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

Tretyakov E.V.

Head - Professor, Dr. Sci. (Chem)
TRETYAKOV Evgeny Victorovich

Phone: (383) 330-91-71
internal phone: т.3-48
email:This email address is being protected from spambots. You need JavaScript enabled to view it.


 

Up to 2015 Laboratoty was headed by Professor, Dr. Sci. Shteingarts Vitaliy Davidovich

The laboratory has been established in 1975 as a result of transformation of the former laboratory of kinetics of homogeneous reactions (Prof. Dr. S.M. Shein). 


Research areas:

Research areas:

  • Investigation of structure, reaction mechanisms and ways of synthetic utilization of anionic forms generated by one- and two-electron reduction of aromatic compounds

     LINIRR 1

    1. R.Yu. Peshkov, E.V. Panteleeva, W. Chunyan, E.V. Tretyakov, V.D. Shteingarts. One-pot synthesis of 4'-alkyl-4-cyanobiaryls on the basis of the terephthalonitrile dianion and neutral aromatic nitrile cross-coupling. Beilstein Journal of Organic Chemistry, 2016, V.12, Pp 1577-1584 doi:10.3762/bjoc.12.153.

    2. 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.

    3. R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, E.V. Tretyakov. Synthesis of 4'-alkyl-[1,1'-biphenyl]-2,3'-dicarbonitriles via dimerisation of phthalonitrile radical anion in liquid ammonia. Arkivoc,2018, part vii, Pp 349-356 doi:10.24820/ark.5550190.p010.764.

    4. R.Yu. Peshkov, E.V. Panteleeva, L.N. Shchegoleva, I.Yu. Bagryanskaya, T.V. Rybalova, N.V. Vasilieva, V.D. Shteingarts. Synthesis of 2-X-, 3-X-4,4'-Dicyanobiphenyls (X = CH3, OCH3, F) by Cross-Coupling of the Terephthalonitrile Dianion with Substituted Benzonitriles. European Journal of Organic Chemistry, V. 2015, N 20, pp 4524-4531, July 2015 doi:10.1002/ejoc.201500295

  • Fluorinated Hetarenes (Our research is focused on preparation of fluorinated (hetero)cyclic compounds, investigating their reactivity and areas of practical application)

     LINIRR 2

    1. L. Politanskaya, E. Tretyakov. p-Toluenesulfonic Acid Induced Conversion of Fluorinated Trimethylsilylethynylanilines into Aminoacetophenones: Versatile Precursors for the Synthesis of Benzoazaheterocycles. Synthesis 2018; 50(03): 555-564 doi:10.1055/s-0036-1591504.

    2. 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.

    3. L. Politanskaya, I. Bagryanskaya, E. Tretyakov. Synthesis of polyfluorinated arylhydrazines, hydrazones and 3-methyl-1-aryl-1H-indazoles. Journal of Fluorine Chemistry, 2018, V. 214, Pp 48-57 doi:10.1016/j.jfluchem.2018.06.011.

    4. L. Politanskaya, N. Troshkova, E. Tretyakov, Ch. Xic. Synthesis of polyfluorinated bezofurans. Journal of Fluorine Chemistry, Volume 227, November 2019, 109371 doi:10.1016/j.jfluchem.2019.109371

    5. L. Politanskaya, E. Tretyakov. Directed synthesis of fluorine containing 2,3-dihydrobenzo[b][1,4]oxathiine derivatives from polyfluoroarenes. Journal of Fluorine Chemistry, 2020, 109592 doi:10.1016/j.jfluchem.2020.109592

  • Application of aromatic nucleophilic substitution as a tool for developing new approaches to the construction and directed functionalization of polyfluorinated arenes (hetarenes) and quinones, including the introduction of radical groups.

     LINIRR 3

    1. 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.

    2. 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.

    3. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov. Synthesis of Nitroxide Diradical Using a New Approach. Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701.

    4. 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

  • Functionally Oriented Synthesis of Organic and Hybrid Compounds (Our goals are to design and synthesize novel molecular structures in order to promote and control interesting chemical and physical properties)

     LINIRR 4

    1. G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva. Trityl-based alkoxyamines as NMP controllers and spin-labels. Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A.

    2. 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.

    3. 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. Stassd, 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.

    4. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov. Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces. J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A

  • Organic Conjugated Paramagnets and High Spin Molecules (Our research is in the area of Synthetic Radical Chemistry with emphasis on the design, synthesis and study of paramagnet molecules with the delocalized spin density)

     LINIRR 5

    1. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin. Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series. Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049.

    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.

    3. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue. (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes. Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085.

