Personal publications by the year

Personal publicalions (DB NIOCh)

Reviews, articles

1. N.A. Grigorieva, I.Yu. Fleitlikh, A.Ya. Tikhonov, V.I. Mamatyuk, E.V. Karpova, O.A. Logutenko
   Recovery of indium from sulfate solutions with D2EHPA in the presence of organic proton-donor additives
   Hydrometallurgy, Available online 11 June 2022, 105925 doi:10.1016/j.hydromet.2022.105925, IF=4.217
2. Н.В. Александрова, Е.Б. Николаенкова, Ю.В. Гатилов, Д.Н. Половяненко, В.И. Маматюк, В.П. Кривопалов
   Синтез и исследование азидо-тетразольной таутомерии 2-азидо-6-фенилпиримидин-4(3H)-она и 2-азидо-4-фенил-6-хлорпиримидина
   Известия Академии наук. Серия химическая.2022, Т. 71, N 6 , Cc. 1266-1272 (Synthesis and study of azide-tetrazole tautomerism in 2-azido-6-phenylpyrimidin-4(3H)-one and 2-azido-4-chloro-6-phenylpyrimidine/ N. V. Aleksandrova, E. B. Nikolaenkova, Yu. V. Gatilov, D. N. Polovyanenko, V. I. Mamatyuk, V. P. Krivopalov// Russian Chemical Bulletin, 2022, V. 71, Pp 1266-1272 doi:10.1007/s11172-022-3529-8), IF=1.704

Reviews, articles

1. Е.Б. Николаенкова, Н.В. Александрова, В.И. Маматюк, В.П. Кривопалов
   Синтез и исследование азидо-тетразольной таутомерии 2-азидо-4-(трифторметил)-6-R-пиримидинов (R = H, 4-CLC6H4)
   Известия Академии наук. Серия химическая. 2018. № 5. С. 893-901. (Synthesis and study of the azide-tetrazole tautomerism in 2-azido-4-(trifluoromethyl)-6-R-pyrimidines (R = H, 4-CLC6H4)/ Е. B. Nikolaenkova, N. V. Aleksandrova, V. I. Mamatyuk, V. P. Krivopalov// Russian Chemical Bulletin, 2018, V. 67, N 5, pp 893-901 doi:10.1007/s11172-018-2154-z), IF=0.781

Reviews, articles

1. Н.В. Плешкова, Е.Б. Николаенкова, В.И. Маматюк, В.П. Кривопалов
   2,6-Дизамещенные 4-азидопиримидины: синтез и определение термодинамических и кинетических параметров азидо-тетразольного равновесия методами спектроскопии ЯМР
   Известия Академии наук. Серия химическая, 2017, N 11, C.2095-2102 (2,6-Disubstituted 4-azidopyrimidines: synthesis, kinetic and thermodynamic studies of azide-tetrazole rearrangement by NMR / N. V. Pleshkova, E. B. Nikolaenkova, V. P. Krivopalov, V. I. Mamatyuk// Russian Chemical Bulletin, 2017, V. 66, N 11, pp 2095-2102 doi:10.1007/s11172-017-1986-2), IF=0.528
2. 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
3. S.F. Vasilevsky, M.P. Davydova, V.I. Mamatyuk, N. Tsvetkov, A. Hughes, D.S. Baranov, I.V. Alabugin
   Full Cleavage of C C Bond in Electron-Deficient Alkynes via Reaction with Ethylenediamine
   AUSTRALIAN JOURNAL OF CHEMISTRY, 2017, V.70, N 4, Pp 421-429 doi:10.1071/CH17026, IF=1.327
4. E. Karpova, A. Nefedov, V. Mamatyuk, N. Polosmak, L. Kundo
   Multi-analytical approach (SEM-EDS, FTIR, Py-GC/MS) to characterize the lacquer objects from Xiongnu burial complex (Noin-Ula, Mongolia)
   Microchemical Journal, Volume 130, January 2017, Pages 336-344 doi:10.1016/j.microc.2016.10.013, IF=3.33

