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Articles (187) More info
1 |
Khusnutdinova E.F.
, Galimova Z.I.
, Petrova A.V.
, Tretyakova E.V.
, Smirnova I.E.
, Slita A.V.
, Fedij S.V.
, Zarubaev V.V.
, Xiao S.
, Ma X.
, Zhou D.
, Rybalova T.V.
, Polovyanenko D.N.
, Kazakova O.B.
Synthesis and Antiviral Activity of 21β-Acetyl-20β,28-Epoxy-18α,19βH-Ursane Derivatives Against Influenza H1N1 and SARS-Cov-2 Spike Pseudovirus Chemistry of Natural Compounds. 2024. V.60. N2. P.275-282. DOI: 10.1007/s10600-024-04302-w |
2 |
KHOROSHUNOVA Y.V.
, MOROZOV D.A.
, RYBALOVA T.V.
, TRAKHININA S.Y.
, ASANBAEVA N.B.
, SOTNIKOVA Y.S.
, KIRILYUK I.A.
1R,5S,7S,8R,12S,13S)-12,13-Dihydroxy-1,8-bis(hydroxymethyl)-6-azadispiro[4.1.4.2]tridecane-6-oxyl - a Chiral Hydrophilic Dispirocyclic Radical with High Stability to Reduction CHEMISTRY FOR SUSTAINABLE DEVELOPMENT. 2024. V.32. N4. P.555-565. DOI: 10.15372/CSD2024588 |
3 |
Kovaleva K.S.
, Abdrakhmanova V.S.
, Yarovaya O.I.
, Gatilov Y.V.
, Rybalova T.V.
, Salakhutdinov N.F.
Facile Stereoselective Synthesis and Structural Study of Camphor‐ and Fenchone‐Based Spirocyclic 1,3,4‐Oxadiazolines European Journal of Organic Chemistry. 2023. e202300811 :1-6. DOI: 10.1002/ejoc.202300811 WOS Scopus РИНЦ |
4 |
Nikolaenkova E.B.
, Grishchenko S.Y.
, Rybalova T.V.
, Tikhonov A.Y.
Preparation of 2-unsubstituted 5-aryl(hetaryl)-1-hydroxy-1H-imidazoles from of 4-aryl(hetaryl)-1-hydroxy-2,5-dihydro-1H-imidazole-2-carboxylic acid 3-oxides Chemistry of Heterocyclic Compounds. 2023. V.59. N11-12. P.752-757. DOI: 10.1007/s10593-024-03268-5 WOS РИНЦ |
5 |
Finke A.O.
, Krasnov V.I.
, Rybalova T.V.
, Chirkova V.Y.
, Belenkaya S.V.
, Volosnikova E.A.
, Shcherbakov D.N.
, Shults E.E.
A straightforward trifluoromethylation at the C6 position of morphinane alkaloids, their modification and evaluation of inhibition of the SARS-CoV-2 main protease Journal of Fluorine Chemistry. 2023. V.271. 110189 :1-10. DOI: 10.1016/j.jfluchem.2023.110189 WOS РИНЦ |
6 |
Khoroshunova Y.V.
, Morozov D.A.
, Kuznetsov D.A.
, Rybalova T.V.
, Glazachev Y.I.
, Bagryanskaya E.G.
, Kirilyuk I.A.
Synthesis and Properties of (1R(S),5R(S),7R(S),8R(S))-1,8-Bis(hydroxymethyl)-6-azadispiro[4.1.4.2]tridecane-6-oxyl: Reduction-Resistant Spin Labels with High Spin Relaxation Times International Journal of Molecular Sciences. 2023. V.24. N14. P.11498. DOI: 10.3390/ijms241411498 WOS Scopus РИНЦ |
7 |
Li-Zhulanov N.S.
, Zaikova N.P.
, Sari S.
, Gülmez D.
, Sabuncuoğlu S.
, Ozadali-Sari K.
, Arikan-Akdagli S.
, Nefedov A.A.
, Rybalova T.V.
, Volcho K.P.
, Salakhutdinov N.F.
Rational Design of New Monoterpene-Containing Azoles and Their Antifungal Activity Antibiotics. 2023. V.12. N5. P.818. DOI: 10.3390/antibiotics12050818 WOS Scopus РИНЦ |
8 |
Trukhanov V.A.
, Kuevda A.V.
, Dominskiy D.I.
, Mannanov A.L.
, Rybalova T.V.
, Tafeenko V.A.
, Sosorev A.Y.
, Konstantinov V.G.
, Kazantsev M.S.
, Borshchev O.V.
, Ponomarenko S.A.
, Pshenichnikov M.S.
