Публікації в міжнародних виданнях

2023 р.

Розділи в зарубіжних монографіях

  • T.V. Tkachenko, D.S. Kamenskyh, Y.V. Sheludko, V.O. Yevdokymenko . Structural and morphological features of nanoсellulose from soybean straw. Nanoobjects & Nanostructuring. Volume I / Edited by Lidiya M. Boichyshyn and Oleksandr. V. Reshetnyak. ‒ Mississauga, Ontario: Nova Printing Inc. 2022. Р. 145-160.
  • S. Konovalov, S. Zubenko, L. Patrylak, A. Yakovenko, V. Povazhnyi, K. Burlachenko. On the Peculiarities of Alkaline-Catalyzed Route of Synthesis of Fatty Acid Monoalkyl Esters. International Symposium on Electric Aircraft and Autonomous Systems.Advances in Electric Aviation.Р. 275-281.
  • Patrylak L.K., Yakovenko A.V., Nizhnik B.O., Pertko O.P., Povazhnyi V.A., Kamenskyh D.S., Melnychuk O.V.. Natural Zeolites Modified with Silver Nanoparticles as Promising Sorbents with Antibacterial Properties. Nanoelectronics, Nanooptics, Nanochemistry and Nanobiotechnology, and Their Applications. Springer Proceedings in Physics. 2023. Р. 87-98.
  • Tsygankova V.A.. Research Advances in Microbiology and Biotechnology. Book Publisher International. SCIENCEDO­MAIN international Ltd. India.United Kingdom. Vol. 3. 2023. 166 p. ISBN 978-81-19102-24-2 (Print) ISBN 978-81-19102-26-6 (eBook). DOI: 10.9734/bpi/ramb/v3.
  • Tsygankova V.A.. Research Advances in Microbiology and Biotechnology. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol. 6. 2023. 183 p. ISBN 978-81-19315-43-7 (Print), ISBN 978-81-19315-40-6 (eBook). Р. 142-158DOI: 10.9734/bpi/ramb/v6.
  • Tsygankova V.A.. Novel Aspects on Chemistry and Biochemistry. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol.1. 2023. 178 p. ISBN 978-81-19217-26-7 (Print), ISBN 978-81-19217-06-9 (eBook). Р. 1-8.DOI: 10.9734/bpi/nacb/v1.
  • Tsygankova V.A.. Novel Aspects on Chemistry and Biochemistry. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. Vol.4. 2023. 178 p. ISBN 978-81-19217-26-7 (Print), ISBN 978-81-19217-06-9 (eBook). Р. 13-24.DOI: 10.9734/bpi/nacb/v1.
  • Tsygankova V.A., Spivak S.I., Shysha E.N., Pastukhova N.L., Biliavska L.A., Iutynska G.A., Kyrylenko V.M., Yemets A.I., Blume Ya.B.. The role of polycomponent biostimulants in increasing plant resistance to the biotic and abiotic stress factors. Chapter in Monograph: Agricultural Research Updates. Nova Science Publishers, Inc., NY, USA. 2023, Ed. Prathamesh Gorawala and Srushti Mandhatri, 307 p. ISBN 979-8-89113-332-7https://novapublishers.com/shop/agricultural-research-updates-volume-46/.