Reviews, articles

1. E. Karpova, V. Vasiliev, V. Mamatyuk, N. Polosmak, L. Kundo
   Xiongnu burial complex: A study of ancient textiles from the 22nd Noin-Ula barrow (Mongolia, first century AD)
   Journal of Archaeological Science, V. 70, June 2016, Pp 15-22 doi:10.1016/j.jas.2016.04.001, IF=2.255
2. 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
3. Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
   Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
   Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875

Reviews, articles

1. 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
2. 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
3. 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
4. М.П. Давыдова, И.В. Сорокина, Т.Г. Толстикова, В.И. Маматюк, Д.С. Фадеев, С.Ф. Василевский
   Синтез новых аналогов комбретастатина A-4 и изучение их противовоспалительной активности
   Биоорганическая химия. 2015. Т. 41. № 1. С. 82-89. (Synthesis of new combretastatin A-4 analogues and study of their anti-inflammatory activity/ M. P. Davydova, I. V. Sorokina, T. G. Tolstikova, V. I. Mamatyuk, D. S. Fadeev, S. F. Vasilevsky// Russian Journal of Bioorganic Chemistry, January 2015, Volume 41, Issue 1, pp 70-76 doi:10.1134/S1068162015010033), IF=0.535

Reviews, articles

1. L.A. Zhukas, S.L. Veber, T.B. Mikenas, M, A. Yurkin, E.V. Karpova, V.P. Maltsev, V.I. Mamatyuk, L.G. Echevskaya, E.G. Bagryanskaya, V.A. Zakharov
   Size-dependent optical properties of polyethylene powders in far-IR region: On the way to universal matrix
   Journal of Quantitative Spectroscopy and Radiative Transfer, 2014, V. 147, Pp 1-7. doi:10.1016/j.jqsrt.2014.05.011, IF=2.288
2. S.i F. Vasilevsky, M.P. Davydova, D.N. Tomilin, L.N. Sobenina, V.I. Mamatuyk, N.V. Pleshkova
   Peculiarities of the cascade cleavage of the polarized C≡C-fragment in α-ketoacetylenes on reaction with ethylene diamine
   ARKIVOС, 2014, V. 2014, Part (v), pp. 132 - 144. doi:10.3998/ark.5550190.p008.663, IF=1.75
3. 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

Reviews, articles

1. 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
2. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, В.И. Маматюк
   Физико-химические свойства стебля у ржи (Secale cereale L.) со стекловидной соломиной
   Вавиловский журнал генетики и селекции, 2013. Т. 17, N 2, С. 303-313. (Physicochemical Properties of Culms in Rye (Secale cereale L.) with a Brittle Stem/ A. A. Konovalov, I. K. Shundrina, E. V. Karpova, and V. I. Mamatyuk// Russian Journal of Genetics: Applied Research, 2013, V. 3, N. 6, pp. 455–463.)
3. А.А. Коновалов, И.К. Шундрина, В.И. Маматюк, Н.П. Гончаров
   Изучение прочности соломы у ржи secale cereale l. методом динамического механического анализа
   Доклады Российской академии сельскохозяйственных наук. -2013. -№ 5. -С. 3-6.

