Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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
- 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