    4. 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

    5. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani. Magnetic edge states and coherent manipulation of graphene nanoribbons. Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7

STAFF

Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Tretyakov Evgeny Viktorovich Lab's Head (Doct. Chem) 216, 310 330-91-71, 330-68-59 3-48, 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Tretyakov Evgeny Viktorovich Chief Researcher (Doct. Chem.) 216, 310 330-91-71, 330-68-59 3-48, 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Panteleeva Elena Valerievna Senior Researcher (Cand. Chem.) 333 330-68-59 2-83 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Politanskaya Larisa Vladimirovna Senior Researcher (Cand. Chem.) 310 330-68-59 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Selivanova Galina Arkadievna Senior Researcher (Cand. Chem.) 333 330-68-59 2-83 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Fedyushin Pavel Andreevich Researcher 310 330-68-59 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Gurskaya Larisa Yurievna Researcher (Cand. Chem.) 131 330-68-59 3-84 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Romanov Vasiliy Evgenievich Researcher (Cand. Chem.) 131 330-68-59 3-84 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Troshkova Nadezhda Mikhailovna Researcher (Cand. Chem.) 310 330-68-59 4-09 This email address is being protected from spambots. You need JavaScript enabled to view it.
10 Mitereva Tatyana Andreevna engineer 210 НТК 330-68-56 2-73 This email address is being protected from spambots. You need JavaScript enabled to view it.
PHD Students
11 Zayakin Igor Alekseevich Junior Researcher 131 330-68-59 3-84
PUBLICATIONS

Publications over the past years

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2020
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. M.A. Gromova, Yu.V. Kharitonov, L.V. Politanskaya, E.V. Tretyakov, E.E. Shults
    A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles
    Journal of Fluorine Chemistry, 2020, V. 236, 109554 doi:10.1016/j.jfluchem.2020.109554, IF=2.332
  8. L. Politanskaya, E. Tretyakov
    Directed synthesis of fluorine containing 2,3-dihydrobenzo[b][1,4]oxathiine derivatives from polyfluoroarenes
    Journal of Fluorine Chemistry, 2020, 109592 doi:10.1016/j.jfluchem.2020.109592, IF=2.332
  9. From spin-labelled fused polyaromatic compounds to magnetically active graphene nanostructures/ Yu A Ten, N M Troshkova, E V Tretyakov// Russian Chemical reviews, 2020, V. 89, N 7, Pp 693-712 doi:10.1070/RCR4923?locatt=label:RUSSIAN, IF=4.75
  10. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
    Synthesis of Nitroxide Diradical Using a New Approach
    Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
  11. Fluorinated benzimidazoles for medicinal chemistry and new materials/ Selivanova, G.A., Tretyakov, E.V.// Russ Chem Bull? 2020, V. 69, N 5, Pp 838-858 doi:10.1007/s11172-020-2842-3, IF=1.061
  12. 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
  13. E. Tretyakov, A. Tkacheva, G. Romanenko, A. Bogomyakov, D. Stass, A. Maryasov, E. Zueva, B. Trofimov, V. Ovcharenko
    (Pyrrole-2,5-Diyl)-Bis(Nitronyl Nitroxide) and-Bis(Iminonitroxide): Specific Features of the Synthesis, Structure, and Magnetic Properties
    Molecules 2020, 25(7), 1503 doi:10.3390/molecules25071503, IF=3.267
  14. Method of preparation of alkylated 1,3-diphenylpropan-2-ones, the components for assembly of graphene nanostructures/ Yu. A. Ten, N. M. Troshkova, E. V. Tretyakov// Russian Chemical Bulletin, 2020, V. 69, Pp 172-175 doi:10.1007/s11172-020-2740-8, IF=1.061
  15. L. Politanskaya, E. Tretyakov, Ch. Xi
    Synthesis of polyfluorinated o-hydroxyacetophenones - convenient precursors of 3-benzylidene-2-phenylchroman-4-ones
    Journal of Fluorine Chemistry, V. 229, January 2020, 109435 doi:10.1016/j.jfluchem.2019.109435, IF=2.332