, Paraschuk D.Y.
Strongly polarized surface electroluminescence from an organic light-emitting transistor Materials Chemistry Frontiers. 2023. V.7. N2. P.238-248. DOI: 10.1039/d2qm01046a WOS РИНЦ |
9 |
Mironov M.E.
, Rybalova T.V.
, Pokrovskii M.A.
, Emaminia F.
, Gandalipov E.R.
, Pokrovskii A.G.
, Shults E.E.
Synthesis of fully functionalized spirostanic 1,2,3-triazoles by the three component reaction of diosgenin azides with acetophenones and aryl aldehydes and their biological evaluation as antiproliferative agents Steroids. 2023. V.190. P.109133. DOI: 10.1016/j.steroids.2022.109133 WOS РИНЦ |
10 |
Yarovaya O.I.
, Kovaleva K.S.
, Borisevich S.S.
, Rybalova T.V.
, Gatilov Y.V.
, Sinegubova E.O.
, Volobueva A.S.
, Zarubaev V.V.
, Salakhutdinov N.F.
Synthesis and antiviral properties of tricyclic amides derived from α-humulene and β-caryophyllene Mendeleev Communications. 2022. V.32. N5. P.609-611. DOI: 10.1016/j.mencom.2022.09.013 WOS Scopus РИНЦ |
11 |
Reshetnikov D.V.
, Burova L.G.
, Rybalova T.V.
, Bondareva E.A.
, Patrushev S.S.
, Evstropov A.N.
, Shults E.E.
Synthesis and Antibacterial Activity of Caffeine Derivatives Containing Amino-Acid Fragments Chemistry of Natural Compounds. 2022. V.58. N5. P.908-915. DOI: 10.1007/s10600-022-03826-3 WOS РИНЦ |
12 |
Stepanova V.A.
, Patrushev S.S.
, Rybalova T.V.
, Shults E.E.
Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent Journal of Molecular Structure. 2022. V.1247. 131373 . DOI: 10.1016/j.molstruc.2021.131373 WOS Scopus РИНЦ |
13 |
Reshetnikov D.V.
, Ivanov I.D.
, Baev D.S.
, Rybalova T.V.
, Mozhaitsev E.S.
, Patrushev S.S.
, Vavilin V.A.
, Tolstikova T.G.
, Shults E.E.
Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors Molecules. 2022. V.27. N24. P.8787. DOI: 10.3390/molecules27248787 WOS РИНЦ |
14 |
Asanbaeva N.B.
, Gurskaya L.Y.
, Polienko Y.F.
, Rybalova T.V.
, Kazantsev M.S.
, Dmitriev A.A.
, Gritsan N.P.
, Haro-Mares N.
, Gutmann T.
, Buntkowsky G.
, Tretyakov E.V.
, Bagryanskaya E.G.
Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization Molecules. 2022. V.27. N10. P.3252. DOI: 10.3390/molecules27103252 WOS Scopus РИНЦ |
15 |
Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations Macroheterocycles. 2021. V.14. N1. P.105-111. DOI: 10.6060/mhc200817s WOS Scopus РИНЦ |
16 |
Borisova M.S.
, Ivankin D.I.
, Sokolov D.N.
, Luzina O.A.
, Rybalova T.V.
, Tolstikova T.G.
, Salakhutdinov N.F.
Synthesis, antiulcerative, and anti-inflammatory activities of new campholenic derivatives-1,3-thiazolidin-4-ones, 1,3-thiazolidine-2,4-diones, and 1,3-thiazinan-4-ones Chemical Papers. 2021. V.75. P.5503–5514. DOI: 10.1007/s11696-021-01741-5 WOS Scopus РИНЦ |
17 |
Avdeeva E.
, Porokhova E.
, Khlusov I.
, Rybalova T.
, Shults E.
, Litvinova L.
, Shupletsova V.
, Khaziakhmatova O.
, Sukhodolo I.
, Belousov M.
Calcium chelidonate: Semi‐synthesis, crystallography, and osteoinductive activity in vitro and in vivo Pharmaceuticals. 2021. V.14. N6. 579 . DOI: 10.3390/ph14060579 WOS Scopus РИНЦ |
18 |
Kharitonov Y.V.
, Shul'ts E.E.
, Rybalova T.V.
, Pavlova A.V.
, Tolstikova T.G.
Synthetic Transformations of Higher Terpenoids. 40. Synthesis and Assessment of Analgesic Activity of N-Containing Derivatives of Lambertianic Acid Chemistry of Natural Compounds. 2021. V.57. N5. P.879-886. DOI: 10.1007/s10600-021-03502-y WOS Scopus РИНЦ |
19 |
Patrushev S.S.
