., Semenova I.A., Korzhenko K.S., Lukashenko A.V., Demidov O.P., Klimochkin Y.N. Eco-friendly synthesis of fused pyrano[2,3- b]pyransviaammonium acetate-mediated formal oxa-[3 + 3]cycloaddition of 4H- chromene-3-carbaldehydes and cyclic 1,3-dicarbonyl compounds // RSC Advances. – 2020. - 10(57). - P. 34344-34354. DOI 10.1039/d0ra06450e

   13. Semenova I.A., Osipov D.V., Popova Y.V., Osyanin, V. A., Demidov O.P., Klimochkin Y.N. Formal [3+3] cycloaddition reaction of 4-hydroxythiocoumarin to 4Н- chromene-3-carbaldehydes: synthesis of thiochromeno[3',4':5,6]pyrano[2,3-b]chromen-6-ones // Chemistry of Heterocyclic Compounds. – 2020. - 56(9). - P.1218-1221. DOI 10.1007/s10593-020-02801-6

   14. Morkovnik A., Zubenko A., Divaeva L., Demidov O., Gribanova T., Sochnev V., Klimenko A., Dobaeva N., Borodkin G., Drobin Y., Fetisov L., Kononenko K. A general method for the synthesis of heterocyclic dithiocarboxylate betaines: Potential precursors of NHC based on a novel type of functionalization of the methyl group // Tetrahedron Letters. – 2020. - 61(35). - P. 152228. DOI 10.1016/j.tetlet.2020.152228

   15. Chernyshev A.V., Voloshin N.A., Rostovtseva I.A., Demidov O.P.,Shepelenko K E., Solovjeva E.V., Gaeva E.B., Metelitsa A.V. Benzothiazolyl substituted spiropyrans with ion-driven photochromic transformation // Dyes and Pigments. – 2020. – 178(108337). DOI 10.1016/j.dyepig.2020.108337

   16. Zhirov A.M., Kovalev D.A., Ulshina D.V., Pisarenko, S.V., Demidov O.P., Borovlev I.V.Diazapyrenes: interaction with nucleic acids and biological activity // Chemistry of Heterocyclic Compounds. – 2020. - 56(6). - P. 674-693. DOI 1007/s10593-020- 02717-1

   17. Kolodina A.A., Tsaturyan A.A., Galkina M.S., Borodkina I.G., Vetrova E.V., Demidov O.P., Berezhnaya A.G., Metelitsa A.V. 6,7-Dihydro-5H-1,2,4-triazolo[3,4- b][1,3,4]thiadiazine Ring Cleavage and Tautomerism of the Products: Experimental and Theoretical Study // ChemistrySelect. – 2020. - 5(12). - P. 3586-3592. DOI 10.1002/slct.202000732

   18. Zubenko A.A., Morkovnik A.S., Divaeva L.N., Demidov O.P., Sochnev V.S., Borodkina I.G., Drobin Y.D., Spasov A.A. New route to bioactive 2- (hetero)arylethylamines via nucleophilic ring opening in fused 7-acyl-2,3- dihydroazepines // Mendeleev Communications. – 2020. - 30(1). - P. 28-30. DOI 10.1016/j.mencom.2020.01.009

   19. Gusakov E.A., Topchu I.A., Mazitova A.M., Dorogan I.V., Bulatov E.R., Serebriiskii I.G., Abramova Z.I., Tupaeva I.O., Demidov O.P., Toan D.N., Lam T.D., Bang D.N., Boumber Y.A., Sayapin Y.A., Minkin V.I. Design, synthesis and biological evaluation of 2-quinolyl-1,3-tropolone derivatives as new anti-cancer agents // RSC Adv . – 2021. –11(8). – P. 4555. DOI: 10.1039/D0RA10610K

   20. Ivakhnenko E.P., Knyazev P.A., Vitkovskaya Y.G., Popov L.D., Lyssenko K.A., Demidov O.P., Starikov A.G., Borodkin G.S., Minkin V.I. Synthesis, staructure and redox properties of cu(II) chelate complexes on the basis of 2-(hydroxyphenyl)-1H- benzo[d]imidazol-1-yl phenol ligands // Eur. J. Inorg. Chem. – 2021. - 2021(21). - P. 2055-2062. https://doi.org/10.1002/ejic.202100184

