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

Department of physical organic chemistry

Половяненко


Head of Center -
Cand. Sci. (Phys.-Math.) Dmitriy N. Polovyanenko
tel.  (383) 330-96-61
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.


Scientific Director
Cand. Sci. (Chem) Victor I. Mamtyuk
tel.  (383) 330-69-60
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

 

The Center of spectral investigations (CSI) has been established on March 11, 2016 on the basis of the Laboratory of Physical Research Methods/
The Centre includes 6 groups.

Purpose:

  • collective use of unique expensive scientific equipment to carry out fundamental and applied research;
     
  • raising the level of experimental work in the field of molecular spectroscopy, structural and analytical research;
     
  • assistance in the implementation of scientific and scientific-applied grants and projects;
     
  • rendering services to organizations and enterprises of the Siberian region;
     
  • education and training of personnel for measurements, operation and maintenance of scientific instruments.
     

 

RESEARCH AREAS


Areas:

  • Analysis and identification of methods of molecular spectroscopy of organic, metal organic and inorganic substances and materials, including nanomaterials with desired properties (plastics, optical, ferromagnetic, biologically active) for science, technology and medicine
  • The study of natural and biological methods of molecular spectroscopy, chromatography, and microanalysis
  • Analysis and identification of substances and materials of synthetic, natural and anthropogenic origin, including nanomaterials
  • Development of physical and chemical methods of analysis of substances and materials
  • Creating databases of molecular spectroscopy data
  • independent expertise

Logistical and methodical base of Spectral Research Center allow us to study the liquid, solid and gaseous substances and carry out sample preparation of complex objects of natural, synthetic and natural origin.

STAFF
The Centre includes 6 groups:

1. Group of Nuclear Magnetic Resonance (GNMR)

Employee Position Room Phone Phone in. email Publications
by years
1 Salnikov Георгий Efimovich Senior Researcher 127 330-55-04 3-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Korchagina Dina Vladimirovna Senior Researcher (Cand. Chem.) 412 НТК 330-55-04 2-58 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Skorova Anna Борисовна Leading Engineer 108 330-55-04 3-32 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Kandaurova Vera Vasilievna technicist 106 330-55-04 3-50 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Ardashova Darya Vladimirovna technicist 108 330-55-04 3-32



2. Group of mass spectrometry (GMS)

Employee Position Room Phone Phone in. email Publications
by years
1 Nefedov Andrey Alekseevich Senior Researcher (Cand. Chem.). Group's Head 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Salnikova Olga Иосифовна Leading Engineer 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Statsenko Olga Борисовна Leading Engineer 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Bondareva Mariya Alexandrovna engineer


3. Group of Optical Spectrometry (GOS)

Employee Position Room Phone Phone in. email Publications
by years
1 Karpova Elena Viktorovna Senior Researcher (Cand. Chem.). Group's Head 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Chuikov Igor Petrovich Researcher (Cand. Chem.) 414 НТК 330-82-51 2-15 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Sagalaeva Natalia Ivanovna Senior Laboratory Assistant 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Kornakova Tatyana Aleksandrovna Leading Engineer 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.


4. Group of X-ray analysis (GXRA)

Employee Position Room Phone Phone in. email Publications
by years
1 Bagryanskaya Irina Yurievna Leading Researcher (Doct.Chem), Group's Head 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Gatilov Yurii Vasilievich Leading Researcher (Doct. Chem) 207 НТК 330-78-64 4-37 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Rybalova Tatyana Valerievna Researcher 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.


5. Group of thermal analysis (GTA)

Employee Position Room Phone Phone in. email Publications
by years
1 Shundrina Inna Kazimirovna Senior Researcher (Cand. Chem.). Group's Head 105 330-78-64 3-46 This email address is being protected from spambots. You need JavaScript enabled to view it.



PUBLICATIONS
 

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2021
  1. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=5.88

2020
  1. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  2. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, First published: 27 July 2020 doi:10.1002/anie.202010041, IF=12.959
  3. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  4. L. Politanskaya, I. Bagryanskaya, E. Tretyakov, Ch. Xic
    Highly efficient synthesis of novel fluorinated 3-amino-2-mercaptobenzothiazole-2(3H)-thione derivatives
    Journal of Fluorine Chemistry, 2020, V.239, 109628 doi:10.1016/j.jfluchem.2020.109628, IF=2.322
  5. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  6. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  7. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi:10.31857/S0044460X20100054, IF=0.716
  8. A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
    2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
    Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
  9. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  10. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  11. V. Romanov, E. Tretyakov, G. Selivanova, J. Li, I. Bagryanskaya, A. Makarov, D. Luneau
    Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
    Crystals 2020, 10(9), 786 doi:10.3390/cryst10090786, IF=2.404
  12. I.V. Oleynik, I.K. Shundrina, I.I. Oleyinik
    Highly active titanium(IV ) dichloride FI catalysts bearing a diallylamino group for the synthesis of disentangled UHMWPE
    Polymers for Advanced Technologies, 2020, V. 31, N 9, Pp 1921-1934 doi:10.1002/pat.4917, IF=2.578
  13. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  14. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  15. S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
    3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
    Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
  16. L. Gurskaya, T. Rybalova, I. Beregovaya, E. Zaytseva, M. Kazantsev, E. Tretyakov
    Aromatic nucleophilic substitution: a case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides
    Journal of Fluorine Chemistry, 2020, V. 237, 109613 doi:10.1016/j.jfluchem.2020.109613, IF=2.322
  17. I. Zayakin, I. Bagryanskaya, D. Stass, M. Kazantsev, E. Tretyakov
    Synthesis and Structure of (Nitronyl Nitroxide-2-ido)(tert-butyldiphenylphosphine)gold(I) and -(Di(tert-butyl)phenylphosphine)gold(I) Derivatives; Their Comparative Study in the Cross-Coupling Reaction
    Crystals 2020, 10(9), 770 doi:10.3390/cryst10090770, IF=2.404
  18. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  19. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  20. Деревянко Д.И., Басистый В.С., Шелковников В.В., Шундрина И.К., Бухтоярова А.Д., Сальников Г.Е., Бережная В.Н., Черноносов А.А.
    Гибридный фотополимерный материал на основе (8-акрилоил-1,4-дитиа-8-азаспиро[4.5]декан-2-ил)метил акрилата и тиол-силоксанового компонента для записи микроструктур: синтез, оптические и термомеханические свойства
    Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 5. С. 382-394. doi:10.31857/S2308113920050046, IF=0.976
  21. Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022, IF=0.716
  22. 2-diethylaminovinyl derivatives of halogenated 1,4-quinones: synthetic and structural aspects/ S. I. Zhivetyeva, I. A. Zayakin, I. Yu. Bagryanskaya & E. V. Tretyakov// Journal of Structural Chemistryб 2020, V. 61, N 8, Pp 1253-1259 doi:10.1134/S0022476620080107 , IF=0.745
  23. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, E.V. Malykhin
    Polyfluorinated hydroxy and carboxy benzenes as a new type of H-donors for self-assembly with 18-crown-6 ether: synthesis, supramolecular structure and stability of co-crystals
    Journal of Fluorine Chemistry, 2020, V. 236, 109577 doi:10.1016/j.jfluchem.2020.109577, IF=2.332
  24. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  25. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  26. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  27. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  28. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  29. Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090, IF=0.976
  30. Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328, IF=0.719
  31. A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
    Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp. 968-972 doi:10.1007/s10593-020-02760-y, IF=1.519
  32. N.S. Li-Zhulanov, A.V. Pavlova, D.V. Korchagina, Yu.V. Gatilov, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis of 1,3-Oxazine Derivatives Based on (-)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 936-941 doi:10.1007/s10593-020-02753-x, IF=1.519
  33. A. M. Genaev, G. E. Salnikov, K.Yu. Koltunov
    Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 892-897 doi:10.1007/s10593-020-02749-7, IF=1.519
  34. I.V. Il'ina, O.S. Patrusheva, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3˙Et2O-H2O Catalytic System
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 867-874 doi:10.1007/s10593-020-02743-z, IF=1.519
  35. A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  36. A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    A NEW Cu(I) IODIDE COMPLEX SHOWING DEEP-RED LUMINESCENCE
    Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  37. Synthesis of polyfluorinated tetraoxacalix[4]arenes by the interaction of pentafluoronitrobenzene with resorcinol, orcinol, and tetrafluororesorcinol/ Kovtonyuk V. N., Han H., Gatilov Yu. V.// Russian Journal of Organic Chemistry, 2020 doi:10.31857/S0514749220070058, IF=0.751
  38. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
  39. A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086, IF=0.745
  40. M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
    Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
  41. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  42. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  43. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  44. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  45. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  46. V.A. Logvinenko, V.P. Fadeeva, B.A. Selivanov, V.D. Tikhova, A.A. Nefedov, A.Ya. Tikhonov
    Thermal decomposition of several N,N'-bis(2-hydroxyiminoalkyl)-α,α'-dinitrones
    Journal of Thermal Analysis and Calorimetry, 2020, V. 140, N 2, Pp 685-693 doi:10.1007/s10973-019-08868-4, IF=2.731
  47. I. Il'ina, E. Morozova, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of aliphatic ketones-derived chiral hexahydro-2H-chromenes
    Medicinal Chemistry Research, 2020, V. 29, N 4, pp 738-747 doi:10.1007/s00044-020-02518-3, IF=1.783
  48. D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
    Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
    Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
  49. 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
  50. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  51. Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety/ M.E. Mironov, A.I. Poltanovich , T.V., Rybalova, M.P. Dolgikh, T.G. Tolstikova, E.E Shults// Russian Chemical Bulletin, 2020, V. 69, Pp 537–546 doi:10.1007/s11172-020-2795-6, IF=1.061
  52. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  53. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
  54. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
    Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
  55. 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
  56. E.B. Nikolaenkova, I.Yu. Bagryanskaya, A.Ya. Tikhonov
    Synthesis of 2-[2-(hydroxyimino)alkyl]-1,2-oxazol-5(2Н)-ones
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 2, Pp 208-212 doi:10.1007/s10593-020-02645-0, IF=1.519
  57. Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1, IF=1.061
  58. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
    Int. J. Mol. Sci. 2020, 21(1), 126. This article belongs to the Special Issue Inhibition of DNA Repair Enzymes as a Valuable Pharmaceutical Approach) doi:10.3390/ijms21010126, IF=4.556
  59. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  60. QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909
  61. I. Il'ina, E. Morozova, D. Korсhagina, K. Volcho, T. Tolstikova, N. Salakhutdinov
    Synthesis and Analgesic Activity of Monoterpenoid Aldehyde-derived Hydro-2H-chromeneols
    Letters in Drug Design & Discovery, 2020, V. 17, N 1, Pp 68-78 doi:10.2174/1570180816666181114131220, IF=1.169