2019
  1. 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
  2. L.Politanskaya, M.Petyuk,E.Tretyakov
    Transformation of fluorinated 2-alkynylanilines by various catalytic systems
    Journal of Fluorine Chemistry, 2019, V. 228, Art. Number 109394 doi:10.1016/j.jfluchem.2019.109394, IF=2.055
  3. L. Politanskaya, N. Troshkova, E. Tretyakov, Ch. Xi
    Synthesis of polyfluorinated bezofurans
    Journal of Fluorine Chemistry, Volume 227, November 2019, 109371 doi:10.1016/j.jfluchem.2019.109371, IF=2.055
  4. O. Zakharova, G. Nevinsky, L. Politanskaya, D. Baev, L. Ovchinnikova, E. Tretyakov
    Evaluation of antioxidant activity and cytotoxicity of polyfluorinated diarylacetylenes and indoles toward human cancer cells
    Journal of Fluorine Chemistry, V. 226, October 2019, 109353 doi:10.1016/j.jfluchem.2019.109353, IF=2.055
  5. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
  6. 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
  7. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
  8. D. Stass, E. Tretyakov
    Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
    Magnetochemistry, 2019, 5(2), 32 (This article belongs to the Special Issue Controlling Molecular Nanomagnets) doi:10.3390/magnetochemistry5020032
  9. Organofluorine chemistry: promising growth areas and challenges/ Politanskaya L.V., Selivanova G.A., Panteleeva E.V., Tretyakov E.V., Platonov V.E., Nikulshin P.V., Vinogradov A.S., Zonov Ya.V., Karpov V.M., Mezhenkova T.V., Vasilyev A.V., Koldobskii A.B., Shilova O.S., Morozova S.M., Burgart Ya.V., Shchegolkov E.V., Saloutin V.I., Sokolov V.B., Aksinenko A.Yu., Nenajdenko V.G., Moskalik M.Yu., Astakhova V.V., Shainyan B.A., Tabolin A.A., Ioffe S.L., Muzalevskiy V.M., Balenkova E.S., Shastin A.V., Tyutyunov A.A., Boiko V.E., Igumnov S.M., Dilman A.D., Adonin N.Yu., Bardin V.V., Masoud S.M., Vorobyeva D.V., Osipov S.N., Nosova E.V., Lipunova G.N., Charushin V.N., Prima D.O., Makarov A.G., Zibarev A.V., Trofimov B.A., Sobenina L.N., Belyaeva K.V., Sosnovskikh V.Ya., Obydennov D.L., Usachev S.A.// RUSSIAN CHEMICAL REVIEWS, 2019, V. 55, N 5, Pp, IF=4.612
  10. 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
  11. 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
  12. V. Morozov, E. Tretyakov
    Spin polarization in graphene nanoribbons functionalized with nitroxide
    Journal of Molecular Modeling, 2019, V.25, N 3, Article 58 doi:10.1007/s00894-019-3944-4, IF=1.335
  13. 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
  14. 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
  15. 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. D. Stass, E. Tretyakov
    Estimation of Absolute Spin Counts in Nitronyl Nitroxide-Bearing Graphene Nanoribbons
    Magnetochemistry, 2019, V.5, N 2, P 32-40 doi:10.3390/magnetochemistry5020032
  2. R.Yu. Peshkov, Ch. Wang, E.V. Panteleeva, E.V. Tretyakov
    Synthesis of 4'-alkyl-[1,1'-biphenyl]-2,3'-dicarbonitriles via dimerisation of phthalonitrile radical anion in liquid ammonia (18-10764UP)
    Arkivoc,2018, part vii, Pp 349-356 doi:10.24820/ark.5550190.p010.764, IF=1.47
  3. 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
  4. 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
  5. L. Politanskaya, I. Bagryanskaya, E. Tretyakov
    Synthesis of polyfluorinated arylhydrazines, hydrazones and 3-methyl-1-aryl-1H-indazoles
    Journal of Fluorine Chemistry, 2018, V. 214, Pp 48-57 doi:10.1016/j.jfluchem.2018.06.011, IF=1.879
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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
  11. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
  12. G. Audran, E. Bagryanskaya, M. Edeleva, S. Marque, D. Parkhomenko, E. Tretyakov, S. Zhivetyeva
    Coordination-Initiated Nitroxide-Mediated Polymerization (CI-NMP)
    Australian Journal of Chemistry, 2018, V. 71, N 5, Pp 334-340 doi:10.1071/CH17570, IF=1.059
  13. A. Vorontsov, E. Tretyakov
    Determination of Graphene Edges Energy using Hexagonal Graphene Quantum Dots and PM7 Method
    Phys. Chem. Chem. Phys., 2018, V. 20, N 21, Pp. 14740-14752 doi:10.1039/C7CP08411K, IF=3.906
  14. 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
  15. M.M. Petrova, S.I. Zhivetyeva, E.V. Tretyakov
    Triplet Diradicals Derived From Quinone-Nitroxides: A Quantum-Chemical Study
    SDRP Journal of Computational Chemistry & Molecular Modelling, 2018, V: 2, N 2 doi:10.25177/JCCMM.2.2.5
  16. 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
  17. 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
  18. 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
  19. 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
  20. L. Politanskaya, E. Tretyakov
    p-Toluenesulfonic Acid Induced Conversion of Fluorinated Trimethylsilylethynylanilines into Aminoacetophenones: Versatile Precursors for the Synthesis of Benzoazaheterocycles
    Synthesis 2018; 50(03): 555-564 doi:10.1055/s-0036-1591504, IF=2.722

2017
  1. 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
  2. A.S. Kondratyev, V.D. Shteingarts, V.V. Litvak, E.V. Tretyakov, A.V. Tkachev
    Domino reaction of (2-haloethyl)polyfluorophenyl sulfides, sulfoxides, and sulfones with ammonia or amines: one-pot synthesis of 3,4-dihydro-2H-1,4-benzothiazines polyfluorinated at the benzene ring and the corresponding 1-oxides and 1,1-dioxides
    Chemistry of Heterocyclic Compounds, 2017, V. 53, N 12, P 1350-1361 doi:10.1007/s10593-018-2217-y, IF=0.893
  3. K. Okada, M. Haraguchi, E. Tretyakov, N. Gritsan, G. Romanenko, D. Gorbunov, A. Bogomyakov, K. Maryunina, S. Suzuki, M. Kozaki, D. Shiomi, K. Sato, T. Takui, S. Nishihara, K. Inoue
    (Azulene-1,3-diyl)-bis(nitronyl nitroxide) and -bis(iminonitroxide) and Their Copper Complexes
    Chemistry - An Asian Journal, 2017, V. 12, N 22, Pp 2929-2941 doi:10.1002/asia.201701085, IF=4.83
  4. 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
  5. 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
  6. Comparative Study of Toxicity of Alkoxyamines In Vitro and In Vivo/ N.A. Popova, G.M. Sysoeva, V.P. Nikolin, V.I. Kaledin, E.V. Tretyakov, M.V. Edeeva, S.M. Balakhnin, E.L. Lushnikova, G. Audran, S. Mark// Bulletin of Experimental Biology and Medicine, November 2017, V. 164, N 1, pp 49-53 doi:10.1007/s10517-017-3924-6, IF=0.456
  7. L.V. Saloutina, E.V. Tretyakov, P.A. Slepukhin, V.I. Saloutin, O.N. Chupakhin
    Synthesis of Cyclic Vicinal Trifluoromethylated Hydroxylamine and Nitrone Based on Perfluorodiacetyl
    Journal of Heterocyclic Chemistry, 2017, V. 54, N 3, Pp 1887-1890 doi:10.1002/jhet.2782, IF=0.893
  8. 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
  9. 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
  10. 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
  11. Synthesis and study of CuII complex with nitroxide, a jumping crystal analog/ R. Z. Sagdeev, S. E. Tolstikov, S. V. Fokin, I. V. Obsharova, S. V. Tumanov, S. L. Veber, G. V. Romanenko, A. S. Bogomyakov, M. V. Fedin, E. V. Tretyakov, M. Halcrow, V. I. Ovcharenko// Russian Chemical Bulletin, February 2017, V. 66, N 2, pp 222-230 doi:10.1007/s11172-017-1722-y, IF=0.528
  12. 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