   21. Demidov O.P., Pobedinskaya D.Y., Borovleva A.А., Avakyan E.K., Ermolenko A.P., Aksenov A.V., Borovlev I.V. SNH-arylamination of 1-methylquinolin-2(1H)-one nitro derivatives // Chem. Heterocycl. Compd. – 2021. – 57. - P. 166-174. https://doi.org/10.1007/s10593-021-02889-4

   22. Zubenko A.A., Morkovnik A.S., Divaeva L.N., Demidov O.P., Kartsev V.G., Sochnev V.S., Klimenko A.I., Dobaeva N.M., Borodkin G.S., Bodryakov A.N., Bodryakova M.A., Fetisov L.N. Thiourea assisted recyclization of 1- (chloromethyl)dihydroisoquinolines: A convenient route to β-(o- thiazolylaryl)ethylamines // Mendeleev. Commun. – 2021. –31(1) – P. 125. DOI: 10.1016/j.mencom.2021.01.040

   23. Osipov D.V., Korzhenko K.S., Rashchepkina D.A., Artemenko A.A., Demidov O.P., Shiryaev V.A., Osyanin V.A. Catalyst-free formal [3 + 2] cycloaddition of stabilized: N, N-cyclic azomethine imines to 3-nitrobenzofurans and 3-nitro-4 H-chromenes: Access to heteroannulated pyrazolo[1,2- A[ pyrazoles // Organic and Biomolecular Chemistry. – 2021. - 19(46). - P. 10156-10168. DOI 10.1039/d1ob01377g

   24. Gusakov E.A., Demidov O.P., Tupaeva I.O., Vetrova E.V., Soldatov M.A., Tereshchenko A.A., Dubonosov A.D., Sayapin Y.A., Metelitsa A.V., Minkin V.I. The first representative of a new class of charge transfer complexes in o-quinone series for organic semiconductors // Mater. Today. Chem. – 2021. – Т.20. DOI 10.1016/j.mtchem.2021.100462

   25. Chernyshev A.V., Soloveva E.V., Voloshin N.A., Demidov O.P., Gaeva E.B., Nepomnyashiy A.S., Metelitsa A.V. Biphotochromic and ionochromic benzoxazolyl- substituted spirobipyrans // J. Photochem. Photobiol. A Chem. – 2021. – Т. 413. DOI 10.1016/j.jphotochem.2021.113259

   26. Zubenko A.A., Morkovnik A.S., Divaeva L.N., Sochnev V.S., Demidov O.P., Bodryakov A.N., Fetisov L.N., Kononenko K.N., Bodryakova M.A., Klimenko A.I. New azepine-furan spirocyclic structures in the reaction of 4-aroyl-1,2- dihydrobenzo[d]azepines and 2-aroyl-4,5-dihydrophenanthreno[1,2-d]azepine with formaldehyde // Russ. J. Gen. Chem. – 2021. – 91(5). – P.792-798. DOI 10.1134/S1070363221050066

   27. Osyanin V.А., Osipov D.V., Korzhenko K.S., Demidov O.P., Klimochkin Y.N. 4H- chromenes as 1,3-bielectrophiles in the reaction with 2-aminobenzimidazole: Synthesis of pyrimido[1,2-a]benzimidazoles // Chem. Heterocycl. Compd . – 2021. – 57(5). – P.588-593. DOI 10.1007/s10593-021-02947-x

   28. Moseev T.D., Lavrinchenko I.A., Varaksin M.V., Pobedinskaya D.Y., Demidov O.P., Borovlev I.V., Charushin V.N., Chupakhin O.N. Meso-functionalization of calix[4]arene with 1,3,7-triazapyrene in the design of novel fluorophores with the dual target detection of Al3+and Fe3+cations // RSC Adv . – 2021. –11(11). – P. 6407-6414. DOI 10.1039/d0ra10605d

   29. Ivakhnenko E., Malay V., Romanenko G., Demidov O., Knyazev P., Starikov A., Minkin V. Michael addition of amines to sterically crowded ortho-benzoquinone completed with unprecedented 1,2-shift of a tert-butyl group // Tetrahedron. – 2021. – Т. 79. DOI 10.1016/j.tet.2020.131841

