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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

Kirilyuk Igor A.



Head - Cand. of Chemical Sciences
Igor A. Kirilyuk
Phone: 8(383) 330-7387


e-mail:This email address is being protected from spambots. You need JavaScript enabled to view it.

 

 

 

The Laboratory of Nitrogen Compounds (LNC) was organized by professor Leonid B. Volodarsky on the basis of research group founded in 1974. Since 1998 the laboratory is headed by professor Igor A. Grigor’ev, who was simultaneously the director of the Novosibirsk Institute of Organic Chemistry SB RAS since 2002 to 2012.

The subject of research activities of the LNC originated from studies of chemistry of hydroxylamine bifunctional organic derivatives. Further evolution of these research resulted in development of original methods for synthesis of various heterocyclic compounds, oximes, nitrones and stable nitroxides.

In 1994 the Russian Federation State Premium for science and technology was awarded to three researchers from LNC for their works on “Imidazoline nitroxides”. The fruitful research activities of Laboratory research fellows allowed them to create from nitroxides a series of high technology products, “a functional spin probes”, the compounds with a set of unique properties which are relevant to various fields of science and technology. These spin probes are designed to monitor local pH values and thiol concentrations, to follow production of nitric oxide NO, formation of superoxide anion radical and other reactive oxygen species. The use of these spin probes allowed LNC in collaboration with researchers from other institutions in Russia and abroad to develop of special methods for analysis and investigation of complex molecular structures, including those related to biological samples on molecular or cellular levels, in isolated organs and tissues. Recently the examples of successful applications of these functional spin probes to noninvasive studies of physiological processes in vivo have been described; the diagnostic procedures are in developmental stage.

Besides that, a broad variety of research is being carried out in LNS currently, including development of new therapeutic agents, new functional materials for applications of organic electronic devices, molecular magnets, mediators of radical polymerization, etc. The range of research activity of LNC is still expanding.

Laboratory of Nitrogen Compounds of NIOCh SB RAS have been renowned in Russia and abroad. The majority of international conferences on EPR biological applications and/or nitroxide chemistry frequently include some scientific contributions by researchers from LNC. The Laboratory of Nitrogen Compounds was the organizer of international conferences on nitroxides in 1989 and in 2005. The LNC is more and more engaged in research collaboration with leading research groups from Russia, USA, Germany, France, Italy, Japan, etc..


 

Research areas:

Research areas:

The major scientific trends  

  • Development of the new methods for synthesis and modification of organic hydroxylamine derivatives (including nitroxides, nitrones, Alkoxyamines, etc.) and a search for the new fields of application of these compounds.
  • Molecular design and synthesis of functional spin probes (i.e., those designed to monitor pH, thiols, nitric oxide NO, etc.) for investigation of various complex systems, including biological samples and models, living animals, sorbents, catalysts, etc..
  • Molecular design and synthesis of specific spin labels for studies of structure and dynamics of molecular and supramolecular systems, including biological macromolecules and their complexes.
  • Molecular design and synthesis of spin traps and spin probes for studies of processes involving short-living free radicals, including biogenic reactive oxygen species.
  • The studies of antioxidant properties of nitroxides, hydroxylamines and nitrones; development of the therapeutic agents on the basis of the above mentioned compounds, for prevention and treatment of various pathologies, which origination and/or development is associated with reactive oxygen species; targeting of nitroxide-based antioxidants using natural and/or synthetic biologically active molecules residues.
  • Development nitroxide and/or alkoxyamine mediators of free radical polymerization of vinyl monomers.
  • Molecular design and synthesis of paramagnetic ligands, paramagnetic liquid crystals and similar nitroxide-containing compounds for preparations of new organic and metalocomplex magnetic materials.
  • Development of nitroxide-based materials for microelectronic components, such as organic accumulators, dye-sensitized solar cells, data storage devices, etc..
  • Molecular design and synthesis of new 1,1-diphosphonate-based calcium metabolism regulators and cytostatic drugs.

Scientific achievements

 

  • The convenient scalable technologies have been developed for preparation of 1,2-hydroxyaminooxymes, 1,2-hydroxyaminoketones, N,N’-bis-hydroxyamines and similar building blocks from easily available chemicals; the utility of these blocks for synthesis of various heterocyclic systems have been demonstrated.
  • As a result of extensive studies of reactivities of nitrone and imine moieties in various heterocyclic systems, the original general methods have been developed for chemical modification and synthesis of practically useful compounds.
  • The original spin probes, the derivatives of stable nitroxides of imidazoline and imidazolidine series, have been developed, which EPR spectra are highly sensitive to pH changes. Based on these compounds, the methods have been developed for local pH monitoring in microvolumes of heterogeneous samples of various origin (in liposomes, polyelectrolyte pores, membrane surfaces, subcellular fractions and compartments, in extracellular media, in isolated organs and living tissues in vivo), for studies of proton transport, for studies of surface potentials of catalysts, sorbents, membranes, biomacromolecules, etc.The methods have been developed for preparation of imidazoline and/or pyrroline nitroxides with bulky substituents or spirocyclic moieties adjacent to nitroxide group; these nitroxides were shown to be resistant to reduction in biological samples.

 

Collaboration with:

 

  • Pacific Institute of Bioorganic Chemistry Far-East Branch of Russian Academy of Science;
  • Institute of Bioorganic Chemistry of the National Academy of Sciences of Belarus;
  • Buryat State University;
  • Institute of Problems of Chemical and Energetic Technologies Siberian Branch of RAS;
  • JSC International research and Production holding “Phytochemistry” (Karaganda, Kazakhstan);
  • Institute of Chemistry and Chemical Technology Mongolian Academy of Sciences;
  • Institute of Organic Chemistry, University of Cologne (Kцln, Germany);
  • Laboratory of Molecular Pharmacology, Center for Cancer Research, NCI, USA.

 

The major scientific trends of current researchs/Priority directions

 

  • Basic. V.36. “Theoretical chemistry and methodology of oranic synthesis development; new methods of physic-chemical investigations”.
  • Interdisciplinary Integration Projects
    • V.37: “Current problems of chemistry of materials, including nanomaterials”.
    • V.41:“Chemical problems of creation of pharmacologically active compounds of new generation”.

 

Current projects

 

  • Headed or coordinated by laboratory researchers
    • RAS basic project V.36.6.8:
      • “Development of methods for synthesis of heteroatom-containing organic compounds for biomedical research and for preparation of new materials”. Headed by Prof. Igor A. Grigor’ev.
    • RFBR Projects No.:
      • 11-03-92107-ЯФ_а “Development of novel all-organic liquid crystalline nitroxide radical compounds showing strong magnetic interactions at high temperatures”. Head from RF – Grigor’ev I.A.
      • 12-03-00718-а “Development of specifically targeted nitroxides and hydroxylamines for red-ox status regulation”. Head – Prof. Grigor’ev I.A.
      • 12-03-00737-а “A new synthetic strategy for sterically hindered nitroxides based on intramolecular 1,3-dipolar cycloaddition in alkenyl nitrones”. Head – Dr. Kirilyuk I.A.
      • 12-03-31330 мол_а “Molecular design, synthesis and properties of new redox systems based on nitroxides”. Head – Mostovich E.A.
  • Projects or programs in which the Laboratory is engaged
    • Federal research program RF “Physico-chemical studies of functional properties of new nitroxides and of nitroxide-based high-tech materials” headed by Prof Bagryanskaya (application 2012-1.2.1-12-000-1005-020).
    • Moscow city regional scientific programs:
      • “Development and practical application of new methods of healthcare, prophylaxis and diagnostics of cancer, infectious and another dangerous diseases”.
      • “Synthesis and studies of diphosphonic acids as a complexones for calcium metabolism regulation in atherosclerosis plaque”.
    • Interdisciplinary Integration Projects of SB RAS, V.37
      • Project No. 1 “Synthesis of functional nitroxides aimed to create new manetoactive compounds and materials” (Coordinated by corresponding member of RAS Ovcharenko V.I., ITC SB RAS).
      • Project No. 129 “A comprehensive study of soft media condition in electromagnetic field aimed to design highly efficient energy converters of new generation” (Coordinated by Dr Sci Klement’ev V.M., ILP SB RAS).
    • Interdisciplinary Integration Project of SB RAS, V.41
      • Project No. 52 “Oncogenesis of glioma and human brain reparation” (Coordinators: Dr Sci Mordvinov V.A. (ICG SB RAS) and corresponding member of RAS Krivoshapkin A.L. (ICG SB RAS).
    • RFBR Projects No.
      • 10-04-91331-ННИО_а “Nano-electrostatics of biological interfaces”. Head from RF– Academician Skulachev V.P. (MSU).
      • 12-03-01042-а “Novel synthetic methodologies for homo- and co-polymer nanostructured materials”. Head – Dr. Edeleva M.V., ITC SB RAS).
      • 12-04-01435-а “Development and application of new spin probes for in vivo EPR tomography and EPR spectroscopy of spin-labeled proteins”. Head – Bagryanskaya E. G. (NIOCh SB RAS).
     