Публікації в зарубіжних виданнях

  1. A.O. Kolodiazhna,O.I. Kolodiazhnyi. Chiral Organophosphorus drugs. Symmetry. 2023. V.15, N. 8. Р.1550. https://doi.org/10.3390/sym15081550
  2. D. Kamenskyh, T. Tkachenko, L. Tecer, Y. Sheludko, V. Povazhny, M. Jafarov, V. Yevdokymenko. Influence of ratio of silicon complex and coagulant on silicon dioxide physicochemical characteristics. Applied Nanoscience. 2023. V. 13, N 10. P. 6967-6999. https://doi.org/10.1007/s13204-023-02841-2
  3. M. Aksylenko, E. Sheludko, V. Yevdokymenko, O. Haidai, N. Khimach. Biostimulating Effect of Polygalacturonates of Biogenic Metals on Growing Winter Wheat. Cutting Edge Research in Biology. 2023. V. 6, N 11., Ch. 1. P. 1-24, https://doi.org/10.9734/bpi/cerb/v6/5047B
  4. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Model Desublimation Conditions. Asian Journal of Chemical Sciences. 2023. V. 13, N 2. P. 1-6.https://doi.org/10.9734/AJOCS/2023/v13i2234
  5. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Chemical Science International Journal. 2023. V. 32, N 3. P. 62-68. https://doi.org/10.9734/CSJI/2023/v32i3849
  6. K. Hutsul, I. Ivanenko, L. Patrylak, O. Pertko, D. Kamenskyh. ZnO/Zeolite composite photocatalyst for dyes degradation. Applied Nanoscience. 2023. Р. 1-9. https://doi.org/10.1007/s13204-023-02950-y
  7. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Evolutions Mech Eng. 2023. V. 4, N 4. EME.000595.2023. https://doi.org/10.31031/EME.2023.04.000595
  8. Vretik L.O., Noskov Yu.V., Chepurna O.M., Ogurtsov N.A., O.A. Nikolaeva, O.A. Marynin, A.I. Ohulchanskyy, A.A. Pud . Dual Stimuli-Responsive Ternary Core-Shell Polystyrene@Pnipam-Pedot Latexes. Particle & Particle Systems Characterization. 2023. Р. 2300096. https://doi.org/10.1002/ppsc.202300096
  9. Petrychuk M.V., Oliynyk V.V., Zagorodnii V.V.,Ogurtsov N.A., Pud A.A.. PVDF/poly(3-methylthiophene)/MWCNT nanocomposites for EMI shielding in the microwave range. Heliyon.2023. V. 9, N 12. Р. e23101
  10. Z.I. Kazantseva, I.A. Koshets, A.V. Mamykin, A.S. Pavluchenko, O.L. Kukla, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, R.V. Rodik, S.G. Vyshnevskyy. Detection of the explosive nitroaromatic compound simulants with chemosensory systems based on quartz crystal microbalance and chemiresistive sensor arrays. Semiconductor Physics, Quantum Electronics & Optoelectronics. 2023. V. 26, N.3. Р. 332-342
  11. N. Redon, N. Davydenko, N. Ogurtsov, M. Jamar, Yu. Noskov, A. Pud, J.-L. Wojkiewicz. PPy & P3MT-MWCNT Nanocomposites-Based Sensors for Nerve Gas Detection at ppb Levels. 2023 IEEE SENSORS proceedings, 2023, Vienna, Austria. Р. 1-4.DOI: 10.1109/SENSORS56945.2023.10325230
  12. I.P. Matushko, Yu.V. Noskov,V.A. Moiseienko,V.Y. Malyshev,L.M. Grishchenko. Electromagnetic Microwave Absorption Performances of PVC/AC Composites. Materials Proceedings. 2023. V. 14, N.1. Р. 15.https://doi.org/10.3390/IOCN2023-14537
  13. D.О. Zhytnyk, I.P. Matushko, Yu.V. Noskov, V.A. Moiseienko, V.Yu. Malyshev, O.О. Barsukov, N.A. Atamas, L.M. Grishchenko. Microwave properties of composite materials based on PVC and oxidized activated carbon. Proceedings of the III International Scientific and Practical Conference “Science in the environment of rapid changes”, 2023, Brussels, Belgium. P. 237-244.
  14. Kobzar O.L.,Tatarchuk, A.V.,Mrug G.P.,Bondarenko S.P., Demydchuk B.A., Frasinyuk M.S.,Vovk A.I.. Carboxylated chalcones and related flavonoids as inhibitors of xanthine oxidase. Medicinal Chemistry Research. 2023. V. 32, N 8. Р. 1804-1815
  15. Velihina Y.,Gesese R.,Zhirnov V.,Kobzar O.,Bui B.,Pilyo S.,Vovk A.,Shen H.Brovarets V.. Design, synthesis and evaluation of the anti-breast cancer activity of 1,3-oxazolo[4, 5-d] pyrimidine and 1, 3-oxazolo[5, 4-d] pyrimidine derivatives. RSC Medicinal Chemistry. 2023. V. 14, N 4.Р. 692-699
  16. Kovalishyn V.,Severin O.,Kachaeva M.,Kobzar O.,Keith K.A.,Harden E.A.,Hartline C.B.,James S.H.,Vovk A.,Brovarets V.. In Silico Design and Experimental Validation of Novel Oxazole Derivatives Against Varicella zoster virus. Molecular Biotechnology. 2023. Р. 1-11
  17. Los O.V.,Sinenko V.O.,Kobzar O.L.,Zhirnov V.V.,Vovk A.I.,Brovarets V.S.. Synthesis and in vitro anticancer potential of new thiazole-containing derivatives of rhodanine. Chemistry of Heterocyclic Compounds. 2023. V. 59, N 6-7. Р. 484-493
  18. Zhirnov V.,Shablykin O., Chumachenko S.,Kornii Y.,Keith K. A.,Harden E. A.,Hartline C.B.,James S.H.,Kobzar O.,Kovalishyn V.,Vovk A.Brovarets V.. In vitro activity of novel 4-iminohydantoin sulfamide derivatives against human cytomegalovirus. Chemical Papers. 2023. Р. 1-8
  19. Hodyna D.,Kovalishyn V., Kachaeva M.,Shulha Y.,Klipkov A.,Shaitanova E.,Kobzar O.,Shablykin O.,Metelytsia L.. In Silico, In Vitro and In Vivo Study of Substituted Imidazolidinone Sulfonamides as Antibacterial Agents. Chemistry & Biodiversity. 2023. Р. e202301267
  20. Derevyanchuk M.Kretynin S., Bukhonska Y., Pokotylo I., Khripach V., Ruelland E., Filepova R., Dobrev P.I., Martinec, J., Kravets V.. Influence of Exogenous 24-Epicasterone on the Hormonal Status of Soybean. Plants. 2023. V.12. N 20. Р. 3586
  21. Kretynin S.V., Kolesnikov Y.S.. The role of calcium in implementation of the effect of brassinosteroids during the induction of oxidative stress in tobacco. Cytology and Genetics. 2023. V. 57. Р. 312-319
  22. Rogalsky S., Tarasyuk O., Vashchuk A., Dzhuzha O., Cherniavska T., Makhno S.. Thermophysical properties and ionic conductivity of new imidazolium based protic ionic liquids. Journal of Molecular Liquids. 2023. V. 382. Р. 121942
  23. Lishchuk P., Vashchuk A., Rogalsky S., Chepela L., Borovyi M., Lacroix D., Isaiev M.. Thermal transport properties of porous silicon filled by ionic liquid nanocomposite system. Scientific Reports. 2023. V.13. Р. 5889
  24. Rogalsky S., Tarasyuk O., Babkina N., Makhno S., Pertko O., Povazhnyi V., Cherniavska T., Fatyeyeva K.. Fabrication of new proton conducting membrane for fuel cell applications based on porous polyimide Matrimid® and hydrophobic protic ionic liquid. Journal of Applied Polymer Science. 2023. V. 140, N 15. Р. e53731
  25. Talaniuk V., Godzierz M., Vashchuk A., Iurhenko M., Chaber P., Sikorska W., Kobyliukh A., Demchenko V., Rogalsky S., Szeluga U., Adamus G.. Development of Polyhydroxybutyrate – Based Packaging Films and Methods to Their Ultrasonic. Materials. 2023. V.16, N 20. Р. 6617
  26. Rogalsky S., Hodyna D., Semenyuta I., Frasinyuk M., Tarasyuk O., Riabov S., Kobrina L., Tetko I., Metelytsia L.. Antibacterial activity of 1-dodecylpyridinium tetrafluoroborate and its inclusion complex with sulfobutyl ether-b-cyclodextrin against MDR Acinetobacter baumannii strains. Innovative Biosystems and Bioengineering. 2023. V.7, N 4.Р. 25-35
  27. Vortman M.Ya., Berezhnytska O.S., Aksenovska O.A., Kobylinskyi S.M., Kobrina L.V., Lemeshko V.N., Shevchenko V.V.. Guanidinium-containing oligoether as a complexing agent of transition metal ions. Functional Materials. 2023. V.30, N 1. Р. 120-127
  28. Patrylak L.,Konovalov S.,Yakovenko A.,Pertko O.,Povazhnyi V.. Polycationic Nanostructured Faujasite Zeolite Catalysts for Glucose Transformation into 5-Hydroxymethylfurfural. Applied Nanoscience. 2023,V. 13. Р. 5743–5754https://doi.org/10.1007/s13204-023-02820-7
  29. Shvets O.V.,Kurmach M.M., Yaremov P.S., Voloshyna Yu.G., Shcherban N.D.. Zeolite nanocomposites with variable acid and basic properties: effective catalysts for fine chemical synthesis and industrial reaction. Applied Nanoscience. 2023. https://doi.org/10.1007/s13204-023-02955-7
  30. Muzychka L.,Boiko I.,Vrynchanu N., Smolii O.. Synthesis, antibacterial, and antibiofilm activities of pulmonarin B analogues. Curr. Chem. Lett. 2024. V. 24. doi:10.5267/j.ccl.2023.11.005
  31. I. Semenyuta, D. Hodyna, V. Kovalishyn, B. Demydchuk, M. Kachaeva,S. Pilyo, V. Brovarets, L. Metelytsia. Development and application of in silico models to design new antibacterial5-amino-4-cyano-1,3-oxazoles against colistin-resistant E. coli strains. Artificial Intelligence Chemistry. 2023. V. 1, N 2. Р. 100024.https://doi.org/10.1016/j.aichem.2023.100024
  32. D. Hodyna, V. Kovalishyn, Y. Romanenko, I. Semenyuta,V. Blagodatny, M. Kachaeva, O. Brazhko L. Metelytsia. Quinoline Hydrazone Derivatives as New Antibacterialsagainst Multidrug Resistant Strains. Chem. Biodiversity 2023. V. 20, N 10. Р. e202300839doi.org/10.1002/cbdv.2023008
  33. D. Hodyna,V. Kovalishyn,I. Semenyuta,M. Kachaeva,Y. Shulha,M. Bugera, V. Blagodatny, O. Shablykin,L. Metelytsia. Design and Biological Evaluation of 4-Iminohydantoin Sulfamides as New Anti-Acinetobacter baumannii Agents. Biointerface Res. Appl. Chem. 2023. V. 13, N 6. P. 511-524.DOI: https://doi.org/1.33263/BRIAC136.511
  34. G. Mrug,D. Hodyna,L. Metelytsia,V. Kovalishyn,O. Trokhimenko, S. Bondarenko,K. Kondratyuk,A. Kozitskiy, M. Frasinyuk. Structure-Activity Relationship Prediction-Based Synthesis and Cytotoxicity Evaluation against the HEp-2 Laryngeal Carcinoma Cell of Isoflavone–Cytisine Mannich Bases. Chemistry & Biodiversity. 2023. V. 20, N 8. Р. e202300560.https://doi.org/10.1002/cbdv.202300560
  35. Pilyo S.G., Demydchuk B.A., Moskvina V.S., Shablykina O.V., Brovarets V.S.. A combinatorial library of substituted 3-sulfonyl-2-imino-1,2-dihydro-5H-dipyrido[1,2-a:2′,3′-d]pyrimidin-5-ones and their anticancer activities. Biopolym. Cell. 2022. V. 38, N 4. Р. 242-256. http://dx.doi.org/10.7124/bc.000A7B
  36. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M.. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension. Adv. Pharm. Bull. 2023. V.13, N 2. С. 399-407. https://doi.org/10.34172/apb.2023.044
  37. Zyabrev V., Demydchuk B., Zhirnov V., Brovarets V.. Synthesis, characterization, and in vitro anticancer evaluation of 2-aryl-4-arylsulfonyl-5-RS-1,3-oxazoles. Biointerface Res. Appl. Chem. 2023. V.13, N 3. P. 300. DOI: 10.33263/BRIAC133.300
  38. Kovalishyn V., Severin O., Kachaeva M., Semenyuta I., Keith K.A., Harden E.A., Hartline C.B., James S.H., Metelytsia L., Brovarets V.. Design and experimental validation of the oxazole and thiazole derivatives as potential antivirals against of human cytomegalovirus. SAR and QSAR in Environmental Res. 2023. V.34, N 7. P. 523-541
  39. Bondar D., Bragina O., Lee Ji Y., Semenyuta I., Jӓrving I., Brovarets V., Wipf P., Bahar I., Karpichev Y.. Hydroxamic Acids as PARP-1 Inhibitors: Molecular Design and Anticancer Activity of Novel Phenanthridinones. Helv. Chim. Acta. 2023. https://doi.org/10.1002/hlca.202300133
  40. Zyabrev V., Pilyo S., Demydchuk B., Kachaeva M., Semenyuta I., Zhirnov V., Velihina Ye., Brovarets V.. Synthesis, characterization and in vitro anticancer evaluation of 5-sulfinyl(sulfonyl)-4-arylsulfonyl substituted 1,3-thiazoles. Chem. Med. Chem. 2023. V.18, N 14. Р. E202300161
  41. Shablykin O.V., Merzhievskyi D.O., Brovarets V.S., Shishkina S.V.. New oxazole to oxazole recyclization. Chem. Het. Compd. 2023. V. 59, N 6. P. 521-524
  42. Konovalenko A.S., Shablykin O.V., Shablykina O.V., Moskvina V.S., Shishkina S.V., Kozytskyi A.V., Brovarets V.S.. Distinctive features of 3-acetyl- and 3-benzoylisocoumarins’ interaction with active primery amines. Chem. Select. 2023. V.8, N 37. Р. e202301380. https://doi.org/10.1002/slct.202301380
  43. Golovchenko O.V., Brusnakov M.V., Shabelko Yu.O., Brovarets V.S., Vydzhak R.M., Bahrieieva O.S., Potikha L.M., Shishkina S.V.. Synthesis and properties of methanesulfonyl derivatives of diethyl esters of 5-(hydroxyalkylamino)-1,3-oxazol-4-yl-phosphonic acids. Phosphorus, Sulfur, and Silicon and the Related Elements. 2023. DOI: 10.1080/10426507.2023.2251639
  44. Shaydyuk Ye.O., Bashmacova N.V., Klishevich G.V., Dmytruk A.M., Kachkovsky O.D., Kuziv Ya.B., Dubey I.Ya., Befield K.D., Bondar M.V.. Nature of linear spectra; properties and fast relaxations in the excited states and two-photon absorption efficiency of 3-thiazolyl and 3-phenylthiazolyl coumarin derivatives.. ACS Publications. 2023. V.18, N 12. P. 11564-11573
  45. Brusnakov M.Yu., Golovchenko O.V., Potikha L.M., Brovarets V.S.. Condenced azole-based organophosphorus heterocycles. Chem. Het. Compd. 2023. V.59, N 4/5. P. 217-236. Doi:10.1007/s10593-023-03184-0
  46. Konovalenko A., Shablykin O., Shablykina O., Kozytskyi A., Brovares V.. Convenient and versatile method of 8-amino-6-(2-R-thiazol-4-yl)1,7-naphthyridines. Curr. Chem. Lett. 2024. V.13, N 1. P. 163-172. Doi: 10.5267/j.ccl.2023.7.004
  47. Nallaparaju J.V., Nikonovich T., Jarg T., Merzhyievskyi D., Aav R., Kananovich D.G.. Mechanochemistry – amended barbier reaction as an expedient alternative to Grignar synthesis. Angew. Chem. Int. Edd. 2023. E202305775.
  48. Dibchak D., Snisarenko M., Mishuk A., Shablykin O., Bortnichuk L., Klymenko-Ulianov O., Kheylik Yu., Sadkova I., Rzepa H.S., Mykhailiuk P.K.. General synthesis of 3‐azabicyclo [3.1.1]heptanes and evaluation of their properties as saturated isosteres. Angewandte Chemie. 2023. V.135, N 39. Р. e202304246. https://doi.org/10.1002/ange.202304246
  49. Kirichok A.,Tkachuk H., Kozyriev Ye., Shablykin O., Datsenko O., Granat D., Yegorova T., Bas Yu., Semirenko V., Pishel I., Kubyshkin V., Lesyk D., Klymenko-Ulianov O., Mykhailiuk P.K.. 1‐Azaspiro[3.3]heptane as a bioisostere of piperidine. Angewandte Chemie. 2023. e202311583. https://doi.org/10.1002/ange.202311583
  50. Krasylov I.V., Moskvina V.S., Khilya V.P.. Unexpected but prominent imines formation in Beckmann rearrangement of (spiro)pyranocoumarin oximes. Tetrahedron Lett. 2023. V. 129. P. 154747. https://doi.org/10.1016/j.tetlet.2023.154747
  51. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S. V., Brovarets V.S.. Use of pyridine and pyrimidine derivatives as new wheat growth regulators. Global Meet on Food Science and Technology”. March 23, 2023. Webinar GMFST 2023, LAS VEGAS, USA. P. 19-20
  52. Chernykh A.V., Kudryk O.V., Olifir O.S., Dobrydnev A.V., Rusanov E., Moskvina V.S., Volochnyuk D.M., Grygorenko O.O.. Expanding the chemical space of 1,2-difunctionalized cyclobutanes. J. Org. Chem. 2023. V. 88, N 5. P. 3109-3131. https://doi.org/10.1021/acs.joc.2c02892
  53. Chen X., Lv X., Gao L., Liu J., Wang W., Guo L., Frasinyuk M. S., Zhang W., Watt D. S., Liu C., Liu X.. Chalcone derivative CX258 suppresses colorectal cancer via inhibiting the TOP2A/Wnt/β-Catenin signaling. Cells. 2023. V.12, N 7. P. 1066. https://doi.org/10.3390/cells12071066
  54. Myshko A., Mrug G., Kondratyuk K., Demydchuk B., Bondarenko S., Frasinyuk M.. An expedient synthesis of functionalized pyrazole-based aurone analogs.. Chemistry Select. 2023. V.8, N 20. Р. e202300257. https://doi.org/10.1002/slct.202300257
  55. Myshko N.V., Mrug G.P., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S.. Coumarin-based homoisoflavonoids as precursors in the synthesis of 8-heteroarylmethylcoumarins. Chem. Heterocycl. Compd. 2023. V. 59, N 6/7. P. 456-464. https://doi.org/10.1007/s10593-023-03216-9
  56. Levterov V., Panasyuk Ya., Sahun K., Stashkevich O., Badlo V., Shablykin O., Sadkova I., Bortnichuk L., Klymenko-Ulianov O., Holota Yu., Lachmann L., Borysko P., Horbatok K., Bodenchuk I., Bas Yu., Dudenko D., Mykhailiuk P.K.. 2-Oxabicyclo [2.2.2]octane as a new bioisostere of the phenyl ring. Nature Commun. 2023. V.14, N 1. P. 5608. https://doi.org/10.1038/s41467-023-41298-3
  57. Goulden T., Bodachivskyi Iu., Padula M.P., Williams D.B.G.. Concentrated ionic liquids for proteomics: Caveat emptor. International Journal of Biological Macromolecules. 2023. V. 253, № 7. Р. 127438. https://doi.org/10.1016/j.ijbiomac.2023.127438.
  58. Kornii Yu., Shablykin O., Tarasiuk T., Stepaniuk O., Matvienko V., Aloshyn D., Zahorodniuk N., Sadkova I.V., Mykhailiuk P.K.. Fluorinatedaliphatic diazirines: preparation, characterization, and model photolabeling studies. J. Org. Chem. 2023. V. 88, N 1. P. 1-17. Doi:10.1021/acs.joc.2c02262
  59. Malets Ye. S., Vashchenko B. V., Moskvina V.S., Golovchenko O.V., Brovarets V.S., Grygorenko O.O.. Parent 5(7)-azachromones and their partially hydrogenated derivatives: synthesis and physiochemical properties. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 494-499
  60. Kukushkina K.V., Moskvina V.S., Shablykina O.V., Khilya V.P.. Expanding the isoflavone, pyrazole, and oxazole chemical space through 2′-carboxamido-2-hydroxy-deoxybenzoin precursors.. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 479-483. https://doi.org/10.1007/s10593-023-03219-6
  61. Lyutenko N.V., Sorochinsky A.E., Soloshonok V.A.. Asymmetric synthesis of pyroglutamic acids via Ni(II) complex methodology. Chem. Heterocycl. Comp. 2023. Р. 332-340. https://doi.org/10.1007/s10593-023-03203-0
  62. Shablykin O.V., Brovarets V.S., Shablykina O.V.. Recyclization of 5-aminooxazoles as a route to new functionalized heterocycles (developments of V.P. Kukhar institute of bioorganic chemistry and petrochemistry of the NAS of Ukraine). Chem. Record. 2023. e202300264. https://doi.org/10.1002/tcr.202300264
  63. Gaponov A.M., Pavlenko O.L., Dmytrenko O.P., Kulish M.P., Ryzhkova A.S., Lesiuk A.I., Obernikhina N.V., Łuszczyńska B., Kachkovsky O.D.. Molecular heteroassociation in films of thiochrome and tryptophan. Mol. Cryst. Liquid Cryst. 2023. https://doi.org/10.1080/15421406.2023.2257515
  64. Tsygankova V.A., Andrusevich Ya.V., Pilyo S.G., Brovarets V.S.. Effect of plant growth regulators and fertilizers of the vegetative growth of sunflowers (Helianthus annuus L). The scientific heritage. 2023.N 116. P. 3-9. DOI: 10.5281/zenodo.8129039
  65. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Use of synthetic plant growth regulators in combination with fertilizers to improve wheat growth. Int J Med Biotechnol Genetics. 2023. S1:02:002:9-14. URL: http://scidoc.org/IJMBGS1V2.php
  66. Tsygankova V.A., Voloshchuk I.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Studying the effect of plant growth regulators Ivin, Methyur and Kamethur on growth and productivity of sunflower. J. Advanc. Agricult. 2023. V.14. P. 17-24. DOI: https://doi.org/10.24297/jaa.v14i.9453
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2022 р.