   30. Demidov O.P., Pobedinskaya D.Y., Borovleva A.А., Avakyan E.K., Ermolenko A.P., Aksenov A.V., Borovlev I.V. SNH-arylamination of 1-methylquinolin-2(1H)-one nitro derivatives // Chem. Heterocycl. Compd. – 2021. DOI 10.1007/s10593-021-02889-4

   31. Korchagin D.V., Ivakhnenko E.P., Demidov O.P Akimov A.V., Morgunov R.B., Starikov A.G., Palii A.V., Minkin V.I., Aldoshin S.M. Field supported slow magnetic relaxation in a quasi-one-dimensional copper(ii) complex with a pentaheterocyclic triphenodioxazine // New Journal of Chemistry. – 2021. - 45(46). - Р. 21912-21918. DOI 10.1039/d1nj03217h

   32. Osipov D.V., Rashchepkina D.А., Аrtemenko A.А., Demidov O.P., Osyanin V.А. Nucleophilic Dearomatization of 3-nitrobenzofurans by the Action of 2-(1- arylethylidene)Malononitriles // Chemistry of Heterocyclic Compounds. – 2021. - 57(10). - Р. 996-1001. DOI 10.1007/s10593-021-03013-2

   33. Smyshliaeva L.A., Varaksin M.V., Fomina E.I., Medvedeva Svalova T.S., Kozitsina A.N., Demidov O.P., Borovlev I.V., Mensch C., Mampuys P., Maes B. U. W., Charushin V.N., Chupakhin O.N. 1,3,7-Triazapyrene-Based ortho-Carborane Fluorophores: Convenient Synthesis, Theoretical Studies, and Aggregation-Induced Emission Properties // Organometallics. – 2021. - 40(16). - Р. 2792-2807. doi.org/10.1021/acs.organomet.1c00234

   34. Metelitsa A., Chernyshev A., Voloshin N., Demidov O., Solov’eva E., Rostovtseva I., Gaeva E. Photo-controlled bipolar absorption switches based on 5-dimethylamino substituted indoline spiropyrans with semipermanent merocyanines // New Journal of Chemistry. – 2021. - 45(30). - Р. 13529-13538. doi.org/10.1039/D1NJ02371C

   35. Zubenko, A.A., Sochnev, V.S., Kartsev, V.G., Divaeva L.N., Demidov O.P., Klimenko A.I., Bodryakov A.N., Bodryakova M.A., Borodkin G.S., Morkovnik A.S. Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion // Mendeleev Communications. – 2021. - 31(4). - Р. 545- 547. doi.org/10.1016/j.mencom.2021.07.036

   36. Chalikidi P.N., Magkoev T.T., Gutnov A.V., Demidov O.P., Uchuskin M.G., Trushkov I.V., Abaev V.T. One-Step Synthesis of Triphenylphosphonium Salts from (Het)arylmethyl Alcohols // Journal of Organic Chemistry. – 2021. - 86(14). - Р. 9838- 9846. doi.org/10.1021/acs.joc.1c00733

   37. Lavrinchenko I. A. Moseev, T. D., Varaksin, M. V., Zyryanov, G. V., Taniya, O. S., Tsmokalyuk, A. N., Demidov O.P., Borovlev I.V., Chupakhin, O. N. A BF 3-mediated C–H/C–Li coupling of 1, 3, 7-triazapyrene with 2-thienyllithium in the design of push–pull fluorophores and chemosensors for nitroaromatics //New Journal of Chemistry. – 2022. – Т. 46. – №. 11. – P. 5121-5128. DOI: 10.1039/d1nj05216k

   38. Ivakhnenko E., Malay V., Demidov O., Starikov A., Minkin V. An access to 1H- cyclopenta [b] pyridine-4, 5-diones via condensation of 6-nitro-1, 2-o-quinone with arylamines and acetone // Tetrahedron. – 2022. – Т. 103. – P. 132575. DOI: 10.1016/j.tet.2021.132575

