Journal publications with high IF

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Journal publications with high IF
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  1. E.G. Bagryanskaya, S.R. A. Marque
    Scavenging of Organic C-Centered Radicals by Nitroxides
    Chem. Rev., 2014, 114 (9), pp 5011-5056. doi:10.1021/cr4000946, IF=45.66
     
  2. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
     
  3. M.P. Davydova, L. Meng, M.I. Rakhmanova, Zh. Jia, A.S. Berezin, I.Yu. Bagryanskaya, Qi. Lin, H. Meng, A.V. Artem'ev
    Strong Magnetically-Responsive Circularly Polarized Phosphorescence And X-Ray Scintillation in Ultrarobust Mn(II)–Organic Helical Chains
    Advanced Materials, 2023, V. 35, N 35, 2303611 doi:10.1002/adma.202303611, IF=29.4
     
  4. Gérard Audran, Elena G. Bagryanskaya, Raphaël Bikanga, Michelle L. Coote, Olga Guselnikova, Chelsey L. Hammill, Sylvain R.A. Marque, Philippe Mellet, Pavel S. Postnikov
    Dynamic Covalent Bond: Modes of Activation of the C—ON Bond in Alkoxyamines
    Progress in Polymer Science, V. 144, September 2023, 101726 doi:10.1016/j.progpolymsci.2023.101726, IF=27.1
     
  5. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
     
  6. M.P. Davydova, T. Xu, A.M. Agafontsev, L. Meng, M. Wolff, M.Yu. Petyuk, I.Yu. Bagryanskaya, A.S. Berezin, A.V. Tkachev, H. Meng, A.V. Artem'ev
    Toward Rhenium-based Circularly Polarized OLEDs Using Tailored Chiral Re(CO)3 Emitters
    Angewandte Chemie International Edition, V.64, N 7, February 10, 2025, e202419788 doi:10.1002/anie.202419788, IF=16.9
     
  7. M.Yu. Petyuk, L. Meng, Zi. Ma, A.M. Agafontsev, I.Yu. Bagryanskaya, A. Berezin, J. Zhang, A. Chu, M.I. Rakhmanova, H. Meng, A.V. Tkachev, V.Wing-Wah. Yam, A.V. Artem'ev
    Outstanding Circularly Polarized TADF in Chiral Cu(I) Emitters: From Design to Application in CP-TADF OLEDs
    Angewandte Chemie International Edition, V. 63, N 52, December 20, 2024, e202412437 doi:10.1002/anie.202412437, IF=16.1
     
  8. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
     
  9. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
     
  10. A.A. Kuzhelev, V. Denysenkov, I.M. Ahmad, O.Yu. Rogozhnikova, D.V. Trukhin, E.G. Bagryanskaya, V.M. Tormyshev, S.Th. Sigurdsson, T.F. Prisner
    Solid-Effect Dynamic Nuclear Polarization in Viscous Liquids at 9.4 T Using Narrow-Line Polarizing Agents
    Journal of the American Chemical Society, 2023, 145, 18, 10268-10274 doi:10.1021/jacs.3c01358, IF=15
     
  11. S.S. Ovcherenko, A.V. Shernyukov, D.M. Nasonov, A.V. Endutkin, D.O. Zharkov, E.G. Bagryanskaya
    Dynamics of 8-Oxoguanine in DNA: Decisive Effects of Base Pairing and Nucleotide Context
    Journal of the American Chemical Society, 2023, 145, 10, 5613-5617 doi:10.1021/jacs.2c11230, IF=15
     
  12. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
     
  13. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
     
  14. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
     
  15. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
    Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
    Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
     
  16. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
     
  17. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
     
  18. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, V.I. Ovcharenko
    Electron paramagnetic resonance of switchable copper-nitroxide-based molecular magnets: An indispensable tool for intriguing systems
    Coordination Chemistry Reviews, 2015, V. 289–290, Pp 341-356, Special Issue: SI doi:10.1016/j.ccr.2014.11.015, IF=12.239
     
  19. E.S. Stoyanov, I.V. Stoyanova
    Features of protonation of the simplest weakly basic molecules, SO2, CO, N2O, CO2, and others, by solid carborane superacids
    Angewandte Chemie International Edition, 2018, V. 57, N 17, Pp 4516-4520 doi:10.1002/anie.201704645, IF=12.102
     
  20. B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
    Selective High-Resolution Detection of Membrane Protein–Ligand Interaction in Native Membranes using Trityl-Nitroxide PELDOR
    Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
     
