Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. A.M. Agafontsev, T.A. Shumilova, P.A. Panchenko, S. Janz, O.A. Fedorova, E.A. Kataev
   Utilizing a pH-Sensitive Dye in the Selective Fluorescent Recognition of Sulfate
   CHEMISTRY - A EUROPEAN JOURNAL, V. 22, N 42, October 10, 2016, Pp 15069-15074 doi:10.1002/chem.201602623, IF=5.77
    
2. A. M. Agafontsev, T. Shumilova, T.Ruffer, H. Lang, E.A. Kataev
   Anthracene-based cyclophanes with selective fluorescent responses for TTP and GTP: insights into recognition and sensing mechanisms
   Chemistry - A European Journal, 2019, V. 25, N 14, Pp 3541-3549 doi:10.1002/chem.201806130, IF=5.16
    
3. A.M. Agafontsev, A. Ravi, T.A. Shumilova, A. Oshchepkov, E.A. Kataev
   Molecular receptors for recognition and sensing of nucleotides
   Chemistry - A European Journal, 2019, V. 25, N 11, Pp 2684-2694 doi:10.1002/chem.201802978, IF=5.16
    
4. A.M. Agafontsev, T.A. Shumilova, A.S. Oshchepkov, F. Hampel, E. A. Kataev
   Ratiometric detection of ATP by fluorescent cyclophanes with bellows-type sensing mechanism
   Chemistry - A European Journal, 2020, V. 26, N 44, Special Issue: Young Chemists 2020, Pp. 9991-9997 doi:10.1002/chem.202001523, IF=4.857
    
5. A.A. Gabrienko, A.V. Ewing, A.M. Chibiryaev, A.M. Agafontsev, K.A. Dubkov, S.G. Kazarian
   New insights into the mechanism of interaction between CO2 and polymers from thermodynamic parameters obtained by in situ ATR-FTIR spectroscopy
   Phys. Chem. Chem. Phys., 2016, 18(9), 6465-6475 doi:10.1039/C5CP06431G, IF=4.448
    
6. A.M. Agafontsev, A.S. Oshchepkov, T.A. Shumilova, E.A. Kataev
   Binding and Sensing Properties of a Hybrid Naphthalimide-Pyrene Aza-Cyclophane towards Nucleotides in an Aqueous Solution
   Molecules 2021, 26(4), 980 doi:10.3390/molecules26040980, IF=4.411
    
7. S.V. Larionov, Yu.A. Bryleva, L.A. Glinskaya, V.F. Plyusnin, A.S. Kupryakov, A.M. Agafontsev, A.V. Tkachev, A.S. Bogomyakov, D.A. Piryazev, I.V. Korolkov
   Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: synthesis, structure, magnetic properties and photoluminescence
   Dalton Trans., 2017, V. 34, N 46, Pp. 11440-11450 doi:10.1039/C7DT01536D, IF=4.28
    
8. T.E. Kokina, M.I. Rakhmanova, N.A. Shekhovtsov, L.A. Glinskaya, V.Y. Komarov, A.M. Agafontsev, A.Y. Baranov, P.E. Plyusnin, L.A. Sheludyakova, A.V. Tkachev, M.B. Bushuev
   Luminescent Zn(ii) and Cd(ii) complexes with chiral 2,2э-bipyridine ligands bearing natural monoterpene groups: synthesis, speciation in solution and photophysics
   Dalton Trans., 2020, V. 49, N 22, Pp 7552-7563 doi:10.1039/D0DT01438A, IF=4.174
    
9. Yu. A. Bryleva, Yu. P. Ustimenko, V. F. Plyusnin, A. V. Mikheilis, A. A. Shubin, L. A. Glinskaya, V. Yu. Komarov, A. M. Agafontsev , A. V. Tkachev
   Ln(III) complexes with a chiral 1H-pyrazolo[3,4-b]pyridine derivative fused with a (-)-α-pinene moiety: synthesis, crystal structure, and photophysical studies in solution and in the solid state
   New J. Chem., 2021,45, 2276-2284 doi:10.1039/D0NJ05277A, IF=3.591
    
10. K.S. Marenin, Yu.V. Gatilov, A.M. Agafontsev, A.V. Tkachev
    Stereoselectivity of formation of monoterpene - Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives
    Steroids, 2016, V. 117, Pp 112-119 doi:10.1016/j.steroids.2016.09.016, IF=2.282
     
11. Yu.P. Ustimenko, A.M. Agafontsev, V.Yu. Komarov, A.V. Tkachev
    Synthesis of chiral nopinane annelated 3-methyl-1-aryl-1H-pyrazolo[3,4-b]pyridines by condensation of pinocarvone oxime with 1-aryl-1H-pyrazol-5-amines
    Mendeleev Communications, 2018, V. 28, N 6, Pp 584-586 doi:10.1016/j.mencom.2018.11.006, IF=2.098
     
12. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
     
13. Yu.P. Ustimenko, A.M. Agafontsev, A.V. Tkachev
    Synthesis of chiral pinopyridines using catalysis by metal complexes
    Chemistry of Heterocyclic Compounds, 2022, V. 58, N 2-3, Pp 135-143 doi:10.1007/s10593-022-03066-x, IF=1.49
     