2019
  1. An unusual fabric from Jety-Asar-2, Eastern Aral sea region, in the context of the central asian textile tradition/ POLOSMAK N.V., KARPOVA E.V., AMOSOV E.V.// doi:10.17746/1563-0102.2020.48.3.050-058
  2. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
  3. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  4. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  5. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  6. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  7. Thermal Reactions of 6-Bromo-, 6-Chloro-, and 6-(Methylsulfanyl)octafluoroindane-5-thioles with Tetrafluorethylene. Synthesis of Dodecafluoro-2H,3H,5H,6H,7H-indeno[5,6-b]thiophene/ P.V. Nikul'shin, A.M. Maksimov, Yu. V. Gatilov, V.E. Platonov// Russian Journal of General Chemistry, 2019, V. 89, N: 12, Pp 2378-2385 doi: 10.1134/S0044460X19120096 doi:10.1134/S1070363219120090, IF=0.643
  8. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  9. G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
    Direct electrophilic fluorination of naproxen with NF-reagents
    Journal of Fluorine Chemistry, 2019, V. 228, 109412 doi:10.1016/j.jfluchem.2019.109412, IF=2.055
  10. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  11. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
    Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
  12. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  13. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  14. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  15. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  16. Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104, IF=0.794
  17. Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125, IF=0.751
  18. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
    Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
    ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
  19. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
    A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
    ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
  20. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  21. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  22. V.A. Savel'ev, A.A. Kotova, T.V. Rybalova, E.E. Shults
    Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles Containing an Anthranilic Acid Motif
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 10, pp 943-955 doi:10.1007/s10593-019-02561-y, IF=1.492
  23. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
    Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
    Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
  24. Study of Plant Coumarins: XVII. Synthesis and Transformations of 6-Carboxamidocoumarins/ E.E.Shults, D.O. Zakharov, A.V. Lipeeva, Yu.V. Gatilov, A.G. Makarov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1518-1526 doi:10.1134/S1070428019100099, IF=0.751
  25. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  26. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
    CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
  27. E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
    Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units
    Molecules 2019, 24(17), 3186 doi:10.3390/molecules24173186, IF=3.59
  28. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  29. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  30. M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 38.* Synthesis of Conjugates Containing β-Carboline and Tricyclic Diterpenoids
    Chemistry of Natural Compounds, 2019, V. 55, N 5, pp 871-877 doi:10.1007/s10600-019-02836-y, IF=0.566
  31. Aliphatic and triterpenoic products of ether extracts saponification of POPULUS NIGRA L/ T. P. Kukina, I. A. Elshin , O. I. Salnikova , I. V. Eltsov// doi:10.14258/jcprm.2019034951
  32. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
  33. A.I. Titkov, O.A. Logutenko, E.Yu. Gerasimov, I.K. Shundrina, E.V. Karpova, N.Z. Lyakhov
    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  34. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  35. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  36. Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118, IF=0.541
  37. V.N. Kovtonyuk, Yu.V. Gatilov, G.E. Salnikov, E.V. Amosov
    Polyfluorinated tetraoxacalixarenes and bicyclooxacalixarenes. Interaction of pentafluorobenzonitrile with resorcinol, orcinol and tetrafluororesorcinol
    Journal of Fluorine Chemistry, 2019, V. 222-223, Pp 59-67 doi:10.1016/j.jfluchem.2019.04.011, IF=2.055
  38. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
    Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
    J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
  39. T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
    Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
    Journal of Antibiotics, 2019, V. 72, pp 590-599 doi:10.1038/s41429-019-0191-y, IF=2.446
  40. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  41. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
    Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
  42. Synthesis and analgesic activity of octahydro-2H-chromenols, derivatives of aliphatic ketones/ I. V. Il'ina, D. V. Korchagina, E. A. Morozova, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1061-1066 doi:10.1007/s11172-019-2520-5, IF=1.014
  43. 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
  44. Effect of Aliphatic Diols and Dicarboxylic Acids on the Properties of Ethylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2019, V. 61, N 5, pp 544-554 doi:10.1134/S0965545X19050146, IF=0.984
  45. On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051, IF=0.751
  46. V.Yu. Shuvalov, A.S. Rupp, A.K. Kuratova, A.S. Fisyuk, A.A. Nefedov, G.P. Sagitullina
    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
    SYNLETT, 2019, V. 30, N 8, Pp 919-923 doi:10.1055/s-0037-1612416, IF=2.418
  47. E.Mozhaitsev,E.Suslov,Yu. Demidova,D. Korchagina,K.Volcho,A. Zakharenko,I. Vasi'eva,M.Kupryushkin,A. Chepanova,D. M. Ayine-Tora,J.Reynisson,N. Salakhutdinov,O. Lavrik
    The Development of Tyrosyl-DNA Phosphodyesterase 1 (TDP1) Inhibitors Based on the Amines Combining Aromatic/Heteroaromatic and Monoterpenoid Moieties
    Letters in Drug Design & Discovery, 2019, V. 6, N 5, Pp 597-605 doi:10.2174/1570180816666181220121042, IF=0.953
  48. V.V. Shelkovnikov, I.Yu. Kargapolova, S.V. Korotaev, N.A. Orlova, T.V. Rybalova, I.P. Chuikov
    Three-color luminescent transformation of the julolidine pyrylo/pyridocyanine dyes in the adsorbed state
    Journal of Photochemistry and Photobiology A: Chemistry, 2019, V. 375 , Pp 181-190 doi:10.1016/j.jphotochem.2019.02.022, IF=3.261
  49. E.S. Mozhaitsev, A.L. Zakharenko, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, I.A. Vasil’eva, A.A. Chepanova, E. Black, J. Patel, R. Chand, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
    Anti-Cancer Agents in Medicinal Chemistry, 2019, V. 19 , N 4 , Pp 463-472 doi:10.2174/1871520619666181207094243, IF=2.18
  50. V. Romanov, I. Bagryanskaya, N. Gritsan, D. Gorbunov, Yu. Vlasenko, M. Yusubov, E. Zaytseva, D. Luneau, E. Tretyakov
    Assembly of Imidazolyl-Substituted Nitronyl Nitroxides into Ferromagnetically Coupled Chains
    Crystals 2019, 9(4), 219 doi:10.3390/cryst9040219, IF=2.061
  51. N.S. Li-Zhulanov, I.V. Il’ina, A. Chicca, P. Schenker, O.S. Patrusheva, E.V. Nazimova, D.V. Korchagina, M. Krasavin, K.P. Volcho, N.F. Salakhutdinov
    Effect of chiral polyhydrochromenes on cannabinoid system
    Medicinal Chemistry Research, 2019, V. 28, N 4, pp 450-464 doi:10.1007/s00044-019-02294-9, IF=1.72
  52. Exploration of SNF-Approach toward Functionalized Nitronyl Nitroxides/ P. Fedyushin, L. Gurskaya, E. Panteleeva, B. Koshcheev, A. Maksimov, T.V. Rybalova, E. Zaytseva, E. Tretyakov// doi:10.17677/fn20714807.2019.02.04
  53. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, V.G. Shubin, H.S. Rzepa
    Elevated reaction order of 1,3,5-tri-tert-butylbenzene bromination as evidence of a clustered polybromide transition state: a combined kinetic and computational study
    Org. Biomol. Chem., 2019, V. 17, N 15, pp 3781-3789 doi:10.1039/C9OB00607A, IF=3.49
  54. Zh. Zhu, G.E. Salnikov, K.Yu. Koltunov
    Cascade reaction of 2,3-naphthalenediol with benzene in the presence of aluminum halides
    Tetrahedron Letters, 2019, V. 60, N 12, Pp 857-859 doi:10.1016/j.tetlet.2019.02.026, IF=2.259
  55. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
  56. Synthesis of diazaadamantanes from 1,5-dimethylbispidinone and some natural ketones/ Suslov E.V.1, Ponomarev K. Yu.1, Korchagina D.V.1, Volcho K.P.1,2, Salakhutdinov N.F.// Russian Chemical Bulletin, 2019, V. 68, N 3, pp 601-605 doi:10.1007/s11172-019-2461-z, IF=1.014
  57. D.O. Prima, A.G. Makarov, I.Yu. Bagryanskaya, A.E. Kolesnikov, L.V. Zargarova, D.S. Baev, T.F. Eliseeva, L.V. Politanskaya, A.Yu. Makarov, Yu.G. Slizhov, A. V. Zibarev
    Fluorine-Containing n-6 and Angulaand Linear n-6-n' (n, n' = 5, 6, 7) Diaza-Heterocyclic Scaffolds Assembled on Benzene Core in Unified Way
    ChemistrySelect, 2019, V. 4, N 8, Pp 2383-2386 doi:10.1002/slct.201803970, IF=1.716
  58. A.V. Artem.ev, E.A. Pritchina, M.I. Rakhmanova, N.P. Gritsan, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Alkyl-dependent self-assembly of the first red-emitting zwitterionic {Cu4I6} clusters from [alkyl-P(2-Py)3]+ salts and CuI: when size matters
    Dalton Trans., 2019, V. 48, N 7, Pp 2328-2337 doi:10.1039/C8DT04328K, IF=4.052
  59. V.Yu. Shuvalovv, A.S. Rupp, A.S. Fisyuk, A.K. Kuratova, A.A. Nefedov, G.P. Sagitullina
    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
    ChemistrySelect, 2019, V. 4, N 5, Pp 1696-1699 doi:10.1002/slct.201803515, IF=1.716
  60. A.G. Ogienko, A.V. Markov, A.V. Sen'kova, E.B. Logashenko, O.V. Salomatina, S.A. Myz, A.A. Ogienko, A.A. Nefedov, E.A. Losev, T.N. Drebushchak, N.F. Salakhutdinov, V.V. Boldyrev, V.V. Vlasov, M.A. Zenkova, E.V. Boldyreva
    Increasing bioavailability of very poorly water-soluble compounds. A case study of an anti-tumor drug, soloxolon methyl
    Journal of Drug Delivery Science and Technology, 2019, V. 49, Pages 35-42 doi:10.1016/j.jddst.2018.10.025, IF=2.606
  61. Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048, IF=0.634
  62. S.M. Adekenov, P.Zh. Zhanimkhanova, Zh.S. Nurmaganbetov, A. Amanzhan, S.V. Chernov, A.Zh. Turmukhambetov, I.Yu. Bagryanskaya, Yu.V. Gatilov, E.E. Shults
    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 2, pp 135-141 doi:10.1007/s10593-019-02429-1, IF=1.492
  63. Generation of Perfluoroand 1-Chloroperfluoroindanyl and -Benzocyclobutenyl Cations with Perfluoroalkyl Groups in the Aliphatic Ring/ T.V. Mezhenkova, V.M. Karpov, Ya.V. Zonov , I.P. Chuikov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 193–201 doi:10.1134/S1070428019020118, IF=0.751
  64. R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, T.V. Rybalova, E.V. Tretyakov
    Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles
    J. Org. Chem., 2019, 84 (2), pp 963-972 doi:10.1021/acs.joc.8b02904, IF=4.745
  65. N. Pushkarevsky, E. Chulanova, L. Shundrin, A. Smolentsev, G. Salnikov, E. Pritchina, A. Genaev, I. Irtegova, I. Bagryanskaya, S. Konchenko, N. Gritsan, J. Beckmann, A. Zibarev
    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
    Chemistry - A European Journal, Chemistry - A European Journal, 2019, V. 25, N 3, Pp 806-816 doi:10.1002/chem.201803465, IF=5.16
  66. O.P. Korobeinichev, A.A. Paletsky, M.B. Gonchikzhapov, R.K. Glaznev, I.E. Gerasimov, Y.K. Naganovsky, I.K. Shundrina, A.Yu. Snegirev, R. Vinu
    Kinetics of Thermal Decomposition of PMMA at Different Heating Rates and in a Wide Temperature Range
    Thermochimica Acta, 2019, V. 671, Pp 17-25 doi:Thermochimica Acta, Available online 30 , IF=2.251
  67. The Xiongnu Gold from Noin-Ula (Mongolia)/ N.V. Polosmak, S.S. Shatskaya, M.V. Zadorozhnyy, L.P. Kundo, E.V. Karpova// Archaeology, Ethnology and Anthropology of Eurasia, 2019, V. 47, N 1, Pp 83-94 doi:10.17746/1563-0110.2019.47.1.083-094
  68. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
  69. M.A. Gromova, Yu.V. Kharitonov, M.A. Pokrovskii, I.Yu. Bagryanskaya, A.G. Pokrovskii, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 37. Synthesis and Cytotoxicity of 4-(Oxazol-2-Yl)-18-Norisopimaranes
    Chemistry of Natural Compounds, 2019, V. 55, N 1, pp 52-59 doi:10.1007/s10600-019-02613-x, IF=0.567
  70. Antimony Complexes {[2,6-(OME)2C6H3]3SBCH2C(O)OET}2[HG2I6]2- and {[2,6-(OME)2C6H3]3SBME}2+[HgI4]2- ˙ DMSO : Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina, I. V. El'tsov, N. V. Kurat'eva// Russian Journal of Inorganic Chemistry, 2019, V. 64, N 1, pp 28-35 doi:10.1134/S0036023619010078, IF=0.822
  71. Reactions of 1,4-naphthoquinone and 5-hydroxy-1,4-naphthoquinone with ninhydrin/ L.M. Gornostaev, O.I. Fominyh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A. Stashina// Russian Chemical Bulletin, V. 68, N 1, pp 86-91 doi:10.1007/s11172-019-2420-8, IF=1.014
  72. P. Fedyushin, E. Panteleeva, I. Bagryanskaya, K. Maryunina, K. Inoue, D. Stass, E. Tretyakov
    An approach to fluorinated phthalonitriles containing a nitronyl nitroxide or iminonitroxide moiety
    Journal of Fluorine Chemistry, 2019, V. 217, Pp 1-7 doi:10.1016/j.jfluchem.2018.10.016, IF=2.055