Reviews, articles

1. 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
2. Д.С. Баранов, В.И. Маматюк, Ю.В. Гатилов, С.Ф. Василевский
   Реакция 2-метил-4-арилбут-3-ин-2-олов с тиомочевиной — новый способ синтеза 5,5-диметил-4-арилметилиден-4,5-дигидротиазол-2-аминов
   Изв. АН, Cер. хим., 2012, Т. 61, № 8, 1554-1558. (Reaction of 4-aryl-2-methylbut-3-yn-2-ols with thiourea as a new approach to the synthesis of 4-arylmethylidene-5,5-dimethyl-4,5-dihydrothiazole-2-amines/ D. S. Baranov, V. I. Mamatyuk, Yu. V. Gatilov, S. F. Vasilevsky// RUSS CHEM B+, 2012, V. 61, N 8, pp. 1570-1574. doi:10.1007/s11172-012-0208-1), IF=0.379
3. B.A. Trofimov, A.V. Artem'Ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, A.O. Korocheva, Y.V. Gatilov, V.I. Mamatyuk
   Expedient one-pot organometallics-free synthesis of tris(2-pyridyl)phosphine from 2-bromopyridine and elemental phosphorus
   Tetrahedron Lett., 2012, V. 53, № 19, 2424-2427. doi:10.1016/j.tetlet.2012.03.004, IF=2.683
4. A.V. Artem'Ev, N.K. Gusarova, S.F. Malysheva, Y.V. Gatilov, V.I. Mamatyuk
   Efficient synthesis of lupininium, anabasinium and quininium thioselenophosphinates via a multi-component reaction between secondary phosphines, sulfur, selenium and alkaloids
   Org. Prep. Proced. Int., 2012, V. 44, N 3, 262-270. doi:10.1080/00304948.2012.676523, IF=1.14
5. D.S. Baranov, A.A. Ryabichev, S.F. Vasilevsky, V.I. Mamatyuk, Y.V. Gatilov, V.G. Kartsev
   Synthesis of 2-amino-5,5-dialkyl-4-arylmethylidene-2-oxazolines from 2-alkyl-4-arylbut-3-yn-2-oles and guanidine
   Mendeleev Commun., 2012, V. 22, N 2, 114-116. doi:10.1016/j.mencom.2012.03.022, IF=0.901
6. A.V. Artem'Ev, S.F. Malysheva, B.G. Sukhov, N.A. Belogorlova, N.K. Gusarova, Y.V. Gatilov, V.I. Mamatyuk
   Unexpected redox reaction of alkali metal diselenophosphinates with elemental iodine
   Mendeleev Commun., 2012, V. 22, N 1, 18-20. doi:10.1016/j.mencom.2012.01.006, IF=0.901

Reviews, articles

1. 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
2. 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
3. A.V. Artem'ev, S.F. Malysheva, A.O. Korocheva, Yu.V. Gatilov, V.I. Mamatyuk, N.K. Gusarova
   Novel atom-economic synthesis of thioselenophosphinates via three-component reaction between secondary phosphine sulfides, elemental selenium and amines
   J. Sulfur Chem., 2011, V. 32, N 3, 599-610. doi:10.1080/17415993.2011.628993, IF=0.75
4. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, B.A. Trofimov
   Reaction of primary phosphines with elemental sulfur and alkali metal hydroxides (MOH, M = Na, K, Cs): a novel and facile three-component synthesis of trithiophosphonates
   Tetrahedron Lett., 2011, V. 52, N 3, 398-400. doi:10.1016/j.tetlet.2010.11.075, IF=2.618
5. S. F.Vasilevsky, A.I. Govdi, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, V.I. Mamatuyk, I.V. Alabugin
   Rapid Access to New Bioconjugates of Betulonic Acid via Click Chemistry
   Bioorg. Med. Chem. Lett., 2011, V. 21, N 1, 62-65. doi:10.1016/j.bmcl.2010.11.072, IF=2.661

