Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
- 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
- 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
- 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
- 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
- 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
- M.V. Edeleva, S.R-A. Marque, O.Yu. Rogozhnikova, V.M. Tormyshev, T.I. Troitskaya, E.G. Bagryanskaya
Radical polymerization of radical‐labeled monomers: The triarylmethyl‐based radical monomer as an example
Journal of Polymer Science Part A: Polymer Chemistry, 2018, V. 56, N 23, Pp 2656-2664 doi:10.1002/pola.29249, IF=2.588
- D.V. Trukhin, O.Yu. Rogozhnikova, T.I. Troitskaya, V.G. Vasiliev, M.l K. Bowman, V.M. Tormyshev
Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals
Synlett, 2016, 27(06), Pp 893-899 doi:10.1055/s-0035-1561299, IF=2.322
- A.A. Kuzhelev, V.M. Tormyshev, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, R.K. Strizhakov, O.A. Krumkacheva, M.V. Fedin, E.G. Bagryanskaya
Triarylmethyl Radicals: An EPR Study of 13C Hyperfine Coupling Constants
Zeitschrift für Physikalische Chemie, 2017, V. 231, N 4, Pp.777-794 doi:10.1515/zpch-2016-0811, IF=1.327
- Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, А.А. Кужелев, Е.В. Амосов, H.J. Halpern, В.В. Коваль, В.М. Тормышев
Новые спиновые зонды: три-и гексакатионные производные стабильных радикалов трис(тетратиаарил)метильного ряда
Журнал органической химии. 2019. Т. 55. № 3. С. 347-353. DOI:10.1134/S0514749219030030 (New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035), IF=0.751
- Д.В. Трухин, О.Ю. Рогожникова, Т.И. Троицкая, С.С. Овчеренко, Е.В. Амосов, В.М. Тормышев
Новые ацетиленовые производные стабильных радикалов трис(тетратиаарил)метильного ряда
Журнал органической химии. 2020. Т. 56. № 11. С. 1693-1699, doi:10.31857/S0514749220110038. (Novel Acetylene Derivatives of Stable Tetrathiatriarylmethyl Radicals/ D. V. Trukhin, O. Yu. Rogozhnikova, T. I. Troitskaya, S. S. Ovcherenko, E. V. Amosov, V. M. Tormyshev// Russian Journal of Organic Chemistry, 2020, V. 56, N 11, Pp 1905-1910 doi:10.1134/S1070428020110032), IF=0.624
- В.М. Тормышев, Т.В. Михалина, О.Ю. Рогожникова, Т.И. Троицкая, Д.В. Трухин
Удобный для применения в комбинаторной химии синтез этиловых эфиров 5-замещенных оксазол-4-карбоновых кислот
Журн. Орган. Химии, 2006, Т. 42, № 7, 1049-1053. (A combinatorially convenient version of synthesis of 5-substituted oxazole-4-carboxylic acid ethyl esters/ V. M. Tormyshev, T. V. Mikhalina, O. Yu. Rogozhnikova, T. I. Troitskaya, D. V. Trukhin// Russian Journal of Organic Chemistry, 2006, V. 42, N 7, pp 1031-1035 doi:10.1134/S1070428006070177), IF=0.419