2018
  1. A.V. Artem'ev, I.Yu. Bagryanskaya
    [Cu4I73-]n: A novel 1-D iodocuprate aggregate
    Journal of Molecular Structure, 2018, V. 1173, Pp. 743-749 doi:10.1016/j.molstruc.2018.07.006, IF=2.011
  2. M.A. Gromova, Yu.V. Kharitonov, I.Yu. Bagryanskaya, E.E. Shults
    Efficient Synthesis of the N-(buta-2,3-dienyl)carboxamide of Isopimaric Acid and the Potential of This Compound towards Heterocyclic Derivatives of Diterpenoids
    ChemistryOpen, 2018, V. 7, N 11, Pp 890-901 doi:10.1002/open.201800205, IF=2.801
  3. K.S. Kovaleva, F.I. Zubkov, N.I. Bormotov, R.A. Novikov, P.V. Dorovatovskii, V.N. Khrustalev, Yu.V. Gatilov, V.V. Zarubaev, O.I. Yarovaya, L.N. Shishkina, N.F. Salakhutdinov
    Synthesis of D-(+)-camphor-based N-acylhydrazones and their antiviral activity
    Med. Chem. Commun., 2018, V. 9, N 12, Pp 2072-2082 doi:10.1039/C8MD00442K, IF=2.342
  4. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Superelectrophilic activation of 1-nitronaphthalene in the presence of aluminum chloride. Reactions with benzene and cyclohexane
    Org. Biomol. Chem., 2018, V.16, N 47, Pp 9129-9132 doi:10.1039/C8OB02653J, IF=3.423
  5. Thermal Reactions of Polyfluoro-ortho-chloroarenethiols with Tetrafluoroethylene/ P. V. Nikul'shin, A. M. Maksimov, Yu. V. Gatilov, V. E. Platonov// Russian Journal of General Chemistry, 2018, V. 88, N 12, pp 2486-2497 doi:10.1134/S107036321812006X, IF=0.658
  6. A. Ogienko, S. Myz, A. Ogienko, A. Nefedov, A.S. Stoporev, M.S. Mel'gunov, A.S. Yunoshev, T. Shakhtshneider, V.V. Boldyrev, E. Boldyreva
    Cryosynthesis of co-crystals of poorly water-soluble pharmaceutical compounds and their solid dispersions with polymers. “Meloxicam - succinic acid” system as a case study
    Cryst. Growth Des. 2018, 18, 12, 7401-7409 doi:10.1021/acs.cgd.8b01070, IF=3.971
  7. A.D. Rogachev, O.I. Yarovaya, A.V. Fatianova, V.A. Lavrinenko, E.V. Amosov, V.V. Zarubaev, A.G. Pokrovsky, N.F. Salakhutdinov
    Untargeted search and identification of metabolites of antiviral agent camphecene in rat urine by liquid chromatography and mass spectrometry and studying their distribution in organs following peroral administration of the compound
    Journal of Pharmaceutical and Biomedical Analysis, 2018, V. 161, Pp 383-392 doi:10.1016/j.jpba.2018.09.003, IF=2.831
  8. R. Ottenbacher, E. Talsi, T. Rybalova, K.P. Bryliakov
    Enantioselective Benzylic Hydroxylation of Arylalkanes with H2O2 in Fluorinated Alcohols in the Presence of Chiral Mn Aminopyridine Complexes
    ChemCatChem, 2018, V.10, N 22, Pp 5323-5330 doi:10.1002/cctc.201801476, IF=4.673
  9. G.A. Selivanova, A.D. Skolyapova, R.I. Dralyuk, E.V. Karpova, I.K. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov, T.V. Basova, E.V. Tretyakov
    Solid-phase transitions of polymorphs of 4-(4-N,N-dialkylaminophenyl)azobiphenyl-2,3'4'-tricarbonitriles and their analogues
    Thermochimica Acta, 2018, V. 669, Pp 88-98 doi:10.1016/j.tca.2018.08.022, IF=2.188
  10. 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
  11. Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts/ A. M. Astakhov, D. V. Antishin, А. А. Nefedov, G. E. Salnikov, E. S. Buka// Russian Journal of Organic Chemistry, 2018, V. 54, N 11, pp 1638-1642 doi:10.1134/S1070428018110039, IF=0.654
  12. A.I. Taratayko, T.V. Rybalova, V.A. Reznikov
    Synthesis of paramagnetic spiropyran derivatives
    Chemistry of Heterocyclic Compounds, 2018, V. 54, N 10, pp 981-983 doi:10.1007/s10593-018-2375-y, IF=1.2
  13. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
  14. Molecular and Supramolecular Structure of 8-(Trifluoromethyl)Benzo[f][1,2,3,4,5] Pentathiepin-6-Amine - A Representative of Condensed Arene Pentathiepines/ T. V. Rybalova, A. D. Rogachev, T. M. Khomenko, K. P. Volcho, N. F. Salakhutdinov// Journal of Structural Chemistry, 2018, V. 59, N 7, pp 1753-1758 doi:10.1134/S0022476618070326, IF=0.521
  15. А.П. Крысин, А.А. Нефедов, Т.Я. Гаврикова, А.С. Кильметьев
    О реакции полисульфидов 2-трет-бутилфенола с каучуком и гептеном-1 в инертной атмосфере и на воздухе
    Химия в интересах устойчивого развития. 2018. Т. 26. № 4. С. 403-410. doi:10.15372/KhUR20180407
  16. S.A. Dobrynin, Yu.I. Glazachev, Yu.V. Gatilov, E.I. Chernyak, G.E. Salnikov, I.A. Kirilyuk
    Synthesis of 3,4-Bis-(hydroxymethyl)-2,2,5,5-tetraethylpyrrolidin-1-oxyl via 1,3-Dipolar Cycloaddition of Azomethine Ylide to Activated Alkene
    J. Org. Chem., 2018, V. 83, N 10, Pp 5392-5397 doi:10.1021/acs.joc.8b00085, IF=4.805
  17. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  18. N.A. Semenov, D.E. Gorbunov, M.V. Shakhova, G.E. Salnikov, I.Yu. Bagryanskaya, V.V. Korolev, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudo Halides CN- and XCN- (X = O, S, Se, Te)
    Chemistry - A European Journal, 2018, V.24, N 49, Pp 12983-12991 doi:10.1002/chem.201802257, IF=5.16
  19. И.Ю. Журавлева, Е.В. Карпова, Л.А. Опарина, Н. Кабос, А.Л. Ксенофонтов, А.С. Журавлева, Н.Р. Ничай, А.В. Богачев-Прокофьев, Б.А. Трофимов, А.М. Караськов
    Ксеноперикард, консервированный дии пентаэпоксидами: молекулярные механизмы сшивки и механические свойства биоматериала
    Патология кровообращения и кардиохирургия. 2018. Т. 22. № 3. С. 56-68. doi:10.21688-1681-3472-2018-3-56-68
  20. V.E. Romanov, I.Yu. Bagryanskaya, D.E. Gorbunov, N.P. Gritsan, E.V. Zaytseva, D. Luneau, E.V. Tretyakov
    A Crystallographic Study of a Novel Tetrazolyl-Substituted Nitronyl Nitroxide Radical
    Crystals 2018, 8(9), 334 doi:10.3390/cryst8090334, IF=2.144
  21. I.V. Kulakov, I.V. Palamarchuk, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, structure and biological activity 3- (arylmethyl) aminopyridine-2 (1H) -ones and 1H-pyrido[2,3-b][1,4]oxazin-2(3H)-ones
    Journal of Molecular Structure, V.1166, 15 August 2018, Pp. 262-269 doi:10.1016/j.molstruc.2018.04.036, IF=2.011
  22. A.I. Titkov, I.K. Shundrina, R.M. Gadirov, A.V. Odod, A.E. Kurtsevich, Yu.M.Yukhin, N.Z. Lyakhov
    Thermal and laser sintering of a highly stable inkjet ink consisting of silver nanoparticles stabilized by a combination of a short chain carboxylic acid and a polymeric dispersant
    Materials Today: Proceedings, 2018, V. 5, N 8, Part 2, Pp 16042-16050 (14th International Conference on Nanosciences & Nanotechnologies (NN17) 4–7 July 2017 | Thessaloniki, Greece) doi:10.1016/j.matpr.2018.05.049
  23. M.B. Bushuev, V.P. Krivopalov, E.B. Nikolaenkova, K.A. Vinogradova, Yu.V. Gatilov
    Hysteretic spin crossover in isomeric iron(II) complexes
    Dalton Trans., 2018, V. 47, N 29, Pp 9585-9591 doi:10.1039/C8DT02223B, IF=4.099
  24. 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
  25. Модификация аминогруппы полифторированных арилендиаминов в реакциях с альдегидами и хинонами/ Т.А. Ваганова, И.П. Чуйков, Е.В. Малыхин// Fluorine notes, 2018, V.119, N 4, Cc 5-6 doi:10.17677/fn20714807.2018.04.03
  26. L. Politanskaya, Z. Duan, I. Bagryanskaya, I. Eltsov, E. Tretyakov, Chanjuan. Xi
    Highly efficient synthesis of polyfluorinated 2-mercaptobenzothiazole derivatives
    Journal of Fluorine Chemistry, 2018, V. 212, Pp 130-136 doi:10.1016/j.jfluchem.2018.06.001, IF=1.879
  27. V.V. Krisyuk, S. Urkasym-Kyzy, T.V. Rybalova, I.A. Baidina, I.V. Korolkov, D.L. Chizhov, D.N. Bazhin, Yu.S. Kudyakova
    Isomerization as a tool to design volatile heterometallic complexes with methoxy-substituted β-diketonates
    JJournal of Coordination Chemistry, 2018, V. 71, N 14, Pp 2194-2208 doi:10.1080/00958972.2018.1479746, IF=1.703
  28. I.K. Shundrina, D.S. Odintsov, I.A. Os'kina, I.G. Irtegova, L.A. Shundrin
    Synthesis, electrochemical reduction and radical anions of 2-{[bis(4-amino(nitro)phenyl)]aminomethyl}-9H-thioxanthene-9-one derivatives
    European Journal of Organic Chemistry, 2018, V. 2018, N 26, Pp 3471-3480 doi:10.1002/ejoc.201800525, IF=2.882
  29. S.I. Zhivetyeva, I.A. Zayakin, I.Yu. Bagryanskaya, E.V. Zaytseva, E.G. Bargyanskaya, E.V. Tretyakov
    Interaction of a lithiated nitronyl nitroxide with polyfluorinated 1,4-naphthoquinones
    Tetrahedron, 2018, V. 74, N 28, Pp 3924-3930 doi:10.1016/j.tet.2018.05.075, IF=2.377
  30. A.L. Zakharenko, E.S. Mozhaitsev, E.V. Suslov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Synthesis and Inhibitory Properties of Imines Containing Monoterpenoid and Adamantane Fragments Against DNA Repair Enzyme Tyrosyl-DNA Phosphodiesterase 1 (Tdp1)
    Chemistry of Natural Compounds, 2018, V. 54, N 4, pp 672-676 doi:10.1007/s10600-018-2443-7, IF=0.449
  31. L. Politanskaya, T. Rybalova, O. Zakharova, G. Nevinsky, E. Tretyakov
    p-Toluenesulfonic acid mediated one-pot cascade synthesis and cytotoxicity evaluation of polyfluorinated 2-aryl-2,3-dihydroquinolin-4-ones and their derivatives
    Journal of Fluorine Chemistry, 2018, V.211, Pp 129-140 doi:10.1016/j.jfluchem.2018.04.005, IF=1.879
  32. A.D. Skolyapova, G.A. Selivanova, E.V. Tretyakov, I.Yu. Bagryanskaya, V.D. Shteingarts
    Synthesis of polyfluorinated aminoquinolines via nitroquinolines
    Journal of Fluorine Chemistry, 2018, V. 211, Pp 14-23 doi:10.1016/j.jfluchem.2018.04.006, IF=1.879
  33. I.V. Ilyina, V.V. Zarubaev, I.N. Lavrentieva, A.A. Shtro, I.L. Esaulkova, D.V. Korchagina, S.S. Borisevich, K.P. Volcho, N.F. Salakhutdinov
