Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, D.S. Fadeev, Yu.V. Gatilov, A.A. Stepanov, N.V. Vasilieva, I.V. Alabugin
   Conformational Flexibility of Fused Tetracenedione Propellers Obtained from One-Pot Reductive Dimerization of Acetylenic Quinones
   J. Org. Chem., 2015, 80 (3), pp 1618-1631 doi:10.1021/jo502543b, IF=4.721
    
2. A.A. Stepanov, L.M. Gornostaev, S.F. Vasilevsky, E.V. Arnold, V.I. Mamatyuk, D.S. Fadeev, B. Gold, I.V. Alabugin
   Chameleonic reactivity of vicinal diazonium salt of acetylenyl-9,10-antraquinones: syntetic application toward two heterocyclic targets
   J. Org. Chem., 2011, 76 (21), pp 8737-8748. doi:10.1021/jo2014214, IF=4.1
    
3. 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
    
4. 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
    
5. O.V. Salomatina, I.I. Popadyuk, A.L. Zakharenko, O.D. Zakharova, D.S. Fadeev, N.I. Komarova, J. Reynisson, H.J. Arabshahi, R. Chand, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
   Novel semisynthetic derivatives of bile acids as effective tyrosyl-DNA phosphodiesterase 1 inhibitors
   Molecules, 2018, V. 23, N 3, art. number 679 doi:10.3390/molecules23030679, IF=3.098
    
6. A.I. Govdi, N.V. Sokolova, I.V. Sorokina, D.S. Baev, T.G. Tolstikova, V.I. Mamatyuk, D.S. Fadeev, S.F. Vasilevsky, V.G. Nenajdenko
   Synthesis of new betulinic acid–peptide conjugates and in vivo and in silico studies of the influence of peptide moieties on the triterpenoid core activity
   MedChemComm, 2015, V.6, N 1, pp. 230-238. doi:10.1039/c4md00236a, IF=2.495
    
7. D.S. Fadeev, I.P. Chuikov, V.I. Mamatyuk
   A study of NMR parameters of para-substituted polyfluorinated benzyl cations and their precursors
   Journal of Fluorine Chemistry, V. 182, February 2016, Pp 53-60 doi:10.1016/j.jfluchem.2015.12.003, IF=2.213
    
8. K.S. Kovaleva, O.I. Yarovaya, D.S. Fadeev, N.F. Salakhutdinov
   One-pot synthesis of 1,5,3-oxathiazepanes via the three-component condensation of primary amines, formaldehyde and 2-mercaptoethanol
   Tetrahedron Letters, 2017, V. 58, N 19, Pp 1868-1870 doi:10.1016/j.tetlet.2017.03.090, IF=2.193
    
9. P.A. Zaikin, O.T. Dyan, D.S. Fadeev, Yu.V. Gatilov, G.I. Borodkin
   1,1-Difluoronaphthalene-2(1H)-ones in Diels-Alder Reaction
   Journal of Fluorine Chemistry, 2017, V. 199, Pp 20-29 doi:10.1016/j.jfluchem.2017.04.008, IF=2.101
    
10. D.S. Fadeev, I.P. Chuikov, V.M. Karpov, V.I. Mamatyuk
    The Investigation of NMR parameters of the heptafluoroindenyl cation
    Journal of Fluorine Chemistry, V. 197, May 2017, Pages 1-5 doi:10.1016/j.jfluchem.2017.02.002, IF=2.101
     
11. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
     
12. O.T. Dyan, P.A. Zaikin, D.S. Fadeev, Y.V. Gatilov, G.I. Borodkin
    1,1-Difluoronaphthalen-2(1H)-ones as building blocks for fluorinated tetraphenes
    Journal of Fluorine Chemistry,2018, V. 210, Pp 88-93 doi:10.1016/j.jfluchem.2018.03.008, IF=1.879
     
13. I.P. Chuikov, D.S. Fadeev, V.I. Mamatyuk, T.A. Vaganova, E.V. Malykhin
    Analysis of ¹⁹F and ¹³C NMR spectra of tetrafluorophthalic anhydride and its derivatives
    J FLUORINE CHEM, 2011, V. 132, N 8, pp 512–515. doi:10.1016/j.jfluchem.2011.04.021, IF=1.718
     
14. O.I. Brusentzeva, Yu.V. Kharitonov, D.S. Fadeev, E.E. Shults
    Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2020, 96, N 3-4, Pp 245-250 doi:10.1007/s10847-019-00965-z, IF=1.56
     
15. D.S. Baranov, D.S. Fadeev
    Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones
    Mendeleev Communications, V. 26, N 2, March-April 2016, Pp 174- 176 doi:10.1016/j.mencom.2016.03.032, IF=1.404
     
16. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatuyk, N.V. Pleshkova, D.S. Fadeev, I. V. Alabugin
    Reaction of α,β-alkynylketones with β-amino alcohols: pseudoephedrine- assisted cleavage of triple bond via formal internal redox process
    Mendeleev Communications, V. 25, N 5, 2015, Pp 377-379 doi:10.1016/j.mencom.2015.09.021, IF=1.34
     
17. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
     
18. И.В. Нечепуренко, Е.Д. Широкова, М.В. Хвостов, Т.С. Фролова, О.И. Синицина, А.М. Максимов, Р.А. Бредихин, Н.И. Комарова, Д.С. Фадеев, О.А. Лузина, Т.Г. Толстикова, Н.Ф. Салахутдинов
    Синтез, гиполипидемическая и противогрибковая активность сульфонатов тетрагидроберберрубина
    Известия Академии наук. Серия химическая, 2019, Т. 68, N 5, Cc. 1052-1060 (Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y), IF=1.014
     
19. С.Ф. Василевский, Т.Ф. Михайловская, А.А. Степанов, В.И. Маматюк, Д.С. Фадеев
    Особенности основно-индуцируемой гетероциклизации вицинальных (R-этинил)фенилгидроксамовых кислот
    Журнал органической химии. 2014. Т. 50. № 4. С. 518-521. (Base-catalyzed heterocyclization of 2-(R-ethynyl)benzohydroxamic acids/ S. F. Vasilevskii, T. F. Mikhailovskaya, A. A. Stepanov, V. I. Mamatyuk, D. S. Fadeev// Russian Journal of Organic Chemistry, 2014, V. 50, N 4, pp 506-509. doi:10.1134/S1070428014040101), IF=0.675
     
20. Д.С. Фадеев, И.П. Чуйков, В.И. Маматюк
    Неэмпирические и DTF-расчеты химических сдвигов в спектрах ЯМР¹⁹F и ¹³C замещенных пентафторбензолов
    Журнал структурной химии, 2013, Т. 54 (Приложение), С.178-183. (Non-empirical and DFT calculations of 19F and 13C chemical shifts in the NMR spectra of substituted pentafluorobenzenes/ D. S. Fadeev, I. P. Chuikov, V. I. Mamatyuk// Journal of Structural Chemistry, 2013, V. 54, N 1 Supplement, pp 180-185. doi:10.1134/S0022476613070196), IF=0.574