Перелік публікацій співробітників Інституту

Список робіт, опублікованих в 2024 р.

Монографії

Tsygankova V.A. Research Perspectives of Microbiology and Biotechnology, Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. 2024. 175 p. DOI: 10.9734/bpi/rpmab/v2

Tsygankova V.A. Recent Developments in Chemistry and Biochemistry Research, Vol. 8. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. 2024. 177 p. DOI: https://doi.org/10.9734/bpi/rdcbr/v8

Розділи в міжнародих монографіях

Patrylak L.K., Yakovenko A.V., Nizhnik B.O.,Pertko O.P., Melnychuk O.V. Antibacterial Properties of Silver Nanoparticles Deposited on Different Carriers. Springer Proceedings in Physics.In: Nanooptics and Nanoelectronics, Nanobiotechnology, and Their Applications. 2024, V. 312. Springer, Cham. Р. 279-289. https://doi.org/10.1007/978-3-031-67527-0_20

M.M. Baran, D.S. Kamenskyh, T.V. Tkachenko, V.G. Burdeinyi, M.M. Filonenko, V.A. Povazhny, V.O. Yevdokymenko. Effect of the low-frequency sound vibrations on the structural and mor-phological properties of the industrial catalysts for the carbon oxides’ hydrogenation. In: Fesenko, O., Yatsenko, L. (eds) Nanomaterials and Nano-composites, and Nanostructure, and Their Applications. NANO 2023. Springer Proceedings in Physics, 2024. Springer, Cham. Chapter 3. Р. 27-39. https://doi.org/10.1007/978-3-031-67519-5_3

Розділи у вітчизняних монографіях

T. Tkachenko, V. Sokol, O. Haidai, D. Kamenskyh, V. Yevdokymenko. Polyethylene packages and polyethylene terephthalate bottles – a source for chemical syntheses precursors. Chemical Technology and Engi-neering ‒ 2023: Monograph. (Atamanyuk V.M. et al., Eds.). Lviv: Rastr-7, 2023. P. 127-134. ISBN 978-617-8296-99-5

Навчальні посібники

Богатиренко В.А., Євдокименко В.О., Каменських Д.С., Ткаченко Т.В., Андрєєва О.В. Основи хімії викопного й альтернативного палива. Навчальний посібник / Київ: Український державний університет імені Михайла Драгоманова, 2024. 117 c.

Збірники наукових праць

А.І. Вовк. Біоактивні сполуки, нові речовини і матеріали. Київ: Інтерсервіс. 2024. 306 с. ISBN 978-966-999-459-2

Статті в міжнародних виданнях

1. Romanenko V.D. Organophosphorus Synthesis beyond P-Cl bond: The Development of Shelf-Stable Reagents for [RP] Transfer. Chemistry. 2024. V. 28, N 19. Р. 1483-1512. DOI: 10.2174/0113852728323258240613061150

      2. Kolodiazhnyi O.І, Kolodiazhna A.O. Stereoselective Syntheses of Organophosphorus Compounds. Symmetry. 2024. V.16, N 3. Р. 342. https://doi.org/10.3390/sym16030342

      3. O.O. Kolodiazhna, D.V. Prysiazhnuk, A.O. Kolodiazhna, O.I. Kolodiazhnyi. Enzymatic resolution of heterocyclic intermediates for biologically active compound preparation. Phosphorus, Sulfur and Silicon and the Related Elements. 2024. https://doi.org/10.1080/10426507.2024.2367033

      4. Kolodiazhnyi O., Kolodiazhna A., Faiziiev O.,Gurova Y. Enzymatic Deracemization of Fluorinated Arylcarboxylic Acids: Chiral Enzymatic Analysis and Absolute Stereochemistry Using Chiral HPLC. Symmetry. 2024. V.16, N 9. Р. 1150. https://doi.org/10.3390/sym16091150.

      5. Krupodorova T., Barshteyn V., Tsygankova V., Sevindik M., Blume Ya. Strain-specific features of Pleurotus ostreatus growth in vitro and some of its biological activities. BMC Biotechnol. 2024. V. 24, N 9(1). P. 1-14. https://doi.org/10.1186/s12896-024-00834-9

      6. Tsygankova V.A., Kopich V.M., Vasylenko N.M., Andrusevich Ya.V., Pilyo S.G., Brovarets V.S. Phytohormone-like effect of pyrimidine derivatives on the vegetative growth of haricot bean (Phaseolus vulgaris L.). Polish Journal of Science. 2024. V. 1, N 71. P. 6-13. DOI: 10.5281/zenodo.10675232.

      7. Tsygankova V.A., Andrusevich Ya.V., Vasylenko N.M., Kopich V.M., Popilnichenko S.V., Pilyo S.G., Brovarets V.S. Auxin-like and cytokinin-like effects of new synthetic pyrimidine derivatives on the growth and photosynthesis of wheat. J. Plant Sci. Phytopathol. 2024. V. 8, N 1. P. 15-24. DOI: https://dx.doi.org/10.29328/journal.jpsp.1001126

      8. Tsygankova V.A., Vasylenko N.M., Andrusevich Ya.V., Kopich V.M., Solomyannyi R.M., Pilyo S.G., Bondarenko O.M., Popilnichenko S.V., Brovarets V.S. New Wheat Growth Regulators Based On Thioxopyrimidine Derivatives. Int. J. Med. Biotechnol. Genetics. 2024. S1:02:004:23-30. https://scidoc.org/IJMBG-2379-1020-S1-02-004.php

      9. Tsygankova V.A., Andrusevich Ya.V., Vasylenko N.M., Kopich V.M., Pilyo S.G., Solomyannyi R.M., Popilnichenko S.V., Bondarenko O.M., Brovarets V.S. The use of thioxopyrimidine derivatives for the regulation of vegetative growth of wheat. Journal of Medicinal Botany. 2024. V. 8.P. 1-7. DOI: https://doi.org/10.25081/jmb.2024.v8.8918.

      10. Tsygankova V.A., Andrusevich Ya.V., Vasylenko N.M., Kopich V.M., Solomyannyi R.M., Popilnichenko S.V., Kozachenko O.P., Pilyo S.G.,Brovarets V.S. The use of thioxopyrimidine derivatives as new regulators of growth and photosynthesis of barley. J. Plant. Sci. Phytopathol. 2024. V. 8, N 2. P. 090-099.  DOI: https://dx.doi.org/10.29328/journal.jpsp.1001139.

      11. Tsygankova V., Andrusevich Ya., Kopich V., Vasylenko N., Solomyannyi R., Popilnichenko S., Kachaeva M., Kozachenko O., Pilyo S., Brovarets V. Wheat growth in the vegetative phase under the regulatory effect of furopyrimidine derivatives. The scientific heritage. 2024. N 140. P. 3-12. DOI: 10.5281/zenodo.12720609

      12. Tsygankova V., Vasylenko N., Andrusevich Ya.., Kopich V., Kachaeva M., Popilnichenko S.,  Kozachenko O., Pilyo S., Brovarets V. Application of thienopyrimidine derivatives as new eco-friendly wheat growth regulators. Sciences of Europe. 2024. N 146.P. 8-18. DOI: 10.5281/zenodo.13267799

      13. Tsygankova V.A., Kopich V.M., Vasylenko N.M., Golovchenko O.V., Pilyo S.G., Malienko M.V., Brovarets V.S. Increasing the productivity of wheat using synthetic plant growth regulators Methyur, Kamethur and Ivin. Znanstvena misel journal. 2024. N 94. P. 22 – 26. DOI:  https://doi.org/10.5281/zenodo.13860706

      14. Azizov I.V., Tsygankova V.A. The basic theoretical principles of improving the environmental situation on planet Earth. Brief opinion. Sciences of Europe. 2024. N 151. P. 20 – 23. DOI: 10.5281/zenodo.13998958

      15. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Pilyo S.H., Brovarets V.S. Application of synthetic plant growth regulators and microfertilizers to improve sunflower cultivation. Proceedings IX International Scientific and Practical Conference. Toronto. Canada. 14-15 March, 2024. P. 11-14. DOI:10.5281/zenodo.10850764

      16. V. Bohatyrenko, D. Kamenskyh, M. Jafarov, T. Tkachenko, V. Yevdokymenko. Investigation of oxidation-reduction processes of nickel hydroxides precipitation and their carbothermical reduction. Phys. Chem. Chem. Phys. 2024. Advance Article. https://doi.org/10.1039/D4CP03077J

      17. V.A. Bohatyrenko, D.S. Kamenskyh, M.A. Jafarov, T.V. Tkachenko, V.O. Yevdokymenko. Synthesis of nickel nano-particles with magnetic properties using the car-bothermy method. Journal of Physics & Space Sciences. 2024. V. 1, N 2. P. 17-30. ISSN: 3006-6123 (ONLINE)

      18. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Brovarets V.S. Improvement of the vegetative growth of rapeseed (Brassica napus L. using synthetic plant growth regulators and microfertilizers.Proceedings XIII International Scientific and Practical Conference «Modern science: theoretical and practical view». Madrid. Spain. 23-24.07.2024. P. 3-6. Doi:10.5281/zenodo.13124742

      19. V. Bratishko, T. Tkachenko, S. Shulga, O. Tigunova. Results of chemical studies of parameters and composition of samples of lignocellulose raw materials of communal origin. Proceedings 23rd International Scientific Conference Engineering for Rural Development 22.-24.05.2024. Jelgava, LATVIA. P. 1008-1015. https://doi.org/10.22616/ERDev.2024.23.TF205

      20. Hodyna D., Klipkov A., Kachaeva M., Shulha Y., Gerus I., Metelytsia L., Kovalishyn V. In Silico Design and In Vitro Assessment of Bicyclic Trifluoromethylated Pyrroles as New Antibacterial and Antifungal Agents. Chemistry & biodiversity. 2024. V. 21, N 8. Р. e202400638. DOI: 10.1002/cbdv.202400638

      21. Semenyuta I., Kovalishyn V., Hodyna D., Startseva Yu., Rogalsky S., Metelytsia L. New QSTR models to evaluation of imidazolium- and pyridinium-contained ionic liquids toxicity, Computational Toxicology. 2024. V. 30. Р. 100309. https://www.sciencedirect.com/science/article/abs/pii/S2468111324000112

      22. 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, Chem. Pap. 2024. V. 78,  N 1. Р. 133-140. DOI:10.1007/s11696-023-03038-1

      23. Kovalishyn V., Severin O., Kachaeva M., Kobzar O., Keith K., Harden E., Hartline C., James S., Vovk A., Brovarets V. In Silico Design and Experimental Validation of Novel Oxazole Derivatives Against Varicella zoster virus. Molecular biotechnology. 2024. V. 66, N 4. Р. 70 7-717. DOI: 10.1007/s12033-023-00670-w

      24. Severin O.O., Kachaeva M.V., Pilyo S.G., Kovalishyn V.V.,Keith K.A., Harden E.A., Hartline C.B., James S.H., Zhirnov V.V., Brovarets V.S. Synthesis, Characterization, and Study of Anti-HPV Activity and Cell Cytotoxicity of Novel 1,3-Oxazole-4Carbonitrile and  4-Sulfonylamide-5-Phenyl-1,3-Thiazole Derivatives in Vitro. Letters in Applied NanoBioScience. 2024. V. 13, N 2. Р. 89. DOI:10.33263/lianbs132.089

      25. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Pilyo S.H., Brovarets V.S. The effect of synthetic plant growth regulators and microfertilizers on the vegetative growth of flax. World science priorities. Proceedings of the X International Scientific and Practical Conference. 16-17 May 2024. Vienna. Austria. 2024. Pp. 16-20. DOI: 10.5281/zenodo.11244638

      26. O. Severin,S. Pilyo,M. Kachaeva, V. Zhirnov,D. Hodyna,O. Bahrieieva,V. Brovarets. Synthesis, characterization of novel N-(4-cyano-1,3-oxazol-5-yl)sulfonamide derivatives and in vitro screening their activity against NCI-60 cancer cell lines. ChemMedChem, 2024. V. 19, N 5. Р. e202300527. https://doi.org/10.1002/cmdc.202300527

      I.V. Semenyuta, D.M. Hodyna, A.V. Griniukova,S.P. Rogalsky, L.O. Metelytsia.