Розділи в зарубіжних монографіях

  • V.A. Tsygankova, Ya.V. Andrusevich, O.I. Shtompel, R.M. Solomyanny, A.O. Hurenko, M.S. Frasinyuk, G.P. Mrug, O.V. Shablykin, S.G. Pilyo, A.M. Kornienko, V.S. Brovarets. New Auxin and Cytokinin Related Compounds Based on Synthetic Low Molecular Weight Heterocycles. Auxins, Cytokinins and Gibberellins Signaling in Plants. Signaling and Communication in Plants. Aftab, T. (Eds). Springer Nature. Switzerland AG. 2022. 377 p. Pp. 353-377.
  • S. Konovalov,S. Zubenko,L. Patrylak, A. Yakovenko, V. Povazhnyi, K. Burlachenko. Revisiting the Synthesis of Fatty Acid Alkyl Esters of Lower Monohydric Alcohols by Homogeneous Base-Catalyzed Transesterification of Vegetable Oils. Chemmotological Aspects of Sustainable Development of Transport. Sustainable Aviation. 2022, Springer, Cham.Р. 49-80 https://doi.org/10.1007/978-3-031-06577-4_4

Публікації в зарубіжних виданнях

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  2. L.O. Metelytsia,D.M. Hodyna, I.V. Semenyuta,V.V. Kovalishyn,S.P. RogalskyY.K. Derevianko, V.S. Brovarets,I.V. Tetko. Theoretical and Experimental Studies of Phosphonium Ionic Liquids as Potential Antibacterials of MDR Acinetobacter baumannii. Journal of Antibiotics. 2022. V. 11. P. 491. https://doi.org/10.3390/antibiotics11040491.
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  4. O.V. Moshynets,T.P. Baranovskyi,O.S. Iungin, N.P. Kysil, L.O. Metelytsia,I. Pokholenko, V.V. Potochilova,G. Potters, K.L. Rudnieva,S.Y. Rymar, I.V. Semenyuta, A.J. Spiers, O.P. Tarasyuk,S.P. Rogalsky eDNA inactivation and biofilm inhibition by the polymeric biocide polyhexamethylene guanidine hydrochloride (PHMG-Cl). International Journal of Molecular Sciences. 2022. V. 23. Р. 731.DOI: 10.3390/ijms23020731.
  5. Obernikhina N.V.,Kachaeva M.V., Kachkovsky O.D.,Brovarets V.S. In silico Study of Conjugated Nitrogen Heterocycles Affinity in their Biological Complexes Chemistry of Heterocyclic Compounds 2022. V. 58, N 8. Р. 412-420.DOI 10.1007/s10593-022-03107-5
  6. D.S. Kamenskyh, T.V. Tkachenko, V.A. Yevdokymenko, Y.V. Sheludko, M.M. Filonenko, V.A. Povazhny, M.M. Baran, O.V. Pavluik, V.I. Kashkovsky Synthesis, characterization and optimization of the aluminum–nickel–molybdenum catalyst for hydrogenation Applied Nanoscience. 2022. P. 1-13. https://doi.org/10.1007/s13204-022-02644-x
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  8. L.K. Patrylak, S.V. Konovalov, A.V. Yakovenko, O.P. Pertko, V.A. Povazhnyi, Yu.G. Voloshyna, O.V. Melnychuk, M.M. Filonenko Micro–mesoporous kaolin-based zeolites as catalysts for glucose transformation into 5-hydroxymethylfurfural Applied Nanoscience. 2022. P.1-14. https://doi.org/10.1007/s13204-022-02620-5
  9. L. Patrylak, S. Zubenko, S. Konovalov, A. Yakovenko, V. Povazhnyi, O. Pertko, Y. Voloshyna, O. Melnychuk Mykhailo Filonenko Іsomerization of limonene on zeolite-containing catalysts based on Кaolin Chemistry Journal of Moldova. 2022. P. 1857-1727. DOI: dx.doi.org/10.19261/cjm.2022.980
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  52. A.V. Mamykin, O.L. Kukla, A.S. Pavluchenko, Z.I. Kazantseva, I.A. Koshets, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, V.I. Kalchenko Electronic nose-type chemosensory systems for detection of gaseous poisonous substances Semiconductor Physics, Quantum Electronics & Optoelectronics. 2022. V.25, No.4. Р. 429-440https://doi.org/10.15407/spqeo25.04.429

2021 р.

