Публикации сотрудника по IF
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Сотрудник:  Рогожникова Ольга Юрьевна
Занимаемые должности:  снс(кхн) ЛМР


 

Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

  1. 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
     
  2. 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
     
  3. 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
     
  4. 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
     
  5. 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
     
  6. L. Lampp, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M.l K. Bowman, N. Devasahayam, M.C. Krishna, K. Mader, P. Imming
    A radical containing injectable in-situ-oleogel and emulgel for prolonged in-vivo oxygen measurements with CW EPR
    Free Radical Biology and Medicine, 2019, V. 130, Pp 120-127 doi:10.1016/j.freeradbiomed.2018.10.442, IF=5.657
     
  7. B. Joseph, S. Ketter, A. Gopinath, O. Rogozhnikova, D. Trukhin, V.M. Tormyshev, E.G. Bagryanskaya
    In situ labeling and distance measurements of membrane proteins in E coli using Finland and OX063 trityl labels
    Chemistry - A European Journal, 2021, V. 27, N 7, Pp 2299-2304 doi:10.1002/chem.202004606, IF=4.857
     
  8. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
     
  9. H. Chen, A.G. Maryasov, O. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, M. Bowman
    Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
    Phys. Chem. Chem. Phys., 2016,18, 24954-24965 doi:10.1039/C6CP02649D, IF=4.448
     
  10. Y. Talmon, L. Shtirberg, W. Harneit, O.Yu. Rogozhnikova, V. Tormyshev, A. Blank
    Molecular diffusion in porous media by PGSE ESR
    Chem.Phys.Phys.Chem., 2010, 12(23), 5998–6007. doi:10.1039/b922060g, IF=4.116
     
  11. N.B. Asanbaeva, A.A. Sukhanov, A.A. Diveikina, O.Y. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, A.G. Maryasov, A.M. Genaev, A.V. Shernyukov, G.E. Salnikov, A.A. Lomzov, D.V. Pyshnyi, E.G. Bagryanskaya
    Application of W-band 19F electron nuclear double resonance (ENDOR) spectroscopy to distance measurement using a trityl spin probe and a fluorine label
    Phys. Chem. Chem. Phys., 2022, 24 (10), 5982-6001 doi:10.1039/D1CP05445G, IF=3.945
     
  12. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
    Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
    Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
     
  13. O.Yu. Rogozhnikova, V.G. Vasiliev, T.I. Troitskaya, D.V. Trukhin, T.V. Mikhalina, H.J. Halpern, V.M. Tormyshev
    Generation of Trityl Radicals by Nucleophilic Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations and Practical and Convenient Large-Scale Synthesis of Persistent Tris(4-carboxy-2,3,5,6-tetrathiaaryl)methyl Radical
    European Journal of Organic Chemistry, 2013, V. 2013, N 16, P. 3347-3355. doi:10.1002/ejoc.201300176, IF=3.344
     
  14. G. Yu. Shevelev, O. A. Krumkacheva, A. A. Lomzov, A. A. Kuzhelev, D. V. Trukhin, O. Yu. Rogozhnikova, V. M. Tormyshev, D. V. Pyshnyi, M. V. Fedin, E.G. Bagryanskaya
    Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
    J. Phys. Chem. B, 2015, 119 (43), pp 13641-13648 doi:10.1021/acs.jpcb.5b03026, IF=3.302
     
  15. A.A. Kuzhelev, D.V. Trukhin, O.A. Krumkacheva, R.K. Strizhakov, O.Yu. Rogozhnikova, T.I. Troitskaya, M.V. Fedin, V.M. Tormyshev, E. G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Triarylmethyl Radicals at the X- and Q-Bands
    J. Phys. Chem. B, 2015, 119 (43), pp 13630-13640 doi:10.1021/acs.jpcb.5b03027, IF=3.302
     
  16. V.M. Tormyshev, A.M. Genaev, G.E. Sal'nikov, O.Yu. Rogozhnikova, T.I. Troitskaya, D.V. Trukhin, V.I. Mamatyuk, D.S. Fadeev, H.J. Halpern
    Triarylmethanols with Bulky Aryl Groups and the NOESY/EXSY Experimental Observation of a Two-Ring-Flip Mechanism for the Helicity Reversal of Molecular Propellers
    Eur.J. Org. Chem., 2012, N 3, 623-629. doi:10.1002/ejoc.201101243, IF=3.206
     
  17. V. M. Tormyshev, O.Yu. Rogozhnikova, M. K. Bowman, D. V. Trukhin, T. I. Troitskaya, V. G. Vasiliev, L. A. Shundrin, H. J. Halpern
    Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
    European Journal of Organic Chemistry, 2014, V. 2014, N 2, pp 371-380. doi:10.1002/ejoc.201301161, IF=3.154
     
  18. Z. Yang, M.D. Bridges, C.J. Lopez, O.Yu. Rogozhnikova, D.V. Trukhin, E.K. Brooks, V. Tormyshev, H.J. Halpern, W.L. Hubbell
    A Triarylmethyl Spin Label for Long-Range Distance Measurement at Physiological Temperatures Using T1 Relaxation Enhancement
    Journal of Magnetic Resonance, V. 269, August 2016, Pp 50-54 doi:10.1016/j.jmr.2016.05.006, IF=2.888
     
  19. V.M. Tormyshev, D.V. Trukhin, O.Yu. Rogozhnikova, T.V. Mikhalina, T.I. Troitskaya, A. Flinn
    Aryl Alkyl Ketones in One-Pot Gewald Synthesis of 2-Aminothiophenes
    SynLett., 2006, V. 3, N 16, 2559-2564. doi:10.1055/s-2006-951484, IF=2.69
     
  20. K. Sato, R. Hirao, I. Timofeev, O.A. Krumkacheva, E. Zaytseva, O.Yu. Rogozhnikova, V.M. Tormyshev, D.V. Trukhin, E.G. Bagryanskaya, T. Gutmann, V. Klimavicius, G. Buntkowsky, K. Sugisaki, Sh. Nakazawa, H. Matsuoka, K. Toyota, D. Shiomi, T. Takui
    Trityl-Aryl-Nitroxide Based Genuinely g-Engineered Biradicals, as Studied by Dynamic Nuclear Polarization, Multi-Frequency ESR/ENDOR, Arbitrary Wave Generator Pulse Microwave Waveform Spectroscopy and Quantum Chemical Calculations
    The Journal of Physical Chemistry A, 2019, V. 123, N 34, Pp 7507-7517 doi:10.1021/acs.jpca.9b07169, IF=2.641
     


Актуальные новости

13-01-2023

Категория: семинары НИОХ СО РАН

Семинар Отдела медицинской химии № 1, 25.01.2023 г. в 15-00 Доклад по диссертационной работе Решетникова Д. В.