2016
  1. 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
  2. E. Tretyakov, K. Okada, S. Suzuki, M. Baumgarten, G. Romanenko, A. Bogomyakov, V. Ovcharenko
    Synthesis, structure and properties of nitronyl nitroxide diradicals with fused-thiophene couplers
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY. V. 29, N 12, December 2016, Pp.725-734 doi:10.1002/poc.3561, IF=1.514
  3. G. Audran, E.G. Bagryanskaya, P. Bremond, M.V. Edeleva, S.R.A. Marque, D.A. Parkhomenko, O.Yu. Rogozhnikova, V.M. Tormyshev, E.V. Tretyakov, D.V. Trukhin, S.I. Zhivetyeva
    Trityl-based alkoxyamines as NMP controllers and spin-labels
    Polym. Chem., 2016, 42(7), 6490-6499 doi:10.1039/C6PY01303A, IF=5.687
  4. 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
  5. S.E. Tolstikov, E.V. Tretyakov, D.E. Gorbunov, I.F. Zhurko, M.V. Fedin, G.V. Romanenko, A.S. Bogomyakov, N.P. Gritsan, D.G. Mazhukin
    Reaction of Paramagnetic Synthon, Lithiated 4,4,5,5-Tetramethyl-4,5-dihydro-1H-imidazol-1-oxyl 3-oxide, with Cyclic Aldonitrones of the Imidazole Series
    Chemistry - A European Journal, 2016, V. 22, N 41, Pp 14598-14604 doi:10.1002/chem.201602049, IF=5.77
  6. Synthesis of 4-(ω-X-alkyl)benzonitriles (X=1,3-dioxan-2-yl, CN, (CO2Et) by the reaction of terephthalonitrile dianion with ω-X-alkyl bromides in liquid ammonia/ R. Yu. Peshkov, Chynyan Wang, E. V. Panteleeva, E. V. Tretyakov, V. D. Shteingarts// Russian Chemical Bulletin, 2016, V. 65, N 10, pp 2430-2436 doi:10.1007/s11172-016-1602-x, IF=0.579
  7. L.V. Politanskaya, V.D. Shteingarts, E.V. Tretyakov
    General and efficient synthesis of polyfluorinated 2-aminotolans and 2-arylindoles
    Journal of Fluorine Chemistry, Journal of Fluorine Chemistry, 2016, V. 188, August 2016, Pp 85-98 doi:10.1016/j.jfluchem.2016.06.010, IF=2.213
  8. R.Yu. Peshkov, E.V. Panteleeva, W. Chunyan, E.V. Tretyakov, V.D. Shteingarts
    One-pot synthesis of 4'-alkyl-4-cyanobiaryls on the basis of the terephthalonitrile dianion and neutral aromatic nitrile cross-coupling
    Beilstein Journal of Organic Chemistry, 2016, V.12, Pp 1577-1584 doi:10.3762/bjoc.12.153, IF=2.697
  9. E.V. Tretyakov, R.Yu. Peshkov, E.V. Panteleeva, A.S. Scrypnik, D.V. Stass, G.V. Romanenko, V.I. Ovcharenko
    Addition of Cyanomethyl Anion to the Cyano Group of 2-Cyano-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl, a Nitronyl Nitroxide
    Tetrahedron Letters, V. 57, N 21, 25 May 2016, Pp 2327-2330 doi:10.1016/j.tetlet.2016.04.070, IF=2.346
  10. L.Yu. Gurskaya, D.S. Belyanskaya, D.S. Ryabukhin, D.I. Nilov, I.A. Boyarskaya, A.V. Vasilyev
    Reactions of N,3-diarylpropiolamides with arenes under superelectrophilic activation: synthesis of 4,4-diaryl-3,4-dihydroquinolin-2(1H)-ones and their derivatives
    Beilstein J. Org. Chem. 2016, 12, 950-956. doi:10.3762/bjoc.12.93, IF=2.697
  11. 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
  12. 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
  13. O.D. Zakharova, L.P. Ovchinnikova, S.I. Zhivetyeva, L.I. Goryunov, V.D. Shteingarts, E.V. Tretyakov, G.A. Nevinsky
    Synthesis and Evaluation of Cytotoxicity and Antioxidant Properties of Polyfluorinated Phosphorus-containing 1,4-Benzoquinones and 1,4-Naphthoquinones
    Adv. Res., 2016, 6(6), 1-12 doi:10.9734/AIR/2016/24265
  14. 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