 

 



 

STAFF

Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Kirilyuk Igor Anatolievich Lab's Head (Cand. Chem) 207 330-73-87 2-74 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Grigor'ev Igor Alekseevich Chief Researcher (Doct. Chem.) 212 НТК 330-73-87 4-40 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Kirilyuk Igor Anatolievich Leading Researcher (Cand. Chem) 207 330-73-87 2-74 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Glazachev Yurii Ivanovich Senior Researcher (Cand. Phys. Math.)
5 Mazhukin Dmitry Gennadievich Senior Researcher (Cand. Chem.) 317 НТК, 335 330-68-52 2-56, 2-41 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Morozov Denis Aleksandrovich Senior Researcher (Cand. Chem.) 208 330-73-87 4-11 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Polienko Yulia Fedorovna Senior Researcher (Cand. Chem.) 206 330-73-87 4-12 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Taratayko Andrey Igorevich Senior Researcher (Cand. Chem.) 231 330-73-87 4-10 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Dobrynin Sergey Aleksandrovich Researcher (Cand. Chem.) 207 330-73-87 2-74 This email address is being protected from spambots. You need JavaScript enabled to view it.
10 Zhurko Irina Fridrikhovna Researcher (Cand. Chem.) 207 330-73-87 2-74 This email address is being protected from spambots. You need JavaScript enabled to view it.
11 Trofimov Dmitry Gennadievich Researcher (Cand. Chem.) 231 330-73-87 4-10 This email address is being protected from spambots. You need JavaScript enabled to view it.
12 Shevelev Oleg Borisovich Junior Researcher
Students
13 Usatov Mikhail Sergeevich laboratory assistant 207 This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
14 Khoroshunova Yulia Vladislavovna Junior Researcher 208 330-73-87 4-11 This email address is being protected from spambots. You need JavaScript enabled to view it.
PUBLICATIONS
 

Publications over the past years

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2020
  1. T.V. Popova, O.A. Krumkacheva, A.S. Burmakova, A.S. Spitsyna, O.D. Zakharova, V.Al. Lisitskiy, I.A. Kirilyuk, V.N. Silnikov, M. Bowman, E. Bagryanskaya, T. Godovikova
    Protein modification by thiolactone homocysteine chemistry: a multifunctionalized human serum albumin theranostic
    RSC Med. Chem., 2020, Accepted Manuscript doi:10.1039/C9MD00516A
  2. N.E. Sannikova, O. Timofeev, A.S. Chubarov, N.Sh. Lebedeva, A.S. Semeikin, I.A. Kirilyuk, Yu.P. Tsentalovich, M.V. Fedin, E.G. Bagryanskaya, O.A. Krumkacheva
    Application of EPR to porphyrin-protein agents for photodynamic therapy
    Journal of Photochemistry and Photobiology B: Biology, 2020, V. 211, 112008 doi:10.1016/j.jphotobiol.2020.112008, IF=4.383
  3. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  4. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  5. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, N. Bannova
    P-3 Features of metabolic profiles of blood serum and erythrocyte membranes associated with metastasis in colorectal cancer
    Annals of Oncology, 2020, V. 31, Suppl.3, Pp S89-S90 doi:10.1016/j.annonc.2020.04.085
  6. 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
  7. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  8. E.N. Golubeva, N.A. Chumakova, S.V. Kuzin, I.A. Grigoriev, T. Kalai, A.A. Korotkevich, S.E. Bogorodsky, L.I. Krotova, V.K. Popov, V.V. Lunin
    Paramagnetic bioactives encapsulated in poly(D,L-lactide) microparticules: Spatial distribution and in vitro release kinetics
    The Journal of Supercritical Fluids, 2020, V. 158, Art. Number 104748 doi:10.1016/j.supflu.2019.104748, IF=3.744
  9. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  10. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267

2019
  1. 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
  2. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
  3. V.I. Borovkov, A.I. Taratayko, Yu.N. Molin
    Radiation-Induced Fluorescence from Doped Polyolefins on a Nanosecond Timescale: Kinetics of the Processes Involving Geminate Radical Ions
    The Journal of Physical Chemistry B, Just Accepted ( June 17, 2019) doi:10.1021/acs.jpcb.9b03914, IF=2.923
  4. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
    Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
  5. 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
  6. E.V. Parkhomchuk, E.A. Prokopyeva, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, P.N. Kalinkin, S.A. Rastigeev, D.V. Kuleshov, K.A. Sashkina, V.V. Parkhomchuk
    Ultrafine organic aerosol particles inhaled by mice at low doses remain in lungs more than half an year
    Journal of Labelled Compounds & Radiopharmaceuticals, 2019, V. 62, N 11, Pp 785-793, SI doi:10.1002/jlcr.378810.1002/jlcr.3788, IF=1.291
  7. Yu.V. Khoroshunova, D.A. Morozov, A.I. Taratayko, P.D. Gladkikh, Yu.I. Glazachev, I.A. Kirilyuk
    Synthesis of 1-azaspiro[4.4]nonan-1-oxyls via intramolecular 1,3-dipolar cycloaddition
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2036-2042 doi:10.3762/bjoc.15.200, IF=2.595
  8. T. Yokoyama, A. Taguchi, H. Kubota, N.J. Stewart, Sh. Matsumoto, I.A. Kirilyuk, H. Hirata
    Simultaneous T2* mapping of 14N- and 15N-labeled dicarboxy-PROXYLs using CW-EPR-based single-point imaging
    Journal of Magnetic Resonance, 2019, V. 305, Pp 122-130 doi:10.1016/j.jmr.2019.06.012, IF=2.689
  9. E. Zaytseva, I. Timofeev, O. Krumkacheva, D. Parkhomenko, D. Mazhukin, K. Sato, H. Matsuoka, T. Takui, E. Bagryanskaya
    EPR and DEER Characterization of New Mixed Weakly Coupled Nitroxide Triradicals for Molecular Three-Spin Qubits
    Applied Magnetic Resonance, 2019, V. 50, N 8, pp 967-976 doi:10.1007/s00723-019-01125-9, IF=0.78
  10. M. Edeleva, D. Morozov, D. Parkhomenko, Yu. Polienko, A. Iurchenkova, I. Kirilyuk, E. Bagryanskaya
    Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization
    Chem. Commun., 2019,V. 55, N 2, Pp 190-193 doi:10.1039/C8CC08541B, IF=6.164