Reviews, articles

1. A.П. Крысин, Н.У. Халикова, T.B. Хлебникова, Н.И. Ногина, В.И. Маматюк
   γ-Гидроксипропилирование 2,6-диалкил(арил)фенолов аллиловым спиртом и его производными
   Журнал общей химии, 2010, Т. 80, N 11, C. 1826-1833. (γ-hydroxypropylation of 2,6-dialkyl(aryl)phenols with allyl alcohol and its derivatives/ A. P. Krysin, N. U. Khalikova, T. B. Khlebnikova, N. I. Nogina, V. I. Mamatyuk// RUSS J GEN CHEM+, 2010, V. 80, N 11, pp 2290-2297 doi:10.1134/S1070363210110101), IF=0.393
2. A.V. Artem'ev, N.K. Gusarova, S.F. Malysheva, V.I. Mamatyuk, Yu.V. Gatilov, I.A. Ushakov, B.A. Trofimov
   One-Pot Atom-Economic Synthesis of Thioselenophosphinates via a New Multi-Component Reaction of Secondary Phosphanes with Elemental Sulfur, Selenium and Amines
   Eur. J. Org. Chem., 2010, 32, 6157-6160. doi:10.1002/ejoc.201001189, IF=3.95
3. V.V. Yanshole, P.S. Sherin, N.P. Gritsan, O.A. Snytnikova, V.I. Mamatyuk, J. Grilj, E. Vauthey, R.Z. Sagdeev, Yu.P. Tsentalovich
   Photoinduced tautomeric transformations of xanthurenic acid
   Phys. Chem. Chem. Phys., 2010, 12(32), 9502-9515. doi:10.1039/c000735h, IF=4.116
4. В.А. Лоскутов, В.И. Маматюк, И.В. Береговая
   Синтез 2-и 3-хлор-1,4-дигидрокситиоксантен-9-онов.
   Журнал органической химии, 2010, Т. 46, N 2, C. 247-251. (Syntesis of 2- and 3-chloro-1,4-dihydroxythioxanthen-9-ones/ V. A. Loskutov, V. I. Mamatyuk, I. V. Beregovaya// RUSS J ORG CHEM+, 2010, V. 46, N 2, pp 241-245. doi:10.1134/S1070428010020168), IF=0.524

Reviews, articles

1. D.S. Baranov, S.F. Vasilevsky, V.I. Mamatyuk, Yu.V. Gatilov
   Multichannel reaction of 1-(3'-hydroxy-3'-methylbutynyl)-9,10-anthraquinone with guanidine
   Mendeleev Commun., 2009, V. 19, N 6, 326–328. doi:10.1016/j.mencom.2009.11.011, IF=0.609
2. S.F. Vasilevsky, T.F. Mikhailovskaya, G.E. Salnikov, V.I. Mamatyuk, G.A. Bogdanchikov, M. Manoharan, I.V. Alabugin
   Competition between 5-Exo and 6-Endo-dig Anionic Cyclizations of Hydrazides of o-Acetylenyl Benzoic Acids and Based-catalyzed Fragmentation/Recyclization of the Initial 5-Exo-Dig Products.
   J. Org. Chem. 2009, V. 74, N 21, pp 8106-8117. doi:10.1021/jo901551g, IF=3.951
3. S.F. Vasilevsky, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov, I.V. Alabugin
   An Unexpected Rearrangement That Disassembles Alkyne Moiety Through Formal Nitrogen Atom Insertion between Two Acetylenic Carbons and Related Cascade Transformations: New Approach to Sampangine Derivatives and Polycyclic Aromatic Amides
   J. Org. Chem., 2009, V. 74, N 16, 6143–6150. doi:10.1021/jo9008904, IF=3.951