    Highly potent activity of isopulegol-derived substituted octahydro-2H-chromen-4-ols against influenza A and B viruses
    Bioorganic & Medicinal Chemistry Letters, 2018, V. 28, N 11, Pp 2061-2067 doi:10.1016/j.bmcl.2018.04.057, IF=2.371
  34. A.V. Karakulov, E.A. Karpova, V.G. Vasiliev
    Ecological and geographical variation of morphometric parameters and flavonoid composition of Rhododendron parvifolium
    Turczaninowia, 2018, V. 21, N 2, Pp 133-144 doi:10.14258/turczaninowia.21.2.14
  35. Tris(2,6-dimethoxyphenyl)antimony Diazide: Synthesis and Structure/ I. V. Egorova, V. V. Zhidkov, I. P. Grinishak, I. Yu. Bagryanskaya, N. V. Pervukhina// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 6, pp 781-785 doi:10.1134/S0036023618060086, IF=0.709
  36. The content of biologically active polyphenols Lonicera Caerulea Subsp. Pallasll in Natural Conditions and the introduction/ I.G. Boyarskikh, K.G. Vasiliev, T.A. Kukushkina// Khimiya Rastitel'nogo Syr'ya, 2018, N 2, Pp 89-96 doi:10.14258/jcprm.2018023452
  37. 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
  38. S. Bothe, J. Nowag, V. Klimavicius, M. Hoffmann, T.I. Troitskaya, E.V. Amosov, V.M. Tormyshev, I. Kirilyuk, A. Taratayko, A.A. Kuzhelev, D. Parkhomenko, E.G. Bagryanskaya, T. Gutmann, G. Buntkowsky
    Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
    J. Phys. Chem. C, 2018, 122 (21), pp 11422-11432 doi:10.1021/acs.jpcc.8b02570, IF=4.484
  39. A.V. Artem'ev, E.P. Doronina, I.Yu. Bagryanskaya, L.V. Klyba
    Bis(dicyclohexylselenophosphinyl)selenide, [Cy2P(Se)]2Se: Synthesis, molecular structure and application for self-assembly of a tetrahedral Cu(I) cluster
    Journal of Molecular Structure, 2018, V. 1160, Pp 208-214 doi:10.1016/j.molstruc.2018.02.007, IF=2.011
  40. G. Audran, E.G. Bagryanskaya, I.Yu. Bagryanskaya, M. Edeleva, P. Kaletina, S.R-A. Marque, D. Parkhomenko, E.V. Tretyakov, S.I. Zhivetyeva
    The effect of the oxophilic Tb(III) cation on Csingle bond-ON bond homolysis in alkoxyamines
    Inorganic Chemistry Communications, 2018, V. 91, Pp 5-7 doi:10.1016/j.inoche.2018.02.019, IF=1.81
  41. Synthesis and Structure of Cyclohexenes Functionalized by Nitro and Trifluoro(chloro)methyl Groups/ N. A. Anisimova, E. K. Slobodchikova, V. M. Berestovitskaya, M. E. Ivanova, A. A. Kuzhaeva, T. V. Rybalova// Russian Journal of General Chemistry, 2018, V. 88, N 5, Pp 883-891 doi:10.1134/S1070363218050079, IF=0.658
  42. Hexa(isothiocyanato)chromates(III) of Some Yttrium Group Lanthanide(III) and Europium Complexes with Nicotinic Acid: Synthesis and Crystal Structures/ E. V. Cherkasova, N. V. Pervukhina, N. V. Kuratieva, I. Yu. Bagryanskaya, T. G. Cherkasova// Russian Journal of Inorganic Chemistry, 2018, V. 63, N 5, pp 626-630 doi:10.1134/S003602361805011X, IF=0.709
  43. Configurational Stability of 1,1'-Bi-2-naphthol in Superacid System HSO3F-SBF5-SO2ClF/ G. E. Salnikov, A. M. Genaev, A. V. Shernyukov, Z. Zhu, N. V. Tkachenko, K. Yu. Koltunov// Russian Journal of Organic Chemistry, 2018, V. 54, N 5, pp 792-794 doi:10.1134/S1070428018050214, IF=0.655
  44. M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
    Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
    Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
  45. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
  46. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
  47. D. Sadyrbekov, T. Saliev, Yu. Gatilov, I. Kulakov, R. Seidakhmetova, T. Seilkhanov, S. Askarova
    Spatial Structure and Antimicrobial Activity of Cyclopropane Derivative of Limonene
    Natural Product Communications, 2018, V. 13, N 4, Pp: 387-388 WOS:000433651900001, IF=0.809
  48. A.O. Finke, M.E. Mironov, A.B. Skorova, E.E. Shults
    Copper-catalyzed 1,3-dipolar cycloaddition reaction of spirosolanederived azide for the preparation of modified solasodine alkaloid
    Chemistry of Heterocyclic Compounds, 2018, V. 54, N 4, pp 411-416 doi:10.1007/s10593-018-2284-0, IF=1.201
  49. I.V. Kulakov, D.N. Ogurtsova, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis, Structure, and Some Transformations of Novel 1,5-methanonaphtho[1,2-g][1,3,5]oxadiazocine Derivatives
    Journal of Heterocyclic Chemistry, 2018, V. 55, N 4, Pp 923-928 doi:10.1002/jhet.3119, IF=1.141
  50. M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 36.* Synthesis of 13-(Oxazol-5-Yl)-15,16-Bisnorisopimaranes
    Chemistry of Natural Compounds, 2018, V. 54, N 2, pp 293-300 doi:10.1007/s10600-018-2327-x, IF=0.45
  51. Reaction of Perfluorobenzocyclobutene with Excess Pentafluorobenzene in SbF5/ T.V. Mezhenkova, V.R. Sinyakov, V.M. Karpov, Ya.V. Zonov, Yu.V. Gatilov, V.E. Platonov// Russian Journal of Organic Chemistry, 2018, V. 54, N 4, pp 545-553 doi:10.1134/S107042801804005X, IF=0.655
  52. A.Yu. Makarov, I.Yu. Bagryanskaya, Yu.M. Volkova, M.M. Shakirov, A.V. Zibarev
    Salts of Sterically-Hindered Chalcogen-Varied Herz Cations Including Those with New Anions [Te3Cl14]2- and [Te4Cl18]2- Anions
    European Journal of Inorganic Chemistry, 2018, V. 2018, N 11, Pp 1322-1332 doi:10.1002/ejic.201701470, IF=2.507
  53. V.S. Glukhacheva, S.G. Il'yasov, A.A. Obraztsov, Yu.V. Gatilov, I.V. Eltsov
    A New Synthetic Route to Heteroanthracenes
    European Journal of Organic Chemistry, 2018, V. 2018, N 10, Pp 1265-1273 doi:10.1002/ejoc.201701689, IF=2.882
  54. 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
  55. Molecular and Crystal Structure of 2-Amino-Polyfluorophenyl-4,4,5,5-Tetramethyl-4,5-Dihydro-1H-Imidazol- 3-Oxide-1-Oxyls/ E.V. Tretyakov, T.V. Makhneva, L.V. Politanskaya, I.Yu. Bagryanskaya, D.V. Stass// Journal of Structural Chemistry, 2018, V. 59, N 3, pp 689-696 doi:10.1134/S0022476618030289, IF=0.521
  56. А.П. Крысин, В.П. Фадеева, О.Н. Никуличева, А.А. Нефедов
    Решение алгоритма: фенольные антиоксиданты - путь к улучшению механических свойств полимерных материалов
    Химия в интересах устойчивого развития. 2018. Т. 26. № 2. С. 149-155 doi:10.15372/KhUR20180205
  57. P.A. Fedyushin, R.Yu. Peshkov, E.V. Panteleeva, E.V. Tretyakov, I.V. Beregovaya, Yu.V. Gatilov, V.D. Shteingarts
    Purposeful regioselectivity control of the Birch reductive alkylation of biphenyl-4-carbonitrile
    Tetrahedron, 2018, V. 74, N 8, Pages 842-851 doi:10.1016/j.tet.2017.12.046, IF=2.377
  58. A.V. Artem'ev, M.R. Ryzhikov, I.V. Taidakov, M.I. Rakhmanova, E.A. Varaksina, I.Yu. Bagryanskaya, S.F. Malysheva, N.A. Belogorlova
    Bright green-to-yellow emitting Cu(I) complexes based on bis(2-pyridyl)phosphine oxides: synthesis, structure and effective thermally activated-delayed fluorescence
    Dalton Trans., 2018, V.47, N 8, Pp 2701-2710 doi:10.1039/C7DT04758D, IF=4.099
  59. K.Yu. Ponomarev, E.V. Suslov, A.L. Zakharenko, O.D. Zakharova, A.D. Rogachev, D.V. Korchagina, A. Zafar, J. Reynisson, A.A. Nefedov, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Aminoadamantanes Containing Monoterpene-derived Fragments as Potent Tyrosyl-DNA phosphodiesterase 1 Inhibitors
    Bioorganic Chemistry, V.76, February 2018, Pp. 392-399 doi:10.1016/j.bioorg.2017.12.005, IF=3.929
  60. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, I.P. Chuikov, E.V. Malykhin
    Controlled self-assembly of π-stacked/H-bonded 1D crystal structures from polyfluorinated arylamines and 18-crown-6 (2:1).Associate vs. co-former fluorescence properties
    CrystEngComm, 2018, V. 20, N 6, Pp 807-817 doi:10.1039/C7CE01851G, IF=3.304
  61. Synthesis of Nickel Nanoparticles by the Reduction of Its Salts Using the Modified Polyol Method in the Presence of Sodium Polyacrylates with Various Molecular Weights/ O. A. Logutenko, A. I. Titkov, A. M. Vorob'ev, I. K. Shundrina, Yu. M. Yukhin, N. Z. Lyakhov// Russian Journal of General Chemistry, 2018, V. 88, N 2, pp 288-294 doi:10.1134/S1070363218020160, IF=0.658
  62. X-Ray Diffraction Study of Perfluoro- 9,10-Diphenylanthracene and Perfluoro- 9,10-Diphenyldihydroanthracenes/ Yu. V. Gatilov, T.V. Mezhenkova, V.M. Karpov// Journal of Structural Chemistry, 2018, V. 59, N 2, pp 449-454 (doi: 10.1134/S0022476618020282) doi:10.1134/S0022476618020282, IF=0.521
  63. S.I. Zhivetyeva, E.V. Tretyakov, I.Yu. Bagryanskaya
    Synthesis of novel phosphonium betaines and bis-betaines derived from hexafluoro-1,4-naphthoquinone
    Journal of Fluorine Chemistry, V. 206, February 2018, Pp. 19-28 doi:10.1016/j.jfluchem.2017.11.010, IF=1.879
  64. Yu.V. Yushkova, E.I. Chernyak, Yu.V. Gatilov, V.G. Vasil'ev, S.V. Morozov, I.A. Grigor'ev
    Synthesis, Structure, Antioxidant Activity, and Water Solubility of Trolox Ion Conjugates
    Saudi Pharmaceutical Journal, 2018, V. 26, N 1, Pp 84-92 doi:10.1016/j.jsps.2017.10.008, IF=3.11
  65. Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release/ L. S. Konstantinova, E. A. Knyazeva, Yu. V. Gatilov, S. G. Zlotin, O. A. Rakitin// Russian Chemical Bulletin, 2018, V. 67, N1, pp 95-101 doi:10.1007/s11172-018-2042-6, IF=0.781
  66. Oximation of 2-(R1-Amino)-4-(R2-imino)naphthalen-1(4H)-ones/ L. M. Gornostaev, T. A. Rukovets, E. V. Arnold, Yu. G. Khalyavina, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2018, V. 54, N 1, pp 78-86 doi:10.1134/S1070428018010062, IF=0.655