2018
  1. 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
  2. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
  3. Yu. Takemoto, E. Zaytseva, K. Suzuki, N. Yoshioka, Y. Takanishi, M. Funahashi, Y. Uchida, T. Akita, Ja. Park, Sh. Sato, S. Clevers, G. Coquerel, D.G. Mazhukin, S. Shimono, M. Sugiyama, H. Takahashi, J. Yamauchi, R. Tamura
    Unique Superparamagnetic-like Behavior Observed in Non-π-delocalized Nitroxide Diradical Compounds Showing Discotic Liquid Crystalline Phase
    Chemistry - A European Journal, 2018, V. 24, N 65, Pp 17293-17302 doi:10.1002/chem.201803534, IF=5.16
  4. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  5. A.I. Taratayko, T.V. Rybalova, V.A. Reznikov
    Synthesis of paramagnetic spiropyran derivatives
    Chemistry of Heterocyclic Compounds, 2018, V. 54, N 10, pp 981-983 doi:10.1007/s10593-018-2375-y, IF=1.2
  6. 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
  7. S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
    Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
    J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
  8. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  9. E.V. Zaytseva, Yu.V. Gatilov, D.G. Mazhukin
    The synthesis of new functionalized 1,3,5-triazine-based stable bi- and trinitroxides of the 2,5-dihydroimidazole series
    Arkivoc, 2018, part v, 359-374 doi:10.24820/ark.5550190.p010.614, IF=1.048
  10. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
  11. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  12. 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
  13. I.Y. Zhuravleva, N.R. Nichay, Yu.Y. Kulyabin, T.P. Timchenko, A.A. Korobeinikov, Yu.F. Polienko, S.S. Shatskaya, E.V. Kuznetsova, A.V. Voitov, A.V. Bogachev-Prokophiev, A.M. Karaskov
    In search of the best xenogeneic material for a paediatric conduit: an experimental study
    Interactive CardioVascular and Thoracic Surgery, 2018, V. 26, N 5, Pp 738-744 doi:10.1093/icvts/ivx445, IF=1.756
  14. 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
  15. 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
  16. M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
    Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
    Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
  17. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
  18. V.N. Verkhovlyuk, V.I. Borovkov, V.A. Bagryansky, S.B. Zikirin, A.I. Taratayko, O.A. Anisimov, Yu.N. Molin
    Hyperfine Structure in the OD ESR Spectra of Recombining Charge Pairs in Doped Polyethylene Matrices
    Applied Magnetic Resonance, 2018, V. 49, N 4, pp 345-355 doi:10.1007/s00723-018-0978-1, IF=0.835
  19. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767
  20. Т.С. Фролова, С.Ж. Шарапов, О.И. Синицина, Т.Г. Толстикова, И.А. Григорьев, С.В. Морозов, Ю.В. Юшкова
    Новые ионные конъюгаты на основе a-токоферилсукцината как потенциальные цитотоксические агенты1
    Биоорганическая химия. 2018. Т. 44. № 3. С. 325-332. doi:10.7868/S0132342318030089, IF=0.838
  21. S.I. Dikalov, A.E. Dikalova, D.A. Morozov, I.A. Kirilyuk
    Cellular accumulation and antioxidant activity of acetoxymethoxycarbonyl pyrrolidine nitroxides
    Free Radical Research, 2018, V. 52, N 3: International Conference on Electron Paramagnetic Resonance Spectroscopy and Imaging of Biological Systems (EPR-2017), Pp 339-350 doi:10.1080/10715762.2017.1390744, IF=3.038
  22. Yu.V. Yushkova, E.I. Chernyak, Yu.V. Gatilov, V.G. Vasil'ev, S.V. Morozov, I.A. Grigor'ev
    Synthesis, Structure, Antioxidant Activity, and Water Solubility of Trolox Ion Conjugates
    Saudi Pharmaceutical Journal, 2018, V. 26, N 1, Pp 84-92 doi:10.1016/j.jsps.2017.10.008, IF=3.11

2017
  1. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigor'ev
    Synthesis of Conjugates of Ursolic Acid 3-O-Succinate with NO-H2S Donors
    Chemistry of Natural Compounds, с. 1-3, Article in Press doi: 10.1007/s10600-017-2061-9, IF=0.46
  2. И.Ю. Журавлева, М.Б. Васильева, Т.П. Тимченко, Е.В. Кузнецова, Ю.Ф. Полиенко, И.Р. Ничай, И.А. Григорьев, А.В. Богачев-Прокофьев
    Кальцификация эластин-содержащих ксеногенных биоматериалов: влияние консервантов и бисфосфонатов
    Сибирский научный медицинский журнал, 2017, N. 37, № 6, Стр. 28-37 (http://sibmed.net/article.php?lang=rus&id_article=562)
  3. L.Bales. Barney, M.M. Bakirov, R.T. Galeev, I.A. Kirilyuk, A.I. Kokorin, K.M. Salikhov
    The Current State of Measuring Bimolecular Spin Exchange Rates by the EPR Spectral Manifestations of the Exchange and Dipole–Dipole Interactions in Dilute Solutions of Nitroxide Free Radicals with Proton Hyperfine Structure
    Applied Magnetic Resonance, 2017, V. 48, N 11-12, pp 1399-1445 doi:10.1007/s00723-017-0958-x, IF=0.864
  4. Yu.V. Yushkova, S.V. Morozov, E.I. Chernyak, I.A. Grigor'ev
    Covalent and Ionic Conjugates of Trolox and α-Tocopherol with 1-Aminoadamantane
    Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1059-1065 doi:10.1007/s10600-017-2201-2, IF=0.46
  5. N.V. Mamontova, E.I. Chernyak, E.V. Amosov, Yu.V. Gatilov, V.I. Vinogradova, S.F. Aripova, S.V. Morozov, I.A. Grigor'ev
    First Ionic Conjugates of Dihydroquercetin Monosuccinate with Amines
    Chemistry of Natural Compounds, 2017, V. 53, N 6, pp 1045-1051 doi:10.1007/s10600-017-2198-6, IF=0.46
  6. Yu.V. Yushkova, S.V. Morozov, E.I. Chernyak, N.A. Grigor'ev
    Synthesis of New Trolox-Based Antioxidants Containing Amino-bis-Phosphonic Acids
    Chemistry of Natural Compounds,2017, V. 53, N 4, pp 764-766 doi:10.1007/s10600-017-2115-z, IF=0.46
  7. H. Kubota, D.A. Komarov, H. Yasui, S. Matsumoto, O. Inanami, I.A. Kirilyuk, V.V. Khramtsov, H. Hirata
    Feasibility of in vivo three-dimensional T2* mapping using dicarboxy-PROXYL and CW-EPR-based single-point imaging
    Magnetic Resonance Materials in Physics, Biology and Medicine, 2017, V. 30, N 3, pp 291-298 doi:10.1007/s10334-016-0606-8, IF=1.718
  8. E.G. Kovaleva, L.S. Molochnikov, D.P. Stepanova, A.V. Pestov, D.G. Trofimov, I.A. Kirilyuk, A.I. Smirnov
    Interfacial Electrostatic Properties of Hydrated Mesoporous and Nanostructured Alumina Powders by Spin Labeling EPR
    Cell Biochemistry and Biophysics, 2017, V. 75, N 2, pp 159-170 doi:10.1007/s12013-016-0767-0, IF=1.32
  9. M.A. Voinov, C.T. Scheid, I.A. Kirilyuk, D.G. Trofimov, A.I. Smirnov
    IKMTSL-PTE, a Phospholipid-Based EPR Probe for Surface Electrostatic Potential of Biological Interfaces at Neutral pH: Effects of Temperature and Effective Dielectric Constant of the Solvent
    Journal of Physical Chemistry B, 2017, V. 121, N 11, Pp 2443-2453 doi:10.1021/acs.jpcb.7b00592, IF=3.177
  10. V.V. Annenkov, E.N. Danilovtseva, S.S. Khutsishvili, V.A. Pal'shin, Yu.F. Polienko, V.V. Saraev, T.I. Vakul'skaya, S.N. Zelinskiy, I.A. Grigor'ev
    Polyamine-based spin probes for the study of siliceous structures
    Microporous and Mesoporous Materials, 2017, V. 242, Pages 74-81 doi:10.1016/j.micromeso.2017.01.010, IF=3.615
  11. A.G. Matveeva, Yu.V. Yushkova, S.V. Morozov, I.A. Grygor'ev, S.A. Dzuba
    Multi-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency DomainMulti-Gaussian Monte Carlo Analysis of PELDOR Data in the Frequency Domain
    Zeitschrift fur Physikalische Chemie, 2017б V. 231, N 3, Pp 671-688 doi:10.1515/zpch-2016-0830, IF=1.327
  12. A.I. Kokorin, B.Y. Mladenova-Kattnig, I.A. Grigor'ev, G. Grampp
    Unexpected Features of the Intramolecular Spin Exchange in Imidazoline Nitroxide Biradicals Dissolved in Ionic Liquids
    Applied Magnetic Resonance, 2017, V. 48, N 3, Pp 287-296 doi:10.1007/s00723-016-0858-5, IF=0.864
  13. Organic Hydrogen Sulfide Donor Compounds with Cardioprotective Properties (Review)/ N. I. Tkacheva, S. V. Morozov, B. B. Lomivorotov, I. A. Grigor'ev// Pharmaceutical Chemistry Journal, 2017, V. 51, N 3, pp 165-174 doi:10.1007/s11094-017-1576-5, IF=0.444
  14. V. Borovkov, A. Taratayko, A. Bessmertnykh, V. Bagryansky, Yu. Molin
    Solvent Radical Anions in Irradiated Aliphatic Ketones and Esters as Observed Using Time-Resolved Magnetic Field Effects in the Recombination Fluorescence
    Zeitschrift fur Physikalische Chemie, 2017,V. 231, N 2, Pp. 311-323 doi:10.1515/zpch-2016-0818, IF=1.327
  15. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, И.А. Григорьев, Н.И. Ткачева, В.И. Родионов
    Оценка эффективности действия нового местного гемостатического ванкомицин-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сиб. мед. журнал.-2017. - Т. 32, № 1. - С. 108-111.
  16. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  17. А.М. Чернявский, И.А. Григорьев, С.В. Морозов, А.Р. Таркова
    Первый российский комплексный гемостатик
    Наука из первых рук. 2017. Т. 73. № 1. С. 84-89.