      Long-chain N-substituted imidazole derivatives with anticancer activity against chronic myeloid leukemia. Proceedings of the VI Intern. Scientific and Practical Conf. “Education and science of today: intersectoral issues and development of sciences”, Cambridge, March 29, 2024. Р. 175-180. doi: 10.36074/logos-29.03.2024.041

      Babenko L., Futorna O., Romanenko K., Smirnov O., Rogalsky S., Kosakivska I., kwarek E., Wiśniewska M. Exogenous N-hexanoyl-L-homoserine lactone mitigates acid rain stress effects through modulation of structural and functional changes in Triticum aestivum leaf. Applied Soil Ecology.2024. V. 193. Р. 105151. https://doi.org/10.1016/j.apsoil.2023.105151

      Zubova G., Melnyk H., Zaets I., Sergeyeva T., Havryliuk O., Rogalsky S., Khirunenko ., Zaika L., Ruban T., Antonenko S., Kozyrovska N. Halochromic Bacterial Cellulose/Anthocyanins Hybrid Polymer Film with Wound-Healing PotentialPolymers. 2024. V.16, N 16. Р. 2327. https://doi.org/10.3390/polym16162327

      Kobrina L., Boiko V., Shtompel V., Hudzenko N., Rogalsky S., Frasinyuk M., Kozitskiy A., Riabov S. Inclusion complex of ionic liquid

      1-dodecylpyridinium tetrafluoroborate with sulfobutyl ether-β-cyclodextrin: preparation and characterization. Journal of Molecular Structure. 2024. V. 1309.

      Р. 138137. https://doi.org/10.1016/j.molstruc.2024.138137

      Rogalsky S., Moshynets O., Dzhuzha O., Tarasyuk O., Hubina A., Darbut A.M., Lobko Y., Morozovska I., Protasov O.  Bardeau J.-Fr. Preparation and characterization of antifouling coating based on commercial alkyd paint modified with hydrophobic cationic biocide. Journal of Coatings Technology and Research. 2024. V. 21, N 3. Р. 939-953. Doi:10.1007/s11998-023-00862-8

      Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Brovarets V.S. Regulation of wheat growth using synthetic pyridine and pyrimidine derivatives and fertilizers. Proceedings VIII International Scientific Conference. Toronto. Canada. 02-03.07.2024. P. 4-8. DOI:10.5281/zenodo.12688843

      Semenyuta I., Hodyna D., Gryniukova A., Rogalsky S., Metelytsia L. Antitumor activity of long-chain N-substituted 3-methylimidazolium ionic liquids against neuroblastoma cancer cells. International scientific journal «Grail of Science». 2024.

      V. 39.Р. 288-291. DOI:10.36074/grail-of-science.10.05.2024.041

      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 synthesis. Curr. Chem. Lett. 2024. V.13, N 1. P. 163-172. http://dx.doi.org/10.5267/j.ccl.2023.7.004

      Prysiazhniuk K., Datsenko O., Polishchuk O., Shulha S., Shablykin O., Nikandrova L., orbatok K., Bodenchuk I., Borysko P., Shepilov D., Pishel I., Kubyshkin V., Mykhailiuk P. Spiro[3.3]heptane as a saturated benzene bioisostere. Angewandte Chemie. Int. Ed. 2024. V. 63, N 9. Р. e202316557. https://doi.org/10.1002/anie.202316557

      Gaponov A. M., Pavlenko O. L., Dmytrenko O. P., Kulish M. P., Ryzhkova A. S., Lesiuk A.I., Obernikhina N.V., Łuszczyńska B., Kachkosky O. D. Molecular heteroassociation in films of thiochrome and tryptophan. Mol. Cryst. Liquid Cryst. 2024. V. 768, N 3. P. 71-77. https://doi.org/10.1080/15421406.2023.2257515

      Severin O.,Pilyo S., Moskvina V., Shablykina O., Karpichev Y., Brovarets V. Synthesis and in vitro anticancer evaluation of functionalized 5-(4-piperazin-1-yl)-2-aryloxazoles, and 5-(4-arylsulfonyl)piperazine-1-yl)-2-phenoloxazoles. Chem Heterocycl Comp. 2024. V. 60, N 1/2. P. 68-74. https://doi.org/10.1007/s10593-024-03295-2

      Zyabrev V., Demydchuk B., Pilyo S., Zhirnov V., Liavynets O., Brovarets V. Synthesis, characterization, and in vitro anticancer evaluation of 2,4-disulfonyl-substituted 5-aminothiazoles. Curr Chem Lett. 2024. V. 13, N 3. P. 557-568. https://doi.org/10.5267/j.ccl.2024.2.003

      Nallaparaju J.V., Satsi R., Merzhyievskyi D., Jarg T., Aav R., Kananovich D.G. Mechanochemical birch reduction with low reactive alkaline earth metals.  Angew Chem Intern Ed. 2024. V. 63, N 20.  Р. e202319449. https://doi.org/10.1002/anie.202319449

      Semenyuta I., Golovchenko O., Bagreeva O., Vydzhak R., Zhirnov V., Brovarets V.

      Synthesis, characterization, in vitro anticancer evaluation, ADMET properties, and molecular docking of novel 5-sulfonyl substituted (thiazol-4-yl)posphonium salts. ChemMedChem. 2024. E202400205. P. 1-11. https://doi.org/10.1002/cmdc.202400205

      Bondarchuk T., Vaskiv D., Zhuravel E., Shyshlyk O., Hrynyshyn Ye., Nedialko O., okholenko O., Pohribna A., Kuchuk O., Brovarets V., Zozulya S. Synthetic amine lincers for efficient sortagging. Bioconjugate Chem. 2024. V. 35, N 8. P. 1172-1181. https://doi.org/10.1021/asc.bioconjchem.4c00143

      Sinenko V.O., Los O.V., Potikha L.M., Brovarets V.S. Functionalized 1,3-thiazoles by combined halogen dance. Curr Chem Lett. 2024. V. 13, N 4. P. 695-706.

      https://doi.org/10.5267/j.ccl.2024.5.001

      Sosnovich B.D., Timokhin O.S., Kucha O.V., Demianyuk N.Y., Hys D.V.,

      Zvarych .A., Smolii O.B., Vashchenko B.V., Grygorenko O.O. Synthesis and enzymatic resolution of novel analogues of alicyclic and heterocyclic mandelic acid derivatives. Tetrahedron. 2024. V. 161. P. 134068. https://doi.org/10.1016/j.tet.2024.134068

      Shablykin O.V., Chumachenko S.A., Konovalenko A.S., Shablykina O., Shishkina S.V., Kozytskyi A.V., Brovarets V.S. Interactions of 3-acylisocoumarines: a simple route to 3,4-dihydro-6H-pyrazino[1,2-b]isoquinolin-6-ones and their hydrogenated derivatives. Chemistry Select. 2024. V. 9, N 40. 2024. Р. e202403740.

      https://doi.org/10.1002/slct.202403740

      Obernikhina N., Severin O., Pilyo S., Kachaeva M., Kachkovsky O., Kozachenko O., Brovarets V., Bodachivskii Yu. A comparative in vitro and in silico study of the anticancer action of 1,3-oxazol-5-sulfonylamides and new 1-(1,3-oxazol-5-yl)piperidine-sulfonylamides. Chemistry Select. 2024. V.9, N 41. Р. e202403531. https://doi.org/10.1002/slct.202403531

      Levterov V.V., Panasiuk Ya., Shablykin O., Stashkevych O., Sahun K., Rassokhin A., Sadkova I., Lesyk D., Anisiforova A., Holota Yu., Borysko P., Bodenchuk I., oloshchuk N.M., Mykhailiuk P.K. 2-Oxabicyclo[2.1.1]hexanes: synthesis, properties, and validation as bioisosteres of ortho- and meta-benzenes. Angew. Chem. Int. Ed. 2024. V. 63, N 19.  Р. e202319831. https://doi.org/10.1002/anie.202319831

      Prysiazhniuk K., Datsenko O.P., Polishchuk O., Shulha S., Shablykin O.,

      Nikandrova e., Horbatok K., Bodenchuk I., Borysko P., Shepilov D., Pishel I., Kubyshkin V., Mykhailiuk P.K.  Spiro[3.3]heptane as a saturated benzene bioisostere. Angew. Chem. Int. Ed. 2024. V. 63, N 9.  Р. e202316557. https://doi.org/10.1002/anie.202316557

      Myshko A.S., Mrug G.P., Bondarenko S.P., Kondratyuk K.M., Kobzar O.L., Buldenko .M., Kozytskiy A.V., Vovk A.I., Frasinyuk M.S. Trapping of thermally generated ortho– and para-quinone methides by imidazoles and pyrazoles: a simple route to green synthesis of benzopyrone-azole hybrids and their evaluation as α-glucosidase inhibitors. RSC Adv. 2024. V.14. P. 27809-27815. https://doi.org/10.1039/d4ra05230g

      Govor E. V., Naumchyk V., Nestorak I., Radchenko D.S., Dudenko D., Moroz Yu.S., Kachkovsky O.D., Grygorenko O.O. Generation of multimillion chemical space based on the parallel Groebke–Blackburn–Bienaymé reaction. Beilstein J. Org. Chem. 2024. V. 20. P. 1604-1613. https://doi.org/10.3762/bjoc.20.143

      Gaponov A.M., Ryzhkova A.S., Pavlenko O.L., Dmytrenko O.P., Kulish M.P.,

       Lesiuk .I., Kolomys O.F., Obernikhina N.V., Kachkovsky O.D. Spectral features of films of bovine serum albumin with thiochrome. Mol. Cryst. Liquid Cryst. 2024. https://doi.org/10.1080/15421406.2024.2355394

      Shablykin O., Herasimov E., Shablykina O., Kozytsky A. Synthesis of 2-R-5-amino-4-(1H-tetrazol-5-yl)-1,3-oxazoles from 2-R-5-amino-1,3-oxazole-4-carbonitriles. Curr. Chem. Lett. 2025. V.14, N 1. P. 233-238.  https://doi.org 10.5267/j.ccl.2024.6.003

      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-ylphosphonic acids. Phosph. Sulph. Silicon and Relat. Elem. 2024. V. 199, N 1.

