Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. 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
    
2. S.A. Dobrynin, M.M. Gulman, D.A. Morozov, I.F. Zhurko, A.I. Taratayko, Yu.S. Sotnikova, Yu.I. Glazachev, Yu.V. Gatilov, I.A. Kirilyuk
   Synthesis of Sterically Shielded Nitroxides Using the Reaction of Nitrones with Alkynylmagnesium Bromides
   Molecules 2022, 27(21), 7626 doi:10.3390/molecules27217626, IF=4.927
    
3. 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
    
4. Yu.V. Khoroshunova,D. A. Morozov,A. I. Taratayko,S. A. Dobrynin,I. V. Eltsov,T. V. Rybalova,Yu. S. Sotnikova,D. N. Polovyanenko,N. B. Asanbaeva,I. A. Kirilyuk
   The Reactions of 6-(Hydroxymethyl)-2,2-dimethyl-1-azaspiro[4.4]nonanes with Methanesulfonyl Chloride or PPh3-CBr4
   Molecules 2021, 26(19), 6000 doi:10.3390/molecules26196000, IF=4.411
    
5. S.A. Dobrynin, M.S. Usatov, I.F. Zhurko, D.A. Morozov, Yu.F. Polienko, Yu.I. Glazachev, D.A. Parkhomenko, M.A. Tyumentsev, Yu.V. Gatilov, E.I. Chernyak, E.G. Bagryanskaya, I.A. Kirilyuk
   A Simple Method of Synthesis of 3-Carboxy-2,2,5,5-Tetraethylpyrrolidine-1-oxyl and Preparation of Reduction-Resistant Spin Labels and Probes of Pyrrolidine Series
   Molecules 2021, 26(19), 5761 doi:10.3390/molecules26195761, IF=4.41
    
6. P. Fehling, K. Buckenmaier, S.A. Dobrynin, D.A. Morozov, Yu.F. Polienko, Yu.V. Khoroshunova, Yu. Borozdina, P. Mayer, J. Engelmann, K. Scheffler, G. Angelovsk, I.A. Kirilyuk
   The effects of nitroxide structure upon 1H Overhauser dynamic nuclear polarization efficacy at ultralow-field
   J. Chem. Phys., 2021, V. 155, N 14, 144203 doi:10.1063/5.0064342, IF=3.487
    
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. S. Cherkasov, D. Parkhomenko, A. Genaev, G. Salnikov, M. Edeleva, D. Morozov, T. Rybalova, I. Kirilyuk, S.R-A. Marque, E. Bagryanskaya
   NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines
   Molecules 2020, 25(21), 5080 doi:10.3390/molecules25215080, IF=3.266
    
9. 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
    
10. 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
     
11. 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
     
12. S.A. Cherkasov, A.D. Semikina, P.M. Kaletina, Yu.F. Polienko, D.A. Morozov, A.M. Maksimov, I.A. Kirilyuk, E.G. Bagryanskaya, D. Parkhomenko
    The Kinetics of 1,3-Dipolar Cycloaddition of Vinyl Monomers to 2,2,5,5-Tetramethyl-3-imidazoline-3-oxides
    ChemPhysChem, 2021, V.86, N 8, Pp 1080-1086 doi:10.1002/cplu.202100266, IF=2.862
     
13. 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
     
14. 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
     
15. И.А. Кирилюк, Д.А. Морозов, Ю.С. Табатчикова, В.С. Медведев, А.В. Лебедев, Г.В. Романенко, Т.В. Рыбалова, И.А. Григорьев
    Синтез 4Н-имидазол-5-карбальдоксим-3-оксидов и 4Н-имидазол-5-карбонитрил-3-оксидов
    Известия Академии наук. Серия химическая., 2008, Т. 57, N 7, 1487–1503. (Synthesis of 4Н--imidazole-5-carbaldoxime 3-oxides and 4Н--imidazole-5- carbonitrile 3-oxides/ I.A. Kirilyuk, D.A. Morozov, Yu.S. Tabatchikova, V.S. Medvedev, A.V. Lebedev, T.V. Rybalova, I.A. Grigor'Ev, G.V. Romanenko// Russian Chemical Bulletin, 2008, V. 57, N 7, Pp 1516-1533 doi:10.1007/s11172-008-0196-3), IF=0.537
     
16. И.А. Григорьев, Д.А. Морозов, В.А. Святченко, Н.Н. Киселев, В.Б. Локтев, Е.А. Лукьянец, Г.Н. Ворожцов
    Синтез и изучение противоопухолевой активности тетраэтил-2-(2,2,6,6-тетраметилпиперидин-4-иламино)- этилиден-1,1-бисфосфоната
    Доклады Академии наук. 2014. Т. 457. № 3. С. 300-303. (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