2016
  1. А.Р. Таркова, С.В. Морозов, Н.И. Ткачева, В.И. Родионов, И.А. Григорьев, А.М. Чернявский
    Оценка гемостатических свойств нового местного антибиотик-содержащего средства на основе окисленной целлюлозы в эксперименте
    Сибирский научный медицинский журнал, 2016, т.36, № 6, 12-17
  2. Yu.V. Yushkova, S.V. Morozov, Chernyak, I.A. Grigor'ev
    Synthesis of Ionic Biologically Active Conjugates from Trolox and α-Tocopherol Succinates
    Chemistry of Natural Compounds, 2016, V. 52, N 6, pp 1015-1019 doi:10.1007/s10600-016-1850-x, IF=0.472
  3. O.D. Zakharova, T.S. Frolova, Yu.V. Yushkova, E.I. Chernyak, A.G. Pokrovsky, M.A. Pokrovsky, S.V. Morozov, O.I. Sinitsina, I.A. Grigor'ev, G.A. Nevinsky
    Antioxidant and antitumor activity of trolox, trolox succinate, an α-tocopheryl succinate conjugates with nitroxides
    European Journal of Medicinal Chemistry, 2016, V. 122, Pages 127-137 doi:10.1016/j.ejmech.2016.05.051, IF=3.901
  4. 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
  5. E.V. Parkhomchuk, D.G. Gulevich, A.I. Taratayko, A.M. Baklanov, A.V. Selivanova, T.A. Trubitsyna, I.V. Voronova, P.N. Kalinkin, A.G. Okunev, S.A. Rastigeev, V.A. Reznikov, V.S. Semeykina, K.A. Sashkina, V.V. Parkhomchuk
    Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry
    Chemosphere, V. 159, September 2016, Pp 80-88 doi:10.1016/j.chemosphere.2016.05.078, IF=3.697
  6. А.Р. Таркова, А.М. Чернявский, С.В. Морозов, Н.И. Ткачева, И.А. Григорьев, В.И. Родионов
    Экспериментальная оценка гемостатической активности нового антибиотик-содержащего средства местного действия на основе окисленной целлюлозы
    Современная медицина: актуальные вопросы. 2016. № 8 (50). С. 19-26.
  7. A.A. Gorodetsky, I.A. Kirilyuk, V.V. Khramtsov, D.A. Komarov
    Functional electron paramagnetic resonance imaging of ischemic rat heart: Monitoring of tissue oxygenation and pH
    Magnetic Resonance in Medicine, 2016,V. 76, N 1, Pp 350-358 doi:10.1002/mrm.25867, IF=3.782
  8. Yu.F. Polienko, O.A. Snytnikova, V.V. Yanshole, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev, Yu.P. Tsentalovich
    Effect of the spacer length and nitroxide sterical shielding upon photostability of spin-labeled kynurenines
    Journal of Photochemistry and Photobiology A: Chemistry, V.322-323, 15 May-1 June 2016, Pp 76-84 doi:10.1016/j.jphotochem.2016.03.007, IF=2.476
  9. А.М. Чернявский, А.Р. Таркова, Т.М. Рузматов, С.В. Морозов, И.А. Григорьев
    Инфекции в кардиохирургии
    Хирургия. Журнал им. Н.И. Пирогова. 2016. № 5. С. 64-68.
  10. A.A. Kuzhelev, R.K. Strizhakov, O.A. Krumkacheva, Y.F. Polienko, D.A. Morozov, G.Yu. Shevelev, D.V. Pyshnyi, I.A. Kirilyuk, M.V. Fedin, E.G. Bagryanskaya
    Room-Temperature Electron Spin Relaxation of Nitroxides Immobilized in Trehalose: Effect of Substituents Adjacent to NO-group
    Journal of Magnetic Resonance, V. 266, May 2016, Pages 1-7 doi:10.1016/j.jmr.2016.02.014, IF=2.888
  11. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigor'ev
    Synthesis of Ursolic Acid Conjugates Containing a Furoxan Moiety
    Chemistry of Natural Compounds, 2016, V. 52, N 3, pp 555-557 doi:10.1007/s10600-016-1708-2, IF=0.472
  12. 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
  13. S.A. Popov, L.M. Kornaukhova, A.V. Shpatov, I.A. Grigorev
    Synthesis of Conjugate Esters of 5-(4-Hydroxyphenyl)-3H-1,2-Dithiole-3-Thione and Ursolic Acid 3-O-ACYL Derivatives
    Chemistry of Natural Compounds, 2016, V. 52, N 1, pp 183-185 doi:10.1007/s10600-016-1588-5, IF=0.472

