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Федеральное государственное бюджетное учреждение науки
Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук

(2006 - 2017 )

  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.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
     
  3. 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, 2016, V. 128, N 38, Pp 11710-11714 doi:10.1002/ange.201606335, IF=11.709
     
  4. 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
     
  5. 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
     
  6. 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
     
  7. 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
     
  8. 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
     
  9. C. Gmeiner, D. l 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
     
  10. 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
     
  11. 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. Seppeltb, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
     
  12. 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
     
  13. 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
     
  14. 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
     
  15. 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
     
  16. 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
     
  17. 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
     
  18. 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
     
  19. 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
     
  20. 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
     
  21. 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
     
  22. 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
     
  23. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
     
  24. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
     
  25. A. Samouilov, O.V. Efimoya, A.A. Bobko, Z. Sun, S. Petryakov, T.D. Eubank, D.G. Trofimov, I.A. Kirilyuk, I.A. Grigor'ev, W. Takahashi, J.L. Zweier, V.V. Khramtsov
    In Vivo Proton–Electron Double-Resonance Imaging of Extracellular Tumor pH Using an Advanced Nitroxide Probe
    Anal. Chem., 2014, 86 (2), pp. 1045-1052., 2014, 86, 2, 1045-1052 doi:10.1021/ac402230h, IF=5.824
     
  26. O.V. Zalomaeva, A.M. Chibiryaev, K.A. Kovalenko, O.A. Kholdeeva, B.S. Balzhinimaev, V.P. Fedin
    Cyclic carbonates synthesis from epoxides and CO2 over metal-organic framework Cr-MIL-101
    Journal of Catalysis, 2013, V. 298, pp 179-185. doi:10.1016/j.jcat.2012.11.029, IF=5.787
     
  27. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
    Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
    CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
     
  28. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
     
  29. M. Kozuleva, I. Klenina, I. Mysin, I. Kirilyuk, V. Opanasenko, I. Proskuryakov, B. Ivanov
    Quantification of superoxide radical production in thylakoid membrane using cyclic hydroxylamines
    Free Radical Biology and Medicine, V. 89, 2015, Pp 1014-1023 doi:10.1016/j.freeradbiomed.2015.08.016, IF=5.736
     
  30. G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva
    Trityl-based alkoxyamines as NMP controllers and spin-labels
    Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A, IF=5.687
     
  31. M.N. Simonov, P.A. Zaikin, I.L. Simakova
    Highly selective catalytic propylene glycol synthesis from alkyl lactate over copper on silica: Performance and mechanism
    Appl. Cat. B, 2012, V.119–120, 340-347. doi:10.1016/j.apcatb.2012.03.003, IF=5.625
     
  32. A.A. Bobko, I.A. Kirilyuk, I.A. Grigor’ev, J.L. Zweier, V.V. Khramtsov
    Reversible reduction of nitroxides to hydroxylamines: roles for ascorbate and glutathione
    Free Radic.Biol. Med., 2007, V. 42, N 3, 404-412. doi:10.1016/j.freeradbiomed.2006.11.007, IF=5.44
     
  33. N.E. Polyakov, T.V. Leshina, N.F. Salakhutdinov, T.A. Konovalova, L.D. Kispert
    Antioxidant and redox properties of supramolecular complexes of carotenoids with beta-glycyrrhizic acid
    Free Radical Bio. Med., 2006, V. 40, N 10, 1804-1809. doi:10.1016/j.freeradbiomed.2006.01.015, IF=5.399
     
  34. S.N. Konchenko, S.V. Klementieva, N.P. Gritsan, M.M. Khusniyarov, A. Witt, A.A. Dmitriev, E.A. Suturina, N.D. Hill, T.L. Roemmelete, T. Michael, R.T. Boere, P.W. Roesky, A.V. Zibarev
    The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
    Chemistry - A European Journal, V. 23, N 6, January 26, 2017, Pp 1278-1290 doi:10.1002/chem.201604340, IF=5.316
     
  35. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, .N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
     
  36. N.A. Pushkarevsky, P.l A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca. S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
     
  37. Yu.B. Borozdina, E.A. Mostovich, P.T. Cong, L. Postulka, B. Wolf, M. Lang, M. Baumgarten
    Spin-dimer networks: engineering tools to adjust the magnetic interactions in biradicals
    J. Mater. Chem. C, 2017,5(35), 9053-9065 doi:10.1039/C7TC03357E, IF=5.256
     
  38. O.V. Ardashov, A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, E.V. Karpova, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in animal models of Parkinson's disease
    J. Med. Chem., 2011, V. 54, N 11, 3866-74. doi:10.1021/jm2001579, IF=5.206