2017
  1. A.V. Artem'ev, Ju.A. Eremina, E.V. Lider, O.V. Antonova, E.V. Vorontsova, I.Yu. Bagryanskaya
    Luminescent Ag(I) scorpionates based on tris(2-pyridyl)phosphine oxide: Synthesis and cytotoxic activity evaluation
    Polyhedron, 2017, V. 138, Pp 218-224 doi:10.1016/j.poly.2017.09.041, IF=1.925
  2. V. Romanov, A. Vorob'ev, I. Bagryanskaya, D. Parkhomenko, E. Tretyakov
    1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines
    Australian Journal of Chemistry, 2017, 70(12) 1317-1320 doi:10.1071/CH17476, IF=1.327
  3. A. V. Artem'ev, V. A. Kuimov, E. A. Matveeva, I. Yu. Bagryanskaya, A. I. Govdi, S. F. Vasilevsky, M.I. Rakhmanova, D. O. Samultsev, N. K. Gusarova, B. A. Trofimov
    A new access to tri(1-naphthyl)phosphine and its catalytically active palladacycles and luminescent Cu(I) complex
    Inorganic Chemistry Communications, 2017, V. 86, 2017, Pp 94-97 doi:10.1016/j.inoche.2017.09.008, IF=1.639
  4. K.Yu. Ponomarev, E.A. Morozova, E.V. Suslov, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 5,7- and 6-Substituted Diazaadamantanes Containing Monoterpene Moieties
    Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1131-1136 doi:10.1007/s10600-017-2216-8, IF=0.46
  5. O.S. Patrusheva, A.V. Pavlova, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties
    Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1066-1071 doi:10.1007/s10600-017-2202-1, IF=0.46
  6. L.S. Konstantinova, I.V. Baranovsky, E.A. Pritchina, M.S. Mikhailov, I.Yu. Bagryanskaya, N.A. Semenov, I.G. Irtegova, G.E. Salnikov, K.A. Lyssenko, N.P. Gritsan, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
    Chemistry - A European Journal, 2017, V. 23, N 67, Pp 17037-17047 doi:10.1002/chem.201703182, IF=5.316
  7. Development and Validation of a Method for Determination of a New Effective Inhibitor of Influenza Virus H1N1 in Blood Plasma/ A. S. Sokolova, O. I. Yarovaya, A. A. Nefedov, N. F. Salakhutdinov// Pharmaceutical Chemistry Journal, 2018, V. 51, N 12, pp 1102-1105 doi:10.1007/s11094-018-1748-y, IF=0.444
  8. P.A. Abramov, K. A. Brylev, A.Yu. Vorob'ev, Yu. V. Gatilov, G. I. Borodkin, N. Kitamura, M. N. Sokolov
    Emission tuning in Re(I) complexes: Expanding heterocyclic ligands and/or introduction of perfluorinated ligands
    Polyhedron, 2017, V.137, Pp 231-237 doi:10.1016/j.poly.2017.08.046, IF=1.925
  9. V.Yu. Shuvalov, I.V. Eltsov, N.A. Tumanov, E.V. Boldyreva, A.A. Nefedov, G.P. Sagitullina
    [6]-[9]Metacyclophanes: a New Synthesis, Crystal Structures, NMR- and UV-Research
    European Journal of Organic Chemistry, 2017, V. 2017,N 36, Pp 5410-5416 doi:10.1002/ejoc.201700946, IF=2.834
  10. E. Tretyakov, A. Keerthi, M. Baumgarten, S. Veber, M. Fedin, D. Gorbunov, I. Shundrina, N. Gritsan
    The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes
    ChemistryOpen, 2017, V. 6, N 5, Pp 642-652 doi:10.1002/open.201700110, IF=2.917
  11. I.V. Kulakov, A.A. Karbainova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov, A.S. Fisyuk
    Synthesis and Analgesic Activity of bis(3,4-dihydroquinoxalin-2(1H)-one) and bis(3,4-dihydro-2H-1,4-benzoxazin-2-one) Derivatives
    Chemistry of Heterocyclic Compounds, 2017, V.53, N 10, pp 1094-1097 doi:10.1007/s10593-017-2178-6, IF=0.893
  12. E. Suslov, V.V. Zarubaev, A.V. Slita, K. Ponomarev, D. Korchagina, D.M. Ayine-Tora, J. Reynisson, K. Volcho, N. Salakhutdinov
    Anti-Influenza Activity of Diazaadamantanes Combined with Monoterpene Moieties
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 19, Pp 4531-4535 doi:10.1016/j.bmcl.2017.08.062, IF=2.453
  13. A.M. Sheveleva, A.V. Anikeenko, A.S. Poryvaev, D.L. Kuzmina, I.K. Shundrina, D.I. Kolokolov, A. G. Stepanov, M.V. Fedin
    Probing Gas Adsorption in Metal-Organic Framework ZIF-8 by EPR of Embedded Nitroxides
    J. Phys. Chem. C, Just Accepted Manuscript doi:10.1021/acs.jpcc.7b06884, IF=4.535
  14. Yu.M. Deryabina, T.A. Kornakova, N.L. Bazhina, V.D. Tikhova
    Comparative Infrared Spectra Analysis of One Territory Soil Humic Acids by IR-EXPERT Computer System
    IInt. J. Green. Pharm. 2017 (Suppl); 11(3), pp S465-S469 (http://greenpharmacy.info/index.php/ijgp/article/view/1158) doi:10.22377/ijgp.v11i03.1158
  15. D.O. Prima, D.S. Baev, E.V. Vorontsova, T.S. Frolova, I.Yu. Bagryanskaya, Yu.G. Slizhov, T.G. Tolstikova, A.Yu. Makarov, A.V. Zibarev
    New cancer cells apoptosis agents: Fluorinated aza-heterocycles
    AIP Conference Proceedings, V. 1882, N 1, 020057 (2017) (Proceedings of the International Conference on Physics of Cancer: Interdisciplinary Problems and Clinical Applications (PC IPCA’17), 23-26 May 2017, Tomsk, Russia) doi:10.1063/1.5001636
  16. A.V. Artem'ev, I.Yu. Bagryanskaya, E.P. Doronina, P.M. Tolstoy, A.L. Gushchin, M.I. Rakhmanova, A.Yu. Ivanov, A.O. Suturina
    A new family of clusters containing a silver-centered tetracapped [Ag@Ag4(μ3-P)4] tetrahedron, inscribed within a N12 icosahedron
    Dalton Trans., 2017,46, 12425-12429 doi:10.1039/C7DT02597A, IF=4.28
  17. High-temperature adsorption layers based on fluoridated polyimide and diatomite carrier/ E.Yu. Yakovleva, I.K. Shundrina, E.Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2017, V. 91, N 9, pp 1797-1804 doi:10.1134/S0036024417090321
  18. T.P. Kukina, I.A. Elshin, O.I. Sal'nikova
    Comparative Analysis of Aliphatic, Phenolcarboxylic, and Triterpenic Acids from Populus nigra and Salix alba Barks
    Chemistry of Natural Compounds, 2017, V. 53, N 5, pp 941-943 doi:10.1007/s10600-017-2162-5, IF=0.46
  19. D.O. Prima, E.V. Vorontsova, A.G. Makarov, A.Yu. Makarov, I.Yu. Bagryanskaya, T.F. Mikhailovskaya, Yu.G. Slizhov, A.V. Zibarev
    Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis
    Mendeleev Communications, 2017, V. 27, N 5, Pp 439-442 doi:10.1016/j.mencom.2017.09.002, IF=1.741
  20. N.A. Pushkarevsky, P. A. Petrov, D.S. Grigoriev, A.I. Smolentsev, L.M. Lee, F. Kleemiss, G.E. Salnikov, S.N. Konchenko, I. Vargas-Baca, S. Grabowsky, J. Beckmann, A.V. Zibarev
    Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
    Chemistry - A European Journal, 2017, V. 23, N 46, Pp 10987-10991 doi:10.1002/chem.201703018, IF=5.316
  21. K. Ponomarev, E. Morozova, A. Pavlova, E. Suslov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and Analgesic Activity of Amines Combining Diazaadamantane and Monoterpene Fragments
    Medicinal Chemistry, 2017, V. 13 , N 8, Pp 773 - 779 doi:10.2174/1573406413666170525124316, IF=2.331
  22. I.V. Kulakov, A.L. Shatsauskas, M.V. Matsukevich, I.V. Palamarchuk, T.M. Seilkhanov, Y.V. Gatilov, A.S. Fisyuk
    A New Approach to the Synthesis of Benzo[ c ][1,7]naphthyridin-4(3 H )-ones
    Synthesis (Germany), 2017, 49(16): 3700-3709 doi:10.1055/s-0036-1590470, IF=2.65
  23. T.A. Vaganova, V.I. Rodionov, I.P. Chuikov, E.A. Chochrina, E.V. Malykhin
    Selective one-pot synthesis of aminopolyhalobenzonitriles from polyhalobenzotrichlorides in anhydrous ammonia
    Journal of Fluorine Chemistry, Volume 200, August 2017, Pages 84-90 doi:10.1016/j.jfluchem.2017.06.005, IF=2.101
  24. V. Shelkovnikov, G. Selivanova, G. Lyubas, S. Korotaev, I. Shundrina, E. Tretyakov, E. Zueva, A. Plekhanov, S. Mikerin, A. Simanchuk
    Second-order nonlinear optical properties of composite material of an azo-chromophore with a tricyanodiphenyl acceptor in a poly(styrene-co-methyl methacrylate) matrix
    Optical Materials, 2017, V. 69, Pp 67-72 doi:10.1016/j.optmat.2017.04.008, IF=2.237
  25. A.N. Blaznov, E.V. Atyasova, I.K. Shundrina, V.V. Samoilenko, V.V. Firsov, A.S. Zubkov
    Thermomechanical characterization of BFRP and GFRP with different degree of conversion
    Polymer Testing, 2017, V. 60, Pp 49-57 doi:10.1016/j.polymertesting.2017.03.011, IF=2.463
  26. I. Il'ina, A. Pavlova, D. Korchagina, O. Ardashov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of monoterpenoid-derived alkyl-substituted chiral hexahydro-2H-chromenes
    Medicinal Chemistry Research, 2017, V. 26, N 7, pp 1415-1426 doi:10.1007/s00044-017-1847-4, IF=1.276
  27. T.P. Kukina, D.N. Shcherbakov, K.V. Gensh, E.A. Tulysheva, O.I. Salnikova, A.E. Grazhdannikov, E.A. Kolosova
    Bioactive Components of Sea Buckthorn Hippophae rhamnoides L. Foliage
    Russian Journal of Bioorganic Chemistry, 2017, Vol. 43, No. 7, pp. 747-751, IF=0.689
  28. V.N. Kovtonyuk, Yu.V. Gatilov
    Polyfluorinated oxacalixarenes. Interaction of perfluoro-m-xylene with resorcinol and tetrafluororesorcinol
    Journal of Fluorine Chemistry, 2017, V. 199, Pp 52-59 doi:10.1016/j.jfluchem.2017.04.010, IF=2.101
  29. 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
  30. T.M. Khomenko, V.V. Zarubaev, I.R. Orshanskaya, R.A. Kadyrova, V.A. Sannikova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-containing substituted coumarins
    Bioorganic & Medicinal Chemistry Letters, 2017, V. 27, N 13, Pp 2920-2925 doi:10.1016/j.bmcl.2017.04.091, IF=2.453
  31. A.E. Paromov, S.V. Sysolyatin, Y.V. Gatilov
    An Acid-Catalyzed Cascade Synthesis of Oxaazatetracyclo [5.5.0.03,11.05,9]dodecane Derivatives
    Journal of Energetic Materials, 2017, V.35, N 3, Pp. 363-373 doi:10.1080/07370652.2016.1194499, IF=1.557
  32. А.А. Коновалов, И.К. Шундрина, Е.В. Карпова, И.В. Ельцов, Е.А. Орлова, Н.П. Гончаров