2015
  1. I. A. Kirilyuk, A. A. Bobko, S. V. Semenov, D. A. Komarov, I. G. Irtegova, I. A. Grigor'ev, E. G. Bagryanskaya
    The effect of sterical shielding on the redox properties of imidazoline and imidazolidine nitroxides
    J. Org. Chem., 2015, 80 (18), pp 9118-9125 doi:10.1021/acs.joc.5b01494, IF=4.721
  2. 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
  3. Efficacy of different forms of local hemostatic materials based on oxidize cellulose in the experiment/ A.R. Tarkova, A.M. Chernyavskiy, I.A. Grigor'ev, S.V. Morozov, V.I. Rodionov, N.I. Kravchenko// Вестник хирургии им. И.И. Грекова, 2015, Т. 174. № 6. С. 56-59.(in Russian)
  4. Yu.V. Yushkova, E.I. Chernyak, S.V. Morozov, I.A. Grigor'ev
    Antioxidants Based on Covalently and Ionically Bound Trolox Conjugates
    Chemistry of Natural Compounds, November 2015, V. 51, N 6, pp 1070-1073 doi:10.1007/s10600-015-1494-2, IF=0.509
  5. K.S. Taletskiy, V.I. Borovkov, L.N. Schegoleva, I.V. Beregovaya, A.I. Taratayko, Y.N. Molin
    Radical Cationic Pathway for the Decay of Ionized Glyme Molecules in Liquid Solution
    Journal of Physical Chemistry B, 2015, V. 119, N 45, Pages 14472-14478 doi:10.1021/acs.jpcb.5b06086, IF=3.302
  6. А.Р. Таркова, А.М. Чернявский, И.А. Григорьев, С.В. Морозов, В.И. Родионов
    Исследование местных гемостатических средств с целью профилактики осложнений срединной стернотомии в эксперименте
    В сборнике: Современные аспекты диагностики и лечения в кардиохирургии Материалы научно-практической конференции с международным участием. 2015. С. 78-80.
  7. Studies of Carbomer Gels Using Rotational Viscometry and Spin Probes/ A. N. Lyapunov, E. P. Bezuglaya, N. A. Lyapunov, I. A. Kirilyuk// Pharmaceutical Chemistry Journal, 2015, V. 49, N 9, pp 639-644 doi:10.1007/s11094-015-1344-3, IF=0.451
  8. C. Becker, N. Chukanov, I. Grigor’ev
    New amino-bisphosphonate building blocks in the synthesis of bisphosphonic derivatives based on lead compounds
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2015, V. 190, N 7, 1201-1212. 10.1080/10426507.2014.979989 doi:10.1080/10426507.2014.979989, IF=0.561
  9. T.S. Frolova, O.D. Zakharova, Y.F. Polienko, Y.V. Yushkova, E.I. Chernyak, S.V. Morozov, O.I. Sinitsina, I.A. Grigor’ev, G.A. Nevinsky
    Conjugates of trolox and alpha-tocopheryl succinate with nitroxides: Synthesis, antioxidant and antitumor activity
    International Journal of Medicine and Pharmaceutical Sciences. 2015. Vol. 5. No. 3. P. 9-24.
  10. A.E. Dikalova, I.A. Kirilyuk, S.I. Dikalov
    Antihypertensive effect of mitochondria-targeted proxyl nitroxides
    Redox Biology, V. 4, 2015, Pp 355-362 doi:10.1016/j.redox.2014.12.012
  11. Local hemostatic agent based on oxidized cellulose/ A.R. Tarkova, A.M. Chernyavskiy, S.V. Morozov, I.A. Grigor’ev, N.I. Tkacheva, V.I. Rodionov// The Siberian Scientific Medical Journal, 2015, V. 35, № 2, Pp 11-15
  12. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigoriev
    Electrical potential near hydrated surface of ordered mesoporous molecular sieves assessed by EPR of molecular pH-probes
    Microporous and Mesoporous Materials, Volume 203, February 2015, Pages 1-7 doi:10.1016/j.micromeso.2014.10.010, IF=3.453
  13. About the mechanism of membrane permeability enhancement by substances in their intermolecular complexes with polysaccharide arabinogalactan from larches Larix sibirica and Larix gmelinii/ A. V. Dushkin, Yu. S. Chistyachenko, D. A. Komarov, M. V. Khvostov, T. G. Tolstikova, I. F. Zhurko, I. A. Kirilyuk, I. A. Grigor’ev, N. Z. Lyakhov// Doklady Biochemistry and Biophysics, January 2015, Volume 460, Issue 1, pp 9-12 doi:10.1134/S1607672915010020, IF=0.343
  14. S.A. Popov, A.V. Shpatov, I.A. Grigor’ev
    Synthesis of Substituted Esters of Ursolic, Betulonic, and Betulinic Acids Containing the Nitroxyl Radical 4-Amino-2,2,6,6-Tetramethylpiperidine-1-Oxyl
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 87-90 doi:10.1007/s10600-015-1209-8, IF=0.509
  15. Sh.N. Zhurakulov, V.A. Babkin, E.I. Chernyak, S.V. Morozov, I.A. Grigor’ev, M.G. Levkovich, V.I. Vinogradova
    Aminomethylation of 1-Aryl-6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinolines by Dihydroquercetin
    Chemistry of Natural Compounds, January 2015, V. 51, N 1, pp 57-61 doi:10.1007/s10600-015-1203-1, IF=0.509

2014
  1. X-ray emission and X-ray photoelectron study of the electronic structure of paramagnetic and diamagnetic derivatives of 3-imidazoline/ L. N. Mazalov, A. D. Fedorenko, N. A. Kryuchkova, Yu. P. Dikov, Yu. F. Polienko, I. A. Grigor'ev// Journal of Structural Chemistry, November 2014, Volume 55, Issue 6, pp 1044-1056 doi:10.1134/S0022476614060079, IF=0.5
  2. Первые спин-меченые сукцинильные производные α-токоферола и тролокса/ Ю.В. Юшкова, Е.И. Черняк, С.В. Морозов, И.А. Григорьев// Химия природных соединений. 2014, № 5, С. 718-722 doi:10.1007/s10600-014-1093-7, IF=0.5
  3. E.V. Zaytseva, A.V. Shernyukov, A.M. Genaev, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
    New spirocyclic nitroxides of 2,5-dihydroimidazole series flanked by two mesogenic fragments
    ARKIVOC, 2014, (vi) 10-24. http://www.arkat-usa.org/get-file/51547/ doi:10.3998/ark.5550190.p008.808, IF=1.75
  4. L.A. Shundrin, I.A. Kirilyuk, I.A. Grigor'ev
    3-Carboxy-2,2,5,5-tetra(2H3)methyl-[4-2H(1H)]-3-pyrroline-(1-15N)-1-oxyl as a spin probe for in vivo L-band electron paramagnetic resonance imaging
    Mendeleev Communications, V. 24, N 5, September–October 2014, Pp 298-300. doi:10.1016/j.mencom.2014.09.017, IF=1.154
  5. Local hemostasis control by using of oxidized cellulose drugs/ A.M. Cherniavskii, I.A. Grigor'ev, S.V. Morozov, A.R. Tarkova, N.I. Tkacheva// Хирургия. Журнал им. Н.И. Пирогова. 2014. № 8. С. 71-75
  6. I.A. Grigor'ev, N.I. Tkacheva, S.V. Morozov
    Conjugates of Natural Compounds with Nitroxyl Radicals as a Basis for Creation of Pharmacological Agents of New Generation
    Current Medicinal Chemistry, 2014, 21(24), pp 2839-2852. doi:10.2174/0929867321666140304153104, IF=3.714
  7. Синтез диастереомерных спироциклических нитроксильных радикалов ряда 3-имидазолина с двумя мезогенными группами/ Е.В.Зайцева, А.В.Шернюков, С.А.Амитина, Р.Тамура, И.А.Григорьев// Хим.Гетероцикл.Соедин., 2014, N 8, 1207-1220. doi:10.1007/s10593-014-1571-7, IF=0.698
  8. Синтез первых конъюгатов флавоноида дигидрокверцетина в алкалоидом цитизином/ Н.В. Кошелева, Е.И. Черняк, С.В. Морозов, В.И. Виноградова, Ш.Ш. Сагдуллаев, Н.Д. Абдуллаев, И.А. Григорьев// Химия природных соединений, 2014, № 3, С.383-385 doi:10.1007/s10600-014-0982-0, IF=0.5
  9. Synthesis and study of antitumor activity of tetraethyl 2-(2',2',6',6'-Tetramethylpiperidin-4'-ylamino)ethylidene-1,1-bisphosphonate/ I. A. Grigor’ev, D. A. Morozov, V. A. Svyatchenko, N. N. Kiselev, V. B. Loktev, E. A. Luk’yanets, G. N. Vorozhtsov// Doklady Chemistry, July 2014, V. 457, N 1, pp 137-140. doi:10.1134/S0012500814070064, IF=0.351
  10. Effect of the surface charge on the complexing and catalytic properties of Сu2+-containing composite materials based on zirconia and powdered cellulose/ E. G. Kovaleva, L. S. Molochnikov, E. V. Parshina, A. B. Shishmakov, Yu. V. Mikushina, I. A. Kirilyuk, I. A. Grigor’ev// Russian Journal of Physical Chemistry B, 2014, V. 8, N 3, pp 317-325. doi:10.1134/S199079311403021X, IF=0.335
  11. E.S. Babaylova, A.V. Ivanov, A.A. Malygin, M.A. Vorobjeva, A.G. Venyaminova, Yu.F. Polienko, I.A. Kirilyuk, O.A. Krumkacheva, M.V. Fedin, G.G. Karpov, E.G. Bagryanskaya
    A versatile approach for site-directed spin labeling and structural EPR studies of RNAs
    Org. Biomol. Chem., 2014, 12(19), 3129-3136. doi:10.1039/C3OB42154F, IF=3.486
  12. Использование реакции Манниха для синтеза спин-меченых производных природного флаваноида дигидрокверцетина/ Н.В. Кошелева, Е.И. Черняк, Ю.Ф. Полиенко, С.В. Морозов, И.А. Григорьев// Химия природных соединений, 2014, № 2, С. 231-235 doi:10.1007/s10600-014-0927-7, IF=0.5
  13. M.V. Edeleva, D.A. Parkhomenko, D.A. Morozov, S.A. Dobrynin, D.G. Trofimov, B. Kanagatov, I.A. Kirilyuk, E.G. Bagryanskaya
    Controlled/living polymerization of methyl methacrylate using new sterically hindered imidazoline nitroxides prepared via intramolecular 1,3-dipolar cycloaddition reaction
    Journal of Polymer Science Part A: Polymer Chemistry, 2014, V. 52, N 7, pp 929-943. doi:10.1002/pola.27071, IF=3.244
  14. 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
  15. Spirocyclic 2,5-dihydro-1H-imidazole 1-oxyl radicals with a mesogenic substituent on C4. Synthesis and crystal structure/ E. V. Zaytseva, Yu. V. Gatilov, S. A. Amitina, R. Tamura, I. A. Grigor’ev, D. G. Mazhukin// Russian Journal of Organic Chemistry, 2014, V. 50, N 1, pp 72-77. doi:10.1134/S107042801401014X, IF=0.675