2015
  1. S.I. Zhivetyeva, G.A. Selivanova, L.I. Goryunov, I.Yu. Bagryanskaya, V.D. Shteingarts
    Triphenylphosphanodefluorination of Fluoranil and its Derivatives
    Journal of Fluorine Chemistry, V. 180, December 2015, Pp 21-32 doi:10.1016/j.jfluchem.2015.08.018, IF=1.947
  2. I. Yu. Barskaya, S.L. Veber, S.V. Fokin, E.V. Tretyakov, E.G. Bagryanskaya, V.I. Ovcharenko, M.V. Fedin
    Structural specifics of light-induced metastable states in copper(II)-nitroxide molecular magnets
    Dalton Trans., 2015,44, 20883-20888 doi:10.1039/C5DT03683F, IF=4.197
  3. L. V. Politanskaya, I. P. Chuikov, E. V. Tretyakov, V. D. Shteingarts, L. P. Ovchinnikova, O. D. Zakharova, G. A. Nevinsky
    An effective two-step synthesis, fluorescent properties, antioxidant activity and cytotoxicity evaluation of benzene-fluorinated 2,2-dimethyl-2,3-dihydro-1H-quinolin-4-ones
    Journal of Fluorine Chemistry, V. 178, October 2015, Pp 142-153 doi:10.1016/j.jfluchem.2015.07.006, IF=1.947
  4. L. Politanskaya, V. Shteingarts, E. Tretyakov, A. Potapov
    The p-toluenesulfonic acid-catalyzed transformation of polyfluorinated 2-alkynylanilines to 2-aminoarylketones and indoles
    Tetrahedron Letters, V. 56, N 39, 23 September 2015, Pp 5328-5332 doi:10.1016/j.tetlet.2015.07.078, IF=2.378
  5. L. Politanskaya, V. Shteingarts, E. Tretyakov, A. Potapov
    The p-toluenesulfonic acid-catalyzed transformation of polyfluorinated 2-alkynylanilines to 2-aminoarylketones and indoles
    Tetrahedron Letters, V. 56, N 39, 23 September 2015, Pp 5328-5332 doi:10.1016/j.tetlet.2015.07.078, IF=2.378
  6. V.I. Borovkov, I.V. Beregovaya, L.N. Shchegoleva, S.V. Blinkova, D.A. Ovchinnikov, L.Yu. Gurskaya, V.D. Shteingarts, V.A. Bagryansky, Yu.N. Molin
    Structure and Stability of Pentafluoroaniline and 4-Aminononafluorobiphenyl Radical Anions: Optically Detected Electron Paramagnetic Resonance, Time-Resolved Fluorescence, Time-Resolved Magnetic Field Effect, and Quantum Chemical Study
    J. Phys. Chem. A, 2015, 119 (31), pp 8443–8451 doi:10.1021/acs.jpca.5b02617, IF=2.693
  7. R.Yu. Peshkov, E.V. Panteleeva, L.N. Shchegoleva, I.Yu. Bagryanskaya, T.V. Rybalova, N.V. Vasilieva, V.D. Shteingarts
    Synthesis of 2-X-, 3-X-4,4'-Dicyanobiphenyls (X = CH3, OCH3, F) by Cross-Coupling of the Terephthalonitrile Dianion with Substituted Benzonitriles
    European Journal of Organic Chemistry, V. 2015, N 20, pp 4524-4531, July 2015 doi:10.1002/ejoc.201500295, IF=3.65
  8. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Antioxidant Activity and Cytotoxicity of Polyfluorinated 1, 4- Naphthoquinones with Alkylating Functions in the Quinone Moiety
    International Journal of Medicine and Pharmaceutical Sciences (IJMPS), 2015, V.5, N 1, Pp. 11-20 (Paper ID=IJMPSFEB20151)

2014
  1. S.I. Zhivetyeva, L.I. Goryunov, I.Yu. Bagryanskaya, J. Grobe, V.D. Shteingarts, E.U. Wurthwein
    Phosphinodefluorination of polyfluorobenzenes by silylphosphines Ph(R)PSiMe3 (R = Me, Ph): Further experimental and computational evidences for the concerted A(N)D(N) mechanism of aromatic nucleophilic substitution
    Journal of Fluorine Chemistry, 2014, V. 164, Pp. 58-69. doi:10.1016/j.jfluchem.2014.04.012, IF=1.952
  2. N.M. Troshkova, L.I. Goryunov, V.D. Shteingarts, O.D. Zakharova, L.P. Ovchinnikova, G.A. Nevinsky
    Synthesis and cytotoxicity evaluation of polyfluorinated 1,4-naphthoquinones containing amino acid substituents
    Journal of Fluorine Chemistry, 2014, V.164, Pp 18-26. doi:10.1016/j.jfluchem.2014.04.014, IF=1.952

