Head - Cand. Sci. (Chem)
POLITANSKAYA Larisa Vladimirovna

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

   

  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)

   

  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.

   

  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)

   

  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)

   

  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	Politanskaya Larisa Vladimirovna	Lab's Head (Cand. Chem)	405	330-68-59	2-73	This email address is being protected from spambots. You need JavaScript enabled to view it.
2	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.
3	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.
4	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.
5	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.
6	Fedyushin Pavel Andreevich	Researcher (Cand. Chem.)	131	330-68-59	4-09	This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
7	Verkhov Fedor Konstantinovich	laboratory assistant
8	Khasanov Bulat Radikovich	laboratory assistant

PUBLICATIONS

Publications over the past years

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles

2022

1. CYANARYLATION OF FLUORINATED BENZONITRILES WITH TEREPHTHALONITRILE DIANION/ Panteleeva E.V., Peshkov R.Yu.// Chemistry for Sustainable Development. 2022. Т. 30. № 6. С. 617-624. doi:10.15372/CSD2022425
2. L. Politanskaya, B. Khasano, A. Potapov
   Synthetic approaches to fluorinated derivatives of 4-(vinylthio)pyridine
   Journal of Fluorine Chemistry, V. 264, December 2022, 110063 doi:10.1016/j.jfluchem.2022.110063, IF=2.226
3. L. Politanskaya, Ji.Wang, N.Troshkova, I.Chuikov, I. Bagryanskayaa
   One-pot synthesis of fluorinated 2-arylchroman-4-one derivatives from 2-(triisopropylsilyl)ethynylphenols and aromatic aldehydes
   Journal of Fluorine Chemistry V. 263, November 2022, 110045 doi:10.1016/j.jfluchem.2022.110045, IF=2.226
4. N.B. Asanbaeva, L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, M.S. Kazantsev, A.A. Dmitriev, N.P. Gritsan, N. Haro-Mares, T. Gutmann, G. Buntkowsky, E.V. Tretyakov, E.G. Bagryanskaya
   Effects of Spiro-Cyclohexane Substitution of Nitroxyl Biradicals on Dynamic Nuclear Polarization
   Molecules 2022, 27(10), 3252 doi:10.3390/molecules27103252, IF=4.927
5. I.O. Timofeev, L.V. Politanskaya, E.V. Tretyakov, Yu.F. Polienko, V.M. Tormyshev, E.G. Bagryanskaya, O.A. Krumkacheva, M.V. Fedin
   Fullerene-based triplet spin labels: methodology aspects for pulsed dipolar EPR spectroscopy
   Phys. Chem. Chem. Phys., 2022, V.24, N 7, Pp. 4475-4484 doi:10.1039/D1CP05545C, IF=3.945
6. L.Yu. Gurskaya, Yu.F. Polienko, T.V. Rybalova, N.P. Gritsan, A.A. Dmitriev, M.S. Kazantsev, E.V. Zaytseva, D.A. Parkhomenko, I.V. Beregovaya, G.A. Zakabluk, E.V. Tretyakov
   Multispin Systems with a Rigid Ferrocene-1,1'-diyl-Substituted 1,3-Diazetidine-2,4-diimine Coupler: A General Approach
   European journal of organic Chemistry, V. 2022, N 7, February 18, 2022, e202101234 doi:10.1002/ejoc.202101234, IF=3.261
7. G.A. Selivanova, A.D. Skolyapova, J. Wang, E.V. Karpova, I. Shundrina, I.Yu. Bagryanskaya, E.V. Amosov
   Azo dyes containing 1,3,4-thiadiazole fragment: synthesis, properties
   New J. Chem., 2022, 46(4), 1929-1942 doi:10.1039/D1NJ05084B, IF=3.925

2021

1. A.O. Bryzgalov, T.A. Yakovleva, L.V. Politanskaya, I.Yu. Bagryanskaya, T.G. Tolstikova
   Fluorinated 3,4-Dihydro-2H-1,4-Benzothiazin1,1-Dioxide Derivatives with Antiarrhythmic and Hypertensive Effects
   American Journal of Biomedical Science & Research, 2021,13(4),328-338 doi:10.34297/AJBSR.2021.13.001882
2. Azo chromophores for nonlinear-optical application/ G. A. Selivanova// Russian Chemical Bulletin, 2021, V. 70, N 2, Pp 213-238 doi:10.1007/s11172-021-3080-z, IF=1.222
3. L. Politanskaya, E. Tretyakov, Chanjuan. Xi
   Synthesis of polyfluorinated 4-hydroxyquinolin-2(1H)-ones based on the cyclization of 2-alkynylanilines with carbon dioxide
   Journal of Fluorine Chemistry, 2021, V. 242, 109720 doi:10.1016/j.jfluchem.2020.109720, IF=2.05

2020

1. E.M. Kadilenko, N.P. Gritsan, E.V. Tretyakov, S.V. Fokin, G.V. Romanenko, A.S. Bogomyakov, D.E. Gorbunov, D. Schollmeyer, M. Baumgarten, V.I. Ovcharenko
   A black-box approach to the construction of metal-radical multispin systems and analysis of their magnetic properties
   Dalton Trans., 2020, 49(46), 16916-16927 doi:10.1039/D0DT03184D, IF=4.173
2. L.V. Politanskaya, P.A. Fedyushin, T.V. Rybalova, A.S. Bogomyakov, N.B. Asanbaeva, E.V. Tretyakov
   Fluorinated Organic Paramagnetic Building Blocks for Cross-Coupling Reactions
   Molecules 2020, 25(22), 5427 doi:10.3390/molecules25225427, IF=3.266
3. 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, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
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. 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
6. 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
7. 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
8. 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
9. 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
10. 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
11. 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
12. 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
13. 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
14. 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
15. 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
16. 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
17. 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 S_N^F-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. 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
6. 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
7. 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