2013
  1. Hepatoprotective Activity of Betulonic Acid Amides Containing Piperidine or Pyrrolidine Nitroxide Moieties/ I. V. Sorokina, D. S. Baev, N. A. Zhukova, T. G. Tolstikova, A. N. Antimonova, N. I. Petrenko, E. E. Shults, and I. A. Grigor’ev// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 6, pp. 668–670. doi:10.1134/S1068162013060083, IF=0.523
  2. A. I. Taratayko, C.S. Becker,.I. A. Grigor’ev,Y. V. Gatilov, T. V. Rybalova, V. A. Reznikov
    Synthesis of 3,4-dihydro-2H-pyrrole 1-oxide based aldonitrones as potential spin trapping agents
    Arkivoc 2013, (iv), 272-290.full text doi:10.3998/ark.5550190.p008.159, IF=1.57
  3. E.G. Kovaleva, L.S. Molochnikov, E.L. Golovkina, M. Hartmann, I.A. Kirilyuk, I.A. Grigor'ev
    Dynamics of pH-sensitive nitroxide radicals in water adsorbed in ordered mesoporous molecular sieves by EPR Spectroscopy
    Microporous and Mesoporous Materials, 2013, V. 179, P. 258-264. doi:10.1016/j.micromeso.2013.05.019, IF=3.365
  4. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bis-Phosphonic Acid Derivative of Trolox, a New Potential Antioxidant
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 785-786. doi:10.1007/s10600-013-0746-2, IF=0.598
  5. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, V.A. Svyatchenko, N.N. Kiselev, V.B. Loktev, I.A. Grigor’ev
    First bis-Phosphonic Acid Derivatives of the Plant Alkaloid Cytisine
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 781-782. doi:10.1007/s10600-013-0744-4, IF=0.598
  6. 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
  7. Modification of Cellulose as a Promising Direction in the Design of New Materials/ N. I. Tkacheva, S. V. Morozov, I. A. Grigor’ev, D. M. Mognonov, N. A. Kolchanov// Polymer Science Series B, 2013, V. 55, N 7-8, pp 409-429. doi:10.1134/S1560090413070063, IF=0.439
  8. K.S. Bekker, N.V. Chukanov, S.A. Popov, I.A. Grigor'ev
    Conjugates of Bisphosphonates with Derivatives of Ursolic, Betulonic, and Betulinic Acids
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 581-582. doi:10.1007/s10600-013-0680-3, IF=0.598
  9. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bisphosphonate derivative of folic acid
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 495-495. doi:10.1007/s10600-013-0646-5, IF=0.598
  10. Yu.F. Polienko, V.I. Vinogradova, Sh.Sh. Sagdullaev, N.D. Abdullaev, Yu.V. Gatilov, I.A. Grigor'ev
    First spin-labeled cytisine derivatives
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 311-315. doi:10.1007/s10600-013-0588-y, IF=0.598
  11. Yu.V. Yushkova, E.I. Chernyak, Yu.F. Polienko, Yu.V. Gatilov, S.V. Morozov, I.A. Grigor’ev
    Synthesis of spin-labeled amides of 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox)
    Chemistry of Natural Compounds, 2013, V. 49, N 2, P. 253-257. doi:10.1007/s10600-013-0574-4, IF=0.598
  12. Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals/ A. N. Antimonova, N. I. Petrenko, E. E. Shults, Yu. F. Polienko, M. M. Shakirov, I. G. Irtegova, M. A. Pokrovskii, K. M. Sherman, I. A. Grigor’ev, A. G. Pokrovskii, G. A. Tolstikov// Russian Journal of Bioorganic Chemistry, 2013, V. 39, N 2, pp 181-185 doi:10.1134/S1068162013020027, IF=0.523