      P. 71-81. Doi: 10.1080/10426507.2023.2251639

      Hlibov E.K., Gorbulenko N.V., Moskvina V.S., Shablykina O.V., Shokol T.V., Kozytskyi A.V., Khilya V.P. Modified neoflavones based on 7-hydroxyneoflavone-6-enamino ketone and 7-hydroxy-3-hetarylbenzopyran-2- and 4-ones Mannich bases and their recyclization.. Chem. Nat. Compd. 2024. V. 60, N 3. P. 223-228. https://doi.org/10.1007/s10600-024-04293-8

      Gaponov A.M., Pavlenko O.L., Dmytrenko O.P., Neimash V.B., Kachkovsky O.D. Spectral Properties of Thin Films of Squaraine Dyes, Deposited on Silver and Gold Nanoparticles. Springer Proceedings in Physics. 2023. V. 297. P. 339-354. https://doi.org/10.1007/978-3-031-42708-4_22

      Gryniukova A., Borysko P., Myziuk I., Alieksieieva D., Hodyna D., Semenyuta I., ovalishyn V., Metelytsia L., Rogalsky S., Tcherniuk S. Anticancer activity features of imidazole-based ionic liquids and lysosomotropic detergents: in silico and in vitro studies. Molecular Diversity 2024. https://doi.org/10.1007/s11030-023-10779-4

      Demchenko S.,  Sukhovieiev V., Golovchenko O.,  Sukhovieiev J., Yarmoluk S., Demchenko A. Syntheses and evaluation of novel 3-hydroxy-1,3-diaryl-2,3,5,6,7,8-hexahydroimidazo[1,2-a]pyridine-1-ium bromides as potential anticancer agents. Pharmacia. 2024. V.71. P.1-10. https://doi.org/10.3897/pharmacia.71.e135992

      Bondarchuk T., Vaskiv D., Zhuravel E., Shyshlyk O., Hrynyshyn Ye., Nedialko O., Pokholenko O., Pohribna A., Kuchuk O., Brovarets V., Zozulya S. Synthetic amine linkers for efficient sortagging. Bioconj. Chem. 2024. V. 35, N 8. P. 1172-1181. https://doi.org/10.1021/acs.bioconjchem.4c00143

      Shablykin O.V., Brovarets V.S., Shablykina O.V. Recyclization of 5-aminooxazoles as a route to new functionalized heterocycles. Chem. Record: Spec. 2024. V. 24,

       N 2. Р. e202300264. https://doi.org/10.1002/tcr.202300264

      Semenyuta I., Hodyna D., Kovalishin V., Demydchuk B., Pilyo S., Metelytsia L. 5-Amino-4-cyano-1,3-oxazoles as new antibacterials against antibiotic-resistent Escherichia coli strains.  Proceedings “Scientific practice: Modern and classical research methods”. May 26, 2023. Boston, USA. P. 117-121. https://doi.org/10.36074/logos-26.05.2023

      Hodyna D.M., Kovalishin V.V., Derevianko K.Yu. 1,3-Oxazole derivatives as antibacterials against colistin-resistent Acinetobacter Baumannii strains. The process and dinamics of the scientific path.  Proceedings “IV International Scientific and Theoretical Conference”. 16 June, 2023, Athens, Hellenic Republic: European Scientific Platform. P. 83-85.  DOI: 10.3674/scientia-16.06.2023

      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. Use of natural biostimulants to increase the adaptation of wheat to salt and drought stresses.  Збірник статей “International Biotechnology and Nanotechnology Congress”. October 30, 2024. Ardahan: Turkey. P. 819-820. https://doi.org/10.5281/zenodo.14242863

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      Vovk A. Design, synthesis, and xanthine oxidase inhibitory activity of 4‐(5‐aminosubstituted‐4‐cyanooxazol‐2‐yl) benzoic acids. ChemMedChem. 2024.

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      Parkhomenko Y.M.,Vovk A. I.,Protasova Z. S., Pylypchuk S.Y., Chorny S.A.,

      Pavlova O.S., Pylypchuk S.Yu., Stepanenko S.P. Thiazolium salt mimics the non-coenzyme effects of vitamin B1 in rat synaptosomes. Neurochemistry International.

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      Myshko A.S.,Mrug G.P., Bondarenko S.P., Demydchuk B.A., Kobzar O.L.,

      Buldenko V.M.,Vovk A.I.,Frasinyuk M.S. Divergent synthesis of novel 3 (5)‐aminoazole–benzopyrone hybrids and their evaluation as α‐glucosidase inhibitors. ChemMedChem. 2024. Р. e202400525. https://doi.org/10.1002/cmdc.202400525

      Semenyuta I.,Los O.,Sinenko V.,Zhirnov V.,Potikha L.,Kobzar O.,Brovarets V.  Design, synthesis, and antitumor potential of new thiazole-contained 5-fluoro-2-oxindole derivatives as sunitinib analogues. Current Medicinal  Chemistry. 2024.

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      Muzychka L., Muzychka O.,Smolii O. Synthesis and acetylcholinesterase inhibitory activity of novel trilaciclib analogs. Chemistry and Biodiversity. 2024 Р. 02401874 .

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      Muzychka L.V., Humeniuk N.I., Boiko I.O., Vrynchanu N.O., Smolii O.B. Synthesis and in vitro evaluation antibacterial and antibiofilm activities of novel triphenylphosphonium-functionalized substituted pyrimidines. Chemical Biology & Drug Design. 2024. V. 103, N 2. Р. e14483

      DOI: 10.1111/cbdd.14483

      Muzychka L.V., Humeniuk N.I., Boiko I.O.,Vrynchanu N.O., Smolii O.B. Synthesis and antibiofilm activity of novel 1,4-dihydropyrido [1,2-а]pyrrolo[2,3-d]pyrimidine-2-carboxamides. Biopolymers&Cell. 2024. V. 40, N 1. Р. 68-80 http://dx.doi.org/10.7124/bc.000AAB

      Dubina T.F., Kosarevych A.V., Kucher O.V., Sosunovych B.S., Smolii O.B., Vashchenko B.V., Grygorenko O.O. Synthesis and reactions of novel imidazo[4,5-b]pyridine building blocks. Chemistry of Heterocycllic Compounds. 2024. V. 60.

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      Vaskevych A., Shishkina S., Dekhtyar M.,Smolii O.,Vovk M. Access to Seleno-Functionalized Thiazolo­­[3,2-a]Pyrimidinones and Pyrimido[2,1-b][1,3]Thiazinones via Selenocyclization of 2-Alkenylthio­pyrimidinones and Their Fused Analogs. Chemistry Select. 2024. V. 9. Р. e202403699. DOI:10.1002/slct.202403699

      S.I. Vdovenko, I.I. Gerus, M. Pagacz-Kostrzewa, M. Wierzejewska. Comparison of kinetic and thermodynamic parameters of reaction of individual conformers of α‑substituted β‑ethoxyvinyl trifluoromethyl ketones with secondary amines. Reaction Kinetics, Mechanisms and Catalysis. 2024. V. 137, N 2. Р. 1-18. DOI:10.1007/s11144-024-02578-1

      Q. Wang, Y. Bian, G. Dhawan, W. Zhang, A.E. Sorochinsky, A. Makarem,

      V. A. Soloshonok, J. Han. Fluorine-containing drugs approved by the FDA in 2023.  Chinese Chemical Letters. 2024. V. 35. Р. 109780. doi: 10.1016/j.cclet.2024.109780

      Logvinenko I.G., Sadkova I.V., Tolmachova N.A., Shishkina S.V., Daniliuc K.G.,

       Haufe G., Kondratov I.S. 4-Trifluoromethoxy proline: synthesis of stereoisomers and lipophilicity study. Org. Biomol. Chem. 2024.  V. 22. Р. 7982-7988. DOI: 10.1039/D4OB00688G

      Pahl A.,  Grygorenko O.O.,  Kondratov I.S., Waldmann H. Identification of readily available pseudo-natural products. RSC Med. Chem. 2024. V. 15. Р. 2709-2717.

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      F. Liu, A.L. Kaplan, J. Levring, J. Einsiedel, S. Tiedt, K. Distler, N.S. Omattage,

      I.S. Kondratov, Y.S. Moroz, H.L. Pietz, J.J. Irwin, P. Gmeiner, B.K. Shoichet,

       J. Chen. Structure-based discovery of CFTR potentiators and inhibitors. Cell. 2024.

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      P. Janssen, F. Becker, F.T. Füsser, N. Tolmachova, T. Matviiuk, I. Kondratov,

      M.S. Weiss, D. Kümmel, O. Koch. Design and Crystallographic Screening of a Highly Sociable and Diverse Fragment Library Towards Novel Antituberculotic Drugs. ChemRxiv. 2024. doi: 10.26434/chemrxiv-2024-rpst3-v2

      Kolesnikov Ya.S., Kretynin S.V., Filepova R., Dobrev P.I., Martinec J., Kravets V.S. Polyamines metabolism and their biological role in plant cells: what do we really know? Phytochem. Rev. 2024. V. 23. P. 997-1026 . DOI:10.1007/s11101-024-09913-3

      Voloshyna Yu.,Pertko O.,Yakovenko A., Povazhnyi V.,Patrylak L. Metal-containing zeolite composites with separated phases as catalysts for hydroisomerization of linear hexane. J. Porous Mater. 2024. V. 31, N 3.

      P. 1029-1041. https://doi.org/10.1007/s10934-024-01584-x

      O. Pertko,Yu. Voloshyna,L. Patrylak,A. Yakovenko. Oxidative CO2 dehydrogenation of butane on microspherical zeolite-containing composites based on kaolin. ChemRxiv,Preprints. 2024.20 May 2024. DOI : 10.26434/chemrxiv-2024-xqcjg

      A. Yakovenko,L. Patrylak,Yu. Voloshyna,O. Pertko,V. Povazhnyi. Ni/Pd-containing pentasils in n-hexane micropulse hydrocracking and aromatization. Research Square, Preprints. 2024.08 May 2024. https://doi.org/10.21203/rs.3.rs-4375758/v1

      L. Patrylak,Yu. Voloshyna,O. Pertko,A. Yakovenko. n-Alkanes hydroisomerization on Ni-HMFI zeolites of different preparation methods. Research Square, Preprints. 2024.01 April 2024. https://doi.org/10.21203/rs.3.rs-4187059/v1

      L. Patrylak,S. Konovalov,S. Zubenko,A. Yakovenko, D. Davitadze,O. Pertko. Fatty Acid Ethyl Esters as Biodiesel Fuel: Product Quality and Efficiency of Various Purification Techniques. SRNN Preprints, 2024. 3 June 2024. http://dx.doi.org/10.2139/ssrn.4852240

      Yu.Voloshyna,O. Pertko,A. Yakovenko,V. Povazhnyi, L. Patrylak.  Metal-containing zeolite composites with separated phases as catalysts for hydroisomerization of linear hexane. Research Square, Preprints. 2024.12 March 2024. https://doi.org/10.21203/rs.3.rs-3796081/v1

      Povazhnyi V.A., Voloshyna Y.G., Pertko O.P., Melnychuk O.V., Kontsevoi A.L

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      Hutsul,I. Ivanenko, L. Patrylak. Photocatalytic degradation of azo dyes by ZnO/zeolite composite under static conditions. Appl. Nanosci.2023. V. 13, N 12. Р. 7601-7609. https://doi.org/10.1007/s13204-023-02950-y

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      Assessment of the Possibility of Using Lignocellulosic Feedstock for the Production of Sustainable Aviation Fuels. NTAD 2023 – New Trends in Aviation Development 2023: Proceedings 18th International Scientific Conference. Stary Smokovec, 23-24 November 2023. P. 285-288. DOI:10.1109/NTAD61230.2023.10380174

      L. Patrylak,S. Konovalov,S. Zubenko,A. Yakovenko,D. Davitadze,O. Pertko.  Fatty acid ethyl esters as biodiesel fuel: product quality and efficiency of various purification techniques. Chemistry Journal of Moldova. 2024. https://doi.org/10.19261/cjm.2024.1236

      L.M. Grishchenko, D.O. Zhytnyk, I.P. Matushko, V.E. Diyuk, Yu.V. Noskov. V.Yu. Malyshev, V.A. Moiseienko, O.Yu. Boldyrieva, V.V. Lisnyak. Microwave properties of composite films based on polyvinyl chloride and brominated activated carbon. ChemistrySelect.  2024. V. 9, №18. Р. e202400432. https://doi.org/10.1002/slct.202400432

      L.M. Grishchenko, D.О. Zhytnyk, I.P. Matushko, Yu.V. Noskov, V.A. Moiseienko,

      V.V. Klepko, O.Yu. Boldyrieva, Yu.А. Len, N.A. Atamas, V.A. Marianovskyi,

       O.V. Mischanchuk, V.V. Lisnyak. Facile preparation of polyvinyl chloride/activated carbon thin-film composites and study of their microwave absorption at Ka-band frequencies. Molecular Crystals and Liquid Crystals. 2024. V. 768, № 8. P. 139-149.

