Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

1. A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
   Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
   ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
    
2. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
   Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
   Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863
    
3. Zh. Qi, Ya. Guliang, D. Wang, T. Deng, H. Zhou, S.A. Popov, E.E. Shults, Ch. Wang
   Design and Linkage Optimization of Ursane-Thalidomide-Based PROTACs and Identification of Their Targeted-Degradation Properties to MDM2 Protein
   Bioorganic Chemistry, Volume 111, June 2021, 104901 doi:10.1016/j.bioorg.2021.104901, IF=5.275
    
4. D.V. Reshetnikov, I.D. Ivanov, D.S. Baev, T.V. Rybalova, E.S. Mozhaitsev, S.S. Patrushev, V.A. Vavilin, T.G. Tolstikova, E.E. Shults
   Design, Synthesis and Assay of Novel Methylxanthine–Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors
   Molecules 2022, 27(24), 8787 doi:10.3390/molecules27248787, IF=4.927
    
5. Yu.V. Kharitonov, E.E. Shults
   An Approach toward 17-Arylsubstituted Marginatafuran-Type Isospongian Diterpenoids via a Palladium-Catalyzed Heck–Suzuki Cascade Reaction of 16-Bromolambertianic Acid
   Molecules 2022, 27(9), 2643 doi:10.3390/molecules27092643, IF=4.927
    
6. M.E. Mironov, S.A. Borisov, T.V. Rybalova, D.S. Baev, T.G. Tolstikova, E.E. Shults
   Synthesis of Anti-Inflammatory Spirostene-Pyrazole Conjugates by a Consecutive Multicomponent Reaction of Diosgenin with Oxalyl Chloride, Arylalkynes and Hydrazines or Hydrazones
   Molecules 2022, 27(1), 162 doi:10.3390/molecules27010162, IF=4.927
    
7. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
   Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
   Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
    
8. M.A. Lenskiy, E.E. Shul'ts, D.V. Korabel'nikov, A.V. Ozhogin, A.N. Novitskiy
   Pyrocatechol borates: Synthesis, reaction with formaldehyde, and solvent effect on polycondensation process
   Polymer, 2020, V. 183 , 122162 doi:10.1016/j.polymer.2020.122162, IF=4.231
    
9. V.A. Stepanova, S.S. Patrushev, T.V. Rybalova, E.E. Shults
   Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
   Journal of Molecular Structure, V.1247, 5 January 2022, 131373 doi:10.1016/j.molstruc.2021.131373, IF=3.841
    
10. S.F. Vasilevsky, A.I. Govdi, E.E. Shults, M.M. Shakirov, I.V. Sorokina, T.G. Tolstikova, D.S. Baev, G.A. Tolstikov, I.V. Alabugin
    Efficient synthesis of the first betulonic acid -acetylene hybrids and their hepatoprotective and anti-inflammatory activity
    Bioorg. Med. Chem. 2009, V. 17, N 14, 5164-5169. doi:0.1016/j.bmc.2009.05.059, IF=3.75
     
11. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
     
12. M.A. Timoshenko, Yu.V. Kharitonov, M.M. Shakirov, I.Yu. Bagryanskaya, E.E. Shults
    Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
    ChemistryOPEN, V. 5, N 1, pp 65-70, February 2016 doi:10.1002/open.201500187, IF=3.585
     
13. A.V. Lipeeva, M.A. Pokrovsky, D.S. Baev, M.M. Shakirov, I.Y. Bagryanskaya, T.G. Tolstikova, A.G. Pokrovsky, E.E. Shults
    Synthesis of 1H-1,2,3-triazole linked aryl(arylamidomethyl) - dihydrofurocoumarin hybrids and analysis of their cytotoxicity
    European Journal of Medicinal Chemistry, V.100, 2015, Pp 119-128 doi:10.1016/j.ejmech.2015.05.016, IF=3.447
     
14. K.P. Cheremnykh, V.A. Savelyev, E.E. Shults
    An Efficient Access to 3,5-Disubstituted Isoxazoles with Anthranilate Ester Moiety: Alkaloid Lappaconitine – Aryl Conjugates with an Isoxazole Linker
    Asian Journal of Organic Chemistry, V. 10, N 10, Pp. 2638-2643 doi:10.1002/ajoc.202100474, IF=3.319
     
15. N.S. Sirazhetdinova, V.A. Savelyev, T.S. Frolova, D.S. Baev, L.S. Klimenko, I.V. Chernikov, O.S. Oleshko, T.A. Sarojan, A.G. Pokrovskii, E.E. Shults
    1-Hydroxyanthraquinones Containing Aryl Substituents as Potent and Selective Anticancer Agents
    Molecules 2020, 25(11), 2547 doi:10.3390/molecules25112547, IF=3.267
     
16. K.P. Cheremnykh, V.A. Savelyev, S.A. Borisov, I.D. Ivanov, D.S. Baev, T.G. Tolstikova, V.A. Vavilin, E.E. Shults
    Hybrides of Alkaloid Lappaconitine with Pyrimidine Motif on the Anthranilic Acid Moiety: Design, Synthesis, and Investigation of Antinociceptive Potency
    Molecules 2020, 25(23), 5578 doi:10.3390/molecules25235578, IF=3.266
     
17. A.A. Ivanov, E.A. Ukladov, S.A. Kremis, S.Z. Sharapov, S.I. Baiborodin, A.V. Lipeeva, E.E. Shults, T.S. Golubeva
    Investigation of cytotoxic and antioxidative activity of 1,2,3-triazolyl-modified furocoumarins and 2,3-dihydrofurocoumarins
    Protoplasma , 2022, 259 (5), Pp. 1321-1330 doi:10.1007/s00709-022-01739-0, IF=3.186
     
18. S.A. Popov, O.P. Sheremet, L.M. Kornaukhova, A.E. Grazhdannikov, E.E. Shults
    An approach to effective green extraction of triterpenoids from outer birch bark using ethyl acetate with extractant recycle
    Industrial Crops and Products, 2017, V.102, Pp 122-132 doi:10.1016/j.indcrop.2017.03.020, IF=3.18
     
19. A.V. Lipeeva, D.O. Zakharov, L.G. Burova, T.S. Frolova, D.S. Baev, I.V. Shirokikh, A.N. Evstropov, O.I. Sinitsyna, T.G. Tolsikova, E.E. Shults
    Design, Synthesis and Antibacterial Activity of Coumarin-1,2,3-triazole Hybrids Obtained from Natural Furocoumarin Peucedanin
    Molecules 2019, 24(11), 2126 doi:10.3390/molecules24112126, IF=3.06
     
20. Je. Lugiņina, M. Linden, M. Bazulis, V. Kumpiņs, A. Mishnev, S.A. Popov, T.S. Golubeva, S.R. Waldvogel, E.E. Shults, M. Turks
    Electrosynthesis of stable betulin‐derived nitrile oxides and their application in synthesis of cytostatic lupane‐type triterpenoid‐isoxazole conjugates
    European Journal of Organic Chemistry, 2021, V. 2021, N 17, Pp 2557-2577 doi:10.1002/ejoc.202100293, IF=3.021