2012
  1. D.A. Morozov, I.A. Kirilyuk, D.A. Komarov, A. Goti, I.Yu. Bagryanskaya, N.V. Kuratieva, I.A. Grigor’ev
    Synthesis of a Chiral C2-Symmetric Sterically Hindered Pyrrolidine Nitroxide Radical via Combined Iterative Nucleophilic Additions and Intramolecular 1,3-Dipolar Cycloadditions to Cyclic Nitrones
    J. Org. Chem., 2012, V. 77, N 23, 10688-10698. doi:10.1021/jo3019158, IF=4.449
  2. I.A. Khalfina, N.V. Vasilieva, I.G. Irtegova, V.A. Reznikov, L.A. Shundrin
    Reaction of 3,3'-bis(2-phenyl-5,5-dimethyl-4-oxopyrrolinylidene) 1,1'-dioxide with methoxide anion
    Mendeleev Commun., 2012, V. 22, N 6, 327-329. doi:10.1016/j.mencom.2012.11.017, IF=0.901
  3. I.A. Kirilyuk, Yu.F. Polienko, O.A. Krumkacheva, R.K. Strizhakov, Yu.V. Gatilov, I.A. Grigor’ev, E.G. Bagryanskaya
    Synthesis of 2,5-Bis(spirocyclohexane)-Substituted Nitroxides of Pyrroline and Pyrrolidine Series, Including Thiol-Specific Spin Label: An Analogue of MTSSL with Long Relaxation Time
    J. Org. Chem., 2012, V. 77, N 18, 8016–8027. doi:10.1021/jo301235j, IF=4.449
  4. D.A. Komarov, I. Dhimitruka, I.A. Kirilyuk, D.G. Trofimiov, I.A. Grigor’ev, J.L. Zweier, V.V. Khramtsov
    Electron Paramagnetic Resonance Monitoring of Ischemia-Induced Myocardial Oxygen Depletion and Acidosis in Isolated Rat Hearts Using Soluble Paramagnetic Probes
    Magn. Reson. Med., 2012, V. 68, N 2, 649–655. doi:10.1002/mrm.23251, IF=2.963
  5. A.A. Bobko, T.D. Eubank, J.L. Voorhees, O.V. Efimova, I.A. Kirilyuk, S. Petryakov, D.G. Trofimiov, C.B. Marsh, J.L. Zweier, I.A. Grigor’ev, A. Samouilov, V.V. Khramtsov
    In Vivo Monitoring of pH, Redox Status, and Glutathione Using L-Band EPR for Assessment of Therapeutic Effectiveness in Solid Tumors
    Magn. Reson. Med., 2012, V. 67, N 6, 1827-1836. doi:10.1002/mrm.23196, IF=3.266
  6. Defensive effect of tempol in alopecia caused by cyclophosphamide in mice/ N.A. Popova, V.P. Nikolin, V.I. Kaledin, I.A. Kirilyuk, I.A. Grigoryev//
  7. V.I. Borovkov, I.S. Ivanishko, V.A. Reznikov, I.V. Beregovaya
    Turning on the triplet state channel in the excess electron scavenging by nitroxyl radicals in liquid alkanes
    Chem. Phys. Lett., 2012, V. 531, 86-89. doi:10.1016/j.cplett.2012.02.011, IF=2.336
  8. И.А. Кирилюк, В.А. Святченко, Д.А. Морозов, Е.И. Казачинская, Н.Н. Киселёв, С.М. Бакунова, М.А. Войнов, В.Б. Локтев, И.А. Григорьев
    Цитотоксичность нитроксильных радикалов в отношении опухолевых и диплоидных клеток человека in vitro и оценка их противовирусной активности
    Антибиотики и химиотерапия, 2012, № 57 (1-2), 3-12.
  9. Enhanced immunogenic tumor rejection in mice when inhibiting activity of indoleamine 2,3-dioxygenase with ethyl pyruvate/ E.D. Vasilyeva, V.I. Kaledin, V.P. Nikolin, N.А. Popova, I.А. Kirilyuk, I.А. Grigoryev// Сибирский онкологический журнал, 2012, № 1, 41-44. (in russian).

2011
  1. A.V. Pivtsov, L.V. Kulik, N.V. Surovtsev, S.V. Adichtchev, I.A. Kirilyuk, I.A. Grigor’ev, M.V. Fedin, S.A. Dzuba
    Temperature Dependence of Hyperfine Interaction for 15N Nitroxide in a Glassy Matrix at 10–210 K
    Appl. Magn. Reson., 2011, V. 41, N 2-4, 411–429. doi:10.1007/s00723-011-0272-y, IF=1.126
  2. E.A. Mostovich, D.G. Mazhukin, T.V. Rybalova
    Reaction of vicinal aliphatic bis(hydroxylamines) with trifunctionalized methane derivatives
    ARKIVOC, 2011, (xi), 29-42. doi:10.3998/ark.5550190.0012.b03, IF=1.95
  3. Spin statistical factor in the reactions of excess electron scavenging by stable nitroxyl radicals/ V.I. Borovkov, A.G. Matveeva, I.S. Ivanishko, I.V. Beregovaya, V.A. Reznikov// DOKL PHYS CHEM, 2011, V.440, , N 1, pp. 174-177. doi:10.1134/S0012501611090065 Part: 1, IF=0.23
  4. M.V. Edeleva, I.A. Kirilyuk, I.F. Zhurko, D.A. Parkhomenko, Y.P. Tsentalovich, E.G. Bagryanskaya
    pH-Sensitive C_ON Bond Homolysis of Alkoxyamines of Imidazoline Series with Multiple Ionizable Groups As an Approach for Control of Nitroxide Mediated Polymerization
    J. Org. Chem., 2011, 76 (14), pp 5558–5573. doi:10.1021/jo200341m, IF=4.1
  5. Structure and characteristics of chitosan cobalt-containing hybrid systems, the catalysts of olefine oxidation/ A.V. Mekhaev, A.V. Pestov, M.G. Pervova, Y.G. Yaltuk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'Ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 7, pp 1155-1161. doi:10.1134/S0036024411070211, IF=0.503
  6. Investigation of the structure of chitosan hybrid systems by pH-sensitive nitroxyl radical/ A.V. Mekhaev, A.V. Pestov, Yu.G. Yatluk, L.S. Molochnikov, E.G. Kovaleva, I.A. Grigor'ev, I.A. Kirilyuk// RUSS J PHYS CHEM A+, 2011, V. 85, N 6, pp 987-992. doi:10.1134/S0036024411060239, IF=0.503
  7. Luminescent properties of new naphthylnitroxyl radicals/ A.G. Matveeva, E.M. Glebov, V.V. Korolev, I.P. Pozdnyakov, V.F. Plyusnin, D.V. Stass, V.A. Reznikov// HIGH ENERG CHEM+, 2011, V. 45, N 5, pp 416-422. doi:10.1134/S0018143911050134, IF=0.814
  8. M.A. Vershinin, A.B. Burdukov, I.V. Eltsov, V.A. Reznikov, E.G. Boguslavsky, Y.Z. Voloshin
    Unexpected radical substitution of the dichlorine-containing iron(II) clathrochelate with 1,4-dioxane derivatives: Novel approach to functionalization of its macrobicyclic framework
    Polyhedron, 2011, V. 30, N 7, 1233-1237. doi:10.1016/j.poly.2011.01.034, IF=2.32
  9. M. Kozuleva, I. Klenina, I. Proskuryakov, I. Kirilyuk, B. Ivanov
    Production of superoxide in chloroplast thylakoid membranes: ESR study with cyclic hydroxylamines of different lipophilicity
    FEBS Lett., 2011, V. 585, N 7, 1067-1071. doi:10.1016/j.febslet.2011.03.004, IF=3.601
  10. S.I. Dikalov, I.A. Kirilyuk, M.A. Voinov, I.A. Grigor’ev
    EPR detection of cellular and mitochondrial superoxide using cyclic hydroxylamines
    Free Rad. Res., 2011, V. 45, N 4, 417–430. doi:10.3109/10715762.2010.540242, IF=2.805
  11. Medium acidity and catalytic properties of composite materials based on silica and titania and powder cellulose in the presence of Cu2+ ions/ E.V. Parshina, L.S. Molochnikov, E.G. Kovaleva, A.B. Shishmakov, Yu.V. Mikushina, I.A. Kirilyuk, I.A. Grigor'ev// RUSS J PHYS CHEM A+, 2011, V. 85, N 3, pp. 452-456. doi:10.1134/S003602441103023X, IF=0.503
  12. The chemistry of 2,3-dihydroisoxazole derivatives/ N.V. Chukanov, V.A. Reznikov// RUSS CHEM B+, 2011, V. 60, N 3, pp. 379-399. doi:10.1007/s11172-011-0062-6, IF=0.629
  13. Y.P. Tsentalovich, V.V. Yanshole, Y.F. Polienko, S.V. Morozov, I.A. Grigor’ev
    Deactivation of Excited States of Kynurenine Covalently Linked to Nitroxides
    Photochem. Photobiol., 2011, V. 81, N 1, 22-31. doi:10.1111/j.1751-1097.2010.00841.x, IF=2.678
  14. β-Hydroxyalkylation of sterically hindered phenols with epoxides in acid medium/ A. P. Krysin, S. A. Amitina, T. G. Egorova, V. G. Vasiliev// RUSS J ORG CHEM+, 2011, V. 47, N 2, pp. 354-360. doi:10.1134/S1070363211020125, IF=0.393
  15. M.A. Vershinin, A.B. Burdukov, E.G. Boguslavskii, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, V.A. Reznikov, O.A. Varzatskii, Y.Z. Voloshin, Y.N. Bubnov
    The first monoribbed-functionalized tris-dioximate iron(II) clathrochelate with two inherent NH2-substituents, its reactivity, acid–base and coordination-chemical properties
    Inorg. Chim. Acta, 2011, V. 366, N 1, 91-97. doi:10.1016/j.ica.2010.10.012, IF=1.899