, Burova L.G.
, Shtro A.A.
, Rybalova T.V.
, Baev D.S.
, Shirokikh I.V.
, Evstropov A.N.
, Shults E.E.
Modifications of isoalantolactone leading to effective anti-bacterial and anti-viral compounds Letters in Drug Design and Discovery. 2021. V.18. N7. P.686-700. DOI: 10.2174/1570180817999201211193151 WOS Scopus РИНЦ |
20 |
Khoroshunova Y.V.
, Morozov D.A.
, Taratayko A.I.
, Dobrynin S.A.
, Eltsov I.V.
, Rybalova T.V.
, Sotnikova Y.S.
, Polovyanenko D.N.
, Asanbaeva N.B.
, Kirilyuk I.A.
The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4 Molecules. 2021. V.26. N19. 6000 . DOI: 10.3390/molecules26196000 WOS Scopus |
21 |
Patrushev S.S.
, Rybalova T.V.
, Shults E.E.
Synthetic transformations of sesquiterpene lactones. Controllable synthesis of 11,13-dihydroisoalantolactone azides and 13-(1,2,3-triazolyl)eudesmanolides based on sesquiterpene lactones Chemistry of Heterocyclic Compounds. 2021. V.57. N11. P.1116–1129. DOI: 10.1007/s10593-021-03030-1 WOS Scopus |
22 |
Anisimova N.A.
, Slobodchikova E.K.
, Ivanova M.E.
, Rybalova T.V.
Reaction of 3,3,3-Tribromo- and 1,3,3,3-Tetrabromo-1-nitroprop-1-enes with Aliphatic Dienes Russian Journal of General Chemistry. 2020. V.90. N8. P.1388-1397. DOI: 10.1134/S1070363220080022 WOS Scopus РИНЦ |
23 |
Ustimenko Y.P.
, Vasilyev E.S.
, Bizyaev S.N.
, Rybalova T.V.
, Tkachev A.V.
Synthesis of chiral spirodiazafluorenes Chemistry of Heterocyclic Compounds. 2020. V.56. N11. P.1429–1433. DOI: 10.1007/s10593-020-02833-y WOS Scopus РИНЦ |
24 |
Fedyushin P.
, Rybalova T.
, Asanbaeva N.
, Bagryanskaya E.
, Dmitriev A.
, Gritsan N.
, Kazantsev M.
, Tretyakov E.
Synthesis of Nitroxide Diradical Using a New Approach Molecules. 2020. V.25. N11. 2701 . DOI: 10.3390/molecules25112701 WOS Scopus РИНЦ |
25 |
Mironov M.E.
, Poltanovich A.I.
, Rybalova T.V.
, Dolgikh M.P.
, Tolstikova T.G.
, Shults E.E.
Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety Russian Chemical Bulletin. 2020. V.69. N3. P.537-546. DOI: 10.1007/s11172-020-2795-6 WOS Scopus РИНЦ |
26 |
Zhurko I.E.
, Dobrynin S.
, Gorodetskii A.A.
, Glazachev Y.I.
, Rybalova T.V.
, Chernyak E.I.
, Asanbaeva N.
, Bagryanskaya E.G.
, Kirilyuk I.A.
2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties Molecules. 2020. V.25. N4. 845 . DOI: 10.3390/molecules25040845 WOS Scopus РИНЦ |
27 |
Petunin P.V.
, Rybalova T.V.
, Trusova M.E.
, Uvarov M.N.
, Kazantsev M.S.
, Mostovich E.A.
, Postulka L.
, Eibisch P.
, Wolf B.
, Lang M.
, Postnikov P.S.
, Baumgarten M.
A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units ChemPlusChem. 2020. V.85. N1. P.159-162. DOI: 10.1002/cplu.201900709 WOS Scopus |
28 |
Urbagarova B.M.
, Shults E.E.
, Taraskin V.V.
, Radnaeva L.D.
, Petrova T.N.
, Rybalova T.V.
, Frolova T.S.
, Pokrovskii A.G.
, Ganbaatar J.
Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity Journal of Ethnopharmacology. 2020. V.261. 112517 . DOI: 10.1016/j.jep.2019.112517 WOS Scopus РИНЦ |
29 |
Gurskaya L.
, Rybalova T.
, Beregovaya I.
, Zaytseva E.
, Kazantsev M.
, Tretyakov E.
Aromatic nucleophilic substitution: A case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides Journal of Fluorine Chemistry. 2020. V.237. 109613 . DOI: 10.1016/j.jfluchem.2020.109613 WOS Scopus РИНЦ |
30 |
Lubov D.P.