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      М. Kharkhota, М. Kharchuk, А. Kharchuk, G. Grabova, Yu. Noskov, R. Linnik, А. Makeiev, L. Avdieieva. Physico-chemical properties of Priestia endophytica UCM B-5715 fluorescent pigments. Biochemical and Biophysical Research Communications. 2024. V. 741. Р. 151040. DOI: 10.1016/j.bbrc.2024.151040

      2021 р.

      Розділи в зарубіжних монографіях

      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.

      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.

      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.

      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.

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        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.
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        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.
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        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.
        53. A. Adejuwon, V. Tsygankova, M. Donova, O. Odeleye. A Medicinal Plant’s Extract Effective on Tuberculosis in Cases of Osteotic Transformation in Tropical Nigeria. Cancer Biology. 2021. V. 11 (2). P. 106-108. doi:10.7537/marscbj110221.03.
        54. Vasylyuk S.V., Suprun A.D., Shmeleva L.V., Kachkovsky O.D. Configuration of charge waves in polymethine linear dye systems. Springer proceedings in physics. 2021. V. 246. P. 189-201.
        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.
        56. V. Bratishko, T. Tkachenko, S. Shulha, O. Tigunova. Results of composition analysis of non-grain part of major field crops in Ukraine. Proceeding Book of 20th International Scientific Conference Еngineering for rural development. V. 20. May 26-28, 2021. Jelgava, Latvia. Р. 584-588. https://doi.org/10.22616/ERDev.2021.20.TF125.
        57. Starodubtseva A., Kalachova T., Iakovenko O., Stoudková V., Zhabinskii V., Khripach V., Ruelland E., Martinec J., Burketová L., Kravets V. BODIPY Conjugate of Epibrassinolide as a Novel Biologically Active Probe for іn vivo Imaging. International Journal of Molecular Sciences. 2021. V. 22 (3599). Р. 1-12.
        58. Pokotylo I., Hodges M., Kravets V., Ruelland E. A ménage à trois: Salicylic acid, growth inhibition and immunity. Trends in plant Sciences. 2021. TRPLSC2223 https://doi.org/10.1016/j.tplants.2021.11.008.
        59. O.O. Grygorenko, V.S. Moskvina, I. Kleban, O.V. Hryshchyk. Synthesis of saturated and partially saturated heterocyclic boronic derivatives. Tetrahedron. 2021. https://doi.org/10.1016/j.tet.2021.132605.

        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.
        8. M. M.Trush, I. Semenyuta, D. Hodyna, A. Ocheretniuk, S. Vdovenko, S. Rogalsky, L. Kalashnikova, V. Blagodatnyi, O. Kobzar, L. Metelytsia. Functionalized imidazolium-based ionic liquids: biological activity evaluation,toxicity screening, spectroscopic, and molecular docking studies. Medicinal Chemistry Research. 2020. V. 29. Р. 2181-2191.
        9. L. Metelytsia, M. Trush, I. Semenyuta, S. Rogalsky, O. Kobzar, L. Kalashnikova, V. Blagodatny, D. Hodyna. Ionic Liquids with Anti-Candida and Anticancer Dual Activity as Potential N-Myristoyltransferase Inhibitors. Current Bioactive Compounds. 2020. V.16, №7. Р. 1036-1041.
        10. Ghamrawi S., Bouchara J.-Ph., Corbin A., Rogalsky S., Tarasyuk O., Bardeau J.-Fr. Inhibition of fungal growth by silicones modified with cationic biocides. Materials Today Communications. 2020. V. 22. Р. 100716.
        11. Fatyeyeva, K., Rogalsky, S., Makhno, S., Tarasyuk, O., Soto Puente, J.A. Marais, S. Polyimide/Ionic Liquid Composite Membranes for Middle and High Temperature Fuel Cell Application: Water Sorption Behavior and Proton Conductivity. Membranes.2020. V.10. Р.82.
        12. Pokotylo I., Hellal D., Bouceba T., Hernandez-Martinez M., Kravets V., Leitao L., Espinasse C., Kleiner I., Ruelland E.. Deciphering the Binding of Salicylic Acid to Arabidopsis thaliana Chloroplastic GAPDH-A1. International Journal of Molecular Sciences. 2020. V. 21, №13. Р. 4678.
        13. Logvinenko I.G., Markushyna Y., Kondratov I.S., Vashchenko B.V., Kliachyna M., Tokaryeva Yu., Pivnytska V., Grygorenko O. O., Haufe G.. Synthesis, physico-chemical properties and microsomal stability of compounds bearing aliphatic trifluoromethoxy group. Journal of Fluorine Chemistry. 2020. V. 231. Р. 109461.
        14. Bugera M.Ya, Tarasenko K.V., Kondratov I.S., Gerus I. I, Vashchenko B.V., Ivasyshyn V.E. Grygorenko O.O.. (Het)aryl difluoromethyl-substituted β-alkoxyenones: synthesis and heterocyclizations. European Journal of Organic Chemistry. 2020. V. 9. Р. 1069-1077.
        15. Malashchuk A., Chernykh, A.V., Hurmach V.V., Platonov M.O., Onopchenko O., Zozulya S., Daniliuc C.G., Dobrydnev A.V., Kondratov I.S., Moroz Yu.S. Grygorenko O.O. Synthesis, biological evaluation, and modeling studies of 1,3- disubstituted cyclobutane-containing analogs of combretastatin A4. Journal of Molecular Structure. 2020. V. 1210. Р. 128025-128033.
        16. Stepaniuk O.O., Vashchenko B.V., Matvienko V.O., Kondratov I.S., Tolmachev A.A., Grygorenko O.O. Reactions of cyclic β-alkoxyvinyl α-keto esters with heteroaromatic NCC-binucleophiles. Chemistry of Heterocyclic Compounds. 2020. V. 56, № 3. Р. 377-385.
        17. Stepaniuk O.O, Rudenko T.V., Vashchenko B.V., Matvienko V.O., Kondratov I.S., Tolmachev A.A., Grygorenko O.O. Synthesis of Fused Pyridine Carboxylates by Reaction of β-Alkoxyvinyl Glyoxylates with Amino Heterocycles. Synthesis. 2020. V. 52, № 13. Р. 1915-1926.
        18. Feskov I.O., Golub B.O., Vashchenko B.V, Levterov V. V., Kondratov I.S., Grygorenko O.O., Haufe G.. GABA Analogues and Related Mono‐/Bifunctional Building Blocks Derived from the Fluorocyclobutane Scaffold. European Journal of Organic Chemistry. 2020. V. 30. Р. 4755-4767.
        19. Klipkov A.A., Sorochinsky A.E., Tarasenko K.V., Rusanova J.A., Gerus I.I. Synthesis of trifluoromethyl and trifluoroacetyl substituted dihydropyrrolizines and tetrahydroindolizines. Tetrahedron Lett. 2020. V. 61. P. 151633.
        20. Gerus I.I, Zhuk Y.I, Kacharova L.M, Röschenthaler G., Shaitanova E.N., Sorochinskii A.E., Vdovenko S. I., Wojcik Y.. Uncommon fluorination of enones with xenon difluoride. Journal of Fluorine Chemistry. 2020. V. 229. Р. 109413.
        21. Trofymchuk S., Bugera M., Klipkov A., Razhyk B., Semenov S., Tarasenko K., Starova V., Zaporozhets O., Tananaiko O., Alekseenko A., Pustovit Y., Kiriakov O., Gerus I., Tolmachev A., Mykhailiuk P.. Deoxofluorination of (Hetero) aromatic Acids. The Journal of Organic Chemistry. 2020. V. 85, № 5. Р. 3110-3124.
        22. Trofymchuk S.A, Kliukovskyi D.V., Semenov S.V., Khairulin A.R., Shevchenko V.O., Bugera M.Y., Tarasenko K.V., Volochnyuk D.M., Ryabukhin S.V. Semi-Industrial Fluorination of β-Keto Esters with SF4: Safety vs Efficacy. Synlett. 2020. V. 31, № 06. Р. 565-574.
        23. Vretik L.O., Noskov Y.V., Ogurtsov N.A., Nikolaeva O.A., Shevchenko A.V., Marynin A.I., Kharchuk M.S., Chepurna O.M., Ohulchanskyy T.Y., Pud A.A. Thermosensitive ternary core–shell nanocomposites of polystyrene, poly(N-isopropylacrylamide) and polyaniline. Applied Nanoscience. 2020. V. 10, № 12. P. 4951-4964.
        24. Rudenko R.M., Voitsihovska O.O., Poroshin V.M., Petrychuk M.V., Pavlyuk S.P., Nikolenko A.S., Ogurtsov N.A., Noskov Y., Sydorov D.O., Pud A.A.. Specific interactions and charge transport in ternary PVDF/polyaniline/MWCNT nanocomposite films(Article). Composites Science and Technology. 2020. V. 198. Р. 108284.
        25. Kislyuk V., Kotrechko S., Trachevskij V., Melnyk A., Pud A., Ogurtsov N., Noskov Y., Osiponok M., Lytvyn P., Dzyazko Y., Akhmadaliev S., Kentsch U., Krause M., Facsko S. Impact of low energy ion beams on the properties of rr-P3HT films(Article). Applied Surface Science. 1 January 2021. V. 535. Р. 147619.
        26. Hamouda Z., Wojkiewicz J.L., Pud A.A., Bergheul S., Lasri T.. Broadband dielectric characterization of flexible substrates using organic conductive polymer microstrip lines. Microwave and Optical Technology Letters. 2020. V. 62, № 2. P. 688-695.
        27. Binnewerg B., Schubert M., Voronkina A., Muzychka L., Wysokowski M., Petrenko Ia., Djurović M., Kovalchuk V., Tsurkan M., Smolii O.B., Ehrlich H.. Marine biomaterials: Biomimetic and pharmacological potential of cultivated Aplysina aerophoba marine demosponge. Materials Science and Engineering C. 2020. V. 109. Р. 110566.
        28. Mezhenska O., Rebriev A., Kobzar O., Zlatoust N., Vovk A., Parkhomenko Yu. Non-coenzyme properties of thiamine: evaluation of binding affinity to malate dehydrogenase isoforms. Biotechnologia Acta. 2020. V. 13, № 4. P. 26-38.
        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.
        31. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P. Synthesis of Benzofurans Modified by Coumarin and Pyrazole Heterocycles. Chem. Nat. Compd., 2020. V.56. P. 1060-1063.
        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.
        36. Abdurakhmanova E.R., Brusnakov M.Y., Golovchenko O.V., Pilyo S.G., Velychko N.V., Hariden E.A., Prichard M.N., James S.H., Zhirnov V.V., Brovarets V.S. Synthesis and in vitro anticitomegalovirus activity of 5-hydroxyalkylamino-1,3-oxazoles derivatives. Med. Chem. Res., 2020. V.29, № 9. P. 1669-1675.
        37. Выджак Р.Н., Панчишин С.Я., Броварец В.С.. Применение никелевых комплексов 1,3‑дикарбонильных соединений для синтеза конденсированых систем с ядром 4‑аминопиразола. ЖОХ. 2020. T. 90, №8. С. 1231-1239.
        38. L.M. Potikha, V.S. Brovarets. Synthesis of new antineoplastic agents based on imadazo[2,1-a]pyridine. Chem. Heterocycl. Compd. 2020. V.56, № 11. P. 1460-1464.
        39. Potikha L.M., Brovarets V.S.. Synthethis of imidazole[2,1-b][1,3]thiazoles – potential anticancer agents derived from p-bromodipnones. Chem. Heterocycl. Compd. 2020. V.56, № 8. P. 1073-1077.
        40. Grygorenko O.O., Moskvina V.S., Hryshchuk O.V., Tymtsunik A.V. Cycloadditions of alkenylboronic derivatives. Synthesis. 2020. V. 52. P. 2761-2780.
        41. Grygorenko O.O., Hutskalova V., Moskvina V.S. Bicyclic 6-6 systems with one bridgehead (ring junction) nitrogen atom: three extra heteroatoms (2:1). Chapter in collection: “Reference module in chemistry, molecular sciences and chemical engineering”. 2020.
        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.
        43. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.V., Golovchenko O.I.. Synthesis and pharmacological trials of new phosphorylated oxazole derivatives antihypertensive properties. Maced. Pharm. Bull. 2020. V.66, № 1. P. 51-52.
        44. Velihina Ye., Scattolin T., Bondar D., Pil’o S.,Obernikhina N.,Kachkovskyi O.,Semenyuta I., Caligiuri I., Rizzolio F., Brovarets V.,Karpichev Ye.,
        45. Nolan S.P. Synthesis, in silico and in vitro evaluation of novel oxazolopyrimidines as promising anticancer agents. Helv. Chim. Acta. 2020. P. 1‑12.
        46. Obernikhina N., Pavlenko O., Kachkovsky A., Brovarets V.. Quantum-chemical and experimental estimation of non-bonding level (Fermi level) and π‑electron afinity of conjugated systems. Polycycl. Arom. Comp. 2020. P. 1-10.
        47. Blyuss K.B., Al Basir F., Tsygankova V.A. Control of mosaic disease using microbial biostimulants: insights from mathematical modelling. Ricerche Mat. 2020. V.69. P. 437-455.
        48. Adejuwon A.O., Tsygankova V.A., Obayemi O.S., Ogundare H.O. The Anti-microbial Efficacy and Phytochemical Analysis of the Root Bark of Uvaria chamea. Nature and Science. 2020. V.18, № 5. P. 73-80.
        49. Adejuwon A.O., Obayemi O.S., Odeleye O.D., Tsygankova V.A. COVID-19 in Nigeria, West Africa: An Update. Advances in Bioscience and Bioengineering. 2020. V.8, № 2. P. 1-12.
        50. Davydenko I.G., Slominskiy Yu.L., Obernikhina N.V., Kachkovsky A.D., Tolmachev A.. Infrared Polyene Radical-Cation Derived from 7,8-Dihydrobenzo[c,d]Furo[2,3-f]Indole: Synthesis, Spectra and Nature of Electron Transitions. Chemistry Select. 2020. V.5. P. 674-681.
        51. Maiko K.O., Dmitruk I. M., Obernikhina N.V., Kachkovsky A. D. Solitonic‑like excitations in cations of linear conjugated systems. Monatsh. Chem. 2020. V.151, № 4. P. 559-566.
        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.
        53. Adejuwon A.O., Obayemi O.S., Odeleye O.D., Tsygankova V.A., Thonda O.. Inhibitory Actions of a Medicinal Plants’ Extract on SARS-CoV-2 and COVID-19. Cancer Biology. 2020. V.10, № 3. P. 1-3.
        54. Adejuwon A.O., Donova M.V., Obayemi O.S. Tsygankova V.A. SARS-CoV-2 and COVID-19 phyto-activity in individuals with hematopoietic stem cell transplants. Stem Cell. 2020. V.11, № 3. P. 39-41.
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        2019 р.