  21. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
     
  22. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
     
  23. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
     
  24. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
     
  25. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
     
  26. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
     
  27. A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
    Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
    Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147
     
  28. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
     
  29. Zh. Zhao, A.V. Zibarev, Hui. Wang, Ji. Hao, L. Luoa
    Towards efficient CO2RR electrocatalysts: a study of structure and properties of M–N–E active moieties embedded in a biphenylene framework (M = Mn, Fe, Co, Ni, Cu; E = C, B)
    Journal of Materials Chemistry A, 2024, 12(46), 32471-32479 doi:10.1039/D4TA05064A, IF=10.699
     
  30. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
     
  31. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xiu. Hei, K.A. Brylev, O. I. Artyushin, L.E. Zelenkov, I.I. Shishkin, J. Li
    New Approach toward Dual-Emissive Organic–Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=10.383
     
  32. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
     
  33. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
     
  34. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
     
  35. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    lsoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
    ACS Catal., 2015, 5 (8), pp 4673-4679 doi:10.1021/acscatal.5b01212, IF=9.312
     
  36. M.M. Shmakov, S.A. Prikhod'ko, V.N. Panchenko, M.N. Timofeeva, V.V. Bardin, V.N. Parmon, N.Yu. Adonin
    The organoboron compounds: their Lewis acidity and catalytic activity
    Catalysis Reviews, Published online: 03 Apr 2024 doi:10.1080/01614940.2024.2334462, IF=9.3
     
  37. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
     
  38. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Complementary-addressed site-directed spin labeling of long natural RNAs
    Nucl. Acids Res. (19 September 2016), 44(16): 7935-7943. doi:10.1093/nar/gkw516, IF=9.201
     
  39. M.P. Davydova, L. Meng, M.I. Rakhmanova, I.Yu. Bagryanskaya, V.S. Sulyaeva, H. Meng, A.V. Artem'ev
    Highly Emissive Chiral Mn(II) Bromide Hybrids for UV-Pumped Circularly Polarized LEDs and Scintillator Image Applications
    Advanced Optical Materials, 20223, V. 11, N 8, 2202811 doi:10.1002/adom.202202811, IF=9
     
  40. V.V. Chernyshov, I.I. Popadyuk, O.I. Yarovaya, N.F. Salakhutdinov
    Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
    Topics in Current Chemistry, 2022, V. 380, Art. number: 42 doi:10.1007/s41061-022-00399-1, IF=8.904
     
  41. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
    Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
    ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
     
  42. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
     
  43. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
     
  44. A.D. Kuimov, Ch.S. Becker, N.A. Shumilov, I.P. Koskin, A.A. Sonina, V.Yu. Komarov, I.K. Shundrina, M.S. Kazantsev
    Synthetic approach for the control of self-doping in luminescent organic semiconductors
    Mater. Chem. Front., 2022, V. 6, N 16, Pp. 2244-2255 doi:10.1039/D2QM00345G, IF=8.683
     
  45. A.A. Kuzhelev, G. Yu. Shevelev, O.A. Krumkacheva, V.M. Tormyshev, D.V. Pyshnyi, M.V. Fedin, E.G. Bagryanskaya
    Saccharides as Prospective Immobilizers of Nucleic Acids for Room-Temperature Structural EPR Studies
    J. Phys. Chem. Lett., 2016, V. 7, N 12, pp 2544-2548 doi:10.1021/acs.jpclett.6b01024, IF=8.538
     
  46. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
     
  47. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
    Journal of Catalysis, 2022, V. 415, November 2022, Pp 12-18 doi:10.1016/j.jcat.2022.09.020, IF=8.46
     
  48. Ya.V. Demyanov, Z. Ma, Zh. Jia, M.I. Rakhmanova, G.M. Carignan, I.Yu. Bagryanskaya, V.S. Sulyaeva, A.A. Globa, V.K. Brel, L. Meng, H. Meng, Q. Lin, J. Li, A.V. Artemev
    Copper(I)-Arsine Clusters with a Near-Unity Phosphorescence Quantum Yield for X-Ray Scintillation and LED Applications
    Advanced Optical Materials, V.12, N 14, May 16, 2024, 2302904 doi:10.1002/adom.202302904, IF=8
     