Розділи в зарубіжних монографіях

  1. V.D. Romanenko, J.-M. Sotiropoulos. Six-membered rings with two or more heteroatoms with at least one boron.Comprehensive Heterocyclic Chemistry IV, Elsevier. New York. 2021. Р.1-40. DOI: 10.1016/B978-0-12-818655-8.00098-6.
  2. Yakovlieva A., Boichenko S., Zubenko S., Konovalov S. Synthesis and physico-chemical properties of palm kernel oil bioadditives for alternative jet fuel. Systems and means of motor transport. Seleced problems. Seria: Transport. Mono-grafia. Rzeszow (Poland). 2021. Р. 257-264.
  3. Grygorenko O.O., Hutskalova V., Moskvina V.S. Bicyclic 6-6 system with one bridgehead (ring junction) nitrogen atom: three extra heteroatoms (2:1).Chapter in book: “Comprehensive heterocyclic chemistry IV (Fourth edition)”, 2022. P. 216-278. https://doi.org/10.1016/b978-0-12-409547-2.14958-3.
  4. Tsygankova V.A.Characterisation of Endo-Polygalacturonases activities of Rice (Oryza sativa) Fungal Pathogens in Nigeria, West Africa.Chapter in book: Grain and Seed Proteins Functionality (Jimenez-Lopez, J.C. Ed). Chapter 10. 2021. Intechopen Limited, London, United Kingdom. DOI:10.5772/intechopen.94763.