, Lyakin O.Y.
, Samsonenko D.G.
, Rybalova T.V.
, Talsi E.P.
, Bryliakov K.P.
Palladium aminopyridine complexes catalyzed selective benzylic C-H oxidations with peracetic acid Dalton Transactions. 2020. V.49. N32. P.11150-11156. DOI: 10.1039/d0dt02247k WOS Scopus РИНЦ |
31 |
Krisyuk V.V.
, Ursym kyzy S.
, Rybalova T.V.
, Korolkov I.V.
, Sysoev S.V.
, Koretskaya T.P.
, Kuchumov B.M.
, Turgambaeva A.E.
Volatile trinuclear heterometallic beta-diketonates: Structure and thermal properties related to the chemical vapor deposition of composite thin films Polyhedron. 2020. V.191. 114806 . DOI: 10.1016/j.poly.2020.114806 WOS Scopus РИНЦ |
32 |
Cherkasov S.
, Parkhomenko D.
, Genaev A.
, Salnikov G.
, Edeleva M.
, Morozov D.
, Rybalova T.
, Kirilyuk I.
, Marque S.R.A.
, Bagryanskaya E.
NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines Molecules. 2020. V.25. N21. DOI: 10.3390/molecules25215080 WOS Scopus РИНЦ |
33 |
Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Synthetic studies on tricyclic diterpenoids: convenient synthesis of 16-arylisopimaranes Monatshefte für Chemie Chemical Monthly. 2020. V.151. N12. P.1817-1827. DOI: 10.1007/s00706-020-02713-3 WOS Scopus РИНЦ |
34 |
Politanskaya L.V.
, Fedyushin P.A.
, Rybalova T.V.
, Bogomyakov A.S.
, Asanbaeva N.B.
, Tretyakov E.V.
Fluorinated Organic Paramagnetic Building Blocks for Cross-Coupling Reactions Molecules. 2020. V.25. N22. 427 . DOI: 10.3390/molecules25225427 WOS Scopus РИНЦ |
35 |
Babaev M.
, Khusnutdinova E.
, Lobov A.
, Galimova Z.
, Petrova A.
, Rybalova T.
, Nguyen H.T.T.
, Meyers C.
, Prichard M.
, Kazakova O.
Allobetulone rearrangement to l8αH,19βH-ursane triterpenoids with antiviral activity Natural Product Research. 2020. DOI: 10.1080/14786419.2020.1855159 WOS Scopus |
36 |
Mannanov A.A.
, Kazantsev M.S.
, Kuimov A.D.
, Konstantinov V.G.
, Dominskiy D.I.
, Trukhanov V.A.
, Anisimov D.S.
, Gultikov N.V.
, Bruevich V.V.
, Koskin I.P.
, Sonina A.A.
, Rybalova T.V.
, Shundrina I.K.
, Mostovich E.A.
, Paraschuk D.Y.
, Pshenichnikov M.S.
Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals Journal of Materials Chemistry C. 2019. V.7. N1. P.60-68. DOI: 10.1039/c8tc04151b WOS Scopus РИНЦ |
37 |
Peshkov R.Y.
, Wang C.
, Panteleeva E.V.
, Rybalova T.V.
, Tretyakov E.V.
Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles Journal of Organic Chemistry. 2019. V.84. N2. P.963-972. DOI: 10.1021/acs.joc.8b02904 WOS Scopus РИНЦ |
38 |
Shelkovnikov V.V.
, Kargapolova I.Y.
, Korotaev S.V.
, Orlova N.A.
, Rybalova T.V.
, Chuikov I.P.
Three-color luminescent transformation of the julolidine pyrylo/pyridocyanine dyes in the adsorbed state Journal of Photochemistry and Photobiology A: Chemistry. 2019. V.375. P.181-190. DOI: 10.1016/j.jphotochem.2019.02.022 WOS Scopus РИНЦ |
39 |
Avdeeva E.
, Shults E.
, Rybalova T.
, Reshetov Y.
, Porokhova E.
, Sukhodolo I.
, Litvinova L.
, Shupletsova V.
, Khaziakhmatova O.
, Khlusov I.
, Guryev A.
, Belousov M.
Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro Biomolecules. 2019. V.9. N5. 189 . DOI: 10.3390/biom9050189 WOS Scopus РИНЦ |
40 |
Kazantsev M.S.
, Sonina A.A.
, Koskin I.P.
, Sherin P.S.
, Rybalova T.V.
, Benassi E.
, Mostovich E.A.
Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals Materials Chemistry Frontiers. 2019. V.3. N8. P.1545-1554. DOI: 10.1039/c9qm00198k WOS Scopus РИНЦ |
41 |
Petunin P.V.
, Votkina D.E.
, Trusova M.E.
, Rybalova T.V.
, Amosov E.V.
, Uvarov M.N.
, Postnikov P.S.
, Kazantsev M.S.
, Mostovich E.A.
Oxidative addition of verdazyl halogenides to Pd(PPh3)(4) New Journal of Chemistry. 2019. V.43. N38. P.15293-15301. DOI: 10.1039/c9nj03361k WOS Scopus РИНЦ |
42 |
Savel'ev V.A.
, Kotova A.A.
, Rybalova T.V.
, Shults E.E.
Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles Containing an Anthranilic Acid Motif Chemistry of Heterocyclic Compounds. 2019. V.55. N10. P.943-955. DOI: 10.1007/s10593-019-02561-y WOS Scopus РИНЦ |
43 |
Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shul'ts E.E.
Synthetic Transformations of Higher Terpenoids. 38.* Synthesis of Conjugates Containing beta-Carboline and Tricyclic Diterpenoids Chemistry of Natural Compounds. 2019. V.55. N5. P.871-877. DOI: 10.1007/s10600-019-02836-y WOS Scopus РИНЦ |
44 |
Mironov M.E.
, Oleshko O.S.
, Pokrovskii M.A.
, Rybalova T.V.
, Pechurov V.K.
, Pokrovskii A.G.
, Cheresis S.V.
, Mishinov S.V.
, Stupak V.V.
, Shults E.E.
6-(4 '-Aryl-1 ',2 ',3 '-triazolyl)-spirostan-3,5-diols and 6-(4 '-Aryl-1 ',2 ',3 '-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity Steroids. 2019. V.151. 108460 . DOI: 10.1016/j.steroids.2019.108460 WOS Scopus РИНЦ |
45 |
Tretyakov E.
, Fedyushin P.
, Panteleeva E.
, Gurskaya L.
, Rybalova T.
, Bogomyakov A.
, Zaytseva E.
, Kazantsev M.
, Shundrina I.
, Ovcharenko V.
Aromatic S-N(F)-Approach to Fluorinated Phenyl tert-Butyl Nitroxides Molecules. 2019. V.24. N24. 4493 . DOI: 10.3390/molecules24244493 WOS Scopus РИНЦ |
46 |
Talsi E.P.
, Bryliakova A.A.
, Ottenbacher R.V.
, Rybalova T.V.
, Bryliakov K.P.
Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification Research. 2019. V.2019. UNSP 4756025 . DOI: 10.34133/2019/4756025 WOS Scopus РИНЦ |
47 |
Rybalova T.V.
, Rogachev A.D.
, Khomenko T.M.
, Volcho K.P.
, Salakhutdinov N.F.
Molecular and Supramolecular Structure of 8-(Trifluoromethyl)Benzo[f][1,2,3,4,5] Pentathiepin-6-Amine - A Representative of Condensed Arene Pentathiepines Journal of Structural Chemistry. 2018. V.59. N7. P.1753-1758. DOI: 10.1134/S0022476618070326 WOS Scopus РИНЦ |
48 |
Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shul'ts E.E.
Synthetic Transformations of Higher Terpenoids. 36.(*) Synthesis of 13-(Oxazol-5-Yl)-15,16-Bisnorisopimaranes Chemistry of Natural Compounds. 2018. V.54. N2. P.293-300. DOI: 10.1007/s10600-018-2327-x WOS Scopus РИНЦ |
49 |
Ten Y.A.
, Salnikov O.G.
, Amitina S.A.
, Stass D.V.
, Rybalova T.V.
, Kazantsev M.S.
, Bogomyakov A.S.
, Mostovich E.A.
, Mazhukin D.G.
The Suzuki-Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series RSC Advances. 2018. V.8. N46. P.26099-26107. DOI: 10.1039/c8ra05103h WOS Scopus |
50 |
Krisyuk V.V.
, Kyzy S.U.
, Rybalova T.V.
, Baidina I.A.
, Korolkov I.V.
, Chizhov D.L.
, Bazhin D.N.
, Kudyakova Y.S.
Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted -diketonates Journal of Coordination Chemistry. 2018. V.71. N14. P.2194-2208. DOI: 10.1080/00958972.2018.1479746 WOS Scopus РИНЦ |
Identifiers
Scopus ID:
7003650900
, 6507659347
, 55664137400
, 14032096100
ORCID: 0000-0003-2398-5271
ResearcherID: AAO-4376-2020
ORCID: 0000-0003-2398-5271
ResearcherID: AAO-4376-2020