  49. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
     
  50. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
     
  51. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
     
  52. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
     
  53. Г.И. Бородкин
    Механохимический синтез галогенорганических соединений: взгляд синтетика
    Успехи химии. 2023. Т. 92. № 9. RCR5091. (Mechanochemical synthesis of organohalogen compounds: a synthetic chemist's view G I Borodkin/ G I Borodkin// Russian Chemical Reviews, 2023, 92 (9), RCR5091 doi:10.59761/RCR5091), IF=7.7
     
  54. О.И. Яровая, С.С. Лаев, Н.Ф. Салахутдинов
    Противовирусные свойства дитерпенов и их производных
    Успехи химии. 2023. Т. 92. № 1. С. RCR5056. doi:10.57634/RCR5056?locatt=label:RUSSIAN (ANTIVIRAL PROPERTIES OF DITERPENES AND THEIR DERIVATIVES/ O.I. Yarovaya, S.S. Laev, N.F. Salakhutdinov// Russian Chemical Reviews, 2023, 92 (1), RCR5056 doi:10.57634/RCR5056?locatt=label:RUSSIAN), IF=7.7
     
  55. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
     
  56. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
     
  57. A.V. Sen'kova, I.A. Savin, K.V. Odarenko, O.V. Salomatina, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Protective effect of soloxolone derivatives in carrageenan- and LPS-driven acute inflammation: Pharmacological profiling and their effects on key inflammation-related processes
    Biomedicine & Pharmacotherapy, V. 159, March 2023, 114231 doi:10.1016/j.biopha.2023.114231, IF=7.5
     
  58. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
     
  59. R. Nakaoka, K. Kato, K. Yamamoto, H. Yasui, S. Matsumoto, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
    Analytical Chemistry, 2023, 95, 8, 3940–3950, 2023, ACS AuthorChoice doi:10.1021/acs.analchem.2c03194, IF=7.4
     
  60. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
     
  61. R.V. Ottenbacher, D.G. Samsonenko, A.A. Bryliakova, A.A. Nefedov, K.P. Bryliakov
    Manganese Catalyzed Direct Regio- and Stereoselective Hydroxylation of 5α- and 5β-Androstane Derivatives
    Journal of Catalysis, V. 425, September 2023, Pp 32-39 doi:10.1016/j.jcat.2023.06.003, IF=7.3
     
  62. E.O. Zhermolenko, T.Yu. Karogodina, A.Yu. Vorobev, M.A. Panfilov, A.E. Moskalensky
    Photocontrolled release of nitric oxide for precise management of NO concentration in a solution
    Materials Today Chemistry, V. 29, April 2023, 101445 doi:10.1016/j.mtchem.2023.101445, IF=7.3
     
  63. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
     
  64. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
     
  65. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
     
  66. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
     
  67. С.С. Лаев, О.И. Яровая, Н.Ф. Салахутдинов
    Малые молекулы против вирусов, вызывающих геморрагические лихорадки на территории России
    Успехи химии, 2024, 93, RCR5142 doi:10.59761/RCR5142, IF=7
     