    Влияние лигнификации и минерализации тканей листа на устойчивость к бурой ржавчине растений мягкой пшеницы
    Вавиловский журнал генетики и селекции, 2017, Т. 21, N 6, Сс. 686-693 doi:10.18699/VJ17.286
  33. Hexafluorosilicates of cobalt(II) complexes with dimethylsulfoxide and dimethylformamide/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, N.V. Kurat'eva, V.V. Medvedev, E.S. Tatarinova, E.V. Cherkasova// Russian Journal of Inorganic Chemistry, June 2017, V. 62, N 6, pp 760-765 doi:10.1134/S003602361706002X, IF=0.787
  34. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
  35. S.S. Patrushev, T.V. Rybalova, I. D. Ivanov, V.A. Vavilin, E.E. Shults
    Synthesis of a new class of bisheterocycles via the Heck reaction of eudesmane type methylene lactones with 8-bromoxanthines
    Tetrahedron, 2017, V. 73, N 19, Pp 2717-2726 In Press, Accepted Manuscript - Note to users doi:10.1016/j.tet.2017.03.016, IF=2.651
  36. P.A. Zaikin, O.T. Dyan, D.V. Evtushok, A.N. Usoltsev, E.V. Karpova, G.I. Borodkin, V.G. Shubin
    Solvent-free Fluorination of Electron Rich Aromatic Compounds with F-TEDA-BF4 Reagent: Toward "Dry" Processes
    European Journal of Organic Chemistry, 2017, V. 2017, N 17, Pp 2469-2474 doi:10.1002/ejoc.201700179, IF=2.834
  37. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  38. 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
  39. 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
  40. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, S.R.A. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    Zinc(II) Hexafluoroacetylacetonate Complexes of Alkoxyamines: NMR and Kinetic Investigations. First Step for a New Way to Prepare Hybrid Materials
    ChemistrySelect, 2017, V. 2, N 12, Pp 3584-3593 doi:10.1002/slct.201700678
  41. G.E. Salnikov, A.M. Genaev, A.V. Shernyukov, V.G. Shubin
    Protonation of ninhydrin and indan-1,2,3-trione revisited: A combined theoretical and experimental study
    Journal of Molecular Structure, 2017, V. 1134, Pp 1-5 doi:10.1016/j.molstruc.2016.12.057, IF=1.753
  42. I.K. Shundrina, M.A. Matsko, K.I. Baskakova, L.G. Echevskaya, M.I. Nikolaeva, L.A. Shundrin, V.A. Zakharov
    Dynamic mechanical analysis of ethylene/1-hexene copolymers: The effect of the catalyst type on the short-chain branching distribution and properties of the amorphous and crystalline phases
    Journal of Applied Polymer Science, 2017, V. 134, N 14, Article number 44638 doi:10.1002/app.44638, IF=1.86
  43. T.A. Vaganova, Y.V. Gatilov, S.E. Malykhin, D.P. Pishchur, Y.V. Larichev, V.I. Rodionov, E.V. Malykhin
    Design and supramolecular structure of crystal associates of polyfluoroarylenediamines and 18-crown-6 (2:1)
    Journal of Molecular Structure, V. 1133, 5 April 2017, P. 122-134 doi:10.1016/j.molstruc.2016.11.091, IF=1.753
  44. E.V. Tretyakov, P.A. Fedyushin, E.V. Panteleeva, D.V. Stass, I.Yu. Bagryanskaya, I.V. Beregovaya, A.S. Bogomyakov
    Substitution of a Fluorine Atom in Perfluorobenzonitrile by a Lithiated Nitronyl Nitroxide
    J. Org. Chem., 2017, 82 (8), pp 4179-4185 doi:10.1021/acs.joc.7b00144, IF=4.848
  45. A.D. Skolyapova, G.A. Selivanova, E.V. Tretyakov, T.F. Bogdanova, L.N. Shchegoleva, I.Yu. Bagryanskaya, L.Yu. Gurskaya, V.D. Shteingarts
    Interaction of polyfluorinated 2-chloroquinolines with ammonia
    Tetrahedron, 2017, V. 73, N 9, Pp 1219-1229 doi:10.1016/j.tet.2017.01.026, IF=2.651
  46. M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
    Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
    CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
  47. S.A. Prikhod'ko, A.Yu. Shabalin, V.V. Bardin, I.V. Eltsov, I.K. Shundrina, V.N. Parmon, N.Yu. Adonin
    1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties
    RSC Adv., 2017,7, 17497-17504 doi:10.1039/C7RA01709J, IF=3.108
  48. S.M. Adekenov, Zh.R. Shaimerdenova, Yu.V. Gatilov, G.A. Atazhanova
    Two New Sesquiterpene Lactones from Artemisia halophila
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 284-289 doi:10.1007/s10600-017-1971-x, IF=0.46
  49. E.V. Nazimova, A.A. Shtro, V.B. Anikin, O.S. Patrusheva, I.V. Il'ina, D.V. Korchagina, V.V. Zarubaev, K.P. Volcho, N.F. Salakhutdinov
    Influenza Antiviral Activity of Br-Containing [2R,4R(S),4aR,7R,8aR]-4,7-Dimethyl-2-(Thiophen-2-YL)Octahydro-2H-Chromen-4-Ols Prepared from (–)-Isopulegol
    Chemistry of Natural Compounds, 2017, V. 53, N 2, pp 260-264 doi:10.1007/s10600-017-1966-7, IF=0.46
  50. T.A. Vaganova, A.I. Plekhanov, A.E. Simanchuk, S.L. Mikerin, E.V. Spesivtsev, E.V. Karpova, T.S. Frolova, E.V. Malykhin
    Synthesis and characterization of novel polyhalogenaromatic polyimide material for electro-optic applications
    Journal of Fluorine Chemistry, 2017, V. 195, Pp 70-78 doi:10.1016/j.jfluchem.2017.01.010, IF=2.101
  51. E.S. Vasilyev, I.Yu. Bagryanskaya, A.V. Tkachev
    Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9'-bi-4,5-diazafluorenylidene
    Mendeleev Communications, 2017, V. 27, N 2, Pp 128-130 doi:10.1016/j.mencom.2017.03.006, IF=1.741
  52. Cobalt(II) hexaiododimercurate(II) complex with ε-caprolactam: Synthesis and crystal structure/ A.V. Tikhomirova, I.Yu. Bagryanskaya, N.V. Pervukhina, T.G. Cherkasova// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 187-190 doi:10.1134/S0036023617020206, IF=0.787
  53. Double complex [Mn2(C11H13N3O)6(H2O)2][Cr(NH3)2(NCS)4]4: Synthesis and crystal structure/ T.G. Cherkasova, I.Yu. Bagryanskaya, N.V. Pervukhina, A.L. Vornakov, E.V. Cherkasova, N.V. Kuratieva// Russian Journal of Inorganic Chemistry, February 2017, V. 62, N 2, pp 182-186 doi:10.1134/S003602361702005X, IF=0.787
  54. 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
  55. Luminophores of the luminous fungus Neonothopanus nambi/ Y.P. Zernov, T.V. Kobzeva, T.Y. Dranova, D.V. Stas, A.A. Alekseev, A.A. Nefedov// Biophysics (Russian Federation), V, 62, N 2, 1 March 2017, Pp 265-270 doi:10.1134/S0006350917020300
  56. A.V. Shpatov, S.A. Popov, O.I. Salnikova, T.P. Kukina, E.N. Shmidt, B.H. Um
    Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and P. sibirica Du Tour)
    Chemistry & Biodiversity, 2017, V. 14, N 2, Article number e1600203 doi:10.1002/cbdv.201600203, IF=1.44
  57. A.S. Kuzmich, T.M. Khomenko, S.N. Fedorov, T.N. Makarieva, L.K. Shubina, N.I. Komarova, D.V. Korchagina, T.V. Rybalova, K.P. Volcho, N.F. Salakhutdinov
    Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins
    Medicinal Chemistry Research, 2017, V. 26, N 2, pp 397-404 doi:10.1007/s00044-016-1759-8, IF=1.276
  58. A.V. Artem'ev, N.A. Kolyvanov, L.A. Oparina, N.K. Gusarova, A.O. Sutyrina, I.Y. Bagryanskaya, B.A. Trofimov
    Four-Component Reaction between Secondary Phosphines, Primary Amines, Aldehydes, and Chalcogens: A Facile Access to Functionalized α-Aminophosphine Chalcogenides
    Synthesis (Germany), 2017, V. 49, N 3, Pp 677-684 doi:10.1055/s-0036-1588127, IF=2.65
  59. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  60. Yu.M. Volkova, A.Yu. Makarov, S.B. Zikirin, A.M. Genaev, I.Yu. Bagryanskaya, A.V. Zibarev
    3,1,2,4-Benzothiaselenadiazine and related heterocycles: synthesis and transformation into Herz-type radicals
    Mendeleev Communications, 2017, V. 27, N 1, Pp 19-22 doi:10.1016/j.mencom.2017.01.005, IF=1.741
  61. E. A. Chulanova, E.A. Pritchina, L. A. Malaspina, S. Grabowsky, F. Mostaghimi, J. Beckmann, I. Yu. Bagryanskaya, M. V. Shakhova, L. S. Konstantinova, O.A. Rakitin, N. P. Gritsan ,A. V. Zibarev
    New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
    Chemistry - A European Journal, 2017, V. 23, N 4, Pp 852-864 doi:10.1002/chem.201604121, IF=5.316
  62. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
    Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
  63. 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
  64. K.S. Marenin, Yu.V. Gatilov, A.M. Agafontsev, A.V. Tkachev
    Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives
    Steroids, 2016, V. 117, Pp 112-119 doi:10.1016/j.steroids.2016.09.016, IF=2.282
  65. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473
  66. G.A. Atazhanova, A.V. Gering, F.T. Mukasheva, P.E. Sakenova, Yu.V. Gatilov, V.S. Korneev, S.M. Adekenov
    Chemical Study of Pulicaria salviifolia
    Chemistry of Natural Compounds, 2017, V. 53, N 1, pp 178-180 doi:10.1007/s10600-017-1943-1, IF=0.46
  67. Furfural nitrosemicarbazone salts/ V. S. Glukhacheva, S. G. Il'yasov, G. V. Sakovich, Yu. V. Gatilov// Russian Chemical Bulletin, January 2017, V. 66, N 1, pp 83-85 doi:10.1007/s11172-017-1703-1, IF=0.528
  68. Yu.S. Demidova, E.V. Suslov, I.L. Simakova , E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    Selectivity control in one-pot myrtenol amination over Au/ZrO2 by molecular hydrogen addition
    Journal of Molecular Catalysis A: Chemical, V. 426, Part A, January 2017, Pages 60–67 doi:10.1016/j.molcata.2016.10.034, IF=3.957
  69. A.I. Titkov, N.V. Bulina, A.S. Ulihin, I.K. Shundrina, E.V. Karpova, E.Yu. Gerasimov, Yu.M. Yukhin, N.Z. Lyakhov
    N-Lauroylsarcosine capped silver nanoparticle based inks for flexible electronics
    Journal of Materials Science: Materials in Electronics, January 2017, V. 28, N 2, pp 2029-2036 doi:10.1007/s10854-016-5762-0, IF=2.19