Публікації в зарубіжних виданнях

  1. I.G. Logvinenko, I.S. Kondratov, A.V. Dobrydnev, A.V. Kozytskiy, O.O. Grygorenko. Synthesis and reactions of ω-CF3O-substituted aliphatic sulfonyl chlorides.Journal of Fluorine Chemistry. 2021. V. 246. Р. 109799.
  2. J. Han, N. Lyutenko, A. Sorochinsky, A. Okawara, H. Konno, S. White, V. Soloshonok. Tailor-Made Amino Acids in Pharmaceutical Industry: Synthetic Approaches to aza-tryptophane derivatives. Chem. Eur. J. 2021. doi.org/10.1002/chem.202102485
  3. E.N. Shaitanova, O.A. Balabon, A.N. Rybakova, T.S. Khlebnicova, F.А. Lakhvich, I.I. Gerus. Synthesis of functionalized fluoroalkyl pyrimidines and pyrazoles from fluoroalkyl enones. Journal of Fluorine Chemistry. 2021. V. 252. Р. 109905 https://doi.org/10.1016/j.jfluchem.2021.109905
  4. A.A. Homon, O.V. Hryshchuk, O.V. Mykhailenko, B.V. Vashchenko, K.P. Melnykov, O.M. Michurin, C.G. Daniliuc, I.I. Gerus, V.O. Kovtunenko, I.S. Kondratov, O.O. Grygorenko. 4-(Di‐/Trifluoromethyl)‐2‐heterabicyclo[2.1. 1]- hexanes: advanced fluorinated phenyl isosteres and proline analogues. European Journal of Organic Chemistry. 2021 https://doi.org/10.1002/ejoc.202100414
  5. S. Trofymchuk, M. Bugera, A. Klipkov, V. Ahunovych, B. Razhyk, S. Semenov, A. Boretskyi, K. Tarasenko, P. Mykhailiuk. Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4).J. Org. Chem. 2021. V. 86, № 17. Р. 12181-12198 https://doi.org/10.1021/acs.joc.1c01518
  6. V.D. Romanenko. New trends in development of P-C bond forming reactions. Current Organic Chemistry. 2021. V.25, № 17. Р. 1937-1976 DOI: 10.2174/1385272825666210610153954
  7. Noskov Yu., Ogurtsov N., Bliznyuk V., Lvov Yu., Myronyuk I., Pud A. Synthesis and properties of coreshell halloysite–polyaniline nanocomposites. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01812-9
  8. O.I. Kolodiazhnyi. Phosphorus Compounds of Natural Origin: Prebiotic, Stereochemistry, Application. Symmetry. 2021. V. 13(5)., № 889. Р. 1-52.
  9. D.V. Prysiazhnuk, E.B. Rusanov, O.I. Kolodiazhnyi. The absolute configuration of 2-bromo-2,3-dihydro-1H-inden-1-ols. Synthetic communications. 2021. V. 51, № 19. Р. 3023–3031
  10. O.O. Kolodiazhna, D.V. Prysiazhnuk, A.O. Kolodiazhna, O.I. Kolodiazhnyi. Synthesis of optically active vicinal fluorocyclopentanols and fluorocyclopentanamines by enzymatic deracemization. Arkivoc 2022, p. iii. Р. 14-26 https://doi.org/10.24820/ark.5550190.p011.634
  11. O. Kolodiazhnyi, A. Kolodiazhna, E. Grishkun, D. Prysiazhnuk, O. Kolodiazhna, S. Sheiko. Achievements in developments of stereochemistry. Phosphorus, sulfur, and silicon and the related elements. 2021. https://doi.org/10.1080/10426507.2021.2011874
  12. A. Kolodiazhna, D. Prysiazhnuk, O. Kolodiazhnyi. Asymmetric Electrophilic Reactions in Phosphorus Chemistry.Phosphorus, sulfur, and silicon and the related elements. 2021. V. 196. https://doi.org/10.1080/10426507.2021.1989687
  13. A. Kolodiazhna, E. Grishkun, O. Kolodiazhnyi. Synthesis of chiral phosphonobenzaldehydes and phosphonotyrosine. Phosphorus, sulfur, and silicon and the related elements 2021, 196. https://doi.org/10.1080/10426507.2021.1989686
  14. Metelytsia L., Hodyna D., Dobrodub I., Semenyuta I., Zavhorodnii M., Blagodatny V., Kovalishyn V., Brazhko O. Design of (quinolin-4-ylthio)carboxylic acids as new Escherichia coli DNA gyrase B inhibitors: machine learning studies, molecular docking, synthesis and biological testing. Comput. Biol. Chem. 2020. V. 24, № 85. Р. 107224 https://doi.org/10.1016/j.compbiolchem.2020.107224
  15. Metelytsia L.O., Trush M.M., Kovalishyn V.V., Hodyna D.M., Kachaeva M.V., Brovaret V.S., Pilyo S.G., Sukhoveev V.V., Tsyhankov S.A., Blagodatnyi V.M., Semenyuta I.V. 1,3-Oxazole derivatives of cytisine as potential inhibitors of glutathione reductase of Candida spp.: QSAR modeling, docking analysis and experimental study of new anti-Candida agents.. Comput. Biol. Chem. 2021. V. 90. Р. 107407 https://doi.org/10.1016/j.compbiolchem. 2020.107407
  16. Hodyna D., Kovalishyn V., Semenyuta I., Blagodatny V., Rogalsky S., Metelytsia L. In silico and in vitro Studies of Imidazolium Ionic Liquids as Effective Antibacterial Agents against Multidrug Resistant Escherichia coli Strains.. Current Bioactive Comp. 2021. V. 17, № 2. P. 130–144 https://doi.org/10.2174/1573407216999200422115655
  17. Semenyuta I., Trush M., Kovalishyn V., Rogalsky S., Hodyna D., Karpov P., Xia Z., Tetko I., Metelytsia L. Structure-Activity Relationship Modeling and Experimental Validation of the Imidazolium and Pyridinium Based Ionic Liquids as Potential Antibacterials of MDR Acinetobacter Baumannii and Staphylococcus Aureus. Int. J. Mol. Sci. 2021. V.22. Р. 563-576. https://doi.org/10.3390/ijms22020563
  18. T.Tkachenko, Ye.Sheludko, V.Yevdokymenko, D.Kamenskyh, N. Khimach, V. Povazhny, M. Filonenko, M. Aksylenko, V. Kashkovsky. Physico-chemical properties of flax microcrystalline cellulose. Applied Nanoscience (2021). https://doi.org/10.1007/s13204-021-01819-2
  19. O. Pertko, Yu.Voloshyna, A. Kontsevoi, V.Trachevskyi. Ethylbenzene formation and its conversion towards coke in the side-chain methylation of toluene on a basic X zeolite. Journal of Porous Materials. 2021. V.28. P. 1713–1723 https://doi.org/10.1007/s10934-021-01119-8.
  20. L.K. Patrylak, O.P. Pertko, V.A. Povazhnyi, A.V. Yakovenko, S.V. Konovalov. Evaluation of nickel-containing zeolites in the catalytic transformation of glucose in an aqueous medium. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01771-1
  21. L.K. Patrylak, O.P. Pertko, A.V. Yakovenko, Yu.G. Voloshyna, V.A. Povazhnyi, M.M. Kurmach. Isomerization of linear hexane over acid-modified nanosized nickel-containing natural Ukrainian zeolites. Applied Nanoscience. 2021. https://doi.org/10.1007/s13204-021-01682-1.
  22. Kalishyn Ye., Bychko I., Kameneva T., Skoblik O., Polunkin Ye., Strizhak P. Inhibition effect of the α-FeOOH nanoparticles in the benzyl alcohol oxidation.Journal of Cluster Science. 2021. DOI:10.1007/s10876-021-02056-x.
  23. Shatursky O.Ya., Manoilov K.Yu., Gorbatiuk O.B., Usenko M.O., Zhukova D.A., Vovk A.I., Kobzar O.L., Trikash I.O., Borisova T.A., Kolibo D.V., Komisarenko S.V. The geometry of diphtheria toxoid CRM197 channel determined with thiazolium salts and nonelectrolytes. Biophys. J. 2021. V. 120, I. 12. P. 2577-2591.
  24. Kobzar О. L., Shulha Y. V., Buldenko V. M., Mrug G. P., Kolotylo M. V., Stanko O. V., Onysko P.P., Vovk А. I. Alkyl and aryl α-ketophosphonate derivatives as photoactive compounds targeting glutathione-S-transferases. Phosphorus, Sulfur, and Silicon and the Related Elements. 2021. V. 196 (7). Р. 672-678.
  25. Rogalsky S., Bardeau J.-Fr., Lyoshina L., Bulko O., Tarasyuk O., Dzhuzha O., Cherniavska T., Kremenitsky V., Kobrina L., Riabov S. New promising antimicrobial material based on thermoplastic polyurethane modified with polymeric biocide polyhexamethylene guanidine hydrochloride. Materials Chemistry and Physics. 2021. V.267. Р. 124682.
  26. Orlovska I., Podolich O., Kukharenko O., Zaets I., Reva O., Khirunenko L., Zmejkoski D., Rogalsky S., Barh D., Tiwari S., Kumavath R., Góes-Neto A., Azevedo V., Brenig B., Ghosh P., de Vera J.-P., Kozyrovska N. Bacterial Cellulose Retains Robustness but Its Synthesis Declines After Exposure to a Mars-Like Environment Simulated Outside the International Space Station.Astrobiology. 2021. V. 21 (7). P. 706-717.
  27. Rogalsky S., Bardeau J.-Fr., Makhno S., Tarasyuk O., Babkina N., Cherniavska T., Filonenko M., Fatyeyeva K. New polymer-electrolyte membrane for medium-temperature fuel cell applications based on cross-linked polyimide Matrimid and hydrophobic protic ionic liquid.Materials Today Chemistry. 2021. V. 20. P. 100453.
  28. L. Muzychka, A. Voronkina, V. Kovalchuk, O. Smolii, M. Wysokowski, I. Petrenko, D. Youssef, I. Ehrlich, H. Ehrlich. Marine biomimetics: bromotyrosines loaded chitinous skeleton as source of antibacterial agents. Appl. Phys. A Mater. Sci Process. 2021. V. 127, № 1. P. 15.
  29. L.V. Muzychka, E.V. Verves, I.O. Yaremchuk, A.M. Zinchenko, S.V. Shishkina, I.V. Semenyuta, D.M. Hodyna, L.O. Metelytsia, V.Kovalishyn, O.B. Smoliі.Synthesis, QSAR modeling, and molecular docking of novel fused 7-deazaxanthine derivatives as adenosine A2A receptor antagonists. Chem. Biol. Drug Des. 2021. V. 98. P. 1-8
  30. Ключко С.В., Чумаченко С.А., Шаблыкин О.В., Броварец В.С. Синтез новых 1Н-пирроло-[3,4-c]¬пиридин-1,3(2Н)-дионов.ЖОХ. 2021. Т. 91, №3. С. 376-385.
  31. Vydzhak R.N., Panchishin S.Ya., Kachaeva M.V., Pilyo S.G., Moskvina V.S., Shablykina O.V., Kozytskiy A.V., Brovarets V.S. A rapid synthetic approaches to the libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazole-6(1H)-ones.Molecular Diversity. 2021. 10.1007/s11030-021-10234-2.
  32. Shcherbakova V., Dibchak D., Snisarenko M., Skalenko Ye., Denisenko A.V., Kuznetsova A.S., Mykhailiuk P.K. Bicyclic piperidines via [2+2] photocycloaddition. J. Org. Chem. 2021. V.86, №3. P. 2200-2209 doi/10.1021/acs.joc.0c02355.
  33. Slyvchuk S., Pilyo S., Brovarets V., Kartsev V., Angeli A., Pinteala M., Petrou A., Geronikaki A., Supuran C. Chromene-containing aromatic sulfonamides with carbonic anhydrase inhibitory properties.Int. J. Mol. Sci. 2021. V.22, №10. P. 5082 https://doi.org/10.3390/ijms22105082.
  34. Корний Ю.Е., Чумаченко С.А., Шаблыкин О.В., Русанов Э.Б., Броварец В.С. Новые гетероциклизации N’-замещенных N-(2,2-дихлор-1-цианоэтэнил)мочевин с алифатическими аминами.ЖОХ. 2021. –Т. 91, № 6. С. 841-846. doi/10.31857/s0044460х21060020.
  35. Zhirnov V.V., Velihina Ye.S., Mitiukhin O.P., Brovarets V.S. Intrinsic drug potential of oxazolo[5,4-d]pyrimidines and oxazolo[4,5-d]pyrimidines.Chem. Biol. Drug Des. 2021. V.98, № 4. P. 561-581. doi:10.1111/cbdd.13911.
  36. Merzhyievskyi D.O., Shablykin O.V., Shablykin O.V, Kozytskiy A.V., Rusanov E.B., Moskvina V.S., Brovarets V.S. Functionalized 5-amino-4-cyanooxazoles, their hetero and macrocyclic derivatives: preparation and synthetic applications.Eur. J. Org. Chem. 2021. doi.org/10.1002/ejoc.202100412
  37. Angeli A., Kartsev V., Petrou A., Pinteala M., Vydzhak R., Panchishin S., Brovarets V., de Luca V., Capasso C., Geronikaki A., Supuran C. New sulfanilamide derivatives in corporating heterocyclic carboxamide moieties as carbonic anhydrase inhibitors. Pharmaceuticals. 2021. V. 14, № 8. P. 828 https://doi.org/10.3390/ph14080828
  38. Kovalishyn V., Zyabrev V., Kachaeva M., Ziabrev K., Keith K., Harden E., Hartline C., James S., Brovarets V. Design of new imidazole derivatives with anti-HCMV activity: QSAR modeling, synthesis and biological testing.J. Comp.-Aided Mol. Des. 2021. V.35. P.1177-1187. doi.org/10.1007/s10822-021-00428-z.
  39. Шаблыкин О.В., Чумаченко С.А., Броварец В.С. Взаимодействие новых N-(2,2-дихлор-1-цианоэтенил)амидов с алифатическими аминами.ЖОХ. 2021. Т.91, №9. С. 1315-1320.
  40. Velihina E.S., Obernikhina N.V., Pilyo S.G., Kachkovsky O.D., Brovarets V.S. Synhesis, electronic structure and anti-cancer activity of the phenyl substituted pyrazolo[1,5-a][1,3,5]triazines.Current Org. Chem. 2021. V.25, №12. P. 1441-1454.
  41. Maiko K., Merzhyievskyi D., Piryatinski Yu., Obernikhina N., Prostota Ya., Dmitruk I., Kachkovsky O., Brovarets V. Study of excited state relaxation by time-resolved spectroscopy in conjuigated substituted polyene bis-oxazoles.Structural Chem. 2021. V.32, №3. P. 977-987.
  42. Angeli A., Kartsev V., Petrov A., Pinteala M., Brovarets V., Panchishin S., Vydzhak R., Geronikaki A., Supuran C.T. Carbonic anhydrase inhibition with sulfonamides incorporatiny pyrazole- and pyridazinecarboxamide moieties provides examples of isoform-selective inhibitors.Molecules. 2021. V. 26, № 22. P. 7023-7043. https://doi.org/10.3390/molecules26227023.
  43. Ostapiuk Yu.V., Shehedyn M., Barabash O.V., Demydchuk B.A., Batsyts S., Herzberer C., Schmidt A. Bromoarylation of methyl 2-chloroacrylate under Meerwein conditions for the synthesis of substituted 3-hydroxyhiophenes.Synthesis. 2021. Doi: 10.1055/s-0040-1719849.
  44. Shablykina O.V., Shylin S.V., Moskvina V.S., Ischenko V.V., Khilya V.P. Progress in the chemistry of aminoacid derivatives of isocoumarines and 3,4-dihydroisocoumarines.Chem. Nat. Compd. 2021. V. 57, № 2. P. 209-229. Doi:10.1007/s10600-021-03323-z.
  45. Biletska I.M., Mrug G.P., Bondarenko S.P., Kondratyuk K.M., Prostota Y.O., Sviripa V.M., Frasinyuk M.S. Chemoselective synthesis of 3-trifluoromethylpyrazole-deoxybenzoin hybrids.J. Fluorine Chem. 2021. V.242. P. 109698.
  46. Bondarenko S.P., Mrug G.P., Vinogradova V.I., Frasinyuk M.S. Synthesis of new conjugates of coumarins with anabasine and cytisine.Chem. Nat. Compd. 2021. V. 57, № 1. P. 9-13.
  47. Shokol T.V., Moskvina V.S., Hlibov Y. K., Frasinyuk M.S., Khilya V.P. Synthesis of furoneoflavones modified by coumarin and (het)aroyl substituents.Chem. Nat. Compd. 2021. V. 57, № 1. P. 33-37.
  48. Piryatinski Yu.P., Verbitsky A.B., Dmytruk A., Malynovskyi M.B., Lutsyk P.M., Rozhin A.G., Kachkovsky O.D., Prostota Ya.O., Kurdyukov V.V. Excited state relaxation in cationic pentamethine cyanines studied by time-resolved spectroscopy.Dyes Pigm. 2021. V. 193. P. 109539. https://doi.org/10.1016/j.dyepig.2021.109539.
  49. Navozenko O., Yashchuk V., Kachkovsky O., Gudeika D., Butkute R., Slominskii Yu., Azovskyi V. Aggregate formation of boron-containing molecules in thermal vacuum deposited films. Materials. 2021. V. 14, №19. P. 5615. https://doi.org/10.3390/ma14195615.
  50. Bashmakova N.V., Shaydyuk Ye.O., Dmytruk A.M., Swiergosz T., Kachkovsky O.D., Belfield K.D., Bondar M.V., Kasprzyk W. Nature of linear spectral properties and fast electronic relaxations in green fluorescent pyrrolo[3,4-c]pyridine derivative.Int. J. Mol. Sci. 2021. Vol. 22, №11. P. 5592. https://doi.org/10.3390/ijms22115592.
  51. Shaydyuk Ye.O., Bashmakova N.V., Dmytruk A.M., Kachkovsky O.D., Koniev S., Strizhak A.V., Komarov I.V., Belfield K.D., Bondar M.V., Babii O. Nature of fast relaxation processes and spectroscopy of a membrane-active peptide modified with fluorescent amino acid exhibiting excited state intramolecular proton transfer and efficient stimulated emission.ACS Omega. 2021. V. 6, № 15. P. 10119-10128. https://doi.org/10.1021/acsomega.1c00193.
  52. A.O. Adejuwon, O.D. Odeleye, O.A. Odewale, V.A. Tsygankova, M.V. Donova. A Medicinal Plant’s Extract Effective on Osteoarthritis.Biomedicine and Nursing. 2021. V.7 (1). P. 26-28. doi:10.7537/marsbnj070121.04.
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  55. M.D. Aksylenko, V.A. Yevdokymenko, T.V. Tkachenko, D.S. Kamenskyh, V.I. Kashkovsky.Effective organo-mineral fertilizers of prolonged action from the processed organo-containing wastes of various origin. Proceeding Book of III Balkan agricultural congress. August 30-September 1, 2021. Edirne, Turkey. P. 554-564.
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2020 р.