  68. В. Н. Чарушин, Е. В. Вербицкий, О. Н. Чупахин, Д. В. Воробьева, П. С. Грибанов, С. Н. Осипов, А. В. Иванов, С. В. Мартыновская, Е. Ф. Сагитова, В. Д. Дяченко, И. В. Дяченко, С. Г. Кривоколыско, В. В. Доценко, А. В. Аксенов, Д. А. Аксенов, Н. А. Аксенов, А. А. Ларин, Л. Л. Ферштат, В. М. Музалевский, В. Г. Ненайденко, А. В. Гулевская, А. Ф. Пожарский, Е. А. Филатова, К. В. Беляева, Б. А. Трофимов, И. А. Балова, Н. А. Данилкина, А. И. Говди, А. С. Тихомиров, А. Е. Щекотихин, М. С. Новиков, Н. В. Ростовский, А. Ф. Хлебников, Ю. Н. Климочкин, М. В. Леонова, И. М. Ткаченко, В. А. Мамедов, В. Л. Мамедова, Н. А. Жукова, В. Э. Семeнов, О. Г. Синяшин, О. В. Борщев, Ю. Н. Лупоносов, С. А. Пономаренко, А. С. Фисюк, А. С. Костюченко, В. Г. Илькин, Т. В. Березкина, В. А. Бакулев, А. С. Газизов, А. А. Загидуллин, А. А. Карасик, М. Е. Кукушкин, Е. К. Белоглазкина, Н. Е. Голанцов, А. А. Феста, Л. Г. Воскресенский, В. С. Мошкин, Е. М. Буев, В. Я. Сосновских, И. А. Миронова, П. С. Постников, В. В. Жданкин, М. С. Юсубов, И. А. Яременко, В. А. Виль, И. Б. Крылов, А. О. Терентьев, Ю. Г. Горбунова, А. Г. Мартынов, А. Ю. Цивадзе, П. А. Стужин, С. С. Иванова, О. И. Койфман, О. Н. Буров, М. Е. Клецкий, С. В. Курбатов, О. И. Яровая, К. П. Волчо, Н. Ф. Салахутдинов, М. А. Панова, Я. В. Бургарт, В. И. Салоутин, А. Р. Ситдикова, Е. С. Щегравина, А. Ю. Федоров
    Успехи в химии гетероциклических соединений в 21 веке
    Russian Chemical Reviews, 2024, 93 (7), RCR5125 (The chemistry of heterocycles in the 21st century/ V.N. Charushin, E.V. Verbitskiy, O.N. Chupakhin, D.V. Vorobyeva, P.S. Gribanov, S.N. Osipov, A.V. Ivanov, S.V. Kuznetsova, E.F. Sagitova, V.D. Dyachenko, I.V. Dyachenko, S.G. Krivokolylsko, V.V. Dotsenko, A.V. Aksenov, D.A. Aksenov, N.A. Aksenov, A.А. Larin, L.L. Fershtat, V.M. Muzalevskiy, V.G. Nenajdenko, A.V. Gulevskaya, A.F. Pozharskii, E.A. Filatova, K.V. Belyaeva, B.A. Trofimov, I.A. Balova, N.A. Danilkina, A.I. Govdi, A.S. Tikhomorov, A.E. Shchekotikhin, M.S. Novikov, N.V. Rostovskii, A.F. Khlebnikov, Yu.N. Klimochkin, M.V. Leonova, I.M. Tkachenko, V.A. Mamedov, V.L. Mamedova, N.A. Zukova, V.E. Semenov, О.G. Sinyashin, O.V. Borshchev, Yu.N. Luponosov, S.A. Ponomarenko, A.S. Fisyuk, A.S. Kostyuchenko, V.G. Ilkin, T. Beryozkina, V.А. Bakulev, A.S. Gazizov, A. Zagidullin, A.A. Karasik, M.E. Kukushkin, E.K. Beloglazkina, N.E. Golantsov, A.А. Festa, L.G. Voskressensky, V.S. Moshkin, E.M. Buev, V.Ya. Sosnovskikh, I.A. Mironova, P.S. Postnikov, V.V. Zhdankin, M.S. Yusubov, I.A. Yaremenko, V.A. Vil', I.B. Krylov, A.O. Terent'ev, Yu.G. Gorbunova, A.G. Martynov, A.Yu. Tsivadze, P.A. Stuzhin, S.S. Ivanova, O.I. Koifman, O.N. Burov, M.E. Kletskii, С.В. Кurbatov, О.I. Yarovaya, K.P. Bolcho, N.F. Salakhutdinov, M.A. Artemyeva, Ya.V. Burgart, V.I. Saloutin, A.R. Sitdikova, E.S. Shchegravina, A.Yu. Fedorov// Russian Chemical Reviews, 2024, 93 (7), RCR5125 doi:10.59761/RCR5125), IF=7
     
  69. E.A. Katlenok, M.L. Kuznetsov, N.A. Semenov, N.A. Bokach, V.Yu. Kukushkin
    A new look at the chalcogen bond: π-hole-based chalcogen (Se, Te) bonding which does not include a σ-hole interaction
    Inorg. Chem. Front., 2023,10, 3065-3081 doi:10.1039/D3QI00087G, IF=7
     
  70. V.A. Trukhanov, A.V. Kuevda, D.I. Dominskiy, A.L. Mannanov, T.V. Rybalova, V.A. Tafeenko, A.Yu. Sosorev, V.G. Konstantinov, M.S. Kazantsev, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Strongly polarized surface electroluminescence from an organic light-emitting transistor
    Mater. Chem. Front., 2023,7(2), 238-248 doi:10.1039/D2QM01046A, IF=7
     
  71. O.N. Fedyaeva, S.V. Morozov, A.A. Vostrikova
    Supercritical water oxidation of chlorinated waste from pulp and paper mill
    Chemosphere, 2021, V. 238, 131239 doi:10.1016/j.chemosphere.2021.131239, IF=7
     