2016
  1. Photopolymerization kinetics of a thiol-enol composition determined via recording/playback of a transmission holographic diffraction grating/ V. V. Shelkovnikov, D. I. Derevyanko, L. V. Ektova, N. A. Orlova, V. A. Loskutov, E. V. Vasil'iev, E. V. Karpova// Polymer Science Series B, 2016, V. 58, N 5, pp 519-528 doi:10.1134/S1560090416050109, IF=0.736
  2. Remains of tapestry from a Xiongnu (Early 1st Century AD) Burial in Mound 22 at Noin-Ula/ N.V. Polosmak, E.A. Karpova// ARCHAEOLOGY ETHNOLOGY AND ANTHROPOLOGY OF EURASIA,, 2016, V/. 44 № 4 , Pp.76-82 doi:10.17746/1563-0110.2016.44.4.076-082
  3. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, A.O. Sutyrina, I.Yu. Bagryanskaya, P.M. Tolstoy, A.L. Gushchin, A.S. Mazur, N.K. Gusarova, B.A. Trofimov
    Luminescent CuI thiocyanate complexes based on tris(2-pyridyl)phosphine and its oxide: from mono-, di- and trinuclear species to coordination polymers
    New J. Chem., 2016,40, 10028-10040 doi:10.1039/C6NJ02087A, IF=3.276
  4. S.I. Zhivetyeva, O.D. Zakharova, L.P. Ovchinnikova, D.S. Baev, I.Yu. Bagryanskaya, V.D. Shteingarts, T.G. Tolstikova, G.A. Nevinsky, E.V. Tretyakov
    Phosphonium betaines derived from hexafluoro-1,4-naphthoquinone: Synthesis and cytotoxic and antioxidant activities
    Journal of Fluorine Chemistry, V. 192, Part A, December 2016, Pp 68-77 doi:10.1016/j.jfluchem.2016.10.014, IF=2.213
  5. T.V. Mezhenkova, V.M. Karpov, I.V. Beregovaya, Ya.V. Zonov, I.P. Chuikov, V.E. Platonov
    Generation of perfluorinated 1-alkylbenzocyclobuten-1-yl and 1-alkylindan-1-yl cations. On paradoxical stabilizing influence of an electron-withdrawing perfluoroisopropyl group on the relative stabilities of the cations
    Journal of Fluorine Chemistry, 2016, V. 192, Part A, Pp 31-40 doi:10.1016/j.jfluchem.2016.10.009, IF=2.213
  6. G. Audran, E. Bagryanskaya, I. Bagryanskaya, P. Bremond, M. Edeleva, S.R. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    C-ON bond homolysis of alkoxyamines triggered by paramagnetic copper(II) salts
    Inorg. Chem. Front., 2016,3, 1464-1472 doi:10.1039/C6QI00277C, IF=4.532
  7. T. Khomenko, A. Zakharenko, T. Odarchenko, H.J. Arabshahi, V. Sannikova, O. Zakharova, D. Korchagina, J. Reynisson, K. Volcho, N. Salakhutdinov, O. Lavrik
    New inhibitors of tyrosyl-DNA phosphodiesterase I (Tdp 1) combining 7-hydroxycoumarin and monoterpenoid moieties
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pp 5573-5581 doi:10.1016/j.bmc.2016.09.016, IF=2.923
  8. O.S. Patrusheva, V.V. Zarubaev, A.A. Shtro, Ya.R. Orshanskaya, S.A. Boldyrev, I.V. Ilyina, S.Yu. Kurbakova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes
    Bioorganic & Medicinal Chemistry, 2016, V. 24, N 21, Pages 5158-5161 doi:10.1016/j.bmc.2016.08.037, IF=2.923
  9. T.E. Kokina, L.A. Glinskaya, A.V. Tkachev, V.F. Plyusnin, Yu.V. Tsoy, I.Yu. Bagryanskaya, E.S. Vasilyev, D.A. Piryazev, L.A. Sheludyakova, S.V. Larionov
    Chiral zinc(II) and cadmium(II) complexes with a dihydrophenanthroline ligand bearing (-)-α-pinene fragments: synthesis, crystal structures and photophysical properties
    Polyhedron, 2016, V. 117, 15 October 2016, Pp 437-444 doi:10.1016/j.poly.2016.06.018, IF=2.108
  10. Chromosomal localization of aromatic alcohol dehydrogenase fast-migrating isoenzyme Aadh1F (CAD1-F) gene in Triticum aestivum L. bread wheat/ A. A. Konovalov, I.K. Shundrina, E. V. Karpova, N. P. Goncharov, E. Ya. Kondratenko// Russian Journal of Genetics, October 2016, V. 52, N 10, pp 1110-1116 doi:10.1134/S1022795416080056
  11. A.S. Kihkentayeva, E.E. Shults, Yu.V. Gatilov, S.S. Patrushev, S. Karim, G.A. Atazhanova, S.M. Adekenov
    Synthetic Transformations of Sesquiterpene Lactones 10*. Synthesis of 13-Arylguaianolides
    Chemistry of Heterocyclic Compounds, October 2016, V. 52, N 10, pp 788-796 doi:10.1007/s10593-016-1967-7, IF=0.815
  12. 1-Bromo-3,3,3-trifluoro-1-nitropropene: Synthesis and reaction with phenyl azide/ N. A. AnisimovaEmail authorE. K. SlobodchikovaA. A. KuzhaevaE. V. Stukan’I. Yu. BagryanskayaV. M. Berestovitskaya// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1379-1384 doi:10.1134/S1070428016100018, IF=0.759
  13. Formation of ω-(4-oxo-1,4-dihydropyridin-2-yl)alkanamides in the Beckmann rearrangement of spiro-fused cycloalkanone oximes/ V. A. Savel'ev, A. Ya. Tikhonov, T. V. Rybalova// Russian Journal of Organic Chemistry, October 2016, Volume 52, Issue 10, pp 1379-1384 doi:10.1134/S1070428016100134, IF=0.759
  14. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
    Highly-emissive solution-grown furan/phenylene co-oligomer single crystals
    RSC Adv., 2016,6(95), 92325-92329 doi:10.1039/C6RA23160H, IF=3.289
  15. A.B. Burdukov, M.A. Vershinin, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, A.S. Belov, Ya.Z. Voloshin, A.A. Nefedov
    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  16. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  17. A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
    Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
  18. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    Ti-Salalen Mediated Asymmetric Epoxidation of Olefins with H2O2: Effect of Ligand on the Catalytic Performance, and Insight into the Oxidation Mechanism
    Journal of Molecular Catalysis A: Chemical, 2016, V. 421, 2016, Pages 131-137 doi:10.1016/j.molcata.2016.05.019, IF=3.957
  19. G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
    Promotional effect of ionic liquids in electrophilic fluorination of methylated uracils
    RSC Advances, 2016, V. 6, N 6, Pp 60556-60564 doi:10.1039/C6RA10850D, IF=3.289
  20. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
    Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
    Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
  21. Ya.V. Zonov, V.M. Karpov, T.V. Mezhenkova, T.V. Rybalova, Yu.V. Gatilov, V.E. Platonov
    Transformations of perfluorinated 1,2-dialkyl-, 1,1- and 1,2-alkylphenylbenzocyclobutenes to indan-2-one and isochromene derivatives under the action of CO/SbF5
    Journal of Fluorine Chemistry, 2016, V. 188, August 2016, Pp 117-125 doi:10.1016/j.jfluchem.2016.06.014, IF=2.213
  22. A.G. Potapov, I.K. Shundrina
    The influence of different fillers on mechanical and physical properties of high-molecular-weight biodegradable aliphatic polyesters
    Polymer Science Series A, July 2016, V. 58, N 4, pp 585-592 doi:10.1134/S0965545X1604012X, IF=0.759
  23. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  24. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  25. A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
    Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
    J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
  26. E. Nazimova, A. Pavlova, O. Mikhalchenko, I. Il'ina, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Discovery of highly potent analgesic activity of isopulegol-derived (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol
    Medicinal Chemistry Research, 2016, V. 25, N 7, pp 1369-1383 doi:10.1007/s00044-016-1573-3, IF=1.435
  27. Synthesis of polyfluorinated A3B tetraoxacalix[4]arenes/ V.N. Kovtonyuk, Yu.V. Gatilov// Russian Journal of Organic Chemistry, 2016, V. 52, N 7, pp 946-949 doi:10.1134/S1070428016070046, IF=0.759
  28. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  29. D.S. Baranov, Y.V. Gatilov
    Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines
    Mendeleev Communications, 2016, V. 26, N 4, Pp 282-284 doi:10.1016/j.mencom.2016.07.004, IF=1.404
  30. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
    First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
    Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
  31. 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
  32. M.E. Mironov, I.Yu. Bagryanskaya, E.E. Shults
    Synthesis of 3-trimethylsiloxy-1-(furan-3-yl)butadiene and its reactions with dienophiles
    Chemistry of Heterocyclic Compounds, , 2016, V. 52, N 6, pp 364-373 doi:10.1007/s10593-016-1897-4, IF=0.814
  33. Structure of molecular cocrystals of 18-crown-6 and polyhalogeno-meta-phenylenediamines/ T. A. Vaganova, Yu. V. Gatilov, V. I. Rodionov, E. V. Malykhin// Journal of Structural Chemistry, 2016, V. 57, N 6, pp 1225-1234 doi:10.1134/S002247661606024X, IF=0.536
  34. Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026, IF=0.759
  35. L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
    Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
  36. Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101
  37. Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023, IF=0.604
  38. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  39. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  40. I.V. Il'ina, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov
    The Convenient Way for Obtaining Geranial by Acid-Catalyzed Kinetic Resolution of Citral
    Helvetica Chimica Acta, 2016, V. 99, N 5, Pp 373-377 doi:10.1002/hlca.201500266, IF=1.87
  41. O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    A practical way to synthesize chiral fluoro-containing polyhydro-2H-chromenes from monoterpenoids
    Beilstein J. Org. Chem. 2016, 12, 648-653 doi:10.3762/bjoc.12.64, IF=2.697
  42. I.Yu. Bagryanskaya, L.V. Politanskaya, E.V. Tretyakov
    Frequently used, but still unknown: Terbium(III) tris-hexafluoroacetylacetonate dihydrate
    Inorganic Chemistry Communications, April 2016, V. 66, Pp 47-50 doi:10.1016/j.inoche.2016.02.009, IF=1.761
  43. Supramolecular architecture of crystals of perfluorinated 3-alkylphthalides/ T. V. Rybalova, Yu. V. Gatilov, Ya. V. Zonov, V. M. Karpov// Journal of Structural Chemistry, 2016, V. 57, N 4, pp 777-783 doi:10.1134/S0022476616040223, IF=0.536
  44. V.I. Supranovich, A.Yu. Vorob'ev, G.I. Borodkin, Yu.V. Gatilov, V.G. Shubin
    Study on selectivity in the reaction of 2-substituted pyridinium-N-imines with dimethyl acetylenedicarboxylate
    Tetrahedron Letters, V. 57, N 10, 9 March 2016, Pp 1093-1096 doi:10.1016/j.tetlet.2016.01.092, IF=2.346
  45. G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
    X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
    Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
  46. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
  47. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  48. D.V. Trukhin, O.Yu. Rogozhnikova, T.I. Troitskaya, V.G. Vasiliev, M.l K. Bowman, V.M. Tormyshev
    Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals
    Synlett, 2016, 27(06), Pp 893-899 doi:10.1055/s-0035-1561299, IF=2.322
  49. 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
  50. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  51. M.A. Timoshenko, Yu.V. Kharitonov, M.M. Shakirov, I.Yu. Bagryanskaya, E.E. Shults
    Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
    ChemistryOPEN, V. 5, N 1, pp 65-70, February 2016 doi:10.1002/open.201500187, IF=3.585
  52. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  53. Reaction of 3-(R-methylidene)-2-ethoxylindolenines with N,N'-binucleophiles/ V. P. Borovik, Yu. V. Gatilov, O. P. Shkurko// Russian Journal of Organic Chemistry, 2016, V. 52, N 2, pp 228-234 doi:10.1134/S1070428016020123, IF=0.759
  54. 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
  55. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  56. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  57. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  58. 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
  59. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, H.S. Rzepa, V.G. Shubin
    Noncatalytic bromination of benzene: A combined computational and experimental study
    Journal of Computational Chemistry, V. 37, N 2, 15 January 2016, Pp 210-225 doi:10.1002/jcc.23985, IF=3.648
  60. Microwave-Assisted Synthesis of Phthalocyanine Zinc Complexes Derived from Aminotricyanobiphenyl-Based Azo Dyes/ G.A. Selivanova, E. V. Amosov, V. G. Vasilyev, E. A. Lukyanets, E. V. Tretyakov, V.D. Shteingarts// Macroheterocycles 2016 9(1) 80-88 doi:10.6060/mhc151192s, IF=0.804
  61. А.Н. Блазнов, Е.В. Атясова, Н.В. Бычин, И.К. Шундрина, Н.Н. Ходакова, В.В. Самойленко
    Влияние степени отверждения связующего на температуру стеклования композитных материалов
    Южно-Сибирский научный вестник, 2016, № 1 (13), С. 13-20.
  62. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  63. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  64. S.P. Babailov, I.P. Chuikov, A.I. Kruppa
    Activation Energies of Intermolecular Dynamics in Ethylenediaminetetraacetate Complexes with Lanthanides: An Effect of the “Gadolinium Break”
    Inorganica Chimica Acta, V. 439, 1 January 2016, Pp 117-122 doi:10.1016/j.ica.2015.10.009, IF=1.917
  65. И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
    Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
    Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150