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        74. Tsygankova V.A., Andrusevich Ya.V, Shtompel O.I, Kopich V.M, Panchyshyn S.Ya, Vydzhak R.M, Brovarets V.S (2019). Application of Pyrazole Derivatives As New Substitutes of Auxin IAA To Regulate Morphometric and Biochemical Parameters of Wheat (Triticum Aestivum L.) Seedlings. JOURNAL OF ADVANCES IN AGRICULTURE, 10, 1772-1786. https://doi.org/10.24297/jaa.v10i0.8341
        75. Adekunle Odunayo Adejuwon, Victoria Anatolyivna Tsygankova, Abiola Muhammad Adeosun, Adefemi Olawale Falase, Olubunmi Sharon Obayemi, Fatai Ishola Amusa. Phytochemical screening and antimicrobial efficacy of the root bark of Securidaca longipedunculata extracts. AMERICAN JOURNAL OF RESEARCH IN MEDICAL SCIENCES. 2019. Vol. 5, No 1, P. 7 – 13. doi: 10.5455/ajrms.20181204113428.
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        77. Adekunle Odunayo Adejuwon, Victoria Anatolyivna Tsygankova, Olubunmi Sharon Obayemi. ?-Amylase Production Using Aspergilus vadensis Isolated From Pulverized Cocoa Seeds. Life Science Journal 2019; 16(8). P. 64 – 70.
        78. Victoria Tsygankova et al. (2019), Screening of New Effective Regulators of Oilseed Rape Growth Among Derivatives of Oxazole and Oxazolopyrimidine. Proceedings of World Congress and Expo on Chemistry during November 15-17, 2018 in Rome, Italy. Int J Pharm Sci & Scient Res. 5:3, 34.

          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.

        1. Rogalsky S., Bardeau J.-F., Makhno S., Babkina N., Tarasyuk O., Cherniavska T., Orlovska I., Kozyrovska N., Brovko O.. New proton conducting membrane based on bacterial cellulose/polyaniline nanocomposite film impregnated with guanidinium-based ionic liquid. Polymer. – 2018. – Т.142. – P.183-195.
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        3. Vashchuk A., Rios de Anda A., Starostenko O., Grigoryeva O., Sotta P., Rogalsky S., Smertenko P., Fainleib A., Grande D.. Structure ? property relationships in nanocomposites based on cyanate ester resins and 1-heptyl pyridinium tetrafluoroborate ionic liquid. Polymer. – 2018, Vol.148. – P.14-26.
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        12. L.K. Patrylak, M.M. Krylova, O.P. Pertko, Yu.G. Voloshyna . Linear Hexane Isomerization over Ni-Containing Pentasils . J. Porous Mater.- 2018 https://doi.org/10.1007/s10934-018-0685-1.
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        15. Z. Hamouda, J.L. Wojkiewicz, A.A. Pud, L. Kone, S. Bergheul, T. Lasri. Magnetodielectric Nanocomposite Polymer-Based Dual-Band Flexible Antenna for Wearable Applications. IEEE Transactions on Antennas and Propagation.- 2018.- Vol. 66(7).- Р. 3271-3277.
        16. Ogurtsov N.A., Bliznyuk V.N., Mamykin A.V., Kukla O.L., Piryatinski Yu.P., Pud A.A.. Improved Structural and Electronic Properties of Poly(3-Methylthiophene) in Nanocomposites with Poly(Vinylidene Fluoride). Effect of an Electroactive Template”. Physical Chemistry Chemical Physics.- 2018.- Vol. 20.- Р. 6450-6461.
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        18. I.O. Yaremchuk, L.V. Muzychka, O.B. Smolii, O.V. Kucher, S.V. Shishkina. Synthesis of novel 1,2-dihydro-pyrrolo[1,2-a]pyrazin-1(2H)-one derivatives. Tetrahedron Lett.- 2018.- Vol. 59, №5.- P.442-444 19. A.M. Zinchenko, L.V. Muzychka, O.V. Kucher, I.V. Sadkova, P.K. Mykhailiuk, O.B. Smolii. One-Pot Synthesis of 6-Aminopyrido[2,3-d]pyrimidin-7-ones. Eur. J. Org. Chem.- 2018.- № 47 DOI: 10.1002/ejoc.201801204.
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        28. Tolmachova N.A., Kondratov I.S., Dolovanyuk V.G., Pridma S.O., Chernykh A.V., Daniliuc C.G., Haufe G.. Synthesis of new fluorinated proline analogues from polyfluoroalkyl ?-ketoacetals and ethyl isocyanoacetate. Chemical Communications.- 2018.- Vol. 54 (69).- Р. 9683-9686.
        29. Zyabrev V.S., Babii S.B.. Reactions of 5-mesyl-2-phenyl-4-tosyloxazole with N-, C-, and S-nucleophiles. Chem. Heter. Comp.- 2018. – Vol. 54, № 1. – Р. 93-95.
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        34. Kachkovsky A., Obernikhina N., Prostota Y., Naumenko A., Melnyk D., Yashchuk V.. Estimation of the basicity of the donor strength of terminal groups in cationic polymethine dyes. J. Molec. Structure.- 2018. – Vol.1154. – P. 606-618.
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        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.
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        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.
        61. Shokol T.V., Abdullaev E.N., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Synthesis and modification of 6-thiazolyl-4-methylumbelliferone. Chem. Nat. Comp. 2018. – Vol. 54, №3. – P. 439-442.
        62. Tolmachova K., Moroz Y., Konovets A., Platonov M., Vasylchenko O., Borysko P., Zozulya S., Gryniukova A., Bogolubsky A., Pipko S., Mykhailiuk P., Brovarets V., Grygorenko O. . (Chlorosulfonyl)benzenesulfonyl Fluorides—Versatile Building Blocks for Combinatorial Chemistry: Design, Synthesis and Evaluation of a Covalent Inhibitor Library. ACS Comb. Sci.- 2018. – Vol. 20, № 11. – P. 672-680.
        63. Adejuwon A.O., Tsygankova V.A., Alonge O.. Effect of cultivation conditions on activity of ?-amylase from a tropical strain Aspergillus Flavus Link. J. Microbiol. Biotechnol. Food Sci.- 2018. -Vol.7, № 6. – P. 571-575.
        64. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Shablykin O.V., Hurenko A.O., Solomyanny R.M., Mrug G.P., Frasinyuk M.S., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Auxin-like effect of derivatives of pyrimidine, pyrazole, isoflavones, pyridine, oxazolopyrimidine and oxazole on acceleration of vegetative growth of flax. Intern. J. Pharm. Tech. Res.- 2018. – Vol.11, № 3. – P. 274-286.
        65. Zuzana Krckova, Daniela Kocourkova, Michal Danek, J itka Brouzdova, Premysl Pejchar, Martin Janda, Igor Pokotylo, Peter G. Ott, Olga Valentova, Jan Martinec . The Arabidopsis thaliana non-specific phospholipase C2 is involved in the response to Pseudomonas syringae attack. Annals of Botany.- 2018.- 121.- Р. 297–310.
        66. Tsygankova V., Andrusevich Ya., Kopich V., Shtompel O., Pilyo S., Kornienko A.M, BrovaretsV. Use of Oxazole and Oxazolopyrimidine to Improve Oilseed Rape Growth, Scholars Bulletin, 2018; 4(3): 301 – 312. DOI: 10.21276/sb.2018.4.3.8.
        67. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S. Using of [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted of 1,3-oxazole to improve the growth of soybean seedlings. Chemistry Research Journal, 2018, 3(2):165-173.
        68. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S. Acceleration of vegetative growth of wheat (Triticum aestivum L.) using [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted 1,3-oxazole. The Pharmaceutical and Chemical Journal. 2018, 5(2), P.167-175.