  72. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
     
  73. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
     
  74. О.И. Яровая, Н.Ф. Салахутдинов
    Моно- и сесквитерпены в качестве стартовой платформы для создания противовирусных средств
    Успехи химии, 2021, Т. 90, N 4, Сc 488-510 (Mono- and sesquiterpenes as a starting platform for the development of antiviral drugs/ O I Yarovaya, N F Salakhutdinov// RUSS CHEM REV, 2021, 90 (4), 488-510 doi:10.1070/RCR4969), IF=6.926
     
  75. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
     
  76. Yu.A. Frank, Yu.S. Sotnikova, V.Yu. Tsygankov, A.R. Rednikin, M.M. Donets, E.V. Karpova, M.A. Belanov, S. Rakhmatullina, A.D. Borovkova, D.N. Polovyanenko, D.S. Vorobiev
    Pollution of Beach Sands of the Ob River (Western Siberia) with Microplastics and Persistent Organic Pollutants
    J. Xenobiot. 2024, 14(3), 989-1002 doi:10.3390/jox14030055, IF=6.8
     
  77. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
     
  78. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
     
  79. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
     
  80. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
     
  81. M. Barshutina a, N. Doroshina, A. Baizhumanov, E. Nikelshparg, A. Fedotova, A. Popov, A. Semyanov, D. Yakubovsky, G. Tselikov, O. Luneva, I. Kirilyuk, G. Maksimov, V. Volkov, A. Arsenin, N. Brazhe, S. Novikov
    SERS substrates based on rose petal replicas for the oxidative stress detection
    Applied Surface Science, 2023, V. 626, 30 July 2023, 157281 doi:10.1016/j.apsusc.2023.157281, IF=6.7
     
  82. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
     
  83. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
     
  84. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
     
  85. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
     
  86. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
    Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
     
  87. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
     
  88. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
     
  89. S. Dikalov, Yu.F. Polienko, I. Kirilyuk
    Electron Paramagnetic Resonance Measurements of Reactive Oxygen Species by Cyclic Hydroxylamine Spin Probes
    Antioxidants & Redox Signaling, 2018, V. 28, N 15, Pp 1433-1444 doi:10.1089/ars.2017.7396, IF=6.53
     
  90. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
     
  91. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
     
  92. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
     
  93. K.P. Volcho, O.I. Lavrik
    Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach
    Int. J. Mol. Sci. 2023, 24(9), 7954; doi:10.3390/ijms24097954, IF=6.51
     
  94. D.P. Lubov, K.S. Ivanov, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
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    Journal of Catalysis, V. 435, July 2024, 115563 doi:10.1016/j.jcat.2024.115563, IF=6.5
     
  95. A.Yu. Sidorenko, Yu.M. Kurban, I.V. Il'ina, N.S. Li-Zhulanov, O.S. Patrusheva, V.V. Goltsova, M.P. Bei, A. Aho, J. Warna, I. Heinmaa, T.F. Kouznetsova, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Catalytic condensation of α-pinene with formaldehyde
    Journal of Catalysis, 2024, V. 430, February 2024, 115306 doi:10.1016/j.jcat.2024.115306, IF=6.5
     
  96. R.V. Ottenbacher, D.P. Lubov, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Aliphatic C-H Azidation by Mn Based Mimics of α-Ketoglutarate Dependent Enzymes
    Journal of Catalysis, 2024, V. 429, January 2024, 115275 doi:10.1016/j.jcat.2023.115275, IF=6.5
     
  97. I.V. Beregovaya, I.S. Tretyakova, V.I. Borovkov
    An Updated View of Primary Ionization Processes in Polar Liquids
    The Journal of Physical Chemistry Letters, 2021, 12, 47, 11573-11577 doi:10.1021/acs.jpclett.1c03388, IF=6.475
     
  98. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
     
  99. A.Yu. Baranov, E.P. Doronina, M.I. Rakhmanova, I.Yu. Bagryanskaya, K.A. Brylev, T.S. Sukhikh, A.V. Artem'ev
    Coinage metal(I) clusters based on a flexible P,P'(N,N')2-ligand: colorful phosphorescence, abnormal thermal quenching behavior and anticounterfeiting application
    Inorg. Chem. Front., 2025, The article was first published on 16 Jun 2025 doi:10.1039/D5QI00813A, IF=6.4
     
  100. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
     
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