Reviews, articles

1. B.A. Trofimov, S.F. Vasilevskii, N.K. Gusarova, S.F. Malysheva, D.S. Baranov, V.I. Mamatyuk, Yu.V. Gatilov
   Complex of tris(Z-styryl)phosphine with PdCl2: a novel prospective catalyst for the Sonogashira reaction
   Mendeleev Commun., 2008, V. 18, N 6, Pp 318-319. doi:10.1016/j.mencom.2008.11.010, IF=0.73
2. В.А. Лоскутов, Ю.В. Гатилов, В.И. Маматюк
   Хлорирование 1,4-дигидрокситиоксантен-9-она
   Журнал органической химии, 2008, Т. 44, N 4, 630-632. (Chlorination of 1,4-dihydroxythioxanthen-9-one/ V. A. Loskutov, Yu. V. Gatilov, V. I. Mamatyuk// Russian Journal of Organic Chemistry, 2008, V. 44, N 4, pp 626-628 doi:10.1134/S1070428008040295), IF=0.51
3. Г.Е. Сальников, А.М. Генаев, В.И. Маматюк, В.Г. Шубин
   Гомофеналенильные катионы – новые представители гомоароматических систем
   Журнал органической химии, 2008, Т. 44, N 7, 1011-1016. (Homophenalenyl cations, new representatives of homoaromatic systems/ Sal'nikov G. E., Genaev A. M., Mamatyuk V. I., Shubin V.G.// Russian Journal of Organic Chemistry, 2008, V. 44, N 7, P. 1000-1005 doi:10.1134/S1070428008070099), IF=0.51
4. Г.Е. Сальников, А.М. Генаев, В.И. Маматюк, В.Г. Шубин
   Структурная нежесткость гомофеналенильных катионов
   Журнал органической химии, 2008, Т. 44, N 7, 970-974. (Stereochemical nonrigidity of homophenalenyl cations/ G.E. Sal'nikov, A.M. Genaev, V.I. Mamatyuk, V.G. Shubin// Russian Journal of Organic Chemistry, 2008, V. 44, N 7, pp 958-962 doi:10.1134/S107042800807004X), IF=0.51
5. T.A. Vaganova, S.Z. Kusov, V.I. Rodionov, I.K. Shundrina, G.E. Sal’nikov, V.I. Mamatyuk, E.V. Malykhin
   Amination of octafluoronaphthalene in liquid ammonia. 2,6- and 2,7-Diaminohexafluoronaphthalenes selective preparation
   J. Fluor. Chem., 2008, V. 129, N 4, 253-260. doi:10.1016/j.jfluchem.2007.11.010, IF=1.513

Reviews, articles

1. С.А. Амитина, И.А. Григорьев, В.И. Маматюк, А.Я. Тихонов
   Взаимодействие Z-изомеров алкилароматических 1,2-гидроксиламинооксимов с метил- и арилглиоксалями
   Изв. АН, Сер. Хим., 2007, Т. 56, № 6, 1146-1149. (Reactions of Z-isomers of alkylaromatic 1,2-hydroxylamino oximes with methyl- and arylglyoxals/ S. A. Amitina, I. A. Grigor’ev, V. I. Mamatyuk, A. Ya. Tikhonova// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1190-1193 doi:10.1007/s11172-007-0181-2), IF=0.504

Reviews, articles

1. Т.А. Ваганова, П.С. Юферов, Л.И. Горюнов, Е.В. Пантелеева, Г.Е. Сальников, Л.Н. Щеголева, В.И. Маматюк, В.Д. Штейнгарц
   Восстановительная активация аренов. Сообщение 20. Анионные продукты двухэлектронного восстановления толунитрилов в жидком аммиаке: природа и электронное строение
   Изв. АН, Cер. Хим., 2006, Т. 55, № 6, 940-944. (Reductive activation of arenes/ T. A. Vaganova, P. S. Yuferov, L. I. Goryunov, E. V. Panteleeva, G. E. Sal'nikov, L. N. Shchegoleva, V. I. Mamatyuk, V. D. Shteingarts// Russian Chemical Bulletin, 2006, V. 55, N 6, pp 976-980 doi:10.1007/s11172-006-0365-1), IF=0.589
2. G.G. Balakina, V.G. Vasiliev, E.V. Karpova, V.I. Mamatyuk
   HPLC and Molecular Spectroscopic Investigations of the Red Dye Obtained from an Ancient Pazyryk Textile
   Dyes and Pigments, 2006, V. 71, N 1, 54-60. doi:0.1016/j.dyepig.2005.06.014, IF=1.69