        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
        8 . Kovalishyn V., Abramenko N., Kopernyk I., Charochkina L., Metelytsia L., Tetko I.V., Peijnenburg W.,Kustov L. Modelling the toxicity of a large set of metal and metal oxide nanoparticles using the OCHEM platform. // Food and Chemical Toxicology.- 2017. – 17. – S.0278-6915.doi: 10.1016/ j.fct.2017.08.008.
        9 . H.S Sayiner, A. A.S. Abdalrahm, M. A. Basaran, V. Kovalishyn, F. Kandemirli The Quantum Chemical and QSAR Studies on Acinetobacter Baumannii Oxphos Inhibitors. // Medicinal Chemistry.- 2017.-V.13, DOI : 10.2174/1573406413666171002124408
        10 . Абдурахманова Э.Р., Пильо C.Г., Кондратюк К.М., Головченко А.В., Броварец В.С. 1,3-Оксазол¬содер¬жащие про¬извод¬ные цитизина. // ЖОХ.- 2017.- Т.87, №2.- С.268-276.
        11 . Kolodiazhnyi O.I.,Kolodiazhna A.O. Nucleophilic substitution at phosphorus: stereochemistry and Mechanisms. // Tetrahedron: Asymmetry. 2017.- 28,N11; doi.org/10.1016/ j.tetasy.2017.10.02
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        24 . Anna N. Zinchenko, Lyubov V. Muzychka, Igor I. Biletskii, Oleg B. Smolii Synthesis of new 4-amino-substituted 7-iminopyrido[2,3-d]pyrimidines // Chem. Heterocycl. Comp.- 2017.- V.53, №5.- P. 589-596.
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        53 . Krchkova Z., Kotsurkova D., Danek M., Browzdova J., Peykhar P., Yanda M., Pokotilo I., Ot P., Valentyova O., Martynets Ya The Arabidopsis thaliana non-specifc phospholipase C2 is involved in the response to Pseudomonas syringae attack // Annals of Botany DOI: 10.1093/aob/mcx160
        54 . S.K. Kohli, N. Hunda, R. Sharna, H. Kaur, A.K. Thurkul, S. Avrora, V. Кravets, R. Bhardvaj Multigene engineering strategies for crop improvement // Chapter 4 in book: Mechanisms behind phytohormonal signalling and crop abiotic stress response. Р. 61-88.
        55 . Pud A.A., Fedorenko E.A., Vretik L.O., Ogurtsov N.A., Nikolayeva O.A., Kruglyak O.S., Noskov Yu.V. New nanocomposites of polystyrene with polyaniline doped with lauryl sulfuric acid // Nanoscale Research Letters.- 2017.- № 12, paper 493 (11 pages).
        56 . Dimitriev O.P., Grynko D.O., Fedoryak A.M., Doroshenko T.P., Kratzer M., Teichert C., Noskov Yu.V.,Ogurtsov N.A., Pud A.A., Balaz P., Balaz M., Tesinsky M. Macroscopic versus microscopic photovoltaic response of heterojunctions based on mechanochemically prepared nanopowders of kesterite and n-type semiconductors // Semiconductor Physics, Quantum Electronics & Optoelectronics.- 2017.- V. 20, N 4.- P. 418-423.
        57 . Hamouda Z., Wojkiewicz J-L., Pud A.A., Kone L., Bergheul S., Lasri T. A Flexible UWB Organic Antenna for Wearable Technologies Application // IET Microwaves Antennas & Propagation, accepted manuscript.- 2017, DOI: 10.1049/iet-map.2017.0189
        58 . Hamouda Z., Wojkiewicz J-L., Pud A.A., Kone L., Bergheul S., Lasri T. Design, fabrication and characterization of a new wideband antenna based on a Polyaniline/Carbon coated Cobalt composite // Proceedings of the 11th European Conference on Antennas and Propagation (EUCAP), 19-24 March 2017, Р. 2130-2133.DOI: 10.23919/EuCAP.2017.7928153
        59 . Wojkiewicz J.-L, Redon N., Pud A., Mikhaylov S., Ogurtsov N., Noskov Y., Collard C., Li W. Hybrid and Bio Nanocomposites for Ultrasensitive Ammonia Sensors // Proceedings.- 2017.- V.1, №4.- paper 407 (5 pages); DOI:10.3390/proceedings1040407
        60 . Mikhaylov S., Pud A., Wojkiewicz J.-L., Coddeville P. UV-light Induced Solid-phase Photodegradation in PANI Nanocomposites // Proceedings of Nanomaterials: Application & Properties.- 2017.- V. 6, 03NNSA09.
        61 . Myronyuk I., Pud A., Mamykin A., Kukla A. The Specificity of the Core-shell Polyvinylidene/Polyaniline Nanocomposite Sensing Applications // Proceedings of Nanomaterials : Application & Properties.- 2017.- V. 6, 03NNSA19.
        62 . L. Zheleznyi,G. Pop,O. Papeykin,I. Venger, L. Bodachivska Development of compositions of urea greases on aminoamides of fatty acids // Eastern-European Journal of Enterprise Technologies. – 2017, №3/6(87).– С. 9-15.
        63 . Iukhymenko V.V., Chernyak V.Ya.,Hamazin D.K.,Levko D.S.,Bortyshevskyy V.A.,Korzh R.V. Rotating Gliding Discharge Submerged in Liquid // Problems of Atomic Science and Technology. – 2017.-Р. 136-139.
        64 . Hamazin D.K.,Iukhymenko V.V., Chernyak V.Ya.,Prysiazhna O.V.,Martysh E.V.,Bortyshevskyy V.A., Korzh R.V. Properties of Secondary Discharge in Plasma-Liquid System Based on Rotating Gliding Discharge // Problems of Atomic Science and Technology. – 2017.-Р. 167-170.
        65 . Ocheretniuk A.D., Kobzar O.L., Mischenko I.M., Vovk A.I N-Phenacylthiazolium Salts as Inhibitors of Cholinesterases // French-Ukrainian Journal of Chemistry, 2017, Vol 5, №2.- P. 1-14.
        66 . Buldenko V.M., Kobzar O.L.,Trush V.V.,Drapailo A.B., Kalchenko V.I.,Vovk A.I Sulfonyl-bridged Calix[4]arene as an Inhibitor of Protein Tyrosine Phosphatases // French-Ukrainian Journal of Chemistry, 2017, Vol. 5, №2.- P. 144-151.

        2016 р.