14. E.S. Vasilyev, A.M. Agafontsev, A.V. Tkachev
    Microwave-Assisted Synthesis of Chiral Nopinane-Annelated Pyridines by Condensation of Pinocarvone Oxime with Enamines Promoted by FeCl₃ and CuCl₂
    Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry, 2014, V. 44, N 12, pp 1817-1824. doi:10.1080/00397911.2013.877145, IF=0.984
     
15. E.S. Vasilyev, A.M. Agafontsev, V.D. Kolesnik, Yu.V. Gatilov, A.V. Tkachev
    Stereoselective functionalisation of pinopyridine with anisidines and o-phenylenediamine
    Mendeleev Commun., 2011, V. 21, N 5, 253-255. doi:10.1016/j.mencom.2011.09.007, IF=0.814
     
16. A.M. Agafontsev, N.B. Gorshkov, A.V. Tkachev
    Efficient synthesis of β-hydroxy sulfides by microwave-promoted ring opening in (+)-3-carene trans-epoxide with sodium thiolates
    Mendeleev Commun., 2011, V. 21, N 4, 192-193. doi:10.1016/j.mencom.2011.07.006, IF=0.814
     
17. Т.Е. Кокина, Л.А. Глинская, Д.А. Пирязев, А.Ю. Баранов, А.М. Агафонцев, Ю.А. Еремина, Е.В. Воронцова, А.С. Богомяков, Д.Ю. Наумов, А.В. Ткачев, С.В. Ларионов
    Синтез и строение комплексов CuII,I и CгI с производным 2,2'-бипиридина, содержащим фрагмент природного монотерпена (+)-3-карена
    Известия Академии наук. Серия химическая. 2018. № 7. С. 1251-1260. (Synthesis and structures of CuI,II complexes with a 2,2´-bipyridine derivative bearing a (+)-3-carene moiety/ T. E. Kokina. A. Glinskaya, D. A. Piryazev, A. Yu. Baranov, A. M. Agafontsev, Yu. A. Eremina, E. V. Vorontsova, A. S. Bogomyakov, D. Yu. Naumov, A. V. Tkachev, S. V. Larionov// Russian Chemical Bulletin, 2018, V. 67, N 7, pp 1251-1260 doi:10.1007/s11172-018-2209-1), IF=0.781
     
18. Ю.А. Брылева, Д.А. Пирязев, Л.А. Глинская, А.М. Агафонцев, М.И. Рахманова, А.В. Ткачев
    Синтез, структура и фотолюминесцентные свойства комплексов лантанидов(III) с лигандом на основе 1,10-фенантролина и борнеола
    Журнал структурной химии. 2020. Т. 61. № 11. С. 1906-1919. doi:10.26902/JSC_id63269 (Synthesis, structure, and photoluminescent properties of lanthanide(III) complexes with a ligand based on 1,10-phenanthroline and borneol/ Yu. A. Bryleva, D. A. Piryazev, L. A. Glinskaya, A. M. Agafontsev, M. I. Rakhmanova & A. V. Tkachev// Journal of Structural Chemistry, 2020, V. 61, N 11, Pp 1810-1822 doi:10.1134/S0022476620110141), IF=0.745
     
19. I.V. Romanova, A.A. Alekseev, И.В. Романова, А.А. Алексеев, В.А. Рихтер, Н.Е. Грунтенко, А.М. Агафонцев, Е.К. Карпова
    Получение меченного тритием ювенильного гормона и радиометрический анализ уровня его ферментативного гидролиза
    Биоорганическая химия. 2017. Т. 43. № 2. С. 208-213 (A synthesis of tritium-labeled juvenile hormone and / I.V. Romanova, A.A. Alekseev, V.A. Richter, N.E. Gruntenko, A.M. Agafontsev, E.K. Karpova// Russian Journal of Bioorganic Chemistry, 2017, V. 43, N 2, pp 211-215 doi:10.1134/S1068162017020121), IF=0.689
     
20. Т.Е. Кокина, Ю.П. Устименко, М.И. Рахманова, Л.А. Шелудякова, А.М. Агафонцев, П.Е. Плюснин, А.В. Ткачев, С.В. Ларионов
    Люминесцирующие комплексы ZN(II) и CD(II) c хиральными лигандами, содержащими фрагменты 1,10-фенантролина и природных монотерпеноидов (+)-3-карена или (+)-лимонена
    Журнал общей химии. 2019. Т. 89. № 1. С. 98-107. DOI:10.1134/S0044460X19010165 (Luminescent Complexes of Zn(II) and Cd(II) with Chiral Ligands Containing 1,10-Phenanthroline and Natural Monoterpenoids (+)-3-Carene or (+)-Limonene Fragments/ T.E. Kokina, Yu. P. Ustimenko, M.I. Rakhmanova, L.A. Sheludyakova, A.M. Agafontsev, P.E. Plusnin, A.V. Tkachev, S.V.Larionov// Russian Journal of General Chemistry, 2019, V. 89, N 1, pp 87-95 doi:10.1134/S107036321901016X), IF=0.643