2013
  1. L.Yu. Gurskaya, V.D. Shteingarts
    Ortho-hydrodefluorination of polyfluorinated 4-acetamidobiphenyls and synthesis of polyfluorinated 6-phenylquinolines
    Journal of Fluorine Chemistry, 2013, V. 156, P. 214–219 doi:10.1016/j.jfluchem.2013.09.015, IF=1.939
  2. L. V. Politanskaya, I. P. Chuikov, V. D. Shteingarts
    Synthesis of indoles with a polyfluorinated benzene ring
    Tetrahedron, 2013, V. 69., N 39, P. 8477-8486. doi:10.1016/j.tet.2013.07.037, IF=2.802
  3. A.G. Potapov, L.V. Politanskaya
    The study of the adsorption of 1,3-diethers on the MgCl2 surface
    Journal of Molecular Catalysia A-Chemical, 2013, V. 368, P. 159-162. doi:10.1016/j.molcata.2012.12.004, IF=3.187
  4. Synthesis of phthalonitriles containing omega-alkenyl, omega-(alkylsulfanyl)alkyl, and omega-(alkylsulfonyl)alkyl substituents and phthalocyanine derivatives based thereon/ E. V. Panteleeva, A. S. Kondrat’ev, L. I. Goryunov, V. V. Koval’, E. A. Luk’yanets, V. D. Shteingarts// Russian Journal of Organic Chemistry, 2013, V.49, N 1, pp 138-144 doi:10.1134/S1070428013010235, IF=0.513

2012
  1. Alkoxylation of 4-chloronitrobenzene with aliphatic alcohols and glycols in the presence of NaOH/ E.V. Malykhin, V.D. Shteingarts// RUSS J APPL CHEM+, 2012, V. 85, N 8, pp: 1232-123 doi:10.1134/S1070427212080162, IF=0.282
  2. G.A. Selivanova, A.V. Reshetov, I.Yu. Bagryanskaya, V.D. Shteingarts
    Skraup-like cyclization of polyfluoro-2-naphthylamines: Vicarious electrophilic substitution of fluorine
    J. Fluorine Chem., 2012, V. 137, 113–116. doi:10.1016/j.jfluchem.2012.03.001, IF=2.32
  3. G.A. Selivanova, A.V. Reshetov, I.V. Beregovaya, N.V. Vasil’eva, I.Yu. Bagryanskaya, V.D. Shteingarts
    Hydrodefluorination of polyfluoro-2-naphthylamines by Zn in aqueous NH3: A correlation of the product distribution and the computationally predicted regioselectivity of the substrate radical anion fragmentation
    J. Fluorine Chem., 2012, V. 137, 64–72. doi:10.1016/j.jfluchem.2012.02.012, IF=2.32
  4. L.Yu. Gurskaya, G.A. Selivanova, V.D. Shteingarts
    Interaction of quinolines polyfluorinated on the benzene moiety with sodium and potassium amides in liquid ammonia
    J. Fluorine Chem., 2012, V. 136, 32–37. doi:10.1016/j.jfluchem.2012.01.007, IF=2.32
  5. L.V. Politanskaya, I.P. Chuikov, Е.А. Kolodina, M.S. Shvartsberg, V.D. Shteingarts
    Synthesis of polyfluorinated orthoalkynylanilines
    J. Fluorine Chem., 2012, V. 135, 97-107. doi:0.1016/j.jfluchem.2011.09.008, IF=2.32

2011
  1. A.V. Reshetov, G.A. Selivanova, L.V. Politanskaya, I.V. Beregovaya, L.N. Shchegoleva, N.V. Vasil’eva, I.Yu. Bagryanskaya, V.D. Shteingarts
    Hydrodefluorination of N-acetylheptafluoro-2-naphthylamine by zinc in aqueous ammonia: synthetic outcomes and mechanistic considerations
    ARKIVOC, 2011, (viii), 242–262.full text doi:10.3998/ark.5550190.0012.818, IF=1.95
  2. L.I. Goryunov, S.I. Zhivetyeva, G.A. Nevinsky, V.D. Shteingarts
    Synthesis of diphenyl(X)phosphonium betaines (X = CH3, C6H5, 2,5-F2C6H3) from hexafluoro-1,4-naphthoquinone
    ARKIVOC, 2011, (viii), 185-191.full text doi:10.3998/ark.5550190.0012.814, IF=1.95
  3. E.V. Panteleeva, V.D. Shteingarts, I.Yu. Bagryanskaya, G.E. Sal’nikov
    The formation of dicyanoterphenyls by the interaction of terephthalonitrile dianion with biphenylcarbonitriles in liquid ammonia
    ARKIVOC, 2011, (viii), 123-133.full text doi:10.3998/ark.5550190.0012.808, IF=1.95
  4. Synthesis of 2,3',4'-tricyanobiphenyl derivatives and tetraphenylphthalocyanines based thereon/ G.A. Selivanova, E.V. Amosov, L.I. Goryunov, S.V. Balina, V.G. Vasil'ev, G.E. Sal'nikov, E.A. Luk'yanets, V.D. Shteingarts// RUSS J ORG CHEM+, 2011, V. 47, N 8, pp. 1240-1246. doi:10.1134/S1070428011080215, IF=0.634
  5. Synthesis of (2-X,3-Y-Phenyl)dimethylphosphanes (X, Y = Me2P, H; Me2P, F; Br, F) and their complexes with PdCl2/ L.I. Goryunov, V.D. Shteingarts, J. Grobe, R. Mews// RUSS J ORG CHEM+, 2011, V. 47, N 5, pp. 780-782. doi:10.1134/S1070428011050204, IF=0.634
  6. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new polyfluorinated 1,4-naphthoquinones with divers substituents in the quinine moiety
    Bioorg. Med. Chem. 2011, V. 19, 256-260. doi: 10.1016/j.bmc.2010.11.027, IF=2.977