Розділи в зарубіжних монографіях

  1. Romanenko V.D. Rings containing group 15 elements.Ref. Mod. Chem. Molecular Sciences. Elsevier. 2020. Р.1-36.
  2. Parkhomenko Y., Vovk A., Protasova Z. Vitamin B1 and the pyruvate dehydrogenase complex.In Molecular Nutrition. Vitamins. Academic Press. 2020. P. 185-206.
  3. Poda G., Tanchuk V. Computational Methods for the Discovery of Chemical Probes.The Discovery and Utility of Chemical Probes in Target Discovery. RSC Publishing. 2020. P. 39-68.
  4. V.A. Tsygankova, K.B. Blyuss, E.N. Shysha, L.A. Biliavska, G.A. Iutynska, Y.V. Andrusevich, S.P. Ponomarenko, A.I. Yemets, Y.B. Blume. Using Microbial Biostimulants to Deliver RNA Interference in Plants as an Effective Tool for Biocontrol of Pathogenic Fungi, Parasitic Nematodes and Insects.In Monograph «Research Advances in Plant Biotechnology». Series: Plant Science Research and Practices. Chapter 6. Nova Science Publishers, Inc. USA. 2020. 375 p. P. 205-319.
  5. A.O. Adejuwon, V.A. Tsygankova. α-Amylase Production by Toxigenic Strains of Aspergillus and Penicillium.In Monograph “Aflatoxin B1 Occurrence, Detection and Toxicological Effects” Ed. by Xi-Dai Long. IntechOpen, 2020. P. 1-22.

Публікації в зарубіжних виданнях

  1. A.О. Kolodiazhna, O.I. Kolodiazhnyi. Asymmetric Electrophilic Reactions in Phosphorus Chemistry. Symmetry. 2020. V.12, № 1. Р. 108-159.
  2. A.О. Kolodiazhna, А.I Skliarov, A.A. Slastennikova, O.I Kolodiazhnyi. Asymmetric Synthesis of (S,R)- and (R,R)-Methiin Stereoisomers. Phosph., Sulf., Silicon and Relat. Elem. 2020. V.195. P. 713-717.
  3. T. Tkachenko, V. Yevdokymenko, D. Kamenskyh, Y. Sheludko, V. Povazhny, V. Kashkovsky. Physico-chemical properties of biogenic SiO2 nanoparticles obtained from agriculture residue. Applied Nanoscience. 2020. V. 10, № 12. P. 4617 – 4623.
  4. Tigunova O.O., Kamenskyh D.S., Tkachenko T.V., Yevdokymenko V.A., Kashkovskiy V.I., Rakhmetov D.B., Blume Ya.B., Shulga S.M.. Biobutanol Production from Plant Biomass. The Open Agriculture Journal. 2020. V. 14. P. 187-197.
  5. V. Kovalishyn, D. Hodyna, V.O. Sinenko, V. Blagodatny, I. Semenyuta, S. R. Slivchuk, V. Brovarets, G. Poda, L. Metelytsia. Hybrid Design of Isonicotinic Acid Hydrazide Derivatives: Machine Learning Studies, Synthesis and Biological Evaluation of their Antituberculosis Activity. Current Drug Discovery Technologies. 2020. V. 17. Р. 365-375.
  6. M. Trush, V. Kovalishyn, D. Hodyna O. Golovchenko S. Chumachenko I. Tetko V. Brovarets L. Metelytsia. In silico and in vitro studies of a number PILs as new antibacterials against MDR clinical isolate Acinetobacter baumannii. Chem Biol Drug Des. 2020. V. 95. Р. 624-630.
  7. N. Abramenko, L. Kustova, L. Metelytsia, V. Kovalishyn, I. Tetko, W. Peijnenburg. A review of recent advances towards the development of QSAR models for toxicity assessment of ionic liquids. Journal of Hazardous Materials. 2020. V. 384. 121489. Р. 1-14.
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  29. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Synthesis of 7-Hydroxy-8-Methyl-4′-Methoxy-6-Formylisoflavone and Linear Hetarenochromones Based on It. Chem. Nat. Compd. 2020. V.56, № 3. P. 420-422.
  30. Tang B., Frasinyuk M.S., Chikwana V.M., Mahalingan K.K., Morgan C.A., Segvich D.M., Bondarenko S.P., Mrug G.P., Wyrebek P., Watt D.S., DePaoli-Roach A.A., Roach P.J., Hurley T.D. Discovery and Development of Small-Molecule Inhibitors of Glycogen Synthase. J. Med. Chem. 2020. V.63, № 7. P. 3538-3551.
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  32. Bondarenko S.P., Makarenko O.G., Vinogradova V.I., Frasinyuk M.S. Synthesis of 7-(N-12-Cytisinylpropoxy)Isoflavones. Chem. Nat. Compd. 2020. V.56 P. 1040-1043.
  33. Golovchenko O.V., Abdurakhmanova E.R., Vladimirov S.O., Brusnakov M.Y., Krupoder T.O., Sukhoveev V.V., Rusanov E.B., Vydzhak R.N., Brovarets V.S. Interaction of 1-acylamino-2,2-dichloroethenyl(triphenyl)phosphonium chlorides with alkanolamines. Phosph. Sulph. Silicon and Relat. Elem. 2020. V.195, №10. P. 848-857.
  34. Konovalenko A.S., Shablykin O.V., Brovarets V.S., Shablykina O.V., Moskvina V.S., Kozytskiy A.V.. 3-Hetarylisocoumarins in the synthesis of 1‑functionalized 3-hetarylisoquinolines. Chem. Het. Compd. 2020. V.56, № 8. P. 1021-1029.
  35. Omelian T.V., Ostapchuk E.N., Dobrydnev A.V., Malets Y.S., Brovarets V.S., Grygorenko O.O. Strategy for the synthesis of 2,2-disubstituted 8‑azachromanones via Horner-Wadsworth_Emmons. Chem. Het. Compd. 2020. V.56, № 2. P. 213-218.
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  42. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S. The new plant growth regulators based on derivatives of oxazole and oxazolopyrimidine. World J. Pharm. Toxicol. 2020. V.3, № 2. P. 1-5.
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  52. Tsygankova V., Voloshchuk I., Andrusevich Y., Shtompel O., Kopich V., Klyuchko S., Brovarets V. The influence of the derivative of pyrimidine – Methyur on the yield of the maize, beet and oats plants. Збірник статей «Topical issues of the development of modern science» за матеріалами 8-ї Міжнародної наукової та практичної конференції. Видавництво “ACCENT”, Софія, Болгарія. 2020. P. 514-523.
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2019 р.

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    Монографії

    Lutynska G.O., Biliavska L.O., Babych O.A., Tsygankova V.A., Babych A.G. The Monograph “Plant protection and bioregulation in modern agriculture” / Ed. “Diamond trading tour” Warszawa. Poland, 2019.- 100 p. ISBN: 978-83-66030-73-2.

    The Monograph “Advances and Trends in Biotechnology and Genetics Vol. 3” / Eds. Dr. Tsygankova Victoria Anatolyivna; Prof. Dr. Lanzhuang Che. Book Publisher International. SCIENCEDOMAIN international Ltd. 2019. 166 p. DOI 10.9734/bpi/atbg/v3. ISBN9789389562460. (Indexed in Scopus).

2018 р.

