41
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Fedin M.V.
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Interaction of triarylmethyl radicals with DNA termini revealed by orientation-selective W-band double electron-electron resonance spectroscopy
Physical Chemistry Chemical Physics. 2016.
V.18. N42. P.29549-29554. DOI: 10.1039/c6cp05904j
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42
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Chen H.
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Electron spin dynamics and spin-lattice relaxation of trityl radicals in frozen solutions
Physical Chemistry Chemical Physics. 2016.
V.18. N36. P.24954-24965. DOI: 10.1039/c6cp02649d
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43
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Joseph B.
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, Rogozhnikova O.Y.
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, Bagryanskaya E.G.
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Selective High-Resolution Detection of Membrane Protein-Ligand Interaction in Native Membranes Using Trityl-Nitroxide PELDOR
Angewandte Chemie - International Edition. 2016.
V.55. N38. P.11538-11542. DOI: 10.1002/anie.201606335
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44
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Shevelev G.Y.
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, Krumkacheva O.A.
, Fedin M.V.
, Rogozhnikova O.Y.
, Trukhin D.V.
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Spin-labeled oligonucleotides - useful tool for the structural biology
FEBS JOURNAL. 2015.
V.282. NSI. P36-043
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45
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Kuzhelev A.A.
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, Troitskaya T.I.
, Fedin M.V.
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Room-Temperature Electron Spin Relaxation of Triarylmethyl Radicals at the X- and Q-Bands
Journal of Physical Chemistry B. 2015.
V.119. N43. P.13630-13640. DOI: 10.1021/acs.jpcb.5b03027
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46
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Shevelev G.Y.
, Krumkacheva O.A.
, Lomzov A.A.
, Kuzhelev A.A.
, Trukhin D.V.
, Rogozhnikova O.Y.
, Tormyshev V.M.
, Pyshnyi D.V.
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Triarylmethyl Labels: Toward Improving the Accuracy of EPR Nanoscale Distance Measurements in DNAs
Journal of Physical Chemistry B. 2015.
V.119. N43. P.13641-13648. DOI: 10.1021/acs.jpcb.5b03026
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47
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Tormyshev V.M.
, Rogozhnikova O.Y.
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, Vasiliev V.G.
, Shundrin L.A.
, Halpern H.J.
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. N2. P.371-380. DOI: 10.1002/ejoc.201301161
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48
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Shevelev G.Y.
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, Lomzov A.A.
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, Rogozhnikova O.Y.
, Trukhin D.V.
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, Fedin M.V.
, Pyshnyi D.V.
, Bagryanskaya E.G.
Physiological-Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy
Journal of the American Chemical Society. 2014.
V.136. N28. P.9874-9877. DOI: 10.1021/ja505122n
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49
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Rogozhnikova O.Y.
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, Tormyshev V.M.
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. N16. P.3347-3355. DOI: 10.1002/ejoc.201300176
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50
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Trukhan S.N.
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, Tormyshev V.M.
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V.233. P.29-36. DOI: 10.1016/j.jmr.2013.04.017
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51
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Tormyshev V.M.
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, Sal'nikov G.E.
, Rogozhnikova O.Y.
, Troitskaya T.I.
, Trukhin D.V.
, Mamatyuk V.I.
, Fadeev D.S.
, Halpern H.J.
Triarylmethanols with Bulky Aryl Groups and the NOESY/EXSY Experimental Observation of a Two-Ring-Flip Mechanism for the Helicity Reversal of Molecular Propellers
European Journal of Organic Chemistry. 2012.
V.2012. N3. P.623-629. DOI: 10.1002/ejoc.201101243
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52
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Talmon Y.
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Molecular diffusion in porous media by PGSE ESR
Physical Chemistry Chemical Physics. 2010.
V.12. N23. P.5998-6007. DOI: 10.1039/b922060g
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53
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Halevy R.
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Microimaging of Oxygen Concentration near Live Photosynthetic Cells by Electron Spin Resonance
Biophysical Journal. 2010.
V.99. N3. P.971-978. DOI: 10.1016/j.bpj.2010.05.002
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54
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Tormyshev V.M.
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Aryl alkyl ketones in a one-pot Gewald synthesis of 2-aminothiophenes
Synlett. 2006.
N16. P.2559-2564. DOI: 10.1055/s-2006-951484
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55
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Tormyshev V.M.
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A combinatorially convenient version of synthesis of 5-substituted oxazole-4-carboxylic acid ethyl esters
Russian Journal of Organic Chemistry. 2006.
V.42. N7. P.1031-1035. DOI: 10.1134/S1070428006070177
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56
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Тормышев В.М.
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, Рогожникова О.Ю.
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, Трухин Д.В.
Удобный для применения в комбинаторной химии вариант синтеза этиловых эфиров 5-замещенных оксазол-4-карбоновых кислот
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57
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Trukhin D.
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A straightforward and convenient synthesis of Cbz-protected 2-(1-aminoalkyl)oxazole-5-carboxylates
Synlett. 2005.
N13. P.2072-2076. DOI: 10.1055/s-2005-871957
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58
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Slynko N.M.
, Tormyshev V.M.
Simple modification of the familiar method for the preparation of 2-phenoxyethylbromides with high output
Журнал органической химии (RUSS J ORG CHEM+). 2000.
V.36. N2. P.276-279.
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59
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Slyn'ko N.M.
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A simple modification of the known preparation procedure of 2-Phenoxyethyl bromides providing high yields
Russian Journal of Organic Chemistry. 2000.
V.36. N2. P.254-257.
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60
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Romanenko E.P.
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Study of Pd-containing catalytic system of oxidative alkene acetoxylation
Журнал органической химии (RUSS J ORG CHEM+). 1998.
V.34. N11. P.1619-1633.
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