Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
   Сопряженные нитроксильные радикалы
   Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
    
2. 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
    
3. 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
    
4. 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
    
5. L. N. Grigor’eva,A. Ya. Tikhonov,K. A. Lomanovich,D. G. Mazhukin
   Stable Bicyclic Functionalized Nitroxides: The Synthesis of Derivatives of Aza-nortropinone–5-Methyl-3-oxo-6,8-diazabicyclo[3.2.1]-6-octene 8-oxyls
   Molecules 2021, 26(10), 3050 doi:10.3390/molecules26103050, IF=4.411
    
6. E.V. Zaytseva, D.G. Mazhukin
   Spirocyclic Nitroxides as Versatile Tools in Modern Natural Sciences: From Synthesis to Applications. Part I. Old and New Synthetic Approaches to Spirocyclic Nitroxyl Radicals
   Molecules 2021, 26(3), 677 doi:10.3390/molecules26030677, IF=4.411
    
7. 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
    
8. Yo. Uchida, T. Sakaguchi, Sh. Oki, S. Shimono, Ja. Park, M. Sugiyama, Sh. Sato, E. Zaytseva, D.G. Mazhukin, R. Tamura
   Magnetically Manipulable Ionic Liquid Crystals Incorporating Neutral Radical Moiety
   ChemPlusChem,V.87, N. 3, March 2022, e20210035 doi:10.1002/cplu.202100352, IF=3.21
    
9. 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
    
10. E. Chugunova, V. Samsonov, N. Akylbekov, D. Mazhukin
    Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinondioximes with ketones
    Tetrahedron, 2017, V. 73, N 27-28, Pp 3986-3992 doi:10.1016/j.tet.2017.05.078, IF=2.651
     
11. 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
     
12. 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
     
13. 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
     
14. 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
     
15. 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
     
16. 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
     
17. E.A. Mostovich, D.G. Mazhukin, Yu.V. Gatilov, T.V. Rybalova
    Coupling of 1,2-bis(alkoxyamino)cyc-lohexane with 1,3-dicarbonyl com-pounds: first synthesis of 1,4-dialk-oxy-2,3-dihydro-1,4-diazepinium salts
    Mendeleev Commun., 2007, V. 17, N 1, 48-50. doi:10.1016/j.mencom.2007.01.019, IF=0.712
     
18. E.V. Zaitseva, A.V. Shernyukov, S.A. Amitina, R. Tamura, I.A. Grigor’ev, D.G. Mazhukin
    Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups
    Chemistry of Heterocyclic Compounds, November 2014, V. 50, N 8, pp 1113-1125. doi:10.1007/s10593-014-1571-7, IF=0.698
     
19. Е.В. Зайцева, Ю.В. Гатилов, С.А. Амитина, Р. Тамура, И.А. Григорьев, Д.Г. Мажукин
    Спироциклические нитроксильные радикалы 3-имидазолина с мезогенным заместителем при атоме C ⁴гетероцикла. синтез и кристаллическая структура
    Журнал органической химии. 2014. Т. 50. № 1. С. 78-83. (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
     
20. И.В. Машевская, З.Г. Алиев, Д.Г. Мажукин, С.А. Попов, А.Я. Тихонов, А.Н. Масливец
    Пятичленные 2,3-диоксогетероциклы. LXII. Взаимодействие 3-ароил-1Н-пирроло[2,1-c][1,4]бензоксазин-1,2,4-трионов с 1,2-бис(гидроксиамино)циклогексаном. Необычная перегруппировка в системе хиноксалино-спиро-пиррола
    Журнал органической химии, 2008, Т. 44, N 8, 1202-1206. (Five-membered 2,3-dioxo heterocycles: LXII. Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with N,N'-dihydroxycyclohexane-1,2-diamine. Unusual rearrangement in the spiro[quinoxaline-2,2'-pyrrole] system/ I.V. Mashevskaya, A.N. Maslivets, Z.G. Aliev, D.G. Mazhukin, S.A. Popov, A.Ya. Tikhonov// Russian Journal of Organic Chemistry, 2008, V. 44, N 8, P. 1189-1193. doi:10.1134/S1070428008080149), IF=0.51