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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

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Employee:  Mamatyuk Viktor Il'ich
Positions:  Leading Researcher (Cand. Chem), LMRS
Positions:  Leading Researcher (Cand. Chem), LMRBS


 


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Personal publicalions (DB NIOCh)


2018

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

2017

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

2016

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

2015

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

2014

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

2013

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.

2012

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

2011

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

2010

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

2009

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

2008

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

2007

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

2006

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



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