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35. Sinenko V.O., Slivchuk S.R., Brovarets V.S.. Lithiation of 2-Bromo-4-(1,3-dioxolan-2- yl)-13-thiazole. Current Chem. Letters.- 2018. – Vol. 8. – P.1-8.
36. Kachaeva M.V., Pilyo S.G., Demydchuk B.A., Prokopenko V.M., Zhirnov V.V., Brovarets V.S.. 4-Cyano-1,3-oxazole-5-sulfonamides as Novel Promising Anticancer Lead Compounds. Intern. J. Curr. Res.- 2018. – Vol. 10, № 5. – P. 69410-69425.
37. Tsygankova V., Andrusevich Y., Shompel O., Kopich V., Solomyanny R., Bondarenko O., Brovarets V.. Phytohormone-like effect of pyrimidine derivatives on regulation of vegetative growth of tomato. International J. of Botany Studies.- 2018. – Vol. 3, № 2. – P. 91-102.
38. Tsygankova V., Andrusevich Y., Kopich V., Shtompel O., Veligina Ye., Pilyo S., Kachaeva M., Kornienko A., Brovarets V.. Application of Oxazole and Oxazolopyrimidine as New Effective Regulatores of Oilseed Rape Growth. Sch. Bull.- 2018. – Vol. 4, № 3. – P. 301-312.
39. Шаблыкин О.В., Волощенюк М.А., Броварец В.С.. Синтез новых 2-(оксиран-2-ил)-1,3-оксазолов. ЖОХ.- 2018. – Т. 88, № 7. – С. 1207-1210.
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41. Popova A.V., Bondarenko C.P., Frasinyuk M.S., Wen Zhang, Xie Yanji, Martin Zachary M., Cai Xianfeng, Fiandalo Michael V., Mohler James L., Liu Chunming, Watt David S., Sviripa V.M.. Efficient synthesis of aurone Mannich bases and evaluation of their antineoplastic activity in PC-3 prostate cancer cells. Chemical Papers, 2018. – Vol. 72, № 10. – P. 2443-2456.
42. Kachaeva M., Pilyo S., Popilnichenko S., Kornienko A., Rusanov E., Prokopenko V., Zyabrev V., Brovarets V.. Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)oxazole-4-carboxylates and ?-aminoakoles involving the Smiles rearrangement. Current Chem. Letters.- 2018. – Vol. 7, № 4. – P. 101-110.
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45. Velihina Ye., Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S.. Synthesis, Characterization, and Vitro Anticancer Evaluation of 7-Piperazin-substituted [1,3]oxazolo[4,5-d]pyrimidines. Der Pharma Chemica.- 2018. – Vol. 10, № 9. – Р. 1-10.
46. Мруг Г.П., Бондаренко Н.В., Бондаренко С.П., Фрасинюк М.С.. Реакционная способность конденсированных производных изофлавонов по отношению к гидразину. Химия природных соединений.- 2018. – Т.54, №4.- С. 654-659.
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48. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Acceleration on vegetative growth of wheat (Triticum aestivum L.) using [1,3] oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted 1,3-oxazole. Pharm. Chem. J., 2018. – Vol.5, № 2. – P. 167-175.
49. Bogolyubsky A., Savych O., Zhemera A., Khomenko D., Brovarets V., Moroz Yu., Vybornyi M.. A facile one-pot parallel synthesis of 3-amino-1,2,4-triazoles. ACS Combinatorial Science, 2018. – Vol. 20, № 7.– P. 461-466.
50. Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S. Synthesis, characterization, and in vitro anticancer evaluation of 2- substituted 5-arylsulfonyl-1,3-oxazole-4-carbonitriles. Med. Chem. Res.- 2018. – Vol. 22, № 12 https://doi.org/10.1007/s00044-018-2265-y.
51. Mrug G.P., Demydchuk B.A., Bondarenko S.P., Sviripa V.M., Wyrebek P., Mohler J. L., Fiandalo M.V., Liu C., Frasinyuk M.S., Watt D.S.. A Direct Synthesis of 2-(?-Carboxyalkyl)-isoflavones from ortho-Hydroxylated Deoxybenzoins. Eur. J. Org. Chem.- 2018. – Vol. 39. – P. 5460- 5463.
52. Bondarenko S.P., Frasinyuk M.S., Mrug G.P., Vinogradova V.I., Khilya V.P.. Synthesis of Isoflavone-Anabasine Conjugates. Chem. Nat. Comp.- 2018.- Vol. 54, № 6. – P. 1068-1071 https://dx.doi.org/10.1007/s10600-018-2557-y.
53. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Solomyanny R.M., Hurenko A.O., Frasinyuk M.S., Mrug G.P., Shablykin O.V., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Study of auxin-like and cytokinin-like activities of derivatives of pyrimidine, pyrazole, isoflavones, pyridine, oxazolopyrimidine and oxazole on haricot bean and pumpkin plants. Intern. J. Chem. Tech. Res.- 2018. -Vol. 11, № 10. – P. 174-190.
54. Nizhenkovska E.V., Sedko K.V., Golovchenko O.I., Golovchenko O.V.. Efficiency of the application of the 1,3-oxazole-4-ylphosphonic acid derivative on the substained arterial hypertension model in rats. Curr. Topics Pharmacology.- 2018. – Vol. 22, № 63. – P. 63-68.
55. Velihina Ye.S., Kachaeva M.V., Pilyo S.G., Mitiukhin O.P., Zhirnov V.V., Brovarets V.S.. Synthesys, characterization and in vitro anticancer evaluation of 7-(1,4-diazepan)substituted [1,3]oxazolo[4,5]pyrimidines. Chem. Res. J.- 2018 Doi:10.1007/s00044-018-2265-y.
56. Pavlenko O.L., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Sendiuk V.A., Kobzar P.Yu., Strelchuk V.V., Slominskyi Yu.L., Kurdiukov B.V., Kachkovskyi O.D., Prostota Ya.O.. Spectral and Quantum-Chemical Study of Interaction Between Fullerenes and Squaraine Dyes. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol.16, № 1. – P. 31–40. https://www.imp.kiev.ua/nanosys/ua/articles/2018/1/nano_vol16_iss1_p0031p0040_2018_abstract.html
57. Pavlenko E.L., Sendiuk V.A., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Obernihina N.V., Prostota Y.O., Kachkovsky O.D., Brovarets V.S.. Quantum-Chemical Study of Acceptor Properties of Fullerene and Its Bridge Derivatives. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol. 16, № 2. – P. 389-401 https://www.imp.kiev.ua/nanosys/ua/articles/2018/2/nano_vol16_iss2_p0389p0401_2018_abstract.html
58. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Furo[2,3-h]chromones and pyrano[2’,3’:5,6]chromeno[4,3-b]pyridines based on natural isoflavones. Chem. Nat. Comp.- 2018. – Vol. 54, № 6. – Р. 1065-1067 https://dx.doi.org/10.1007/s10600-018-2556-z.
59. Popova A.V., Bondarenko S.P., Frasinyuk M.S.. Synthesis and aminomethylation of regioisomeric 6-hydroxy-4-methyl- and 4-hydroxy-6-methylaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 9. – P. 832- 839.
60. Bondarenko S.P., Frasinyuk M.S.. Observations from aminomethylation of 7-substituted 6-hydroxyaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 8. – P. 765-762.
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2017 р.

1 . V. Tsygankova, Y. Andrusevich, O. Shtompel, O. Romaniuk, M. Yaikova, A. Hurenko, R. Solomyanny, E. Abdurakhmanova, S. Klyuchko, O. Holovchenko, O. Bondarenko, V. Brovarets Application of Synthetic Low Molecular Weight Heterocyclic Compounds Derivatives of Pyrimidine, Pyrazole and Oxazole in Agricultural Biotechnology as a New Plant Growth Regulating Substances. // Int. J. Med. Biotechnol. & Genetics. – 2017. – S2: 002.– P. 10-32.
2 . Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Kopich V.M., Pilyo S.G., Prokopenko V.M, Kornienko A.M, Brovarets V.S. Intensification of Vegetative Growth of Cucumber by Derivatives of [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted of 1,3-oxazole. // Research Journal of Life Sciences, Bioinformatics, Pharmaceutical, and Chemical Sciences(RJLBPCS). – 2017. – V.3, № 4. – P. 107 – 122. DOI://doi.org/10.26479/rjlbpcs
3 . Victoria Tsygankova, Elena Shysha, Anatoly Galkin, Lyudmila Biliavska, Galina Iutynska, Alla Yemets, Yaroslav Blume Impact of Microbial Biostimulants on Induction of Callusogenesis and Organogenesis in the Isolated Tissue Culture of Wheat in vitro. // J. Med. Plants. Stud. – 2017. – V. 5, Issue 3. – P. 155-164.
4 . V.Kovalishyn,V.Brovarets,V.Blagodatnyi,I. Kopernyk,D. Hodyna,S.Chumachenko,O.Shablykin,O. Kozachenko,M. Vovk,M.Barus,M. Bratenko, L.Metelytsia QSAR studies, synthesis and antibacterial assessment of new inhibitors against multidrug-resistant Mycobacterium tuberculosis. // Current Drug Discovery Technologies.- 2017.- V.14, N.1 .- P. 25-38.
5 . Maria M. Trush, Ivan V. Semenyuta, Sergey I. Vdovenko, Sergiy P. Rogalsky, Evgeniya O. Lobko, Larisa O. Metelytsia Synthesis, spectroscopic and molecular docking studies of imidazolium and pyridinium based ionic liquids with HSA as potential antimicrobial agents. // Journal of Molecular Structure.-V.1137, 5.- 2017.- P. 692–699
6 . Protasov Al., Bardeau JF., Morozovskaya I., Boretska M., Cherniavska T., Petrus L., Tarasyuk O., Metelytsia L., Kopernyk I., Kalashnikova L., Dzhuzha O., Rogalsky S. New promising antifouling agent based on polymeric biocide polyhexamethylene guanidine molybdate. // Environ. Toxicol Chem. 2017.- V. 36(9).- P. 2543-2551.
7 . Soares A., Estevao M.S., Marques M.M.B., Kovalishyn V., A.R.S. Latino D., Aires-de-Sousa J., Ramos J., Viveiros M., Martins F. Synthesis and Biological Evaluation of Hybrid 1,5- and 2,5-Disubstituted Indoles as Potentially New Antitubercular Agents. // Medicinal chemistry.- 2017.- 13 (5), Р. 439-447
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27. Rogalsky S. Structural, thermal and antibacterial properties of polyamide 11/polymeric biocide polyhexamethylene guanidine dodecylbenzenesulfonate composites / S. Rogalsky, J.-F. Bardeau, H. Wu[et al.] // J Mater Sci. — 2016. — 51, №16. — P. 7716–7730.
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29. Sokolyuk P. A. Synthesis of diverse pyrazole-4-sulfonyl chlorides starting from 2-(benzylthio)malonaldehyde / P. A. Sokolyuk, I. S. Kondratov, O. V. Gavrylenko, A. A. Tolmachov // Mol. Divers. — 2016. — 20, №1. — P. 1–7.
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36. Derevyanchuk M. Brassinosteroid-induced de novo protein synthesis in zea mays under salinity and bioinformatic approach for identification of heat shock proteins / M. Derevyanchuk, R. Litvinovskaya, V. Khripach, V. Kravets // Plant Growth Regul. — 2016. — 78, №3. — P. 297–305.
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2015 р.