DEVICES:

1. Group of Nuclear Magnetic Resonance (GNMR)

- спектроскопия ядерного магнитного резонанса (ЯМР)>
- спектроскопия электронного парамагнитного резонанса (ЭПР) и ЭПР-томография

Devices:

  • Bruker Avance 300
  • Bruker Avance 400
  • Bruker Avance 600
  • Bruker DRX 500


 

2. Group of mass spectrometry (GMS)

- газовая хроматография
- газовая хромато-масс-спектроскопия (с приставкой термодесорбции)
- жидкостная хроматография
- жидкостная хромато-масс-спектрометрия

Devices:

  • Agilent LC 1100 DAD
  • Agilent LC 1200 + Bruker micro TOF-Q
  • Agilent LC 1100 + MSD G2707
  • Agilent 7200 GC-QTOF
  • Agilent GC-MSD 6890/5973
  • HP GC-MSD 5890/5971
  • Thermo Electron DFS GC-MS


 

3. Group of Optical Spectrometry (GOS)

- ИК-Фурье и КР- спектроскопия
- УФ-Вид спектроскопия
- флуоресцентная спектроскопия
- поляризационная спектроскопия
- электронная микроскопия (с приставкой термодесорбции и элементным анализатором)

Devices:

  • Varian Cary Eclipse Optical Activity PolАAr 3005
  • Electron microscope Hitachi ТМ-1000 + EDS SFIFT
  • Bruker IR+IR-microscope
  • Vector 22 + IFS-66
  • Bruker Raman Sеnterra
  • НР Uv-Vis 8453А DAD
  • Varian Uv-Vis-NIR Cary 5000
  • Varian Cary Eclipse
  • Optical Activity PolАAr 3005
  • Electron microscope Hitachi ТМ-1000 + EDS SFIFT


 

4. Group of X-ray analysis (GXRA)

- X- ray diffraction analysis

Devices:

  • Bruker X-ray САРРА-АРЕХ
  • Bruker X-ray P4


 

5. Group of thermal analysis (GTA)

- thermal analysis: thermogravimetry and differential scanning calorimetry
- dynamic thermomechanical analysis

Devices:

  • Thermoanalyzer STA 409
  • Dynamic mechanical DMA-2420

6. Group of service of scientific equipment (GSSE)



 


 

 


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