   39. Ivakhnenko E. P., Knyazev P. A., Omelichkin N. I., Makarova N. I., Starikov A. G., Aleksandrov A. E., Ezhov A. V., Tameev A. R., Demidov O.P., Minkin V. I. 12Н- quinoxaline [2, 3-b] phenoxazines: Synthesis, optical, electrochemical properties and insight into photovoltaic application // Dyes and Pigments. – 2022. – Т. 197. – P. 109848. https://doi.org/10.1016/j.dyepig.2021.109848

   40. Zubenko, A.A., Morkovnik, A.S., Divaeva, L.N., ...Bodryakova, M.A., Borodkin, G.S. New type of recyclization in 3,4-dihydroisoquinolines in the synthesis of β-(o- indazolylaryl)ethylamines and their 7-azaindazolyl analogues // Mendeleev Communicationsthis link is disabled. – 2022. - 32(2). - Р. 271–273. DOI:10.1016/j.mencom.2022.03.040

   41. Minkin V.I., Ivakhnenko E.P., Knyazev P.A., Starikov A.G., Demidov O.P., Tkachenko, N.V., Boldyrev, A.I. Electronic isomerism (electromerism) of 6,8-di-tert-butyl-3H-phenoxazin-3-one oxime radical // Russian Chemical Bulletin – 2022. - 71(1). - Р. 30–37. doi.org/10.1007/s11172-022-3372-y

   42. Avakyan, E. K., Borovleva, A. A., Pobedinskaya, D. Y., Demidov, O. P., Ermolenko, A. P., Larin, A. N., & Borovlev, I. V. (2022). SNH-Amidation of 5-Nitroisoquinoline: Access to Nitro-and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline. Molecules, 27(22), 7862 DOI doi.org/10.3390/molecules27227862.

   43. Ozhogin I. V. et al. Novel Indoline Spiropyrans Based on Human Hormones β- Estradiol and Estrone: Synthesis, Structure, Chromogenic and Cytotoxic Properties //Molecules. – 2023. – Т. 28. – №. 9. – Р. 3866. doi.org/10.3390/molecules28093866

   44. Filatova E. A. et al. Synthesis, conformational stability and molecular structure of 4- aryl-and 4, 5-diaryl-1, 8-bis (dimethylamino) naphthalenes //Organic and Biomolecular Chemistry. – 2023. – Т. 21. – №. 16. – Р. 3388-3401. doi.org/10.1039/D3OB00286A

   45. Osipov D. V. et al. Reactions of 2-Nitro-1 H-benzo [f] chromenes and 3-Nitro-1- benzofurans with Nucleophiles //Russian Journal of Organic Chemistry. – 2023. – Т. 59. – №. 3. – Р. 422-437. doi.org/10.1134/S1070428023030107

   46. Minkin V. I. et al. Heteropentacyclic quinoxalino [2, 3-b] phenoxazines: the synthesis, optoelectronic, and electrochemical properties //Russian Chemical Bulletin. – 2023. – Т. 72. – №. 3. – Р. 669-680. doi.org/10.1007/s11172-023-3831-4

   47. Zubenko A. A. et al. New β-[o-(5-oxopyrazol-3-yl) aryl] ethylamines and their unusual metastable betaine form //Mendeleev Communications. – 2023. – Т. 33. – №. 2. – Р. 203-205. doi.org/10.1016/j.mencom.2023.02.017

   48. Vlasenko M. P. et al. α-Amino acid-assisted autoxidation of naphthalene proton sponge affording 1, 4-naphthoquinone nitrogen derivatives //Mendeleev Communications. – 2023. – Т. 33. – №. 2. – Р. 197-200. doi.org/10.1016/j.mencom.2023.02.015

   49. Khodykina E. S. et al. Intramolecular Cyclization of the ortho‐Substituted N‐arylquinone Imines under Basic and Thermal Conditions //ChemistrySelect. – 2023. – Т. 8. – №. 3. – Р. e202204317. doi.org/10.1002/slct.202204317

Данные о публикационной активности:

• Scopus: публикаций – 68, цитирование – 228, индекс Хирша – 7
• Web of Science: публикаций – 52, цитирование – 206, индекс Хирша – 8

Web of Science ResearcherID N-6296-2017

ORCID 0000-0002-3586-0487

Scopus Author ID:  6603864038