        1. Hodyna D. Antibacterial activity of imidazolium-based ionic liquids investigated by QSAR modeling and experimental studies / D. Hodyna, V. Kovalishyn, S. Rogalsky[et al.] // Chem. Biol. Drug Des. — 2016. — 88, №3. — P. 422–433.
        2. Tanchuk V. Y. A new, improved hybrid scoring function for molecular docking and scoring based on autodock and autodock vina / V. Y. Tanchuk, V. O. Tanin, A. I. Vovk, G. Poda // Chem. Biol. Drug. Des. — 2016. — 87, №4. — P. 618–625.
        3. Hodyna D. Efficient antimicrobial activity and reduced toxicity of 1-dodecyl-3-methylimidazolium tetrafluoroborate ionic liquid/beta-cyclodextrin complex / D. Hodyna, J.-F. Bardeau, L. Metelytsia[et al.] // Chemical Engineering Journal. — 2016. — 284. — P. 1136–1145.
        4. Bondarenko S. P. A domino reaction for the synthesis of 2H-pyrano-[4″,3″,2″:4′,5′]chromeno[2′,3′:4,5]thieno-[2,3-b]pyridin-2-ones / S. P. Bondarenko, I. V. Zhitnetskyi, S. V. Semenov, M. S. Frasinyuk // Chem. Heterocycl Comp. — 2016. — 52, №4. — P. 262–266.
        5. Mrug G. P. Inverse electron demand diels–alder reactions with aminomethyl derivatives of 3-arylhydroxycoumarins / G. P. Mrug, K. M. Kondratyuk, S. P. Bondarenko, M. S. Frasinyuk // Chem. Heterocycl Comp. — 2016. — 52, №7. — P. 460–466.
        6. Popova A. V. Synthesis and properties of 2-benzylidene-8,9-dihydro-7H-furo[2,3-f][1,3]benzoxazin-3(2h)-one derivatives / A. V. Popova, S. P. Bondarenko, M. S. Frasinyuk // Chem Heterocycl Comp. — 2016. — 52, №8. — P. 592–600.
        7. Shablykin O. V. Interaction of 2-aryl-4-(dichloromethylidene)-1,3-oxazol-5(4H)-ones with methyl 2-isocyanoacetate / O. V. Shablykin, V. M. Prokopenko, V. S. Brovarets // Chem. Heterocycl Comp. — 2016. — 52, №6. — P. 424–426.
        8. Bondarenko S. P. New aloperine–isoflavone conjugates / S. P. Bondarenko, M. S. Frasinyuk, V. P. Khilya // Chem. Nat. Compd. — 2016. — 52, №4. — P. 615–619.
        9. Bondarenko S. P. New aloperine–isoflavone conjugates / S. P. Bondarenko, M. S. Frasinyuk, V. P. Khilya // Chem. Nat. Compd. — 2016. — 52, №4. — P. 615–619.
        10. Bondarenko S. P. Synthesis of 4-aryl-5-[2-hydroxy-4-(2-cytisin-12-ylethoxy)phenyl]isoxazoles / S. P. Bondarenko, M. S. Frasinyuk, V. I. Vinogradova, V. P. Khilya // Chem. Nat. Compd. — 2016. — 52, №3. — P. 463–467.
        11. Bondarenko S. P. Reductive amination as an aminomethylation method for isoflavone ring b / S. P. Bondarenko, I. V. Zhitnetskii, S. V. Semenov, M. S. Frasinyuk // Chem. Nat. Compd. — 2016. — 52, №5. — P. 802–806.
        12. Popova A. V. New heterocyclic pyrano[2′,3′:5,6]chromeno[3,2-c]pyridin-4-ones and furo[2′,3′:5,6]chromeno[3,2-c]pyridin-3(2H)-ones synthesized via a hetero-diels–alder reaction / A. V. Popova, G. P. Mrug, K. M. Kondratyuk[et al.] // Chem. Nat. Compd. — 2016. — 52, №6. — P. 1000–1004.
        13. Frasinyuk M. S. Antineoplastic isoflavonoids derived from intermediate ortho-quinone methides generated from mannich bases / M. S. Frasinyuk, G. P. Mrug, S. P. Bondarenko[et al.] // Chem. Med. Chem. — 2016. — 11, №6. — P. 600–611.
        14. Semenyuta I. 1,3-oxazole derivatives as potential anticancer agents: computer modeling and experimental study / I. Semenyuta, V. Kovalishyn, V. Tanchuk[et al.] // Comput. Biol. Chem. — 2016. — 65. — P. 8–15.
        15. Кazymyr І. Patrylak Coke alternate movement in faujasite based catalysts deactivated from butene alkylation / Кazymyr І. Patrylak, Lyubov К. Patrylak, Olexandra P. Pertko[et al.] // Current Catalysis. — 2016. — 5, №2. — P. 108–115.
        16. Hodyna D. Imidazolium ionic liquids as potential anti-candida inhibitors: QSAR modeling and experimental studies / D. Hodyna, V. Kovalishyn, S. Rogalsky[et al.] // Curr. Drug. Discov. Technol. — 2016. — 13, №2. — P. 109–119.
        17. Kalachova T. The inhibition of basal phosphoinositide-dependent phospholipase c activity in arabidopsis suspension cells by abscisic or salicylic acid acts as a signalling hub accounting for an important overlap in transcriptome remodelling induced by these hormones / T. Kalachova, R. Puga-Freitas, V. Kravets[et al.] // Environmental and Experimental Botany. — 2016. — 123. — P. 37–49.
        18. Haidai O. Improvement of performance characteristics of ethanol motor fuels through use of additives based on nanoscale carbon clusters / O. Haidai, V. Pilyavskiy, Y. Shelud’ko, Y. Polunkin // Current Catalysis. — 2016. — 0, №6. — P. 3–10.
        19. Khimach N. Recycling of carbone oxides (CO, CO2) conversion into methanol at atmospheric pressure over mechanochemical achtivated CuOo-ZnO-Al2O3 catalyst / N. Khimach, V. Yevdokymenko, I. Polunkin // Eureka: Physics and Engineering. — 2016. — 0, №6. — P. 11–18.
        20. Tsygankova V. Using of new microbial bio stimulants for obtaining in vitro new lines of Triticum aestivum L. cells resistant to nematode H. avenae. / V. Tsygankova, E. Shysha, Y. Andrusevich[et al.] // Eur. J. Biotechn. and Biosc. — 2016. — 4, №4. — P. 41–53.
        21. Chernykh A. V. Synthesis and physical-chemical properties of cis- and trans-1-amino-3-fluoro-3-methylcyclobutanecarboxylic acids / A. V. Chernykh, I. O. Feskov, A. V. Chernykh[et al.] // Eur. J. Org. Chem. — 2016. — 2016, №28. — P. 4782–4786.
        22. Fainleib A. Acceleration effect of ionic liquids on polycyclotrimerization of dicyanate esters / A. Fainleib, O. Grigoryeva, O. Starostenko[et al.] // eXPRESS Polymer Letters — 2016. — 10, №9. — P. 722–729.
        23. Tsygankova V. Study of growth regulating activity derivatives of [1,3]Oxazolo[5,4-d]pyrimidine and N-Sulfonyl substituted of 1,3-Oxazole on soybean, wheat, flax and pumpkin plants. / V. Tsygankova, Y. Andrusevich, O. Shtompel[et al.] // Int. J. Chem. Stud. — 2016. — 4, №5. — P. 106–120.
        24. L.O.Biliavska Application of new microbial plant resistance/plant growth protection inducers for increasing chinese cabbage plant tolerance against parasitic nematode heterodera schachtii schmidt / L.O.Biliavska, V.A.Tsygankova, V.E.Kozyritska[et al.] // Int. J. Res. Biosciences. — 2016. — V.5.- N2. – P. 64-82..
        25. Tsygankova V. Screening of five and six-membered nitrogen-containing heterocyclic compounds as new effective stimulants of linum usitatissimum l. organogenesis in vitro / V. Tsygankova, Bayer O. O, Andrusevich Ya. V. [et al.] // Intern. J. Med. Biotechnology Genetics. — 2016. — P. 1–9.
        26. Melnyk A. K. An EPR spin probe study of liposomes from sunflower and soybean phospholipids / A. K. Melnyk, O. V. Sukhoveev, L. A. Kononets[et al.] // J. Liposome Res — 2016. — 26, №1. — P. 80–86.
        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.
        28. Adetola O. Modification of silica gel by heteropolyacids / O. Adetola, L. Golovko, A. Vasiliev // Key Engineering Materials — 2016. — 689. — P. 126–132.
        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.
        30. Kolodiazhna A. O. Synthesis, properties and stereochemistry of 2-halo-1,2-lambda-5-oxaphosphetanes / A. O. Kolodiazhna, O. I. Kolodiazhnyi // Molecules — 2016. — 21, №10. — P. 1371–1392.
        31. Grynko D. A. Hybrid solar cell on a carbon fiber / D. A. Grynko, A. N. Fedoryak, P. S. Smertenko[et al.] // Nanoscale Res. Lett. — 2016. — 11, №1. — P. 265.
        32. Korzh R. Supercritical water as nanomedium for gasification of lignite-water suspension / R. Korzh, V. Bortyshevskyi // NanoScale Res. Lett. — 2016. — 11, №1. — P. 255–263.
        33. Belik M. Y. Resolution of fluorinated aminophosphonic acid enantiomers by precolumn derivatization with following reverse phase liquid chromatography / M. Y. Belik, O. Yegorov, A. E. Sorochinsky, V. P. Kukhar // Phosphorus, Sulfur, and Silicon — 2016. — 191, №3. — P. 423–429.
        34. Kolodiazhnyi O. I. Multiple stereoselectivity in organophosphorus chemistry / O. I. Kolodiazhnyi, A. O. Kolodiazhna // Phosphorus, Sulfur, and Silicon. — 2016. — 191, №3. — P. 444–458.
        35. Povolotskii M. I. Molecular and electronic structure of 1,3,2-diazaphosphinine derivatives / M. I. Povolotskii, O. V. Shablykin, E. B. Rusanov, A. B. Rozhenko // Phosporus, Sulfur, and Silicon. — 2016. — 191, №3. — P. 399–404.
        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.
        37. Kolesnikov Y. S. Molecular mechanisms of gravity perception and signal transduction in plants / Y. S. Kolesnikov, S. V. Kretynin, I. D. Volotovsky[et al.] // Protoplasma. — 2016. — 253, №4. — P. 987–1004.
        38. Chen G. Development of nanostructure–activity relationships assisting the nanomaterial hazard categorization for risk assessment and regulatory decision-making / G. Chen, W. J. G. M. Peijnenburg, V. Kovalishyn, M. G. Vijver // RSC Adv. — 2016. — 6, №57. — P. 52227–52235.
        44. Noskov Y. Acid-dopant effects in the formation and properties of polycarbonate-polyaniline composites / Y. Noskov, S. Mikhaylov, P. Coddeville[et al.] // Synthetic Metals. — 2016. — 217. — P. 266–275.
        45. Kucher O. V. Lipase kinetic enantiomeric resolution of 1-heteroarylethanols / O. V. Kucher, A. O. Kolodyazhnaya, O. B. Smolii[et al.] // Tetrahedron: Asymmetry. — 2016. — 27, №7–8. — P. 341–345.
        46. Ogurtsov N. A. Influence of dispersed nanoparticles on the kinetics of formation and molecular mass of polyaniline / N. A. Ogurtsov, S. D. Mikhaylov, P. Coddeville[et al.] // J. Phys. Chem. B. — 2016. — 120, №38. — P. 10106–10113.
        47. Ogurtsov N. A. Evolution and interdependence of structure and properties of nanocomposites of multiwall carbon nanotubes with polyaniline / N. A. Ogurtsov, Y. V. Noskov, V. N. Bliznyuk[et al.] // J. Phys. Chem. C. — 2016. — 120, №1. — P. 230–242.
        48. Korzh R. Primary reactions of lignite-water slurry gasification under the supercritical conditions / R. Korzh, V. Bortyshevskyi // J. Supercritical Fluids. — 2016. — 117. — P. 64–71.
        49. Kolodiazhnyi O. I. Wiley: asymmetric synthesis in organophosphorus chemistry: synthetic methods, catalysis and applications / O. I. Kolodiazhnyi. — 2016.
        50. Mikhaylov S. The PANI-DBSA content and dispersing solvent as influencing parameters in sensing performances of TiO 2/PANI-DBSA hybrid nanocomposites to ammonia / S. Mikhaylov, N. A. Ogurtsov, N. Redon[et al.] // RSC Adv. — 2016. — 6, №86. — P. 82625–82634.
        51. Tsygankova V. Study of auxin, cytokinin and gibberellin-like activity of heterocyclic compounds derivatives of pyrimidine, pyridine, pyrazole and isoflavones / V. Tsygankova, Y. Andrusevich, O. Shtompel[et al.] // 2016. — 4, №12. — P. 29–44.
        52. Tsygankova V. A. Stimulating effect of five and six-membered heterocyclic compounds on seed germination and vegetative growth of maize (Zea mays L.) / V. A. Tsygankova, Y. Andrusevich, O. Shtompel[et al.] // 2016. — 1, №4. — P. 1–14.

        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.
        3. Chernykh A. V. Synthesis and physicochemical properties of 3-fluorocyclobutylamines / A. V. Chernykh, D. S. Radchenko, A. V. Chernykh[et al.] // Eur. J. Org. Chem. — 2015. — 2015, №29. — P. 6466–6471.
        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.
        13. Kobzar O. L. Phosphonate derivatives of tetraazamacrocycles as new inhibitors of protein tyrosine phosphatases / O. L. Kobzar, M. V. Shevchuk, A. N. Lyashenko[et al.] // Org. Biomol. Chem. — 2015. — 13, №27. — P. 7437–7444.
        14. Kobzar O. L. Polycarboxylic fullerene derivatives as protein tyrosine phosphatase inhibitors / O. L. Kobzar, V. V. Trush, V. Y. Tanchuk[et al.] // Mendeleev Comm. — 2015. — 25, №3. — P. 199–201.
        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.
        21. Kovalishyn V. Efficient variable selection batch pruning algorithm for artificial neural networks / V. Kovalishyn, G. Poda // Chemometrics and Intelligent Lab. Sys. — 2015. — 149, Part B. — P. 10–16.
        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.
        28. Ruelland E. Role of phospholipid signalling in plant environmental responses / E. Ruelland, V. Kravets, M. Derevyanchuk[et al.] // Environmental and Experimental Botany. — 2015. — 114. — P. 129–143.
        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.
        30. Tarasevych A. V. High temperature sublimation of alpha-amino acids: a realistic prebiotic process leading to large enantiomeric excess / A. V. Tarasevych, A. E. Sorochinsky, V. P. Kukhar, J.-C. Guillemin // Chem. Commun. — 2015. — 51, №32. — P. 7054–7057.
        31. Tarasevych A. V. Attrition-induced spontaneous chiral amplification of the gamma polymorphic modification of glycine / A. V. Tarasevych, A. E. Sorochinsky, V. P. Kukhar[et al.] // Cryst. Eng. Comm. — 2015. — 17, №7. — P. 1513–1517.
        32. Trush V. V. Phosphonate monoesters on a thiacalix[4]arene framework as potential inhibitors of protein tyrosine phosphatase 1B / V. V. Trush, S. G. Kharchenko, V. Y. Tanchuk[et al.] // Org. Biomol. Chem. — 2015. — 13, №33. — P. 8803–8806.
        33. Tsygankova V. Genetic control and phytohormonal regulation of plant embryogenesis / V. Tsygankova // Int. J. Medical Biotechnology Genetics (I)MBG — 2015. — P. 9–20.
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        35. Zahanich I. Phenoxymethyl 1,3-oxazoles and 1,2,4-oxadiazoles as potent and selective agonists of free fatty acid receptor 1 (GPR40) / I. Zahanich, I. Kondratov, V. Naumchyk[et al.] // Bioorg. Med. Chem. Lett. — 2015. — 25, №16. — P. 3105–3111.
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        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.
        13. Kaminskyy D. Isothiocoumarin-3-carboxylic acid derivatives: synthesis, anticancer and antitrypanosomal activity evaluation / D. Kaminskyy, A. Kryshchyshyn, I. Nektegayev[et al.] // Eur. J. Med. Chem. – 2014. – 75. – P. 57-66.
        14. Kobelev S. M. Macrobicyclic and macrotricyclic derivatives of N,N’,N”,N”’-tetrasubstituted cyclen and cyclam / S. M. Kobelev, A. D. Averin, A. K. Buryak[et al.] // Heterocycles – 2014. – 90, №2. – P. 989-1017.
        15. Kobzar O. L. Fullerene derivatives as a new class of inhibitors of protein tyrosine phosphatases / O. L. Kobzar, V. V. Trush, V. Y. Tanchuk[et al.] // Bioorg. Med. Chem. Lett. – 2014. – 24, №14. – P. 3175-3179.
        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.
        17. Kolodiazhnyi O. I. Advances in asymmetric hydrogenation and hydride reduction of organophosphorus compounds / O. I. Kolodiazhnyi // Phosphorus, Sulfur, and Silicon – 2014. – 189, №7-8. – P. 1102-1131.
        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.
        27. Kovalishyn V. Qsar studies, design, synthesis and antimicrobial evaluation of azole derivatives / V. Kovalishyn, I. Kopernyk, S. Chumachenko[et al.] // Computational Biology and Bioinformatics. – 2014. – 2, №2. – P. 25.
        28. Kovalishyn V. Prediction of thrombin and factor XA inhibitory activity with associative neural networks / V. Kovalishyn, V. Tanchuk, I. Kopernyk[et al.] // Curr Comput Aided Drug Des. – 2014. – 10, №3. – P. 259-265.
        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.
        31. Kukharenko O. Promising low cost antimicrobial composite material based on bacterial cellulose and polyhexamethylene guanidine hydrochloride / O. Kukharenko, J.-F. Bardeau, I. Zaets[et al.] // European Polymer Journal. – 2014. – 60. – P. 247-254.
        32. Lioshina L. G. Plant regeneration from hairy roots and calluses of periwinkle vinca minor l. and foxglove purple digitalis purpurea l. / L. G. Lioshina, O. V. Bulko // Cytol. Genet. – 2014. – 48, №5. – P. 302-307.
        33. Maestro M. A. Chiral N(H)-tbu and N(H)-ad NiII complexes of glycine schiff bases: deduction of a mode of kinetic diastereoselectivity / M. A. Maestro, F. Avecilla, A. E. Sorochinsky[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №20. – P. 4309-4314.
        34. Martins F. Design, synthesis and biological evaluation of novel isoniazid derivatives with potent antitubercular activity / F. Martins, S. Santos, C. Ventura[et al.] // Eur. J. Med. Chem – 2014. – 81. – P. 119-138.
        35. Pokholenko I. O. Development and characterization of porous functionalized collagen scaffolds for delivery of fgf-2 / I. O. Pokholenko, M. D. Chetyrkina, L. V. Dubey[et al.] // Biopolym. Cell. – 2014. – 30, №3. – P. 216-222.
        36. Pokotylo I. Plant phosphoinositide-dependent phospholipases c: variations around a canonical theme / I. Pokotylo, Y. Kolesnikov, V. Kravets[et al.] // Biochimie. – 2014. – 96. – P. 144-157.
        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.
        38. Prokopenko V. Design and synthesis of new potent inhibitors of farnesyl pyrophosphate synthase / V. Prokopenko, V. Kovalishyn, M. Shevchuk[et al.] // Curr Drug Discov Technol. – 2014. – 11, №2. – P. 133-144.
        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.
        40. Rogalsky S. P. Antimicrobial polycarbonates for biomedical applications / S. P. Rogalsky, O. V. Moshynets, L. G. Lyoshina, O. P. Tarasyuk // EPMA J. – 2014. – 5, №Suppl 1. – P. A133.
        41. Shaitanova E. N. Synthesis of enantiomerically pure 4-polyfluoromethyl-4-hydroxy-homoprolines by intramolecular cyclization of 6-amino-5-polyfluoromethyl-hex-2-enoic acids / E. N. Shaitanova, I. I. Gerus, V. P. Kukhar, G. Haufe // J. Fluorine Chem. – 2014. – 160. – P. 8-11.
        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.
        43. Shishkina S. V. Crystal structure of (S)-1-(1,3-benzo­thia­zol-2-yl)-2,2,2-tri­fluoro­ethanol / S. V. Shishkina, O. V. Kucher, A. O. Kolodiazhnaya[et al.] // Acta Cryst E. – 2014. – 70, №9. – P. o946-o946.
        44. Tsygankova V. A. Impact of new microbial PR/PGP inducers on increase of resistance to parasitic nematode of wild and rnai transgenic rape plants / V. A. Tsygankova, L. O. Biliavska, Y. V. Andrusevich[et al.] // Adv. Biosc. Bioeng. 2014. – 2, №1.
        45. Vasylyshyn R. Y. Efficient synthesis of 1,3,5-benzotriazocines from tetrachloro-2-aza-1,3-dienes / R. Y. Vasylyshyn, B. A. Demydchuk, E. B. Rusanov, V. S. Brovarets // Synthetic Commun. – 2014. – 44, №5. – P. 714-719.
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        48. Zelisko N. Crotonic, cynnamic, and propiolic acids motifs in the synthesis of thiopyrano[2,3-d][1,3]thiazoles via hetero-diels-alder reaction and related tandem processes / N. Zelisko, D. Atamanyuk, O. Vasylenko[et al.] // Tetrahedron. – 2014. – 3, №70. – P. 720-729.

