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. 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
    
3. S.A. Popov, L.P. Kozlova, L.M. Kornaukhova, A.V. Shpatov
   Simple and efficient process for large scale preparation of betulonic acid from birch bark extracts
   Industrial Crops and Products, V. 92, 15 December 2016, Pp 197-200 doi:10.1016/j.indcrop.2016.07.026, IF=3.448
    
4. 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
    
5. 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
    
6. M.D. Semenova, S.A. Popov, I.V. Sorokina, Yu.V. Meshkova, D.S. Baev, T.G. Tolstikova, E.E. Shults
   Conjugates of Lupane Triterpenoids with Arylpyrimidines: Synthesis and Anti-inflammatory Activity
   Steroids, 2022, V. 184, 109042 doi:10.1016/j.steroids.2022.109042, IF=2.76
    
7. S.A. Popov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turksc
   Synthesis of water-soluble ester-linked ursolic acid-gallic acid hybrids with various hydrolytic stabilities
   Synthetic Communications, 2021, V.51, N 16, Pp 2466-2477 doi:10.1080/00397911.2021.1939057, IF=2.6
    
8. E.V. Tretyakov, V.F. Plyusnin, A.O. Suvorova, S.V. Larionov, S.A. Popov, O.V. Antonova, E.M. Zueva, D.V. Stass, A.S. Bogomyakov, G.V. Romanenko, V.I. Ovcharenko
   Luminescence of the nitronyl nitroxide radical group in a spin-labelled pyrazolylquinoline
   Journal of Luminescence, 2014, V. 148, Pp 33-38. doi:10.1016/j.jlumin.2013.11.017, IF=2.367
    
9. S.A. Popov, M.D. Semenova, D.S. Baev, I.V. Sorokina, N.A. Zhukova, T.S. Frolova, T.G. Tolstikova, E.E. Shults, M. Turks
   Lupane-type conjugates with aminoacids, 1,3,4- oxadiazole and 1,2,5-oxadiazole-2-oxide derivatives: synthesis, anti-inflammatory activity and in silico evaluation of target affinity
   Steroids, 2019, V.150, 108443 doi:10.1016/j.steroids.2019.108443, IF=2.136
    
10. M.D. Semenova, S.A. Popov, T.S. Golubeva, D.S. Baev, E.E. Shults, M. Turks
    Synthesis and Cytotoxicity of Sulfanyl, Sulfinyl and Sulfonyl Group Containing Ursane Conjugates with 1,3,4-Oxadiazoles and 1,2,4-Triazoles
    ChemistrySelectб 2021, V. 6, N 7, Pp 6472-6477, This article also appears in:Medicinal Chemistry & Drug Discovery doi:10.1002/slct.202101594, IF=2.109
     
11. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
     
12. S.A. Popov, M.D. Semenova, D.S. Baev, T.S. Frolova, M.A. Shestopalov, Ch. Wang, Zh. Qi, E.E. Shults, M. Turks
    Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
    Steroids, 2020, V. 162, , 108698 doi:10.1016/j.steroids.2020.108698, IF=1.948
     
13. S.A. Popov, M. D. Semenova, D. S. Baev, T. S. Frolova, E. E.Shults,Ch.Wang, M.Turks
    Synthesis of cytotoxic urs-12-ene- and 28-nor-urs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles
    Steroids, 2020, V. 153, 108524 doi:10.1016/j.steroids.2019.108524, IF=1.948
     
14. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.N. Shmidt, S.W. Kang, S.M. Kim, B.H. Um
    Lipophilic Extracts from Needles and Defoliated Twigs of Pinus pumila from Two Different Populations
    Chemistry & Biodiversity, 2013, V. 10, N 2, P. 198-208. doi:10.1002/cbdv.201200009, IF=1.807
     
15. A.V. Shpatov, S.A. Popov, O.I. Salnikova, T.P. Kukina, E.N. Shmidt, B.H. Um
    Composition and Bioactivity of Lipophilic Metabolites from Needles and Twigs of Korean and Siberian Pines (Pinus koraiensis Siebold & Zucc. and P. sibirica Du Tour)
    Chemistry & Biodiversity, 2017, V. 14, N 2, Article number e1600203 doi:10.1002/cbdv.201600203, IF=1.44
     
16. A.V. Shpatov, S.A. Popov, O.I. Salnikova, E.A. Khokhrina, E.N. Shmidt, B.H. Um
    Low-Volatile Lipophilic Compounds in Needles, Defoliated Twigs, and Outer Bark of Pinus thunbergii
    Natural Product Communications, 2013, V. 8, N 12, P. 1759-1762., IF=0.955
     
17. A.V. Shpatov, S.S. Zakharova, S.A. Popov
    Synthesis of New Hybrids of Abietic Acid and 1,3,4-Oxadiazoles
    Chemistry of Natural Compounds, 2022, V. 58, N 2, Pp 290-296 doi:10.1007/s10600-022-03662-5, IF=0.83
     
18. M.D. Semenova, S.A. Popov, E.E. Shul'ts, M. Turks
    Synthesis of New Ursane-Type Hybrids with Morpholinomethyl-, Dialkylamino-, and Hydroxyl-Substituted Azoles
    Chemistry of Natural Compoundsб 2022,58(1),Pp. 65-70 doi:10.1007/s10600-022-03597-x, IF=0.83
     
19. S.A. Popov, C. Wang, Z. Qi, E.E. Shul'ts, M. Turks
    Synthesis and Antioxidant Activity of New N-Containing Hybrid Derivatives of Gallic and Ursolic Acids
    Chemistry of Natural Compounds, 2021, V. 57, N. 6, Pp. 1042-1046 doi:10.1007/s10600-021-03546-0, IF=0.809
     
20. S.A. Popov, V.A. Reznikov
    1,3-Dipolar Cycloaddition or Nucleophilic Addition: Influence of Solvents and Nature of Substituents in the Reagent and Substrate Molecules on the Reaction of 4,5-Dihydro-1H-imidazole 3-oxides with Alkynes
    J. Heterocyclic Chem., 2006. V. 43, N 2, 293-298. doi:10.1002/jhet.5570430207, IF=0.74