2010
  1. Synthesis of Fluorine-Containing Poly(phenylamino)-1,4-naphthoquinones/ N.M. Troshkova, L.I. Goryunov, V.D. Shteingarts// RUSS J ORG CHEM+, 2010, V. 46, N 10, pp 1585-1587. doi:10.1134/S1070428010100271, IF=0.524
  2. O.D. Zakharova, L.P. Ovchinnikova, L.I. Goryunov, N.M. Troshkova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new alkylamino- and phenylamino-containing polyfluorinated derivatives of 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 2321–2326. doi:10.1016/j.ejmech.2010.02.009, IF=3.269
  3. O.A. Zakharova, L.I. Goryunov, N.M. Troshkova, L.P. Ovchinnikova, V.D. Shteingarts, G.A. Nevinsky
    Cytotoxicity of new n-butylamino and sulfur-containing derivatives of polyfluorinated 1,4-naphthoquinone
    Eur. J. Med. Chem., 2010, 45, 270-274. doi:10.1016/j.ejmech.2009.10.00, IF=3.269
  4. L.I. Goryunov, J. Grobe, D. Le Van, V.D. Shteingarts, R. Mews, E. Lork, E.-U. Wurthwein
    Di- and Trifluorobenzenes in Reactions with Me2EM (E = P, N; M = SiMe3, SnMe3, Li) Reagents: Evidence for the Concerted Mechanism of Aromatic Nucleophilic Substitution
    Eur. J. Org. Chem., 2010, 6, 1111–1123. doi:10.1002/ejoc.200900880, IF=3.95
  5. N.M. Troshkova, L.I. Goryunov, Yu.V. Gatilov, G.A. Nevinsky, V.D. Shteingarts
    Aminodefluorination of 2-X-pentafluoro-1,4-naphthoquinones (X = NHnBu, NEt2, and OMe)
    J. Fluorine Chem., 2010, V. 131, N 1, 70-77. doi:10.1016/j.jfluchem.2009.10.007, IF=1.73
  6. V.A. Loskutov, Y.V. Gatilov, V.D. Shteingarts
    An unexpected skeletal transformation of 1,4-dihydroxythioxanthen-9-one on treatment with iodic acid: the first construction of the 2-(5-oxofuran-2-ylidene)-1-benzothienyl-3-one core
    Tetrahedron Letters, 2010, V. 51, N 49, Pp. 6396–6398. doi:10.1016/j.tetlet.2010.09.100, IF=2.66

2009
  1. Reaction of chloropentafluorobenzene and 2,3-and 2,6-difluorobromobenzenes with lithium dimethylphosphide/ L.I. Goryunov, J. Grobe, V.D. Shteingarts, R. Mews, E.U. Wurthwein// Russian Journal of Organic Chemistry, 2009, V. 45, N 12, pp 1859-1861 doi:10.1134/S1070428009120197, IF=0.556
  2. Synthesis of beta-Functionalized Ethyl Polyfluoroaryl Sulfides, Sulfoxides, and Sulfones Underlain by Pentafluorobenzoic Acid/ V.V. Litvak, A.S. Kondrat'ev, V.D. Shteimgarts// Russian Journal of Organic Chemistry, 2009, V. 45, N 11, pp 1637-1643. doi:10.1134/S1070428009110104, IF=0.556
  3. L.Yu. Safina, G.A. Selivanova, K.Yu. Koltunov, V.D. Shteingarts
    Synthesis of polyfluorinated 4-phenyl-3,4-dihydroquinolin-2-ones and quinolin-2-ones via superacidic activation of N-(polyfluorophenyl)cinnamamide
    Tetrahedron Lett., 2009, V. 50, N 37, pp 5245–5247. doi:10.1016/j.tetlet.2009.07.013, IF=2.538
  4. Synthesis of 2-aminopentafluoro-1,4-naphthoquinone derivatives/ L.I. Goryunov, N.M. Troshkova, G.A. Nevinskii, V.D. Shteingarts// Russian Journal of Organic Chemistry, 2009, V. 45, N 6, pp 835-841 doi:10.1134/S1070428009060050, IF=0.556
  5. Reaction of quinolines fluorinated at the benzene ring with nitrogen-centered nucleophiles/ L.Yu. Safina, G.A. Selivanova, I.Yu. Bagryanskaya, V.D. Shteingarts// Russian Chemical Bulletin, 2009, V. 58, N 5, pp 1049-1061 doi:10.1007/s11172-009-0134-z, IF=0.469