        2013 р.

        1. Acena J. L. Unconventional preparation of racemic crystals of isopropyl 3,3,3-trifluoro-2-hydroxypropanoate and their unusual crystallographic structure: the ultimate preference for homochiral intermolecular interactions / J. L. Acena, A. E. Sorochinsky, T. Katagiri, V. A. Soloshonok // Chem. Commun. — 2013. — 49, №4. — P. 373–375.
        2. Acena J. L. Synthesis of fluorine-containing alpha-amino acids in enantiomerically pure form via homologation of Ni(II) complexes of glycine and alanine schiff bases / J. L. Acena, A. E. Sorochinsky, H. Moriwaki[et al.] // Journal of Fluorine Chemistry. — 2013. — 155. — P. 21–38.
        3. Bondarenko S. P. Synthesis of aminomethyl derivatives of chrysin / S. P. Bondarenko, M. S. Frasinyuk // Chem. Nat. Compd. — 2013. — 49, №5. — P. 841–844.
        4. Bondarenko S. P. Synthesis of 4-aryl-5-[2-hydroxy-4-beta-(N,N-dialkylamino) ethoxyphenyl]isoxazoles / S. P. Bondarenko, O. N. Miroshnikov, M. S. Frasinyuk, V. P. Khilya // Chem. Nat. Compd. — 2013. — 49, №5. — P. 826–829.
        5. Bugera M. Y. Synthesis and properties of alpha-bromomethyl-substituted beta-ethoxyvinyl polyfluoroalkyl ketones / M. Y. Bugera, K. V. Tarasenko, V. P. Kukhar[et al.] // Synthesis. — 2013. — 45, №22. — P. 3157–3163.
        6. Chumachenko S. A. Application of the recyclization products of 5-alkyl(aryl)amino-2-(3-phthalimidopropyl)-1,3-oxazole-4-carbonitriles to the synthesis of condensed tricyclic nitrogenous structures / S. A. Chumachenko, O. V. Shablykin, V. S. Brovarets // Chem Heterocycl Comp. — 2013. — 48, №12. — P. 1832–1838.
        8. Grynko D. O. Application of a cds nanostructured layer in inverted solar cells / D. O. Grynko, O. M. Fedoryak, P. S. Smertenko[et al.] // J. Phys. D: Appl. Phys. — 2013. — 46, №49. — P. 495114.
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        11. Jayaratna N. B. Silver(I) and copper(I) adducts of a tris(pyrazolyl)borate decorated with nine trifluoromethyl groups / N. B. Jayaratna, I. I. Gerus, R. V. Mironets[et al.] // Inorg. Chem. — 2013. — 52, №4. — P. 1691–1693.
        12. Kachkovskyi G. Visible light-mediated synthesis of (spiro)anellated furans / G. Kachkovskyi, C. Faderl, O. Reiser // Adv. Synth. Catal. — 2013. — 355, №11–12. — P. 2240–2248.
        13. Kalachova T. Involvement of phospholipase d and nadph-oxidase in salicylic acid signaling cascade / T. Kalachova, O. Iakovenko, S. Kretinin, V. Kravets // Plant Physiol. Biochem. — 2013. — 66. — P. 127–133.
        14. Kalchenko V. I. Calixarene phosphonous acids: synthesis and biological activity / V. I. Kalchenko, S. O. Cherenok, S. O. Kosterin[et al.] // Phosphorus, Sulfur, and Silicon — 2013. — 188, №1–3. — P. 232–237.
        15. Khoroshilov G. E. Simple stepwise route to 1-substituted 2-amino-3-ethoxycarbonylindolizines / G. E. Khoroshilov, N. M. Tverdokhleb, V. S. Brovarets, E. V. Babaev // Tetrahedron. — 2013. — 69, №21. — P. 4353–4357.
        16. Khutova B. M. Reaction of 7-phenyl-7H-pyrazolo-[3,4-d][1,2,3]triazin-4-ol with thionyl chloride / B. M. Khutova, S. V. Klyuchko, A. O. Gurenko[et al.] // Chem. Heterocycl. Comp. — 2013. — 49, №6. — P. 922–929.
        17. Kolodiazhna O. O. Enzymatic preparation of (1S,2R)- and (1R,2S)-stereoisomers of 2-halocycloalkanols / O. O. Kolodiazhna, A. O. Kolodiazhna, O. I. Kolodiazhnyi // Tetrahedron: Asymmetry. — 2013. — 24, №1. — P. 37–42.
        19. Kondratyuk K. M. Synthesis of 5-amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonic acid derivatives and their use in the preparation of phosphorylated peptidomimetics / K. M. Kondratyuk, O. I. Lukashuk, A. V. Golovchenko[et al.] // Tetrahedron. — 2013. — 69, №30. — P. 6251–6261.
        22. Lukashuk O. I. A novel synthetic approach to phosphorylated peptidomimetics / O. I. Lukashuk, K. M. Kondratyuk, A. V. Golovchenko[et al.] // Heteroatom Chem. — 2013. — 24, №4. — P. 289–297.
        23. Lyutenko N. V. Aza-annulation of beta-aminovinyl trifluoromethyl ketones with acryloyl chloride: an efficient synthesis of 5-(trifluoroacetyl)-3,4-dihydro-2(1H)-pyridinones / N. V. Lyutenko, I. I. Gerus // Tetrahedron Letters. — 2013. — 54, №31. — P. 4091–4093.
        24. Mrug G. P. Synthesis and aminomethylation of 7-hydroxy-5-methoxyisoflavones / G. P. Mrug, S. P. Bondarenko, V. P. Khilya, M. S. Frasinyuk // Chem. Nat. Compd. — 2013. — 49, №2. — P. 235–241.
        25. Ogurtsov N. A. Deep impact of the template on molecular weight, structure, and oxidation state of the formed polyaniline / N. A. Ogurtsov, Y. V. Noskov, K. Y. Fatyeyeva[et al.] // J. Phys. Chem. B. — 2013. — 117, №17. — P. 5306–5314.
        26. Pokotylo I. The plant non-specific phospholipase c gene family. novel competitors in lipid signalling / I. Pokotylo, P. Pejchar, M. Potocky[et al.] // Progress in Lipid Research. — 2013. — 52, №1. — P. 62–79.
        27. Ratieuville V. New polyimide based composite films for fuel cells: study of the porous structure / V. Ratieuville, K. Fatyeyeva, C. Chappey[et al.] // Advanced Materials Research. — 2013. — 747. — P. 477–480.
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        29. Shablykina O. V. Synthesis of 3-hetaryl-1H-isochromen-1-ones based on 3-(2-bromoacetyl)-1H-isochromen-1-one / O. V. Shablykina, O. V. Shablykin, V. V. Ishchenko[et al.] // Chem Heterocycl Comp. — 2013. — 48, №11. — P. 1621–1627.
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        32. Sorochinsky A. E. Self-disproportionation of enantiomers of chiral, non-racemic fluoroorganic compounds: role of fluorine as enabling element / A. E. Sorochinsky, J. L. Acena, V. A. Soloshonok // Synthesis — 2013. — 45, №02. — P. 141–152.
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        35. Stepaniuk O. O. Synthesis of new pyrazolo[1,5-a]pyrimidines by reaction of beta,gamma-unsaturated gamma-alkoxy-alpha-keto esters with n-unsubstituted 5-aminopyrazoles / O. O. Stepaniuk, V. O. Matviienko, I. S. Kondratov[et al.] // Synthesis — 2013. — 45, №07. — P. 925–930.
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        40. Vdovenko S. C–H…F hydrogen bond and integral intensities of vinyl C–H vibtations in push-pull beta-dimethylaminotrifluoromethyl ketone and its deuterated analog / S. Vdovenko, I. Gerus, E. Fedorenko, V. Kukhar // ISRN Spectroscopy — 2013. — 2013. — P. e640896.
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