1. Borisova T. Synthesis of new fluorinated analogs of gaba, pregabalin bioisosteres, and their effects on [3H]gaba uptake by rat brain nerve terminals / T. Borisova, N. Pozdnyakova, E. Shaitanova[et al.] // Bioorg. Med. Chem. — 2015. — 23, №15. — P. 4316–4323.
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4. Chumachenko S. A. Interaction of 5-(morpholin-4-yl)-2-(4-phthal-imidobutyl)- and 5-(morpholin-4-yl)-2-(5-phthal-imidopentyl)-1,3-oxazole-4-carbonitriles with hydrazine hydrate / S. A. Chumachenko, O. V. Shablykin, V. S. Brovarets // Chem Heterocycl Comp. — 2015. — 50, №12. — P. 1727–1730.
5. Dahi A. Water sorption properties of room-temperature ionic liquids over the whole range of water activity and molecular states of water in these media / A. Dahi, K. Fatyeyeva, C. Chappey[et al.] // RSC Adv. — 2015. — 5, №94. — P. 76927–76938.
6. Derevyanchuk M. Effect of 24-epibrassinolide on arabidopsis thaliana alternative respiratory pathway under salt stress / M. Derevyanchuk, R. Litvinovskaya, V. Khripach[et al.] // Acta Physiol Plant. — 2015. — 37, №10. — P. 215.
7. Frasinyuk M. S. Synthesis and tautomerization of hydroxylated isoflavones bearing heterocyclic hemi-aminals / M. S. Frasinyuk, S. P. Bondarenko, V. P. Khilya[et al.] // Org. Biomol. Chem. — 2015. — 13, №4. — P. 1053–1067.
8. Frasinyuk M. S. Development of 6H-chromeno[3,4-c]pyrido[3′,2′:4,5]thieno[2,3-e]pyridazin-6-ones as par-4 secretagogues / M. S. Frasinyuk, S. P. Bondarenko, V. M. Sviripa[et al.] // Tetrahedron Lett. — 2015. — 56, №23. — P. 3382–3384.
9. Frasinyuk M. S. Application of mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents / M. S. Frasinyuk, G. P. Mrug, S. P. Bondarenko[et al.] // Org. Biomol. Chem. — 2015. — 13, №46. — P. 11292–11301.
10. Grynko D. O. Multifunctional role of nanostructured cds interfacial layers in hybrid solar cells / D. O. Grynko, O. M. Fedoryak, P. S. Smertenko[et al.] // J Nanosci Nanotechnol. — 2015. — 15, №1. — P. 752–758.
11. Hamouda Z. Dual-band elliptical planar conductive polymer antenna printed on a flexible substrate / Z. Hamouda, J. L. Wojkiewicz, A. A. Pud[et al.] // IEEE Transactions on Antennas and Propagation — 2015. — 63, №12. — P. 5864–5867.
12. Kalachova T. Importance of phosphoinositide-dependent signaling pathways in the control of gene expression in resting cells and in response to phytohormones / T. Kalachova, V. Kravets, A. Zachowski, E. Ruelland // Plant Signal Behav. — 2015. — 10, №5. — P. e1019983.
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15. Kolodiazhna A. O. Synthesis and properties of four-membered phosphorus heterocycles-2-fluoro-1,2lambda5-oxaphosphetanes / A. O. Kolodiazhna, O. I. Kolodiazhnyi // Phosph., Sulfur, Silicon Relat. Elem. — 2015. — 190, №12. — P. 2232–2245.
16. Kolodiazhna O. O. Synthesis of anti-cis-phosphiranes / O. O. Kolodiazhna, O. I. Kolodiazhnyi // Phosph., Sulfur, Silicon Relat. Elem. — 2015. — 190, №7. — P. 1192–1200.
20. Kondratov I. S. Synthesis of trifluoromethyl-containing polysubstituted aromatic compounds by Diels–Alder reaction of ethyl 3-benz­amido-2-oxo-6-(trifluoromethyl)-2H-pyran-5-carboxylate / I. S. Kondratov, N. A. Tolmachova, V. G. Dolovanyuk[et al.] // Eur. J. Org. Chem. — 2015. — 2015, №11. — P. 2482–2491.
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23. Lukashuk O. I. Introduction of chiral 2-(aminoalkyl) substituents into 5-amino-1,3-oxazol-4-ylphosphonic acid derivatives and their use in phosphonodipeptide synthesis / O. I. Lukashuk, E. R. Abdurakhmanova, K. M. Kondratyuk[et al.] // RSC Adv. — 2015. — 5, №15. — P. 11198–11206.
24. Mikhaylov S. Ammonia/amine electronic gas sensors based on hybrid polyaniline–tio2 nanocomposites. the effects of titania and the surface active doping acid / S. Mikhaylov, N. Ogurtsov, Y. Noskov[et al.] // RSC Adv. — 2015. — 5, №26. — P. 20218–20226.
25. Mkrtchyan G. Molecular mechanisms of the non-coenzyme action of thiamin in brain: biochemical, structural and pathway analysis / G. Mkrtchyan, V. Aleshin, Y. Parkhomenko[et al.] // Sci Rep. — 2015. — 5. — P. 12583.
26. Ogurtsov N. A. Effect of multiwalled carbon nanotubes on the kinetics of the aniline polymerization: the semi-quantitative ocp approach / N. A. Ogurtsov, Y. V. Noskov, A. A. Pud // J. Phys. Chem. B. — 2015. — 119, №15. — P. 5055–5061.
27. Pud A. “Anion-chromic” interactions of emeraldine base with hydroxide and halide anions in the solid polymer matrix / A. Pud, I. Duboriz, Y. Piryatinski, O. Dimitriev // Synthetic Metals. — 2015. — 209. — P. 232–239.
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29. Tanchuk V. Y. A new scoring function for molecular docking based on autodock and autodock vina / V. Y. Tanchuk, V. O. Tanin, A. I. Vovk, G. Poda // Curr Drug Discov Technol. — 2015. — 12, №3. — P. 170–178.
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37. Zhirnov V. V. The osmotic resistance, and zeta potential responses of human erythrocytes to transmembrane modification of Ca2+ fluxes in the presence of the imposed low rate radiation field of 90Sr / V. V. Zhirnov, I. N. Iakovenko // Int. J. Radiat. Biol. — 2015. — 91, №1. — P. 117–126.

2014 р.

1. Acena J. L. Asymmetric synthesis of alpha-amino acids via homologation of Ni(II) complexes of glycine schiff bases. Part 3: michael addition reactions and miscellaneous transformations / J. L. Acena, A. E. Sorochinsky, V. Soloshonok // Amino Acids. – 2014. – 46, №9. – P. 2047-2073.
2. Bondarenko S. P. Synthesis of 4-aryl-3-[2-hydroxy-4-(2-cytisin-12-ylethoxy)phenyl]pyrazoles / S. P. Bondarenko, M. S. Frasinyuk, V. I. Vinogradova, V. P. Khilya // Chem. Nat. Compd. – 2014. – 50, №5. – P. 889-891.
3. Brandmaier S. The qspr-thesaurus: the online platform of the cadaster project / S. Brandmaier, W. Peijnenburg, M. K. Durjava[et al.] // Altern Lab Anim. – 2014. – 42, №1. – P. 13-24.
4. Dahi A. Supported ionic liquid membranes for water and volatile organic compounds separation: sorption and permeation properties / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Journal of Membrane Science. – 2014. – 458. – P. 164-178.
5. Dahi A. Polyimide/ionic liquid composite membranes for fuel cells operating at high temperatures / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Electrochimica Acta. – 2014. – 130. – P. 830-840.
6. Derevyanchuk M. V. Influence of brassinosteroids on plant cell alternative respiration pathway and antioxidant systems activity under abiotic stress conditions / M. V. Derevyanchuk, O. I. Grabelnyh, R. P. Litvinovskaya[et al.] // Biopolym. Cell. – 2014. – 30, №6. – P. 436-442.
7. D. Romanenko V. Progress in the development of pyrophosphate bioisosteres: synthesis and biomedical potential of 1-fluoro- and 1,1-difluoromethylene-1,1-bisphosphonates / V. D. Romanenko, V. P. Kukhar // Curr. Org. Chem. – 2014. – 18, №11. – P. 1491-1512.
8. Duboriz I. Polyaniline/poly(ethylene terephthalate) film as a new optical sensing material / I. Duboriz, A. Pud // Sensors and Actuators B: Chemical. – 2014. – 190. – P. 398-407.
9. Frasinyuk M. S. Pentapeptide boronic acid inhibitors of mycobacterium tuberculosis MYCP1 protease / M. S. Frasinyuk, S. Kwiatkowski, J. M. Wagner[et al.] // Bioorg. Med. Chem. Lett. – 2014. – 24, №15. – P. 3546-3548.
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12. Gurenko A. O. Synthesis of novel pyrazolo[3,4-d][1,2,3]triazines / A. O. Gurenko, B. M. Khutova, S. V. Klyuchko[et al.] // Chem. Heterocycl Comp. – 2014. – 50, №4. – P. 528-536.
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16. Kolodiazhnyi O. I. Asymmetric catalysis as a method for the synthesis of chiral organophosphorus compounds / O. I. Kolodiazhnyi, V. P. Kukhar, A. O. Kolodiazhna // Tetrahedron: Asymmetry. – 2014. – 25, №12. – P. 865-922.
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18. Kolodiazhnyi O. I. Recent advances in asymmetric synthesis of р-stereogenic phosphorus compounds / O. I. Kolodiazhnyi // J.-L. Montchamp. – Springer International Publishing, 2014. – P. 161-236.
21. Kondratov I. S. Diels-alder reaction of ethyl 3-benzamido-2-oxo-6-(trifluoromethyl)-2h-pyran-5-carboxylate with alkoxyalkenes as an effective approach to trifluoromethyl-containing 3-aminobenzoic acid derivatives / I. S. Kondratov, N. A. Tolmachova, V. G. Dolovanyuk[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №12. – P. 2443-2450.
22. Kornienko A. N. Reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-1H-pyrazoles and 5-amino-1H-1,2,4-triazole / A. N. Kornienko, S. G. Pil’o, A. P. Kozachenko[et al.] // Chem Heterocycl Comp. – 2014. – 50, №1. – P. 76-86.
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29. Kucher O. V. Enzyme-catalyzed kinetic resolution of 2,2,2-trifluoro-1-(heteroaryl)ethanols: experimental and docking studies / O. V. Kucher, A. O. Kolodiazhnaya, O. B. Smolii[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №34. – P. 7692-7698.
30. Kucher O. V. Enzymatic resolution of chroman-4-ol and its core analogues with burkholderia cepacia lipase / O. V. Kucher, A. O. Kolodyazhnaya, O. B. Smolii[et al.] // Tetrahedron: Asymmetry. – 2014. – 25, №6-7. – P. 563-567.
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37. Pokotylo I. V. Influence of 24-epibrassinolide on lipid signalling and metabolism in brassica napus / I. V. Pokotylo, S. V. Kretynin, V. A. Khripach[et al.] // Plant Growth Regul. – 2014. – 73, №1. – P. 9-17.
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39. Rogalsky S. Antimicrobial properties and thermal stability of polycarbonate modified with 1-alkyl-3-methylimidazolium tetrafluoroborate ionic liquids / S. Rogalsky, K. Fatyeyeva, L. Lyoshina[et al.] // J. Appl. Polym. Sci. – 2014. – 131, №7. – P. n/a-n/a.
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42. Shibata N. Asymmetric mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids / N. Shibata, T. Nishimine, N. Shibata[et al.] // Org. Biomol. Chem. – 2014. – 12, №9. – P. 1454-1462.
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