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. T.N. Drebushchak, N.A. Pankrushina, A.N. Mikheev, M.K. A. Thumm
   Crystalline products of tolbutamide decomposition in water after microwave treatment
   CrystEngComm, 2013, V. 15, N 18, P. 3582-3586. doi:10.1039/c3ce40145f, IF=3.878
    
3. T.N. Drebushchak, V.A. Drebushchak, N.A. Pankrushina, E.V. Boldyreva
   Single-crystal to single-crystal conformational polymorphic transformation in tolbutamide at 313 K. Relation to other polymorphic transformations in tolbutamide and chlorpropamide
   CrystEngComm, 2016,18, 5736-5743 doi:10.1039/C6CE00764C, IF=3.848
    
4. N.E. Polyakov, O.A. Simaeva, M.B. Taraban, T.V. Leshina, T.A. Konovalova, L.D. Kispert, I.A. Nikitina, N.A. Pankrushina, A.V. Tkachev
   CIDNP and EPR Study of Phototransformation of Lappaconitine Derivatives in Solution
   J. Phys. Chem. B., 2010, V. 114, N 13, 4646-4651. doi:10.1021/jp909166r, IF=3.47
    
5. G.Z. Baisalova, N.A. Pankrushina, R.S. Erkasov, M.S. Shengene, K.K. Kulanova, A.D. Spanbayev, R.S. Orazbaeva
   Virus inhibitory activity of methanol extracts of Halimodendron halodendron Voss
   PLANTA MEDICA, 2016, V. 81, N 16, Pp 1507-1507 Аннотация к встрече: PW-52 doi:10.1055/s-0035-1565676, IF=2.151
    
6. N.E. Polyakov, T.V. Leshina, A.V. Tkachev, I.A. Nikitina, N.A. Pankrushina
   Phototransformation products of the alkaloid lappaconitine: Multinuclear NMR study
   J. Photochem. Photobiol. A: Chem., 2008, V. 197, N 2-3, 290-294. doi:10.1016/j.jphotochem.2008.01.006, IF=1.911
    
7. I.E. Paukov, Y.A. Kovalevskaya, A.E. Arzamastcev, N.A. Pankrushina, E.V. Boldyreva
   Heat capacity of methacetin in a temperature range of 6 to 300 K
   J. Therm. Anal. Calorim., 2012, V. 108, N1, 243-247. doi:10.1007/s10973-011-1505-x, IF=1.603
    
8. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, I.V. Eltsov, S.A. Kuznetsova, A.S. Kichkailo, T.P. Shakhtshneider
   Microwave-assisted synthesis and antitumor activity of the supramolecular complexes of betulin diacetate with arabinogalactan
   Chemical Papers, 2018, V. 72, N 5, pp 1257-1263 doi:10.1007/s11696-017-0362-x, IF=0.963
    
9. Yu.N. Malyar, M.A. Mikhailenko, N.A. Pankrushina, A.N. Mikheev, S.A. Kuznetsova, T.P. Shakhtshneider
   Effect of Microwave Irradiation on Arabinogalactan and Its Interaction with Betulin Diacetate
   Russian Journal of Bioorganic Chemistry, 2018, Vol. 44, No. 7, pp. 762-767. doi:10.1134/S1068162018070075, IF=0.838
    
10. N.A. Pankrushina, K.B. Rakhmetali
    Synthesis of lappaconitine N-oxide under microwave activation
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N 11, pp 970-972 doi:10.1007/s10593-017-1995-y, IF=0.814
     
11. T.N. Drebushchak, N.A. Pankrushina, T.P. Shakhtshneider, S.A. Apenina
    4-Benzoyloxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide
    Acta Crystallogr. C, 2006, V. 62, N 7, o429-o431. doi:10.1107/S0108270106020567, IF=0.779
     
12. D. V. Sandanov, N. A. Pankrushina
    Alkaloid content in various parts of Sophora flavescens
    Chem. Nat. Compd., 2011, V. 47, N 4, pp 669-670. doi:10.1007/s10600-011-0029-8, IF=0.693
     
13. N. Pankrushina, I. Nikitina, E. Chernjak, C. Myz, T. Shakhtshneider, V. Boldyrev
    Solvent-free mechanochemical modification of lappakonifine and piroxicam
    Mater. Manuf. Process., 2008, V.23, N 6, 561-565. doi:10.1080/10426910802157870, IF=0.611
     
14. Н.A. Туманов, Н.A. Панкрушина, A.A. Нефедов, Е.В. Болдырева
    Нанопористый сольват N,N-фталоил-глицина
    Журн. cтруктур. химии, 2012, Т. 53, № 3, 611-614. (Nanoporous solvate of N,N-phthaloyl-glycine/ N. A. Tumanov, N. A. Pankrushina, A. A. Nefedov, E. V. Boldyreva// J STRUCT CHEM+, 2012, V. 53, N 3, pp. 606-609. doi:10.1134/S0022476612030298), IF=0.586
     
15. D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov
    Phenolic compounds of Sophora flavescens Soland. of Russian origin
    Russian Journal of Bioorganic Chemistry, 2013, V., N 7, pp 755-760 .(Original Russian Text © D.N. Olennikov, L.M. Tankhaeva, N.A. Pankrushina, D.V. Sandanov, 2012, published in Khimiya Rastitel’nogo Syr’ya, 2012, No. 4, pp. 101–108.) doi:10.1134/S106816201307011X, IF=0.523
     
16. M.O. Korotkikh, N.A. Pankrushina, O.I. Sal'nikova, A.E. Sonnikova
    Alkaloids from the New Species Papaver kuvajevii
    Chemistry of Natural Compounds, July 2015, Volume 51, Issue 4, pp 803-804 doi:10.1007/s10600-015-1418-1, IF=0.509
     
17. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
     
18. A.E. Goncharov, A.A. Politov, N.A. Pankrushina, O.I. Lomovskii
    Isolation of lappaconitine from Aconitum septentrionale roots by adsorption
    Chem. Nat. Compd. (Хим. Природ. Соедин.), 2006, V. 42, N 3, 336-339. doi:10.1007/s10600-006-0114-6, IF=0.31
     
19. Т.Н. Дребущак, Н.А. Панкрушина, Е.В. Болдырева
    Полиморфные превращения нового типа в толбутамиде: необычное низкотемпературное конформационное упорядочение.
    Доклады Академии наук, 2011, Т. 437, № 4, 507-510. (A new type of polymorphic transformation in tolbutamide: Unusual low-temperature conformation ordering/ T. N. Drebushchak, N. A. Pankrushina, E. V. Boldyreva// DOKL PHYS CHEM, 2011, V. 437, N 2, pp. 61-64. doi:10.1134/S0012501611040014), IF=0.256
     
20. G.Zh. Baisalova, N.A. Pankrushina, D.V. Domrachev, O.I. Salnikova, R.Sh. Erkassov
    Volatile Constituents of Halimodendron halodendron Voss. Growing in Kazakhstan
    Journal of Essential Oil Bearing Plants, 2014, V.. 17, N 5, P. 886-890. doi:10.1080/0972060X.2014.935074, IF=0.187