2010
  1. A.A. Bobko, I.A. Kirilyuk, N.P. Gritsan, D.N. Polovyanenko, I.A. Grigor’ev, V.V. Khramtsov, E.G. Bagryanskaya
    EPR and Quantum Chemical Studies of the pH-sensitive Imidazoline and Imidazolidine Nitroxides with Bulky Substituents
    Appl. Magn. Reson., 2010, V. 39, 437–451. doi:10.1007/s00723-010-0179-z, IF=0.819
  2. Nitroxyl Antioxidant TPPA-TEMPO Increases the Efficacy of Antitumor Therapy on the Model of Transplantable Mouse Tumor/ I.A. Kirilyuk, V.I. Kaledin, N.A. Popova, V.P. Nikolin, E.D. Vasil'eva, I.A. Grigor'ev, E.L. Lushnikova, L.M. Nepomnyashchikh// B EXP BIOL MED+, 2010, V. 150, N 1, pp 75-78. doi:10.1007/s10517-010-1073-2, IF=0.264
  3. Structure and magentic properties of novel chelate complexes of copper(II) and nickel(II) with nitroxide radical ethyl-2-(1-oxyl-2,2,5,5-tetramethylimidazolidin-4-yliden)-3-oxopropanoate/ A.B. Burdukov, K.S. Bekker, G.A. Stepanov, A.L. Bogatyrev, N.V. Pervukhina, A.S. Bogomyakov, V.A. Reznikov// J STRUCT CHEM+, 2010, V. 51, N 5, pp 916-922.. doi:10.1007/s10947-010-0139-3, IF=0.453
  4. Mechanism of the migration of the substituent in 1,2,3,7a-tetrahydroimidazo[1,2-b]isoxazole derivatives/ N.V. Chukanov, S.A. Popov, T.N. Drebushchak, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 9, pp 1817-1826. doi:10.1007/s11172-010-0318-6, IF=0.416
  5. Nitroxyl radicals of the imidazoline series as agents of pseudoliving polymerization of styrene/ E.V. Kolyakina, M.A. Lazarev, M.V. Pavlovskaya, I.A. Kirilyuk, I.F. Zhurko, I.A. Grigor'ev, D.F. Grishin// RUSS CHEM B+, 2010, V. 59, N 8, pp 1556-1564 doi:10.1007/s11172-010-0278-x, IF=0.416
  6. Role of the alkyl fragment of initiating alkoxyamine in nitroxide mediated polymerization of styrene/ D. P. Zubenko, I. A. Kirilyuk, S. Marque, I. P. Chuikov, E. G. Bagryanskaya// Polymer Science Series B, 2010, V. 52, N 5-6, pp 327-338. doi:10.1134/S156009041005009X, IF=0.289
  7. N.P. Isaev, L.V. Kulik, I.A. Kirilyuk, V.A. Reznikov, I.A. Grigor’ev, S.A. Dzuba
    Fast stochastic librations and slow small-angle rotations of molecules in glasses observed on nitroxide spin probes by stimulated electron spin echo spectroscopy
    J. Non-Cryst. Solids 2010, 356, 1037-1042. doi:10.1016/j.jnoncrysol.2010.01.018, IF=1.251
  8. Intra- and intermolecular quenching of carbazole photoluminescence by imidazolidine radicals/ A.G. Matveeva, D.V. Stass, E.M. Glebov, V.P. Grivin, V.V. Korolev, V.F. Plusnin, V.A. Reznikov// RUSS CHEM B+, 2010, V. 59, N 4, pp 771-778. doi:10.1007/s11172-010-0160-x, IF=0.416
  9. Synthesis and Electrochemical Reduction of 2,2 '-Diaryl-5,5,5 ',5 '-tetramethyl-3,3 '-bi(pyrrol-3-ylidene)-4,4 '(5H,5 ' H)-dione 1,1 '-Dioxides/ I.A. Khalfina, N.V. Vasil'eva, I.G. Irtegova, L.A. Shundrin, V.A. Reznikov// RUSS J ORG CHEM+, 2010, V. 46, N 12, pp 1772-1775. doi:10.1134/S1070428009120045, IF=0.524
  10. I. Kirilyuk, D. Polovyanenko, S. Semenov, I. Grigor’ev, O. Gerasko, V. Fedin, E. Bagryanskaya
    Inclusion Complexes of Nitroxides of Pyrrolidine and Imidazoline Series with Cucurbit[7]uril
    J. Phys. Chem. B, 2010, V. 114, N 4, 1719-1728. doi:10.1021/jp9103678, IF=3.47
  11. B. Wolf, P.T. Cong, K. Removic-Langer, Y.D. Borozdina, E. Mostovich, M. Baumgarten, M. Lang
    Coupled spin S = 1/2 dimer systems based on nitronyl-nitroxide biradicals
    J. Phys.: Conf. Ser., 2010, V. 200, Iss.1,012225. http://iopscience.iop.org/1742-6596 doi:10.1088/1742-6596/200/1/012225
  12. D.A. Morozov, I.A. Kirilyuk, Yu.V. Gatilov, I.Yu. Bagryanskaya, Ju.Yu. Bozhko, D.A. Komarov, I.A. Grigor'ev
    Intramolecular 1,3-dipolar cycloaddition of alkenylnitrones of the 4H-imidazole series: synthesis of a new nitroxide pH-sensitive spin probe
    Synthesis, 2010, N 2, 343-348. doi:10.1055/s-0029-1217109, IF=2.572
  13. Antioxidative properties of nitroxyl radicals and hydroxyamines in reactions with triplet and deaminated kynurenine/ V.V. Yan'shole, I.A. Kirilyuk, I.A. Grigor'ev, S.V. Morozov, Yu.P. Tsentalovicha// RUSS CHEM B+, 2010, V. 59, N 1, pp 66-74. doi:10.1007/s11172-010-0046-y, IF=0.416

2009
  1. K. Suzuki, D.G. Mazhukin, H. Takahashi, Y. Uchida, R. Tamura, I.A. Grigor’ev
    Synthesis and stereochemistry of novel rigid nitroxide biradicals based on paramagnetic pyrrolidine core
    Heterocycles, 2009, V. 78, 3091-3099. doi:10.3987/COM-09-11821, IF=0.98
  2. M.V. Edeleva, I.A. Kirilyuk, D.P. Zubenko, I.F. Zhurko, S.R. Marque, D. Gigmes, Y. Guillaneuf, E.G. Bagryanskaya
    Kinetic study of H-atom transfer in imidazoline-, imidazolidine-, and pyrrolidine-based alkoxyamines: consequences for nitroxide-mediated polymerization.
    J. Polym. Sci. Pol. Chem., 2009, V. 47, N 23, 6579-6595. doi:10.1002/pola.23701, IF=3.821
  3. L.V. Kulik, L.L. Rapatsky, A.V. Pivtsov, N.V. Surovtsev, S.V. Adichtchev, I.A. Grigor’ev, S.A. Dzuba
    Electron-nuclear double resonance study of molecular librations of nitroxides in molecular glasses : Quantum effects at low temperatures, comparison with low-frequency Raman scattering
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