2008
  1. L.I. Goryunov, J. Grobe, V.D. Shteingarts
    Compounds R1R2EMMe3 (E = P, As; M = Si,Sn) - Convenient and Versatile Reagents for the Synthesis of Tertiary Fluoroarylphosphanes and -Arsanes
    Coll. Czech. Chem. Commun., 2008, V. 73, N 12, 1612–1622. doi:10.1135/cccc20081612, IF=0.879
  2. X-ray and quantum-topological studies of intermolecular interactions in partially fluorinated quinoline crystals/ I. Yu. Bagryanskaya, M. A. Grishina, L. Yu. Safina, G. A. Selivanova, V. A. Potemkin, Yu. V. Gatilov// Journal of Structural Chemistry, 2008, V. 49, N 5, pp 901-908 doi:10.1007/s10947-008-0155-8, IF=0.481
  3. Anionic reduced forms of electron-deficient arenes in reactions with C - C bond formation/ T.A. Vaganova, E.V. Panteleeva, V.D. Shteingarts// Russian Chemical Reviews,2008., V. 77, N 7, Pp 601-619. doi:10.1070/RC2008v077n07ABEH003776, IF=1.893
  4. Reductive activation of arenecarbonitriles for the reactions with some carbon-centered electrophiles: The reaction mechanisms and synthetic applications/ T.A. Vaganova, E.V. Panteleeva, V.D. Shteingarts// Russian Chemical Bulletin, 2008, V. 57, N 4, Pp 768-779. doi:10.1007/s11172-008-0116-6, IF=0.537
  5. N.V. Vasilieva, I.G. Irtegova, T.A. Vaganova, V.D. Shteingarts
    Electrochemical, ESR and quantum chemical study of 1-substituted naphthalenes and their radical anions
    J. Phys. Org. Chem., 2008, V. 21, N 1, 73–78. doi:10.1002/poc.1288, IF=1.593

2007
  1. Arene complexes of transition metals in reactions with nucleophilic reagents: XXX. Reaction of π-halomesitylene [Tetramethyl(ethyl)cyclopentadienyl]rhodium(II) complexes with anions derived from CH acids/ L. I. Goryunov, N. M. Romanova, G. S. Zhilovskii, V. D. Shteingarts// Russian Journal of Organic Chemistry, 2007, V. 43, N 12, pp 1765-1772 doi:10.1134/S1070428007120056, IF=0.492
  2. V.D. Shteingarts
    Recent advances in practice and theory of polyfluoroarene hydrodehalogenation
    J. Fluorine Chem., 2007, V. 128, N 7, 795-805. doi:10.1016/j.jfluchem.2007.02.019, IF=1.514
  3. Reductive activation of arenes - 22. Reactions of the terephthalonitrile radical anion and dianion with alpha,omega-dibromoalkanes. New evidence for the charge transfer complex as a key intermediate in the reactions of the dianion/ E. V. Panteleeva, M. Yu. Lukyanova, L. M. Pokrovsky, V. D. Shteingarts// Russian Chemical Bulletin, 2007, V. 56, N 6, pp 1110-1118 doi:10.1007/s11172-007-0168-z, IF=0.504
  4. Researcher, educator, and science administrator/ V. D. Shteingarts// Herald of the Russian Academy of Sciences, 2007, Volume 77, Issue 3, pp 262-269 doi:10.1134/S1019331607030094, IF=0.149
  5. E.V. Panteleeva, G. Haufe, V.D. Shteingarts
    Short Access to para-Alkenylbenzonitriles. Reaction of Anionic Reduced Forms of Terephthalonitrile with Alkenyl Bromides
    SynLett., 2007, N 10, 1616-1618. doi:10.1055/s-2007-982549, IF=2.838
  6. S.S. Laev, L.Yu. Gurskaya, G.A. Selivanova, I.V. Beregovay, L.N. Shchegoleva, N.V. Vasil'eva, M.M. Shakirov, V.D. Shteingarts
    N-Acetylation as a means to activate polyfluoroarylamines for selectyive ortho-hydrodefluorination by zinc in aqueous ammonia: a concise route to polyfluorobenzo Azaheterocycles
    Eur. J. Org. Chem., 2007, N 2, 306-316. doi:10.1002/ejoc.200600684, IF=2.769

2006
  1. Reductive activation of arenes: XIX. Mechanism and some synthetic applications of the alkylation of phthalodinitrile radical anion/ E. V. Panteleeva, T. A. Vaganova, E. A. Luk'yanets, V. D. Shteingarts// Russian Journal of Organic Chemistry, 2006, V. 42, N 9, pp 1280-1288 doi:10.1134/S1070428006090053, IF=0.419
  2. Reductive activation of arenes/ T. A. Vaganova, E. V. Panteleeva, P. S. Yuferov, Yu. V. Rebitva, V. D. Shteingarts// Russian Chemical Bulletin, 2006, V. 55, N 6, pp 981-986 doi:10.1007/s11172-006-0366-0, IF=0.589
  3. Reductive activation of arenes/ T. A. Vaganova, P. S. Yuferov, L. I. Goryunov, E. V. Panteleeva, G. E. Sal'nikov, L. N. Shchegoleva, V. I. Mamatyuk, V. D. Shteingarts// Russian Chemical Bulletin, 2006, V. 55, N 6, pp 976-980 doi:10.1007/s11172-006-0365-1, IF=0.589

 

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