International publications

2024 р.

   Monographs

1. The Monograph “Research Perspectives of Microbiology and Biotechnology Vol.2” / Ed. Dr. Tsygankova Victoria Anatolyivna. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. 2024. 175 p. ISBN 978-81-972325-7-2 (Print) ISBN 978-81-972325-0-3 (eBook).  DOI: 10.9734/bpi/rpmab/v2.

2. The Monograph “Recent Developments in Chemistry and Biochemistry Research Vol. 8” / Ed. Dr. Tsygankova Victoria Anatolyivna. Book Publisher International. SCIENCEDOMAIN international Ltd. India.United Kingdom. 2024. 177 p. ISBN 978-93-48388-53-7 (Print), ISBN 978-93-48388-10-0 (eBook).  DOI:  https://doi.org/10.9734/bpi/rdcbr/v8.

Статті, опубліковані у міжнародних та вітчизняних фахових журналах, які індексовані в міжнародних наукометричних базах (Web of Science, Scopus, Google Scholar тощо)

1. 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). 24:9(1):1-14. https://doi.org/10.1186/s12896-024-00834-9 (Web of Sciences and Scopus, Q 2; IF 3.5) https://bmcbiotechnol.biomedcentral.com/articles/10.1186/s12896-024-00834-9.

2. 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. Vol. 1, No 71. P. 6 – 13. DOI: 10.5281/zenodo.10675232. (SJIF 5.943).

3. 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. Vol. 8, Issue 1. P. 15 – 24. DOI: https://dx.doi.org/10.29328/journal.jpsp.1001126

4. 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

5. 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. Vol. 8: 1-7. DOI: https://doi.org/10.25081/jmb.2024.v8.8918.

https://updatepublishing.com/journal/index.php/jmb

6. 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. 8(2): 090-099. DOI: https://dx.doi.org/10.29328/journal.jpsp.1001139.

7. 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. No 140. P. 3-12.DOI: 10.5281/zenodo.12720609.

8. 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. No 146. P. 8 – 18.  DOI: 10.5281/zenodo.13267799.   https://doi.org/10.5281/zenodo.13267799.

9. 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. No 94. P. 22 – 26.  DOI:.  https://doi.org/10.5281/zenodo.13860706

10. Azizov I.V., Tsygankova V.A. The basic theoretical principles of improving the environmental situation on planet Earth. Brief opinion. Sciences of Europe. 2024. No. 151. P. 20 – 23.  DOI: 10.5281/zenodo.13998958.  https://doi.org/10.5281/zenodo.13998958

11. Buziashvili А.Yu., Biliavska L.О., Tsygankova V.А., Iutynska G.O.,  Yemets А.І. Investigation of the influence of avermectin-containing preparations on the resistance of tomato lines to fusarium blight in vitro.  Faktori eksperimental noi evolucii organizmiv. 2023. 32: 74-79. DOI:  10.7124/FEEO.v32.1539 https://doi.org/10.7124/FEEO.v32.1539.

2023 р.

Розділи в зарубіжних монографіях

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

Публікації в зарубіжних виданнях

9. A.O. Kolodiazhna,O.I. Kolodiazhnyi. Chiral Organophosphorus drugs. Symmetry. 2023. V.15, N. 8. Р.1550. https://doi.org/10.3390/sym15081550
10. D. Kamenskyh, T. Tkachenko, L. Tecer, Y. Sheludko, V. Povazhny, M. Jafarov, V. Yevdokymenko. Influence of ratio of silicon complex and coagulant on silicon dioxide physicochemical characteristics. Applied Nanoscience. 2023. V. 13, N 10. P. 6967-6999. https://doi.org/10.1007/s13204-023-02841-2
11. M. Aksylenko, E. Sheludko, V. Yevdokymenko, O. Haidai, N. Khimach. Biostimulating Effect of Polygalacturonates of Biogenic Metals on Growing Winter Wheat. Cutting Edge Research in Biology. 2023. V. 6, N 11., Ch. 1. P. 1-24, https://doi.org/10.9734/bpi/cerb/v6/5047B
12. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Model Desublimation Conditions. Asian Journal of Chemical Sciences. 2023. V. 13, N 2. P. 1-6.https://doi.org/10.9734/AJOCS/2023/v13i2234
13. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Chemical Science International Journal. 2023. V. 32, N 3. P. 62-68. https://doi.org/10.9734/CSJI/2023/v32i3849
14. K. Hutsul, I. Ivanenko, L. Patrylak, O. Pertko, D. Kamenskyh. ZnO/Zeolite composite photocatalyst for dyes degradation. Applied Nanoscience. 2023. Р. 1-9. https://doi.org/10.1007/s13204-023-02950-y
15. M.A. Jafarov, V.O. Yevdokymenko, D.S. Kamenskyh, K.A. Rustamov, Z.A. Jafarov. Mathematical Modeling of Hexafluorsilicate Ammonia Desublimation. Evolutions Mech Eng. 2023. V. 4, N 4. EME.000595.2023. https://doi.org/10.31031/EME.2023.04.000595
16. Vretik L.O., Noskov Yu.V., Chepurna O.M., Ogurtsov N.A., O.A. Nikolaeva, O.A. Marynin, A.I. Ohulchanskyy, A.A. Pud . Dual Stimuli-Responsive Ternary Core-Shell Polystyrene@Pnipam-Pedot Latexes. Particle & Particle Systems Characterization. 2023. Р. 2300096. https://doi.org/10.1002/ppsc.202300096
17. Petrychuk M.V., Oliynyk V.V., Zagorodnii V.V.,Ogurtsov N.A., Pud A.A.. PVDF/poly(3-methylthiophene)/MWCNT nanocomposites for EMI shielding in the microwave range. Heliyon.2023. V. 9, N 12. Р. e23101
18. Z.I. Kazantseva, I.A. Koshets, A.V. Mamykin, A.S. Pavluchenko, O.L. Kukla, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, R.V. Rodik, S.G. Vyshnevskyy. Detection of the explosive nitroaromatic compound simulants with chemosensory systems based on quartz crystal microbalance and chemiresistive sensor arrays. Semiconductor Physics, Quantum Electronics & Optoelectronics. 2023. V. 26, N.3. Р. 332-342
19. N. Redon, N. Davydenko, N. Ogurtsov, M. Jamar, Yu. Noskov, A. Pud, J.-L. Wojkiewicz. PPy & P3MT-MWCNT Nanocomposites-Based Sensors for Nerve Gas Detection at ppb Levels. 2023 IEEE SENSORS proceedings, 2023, Vienna, Austria. Р. 1-4.DOI: 10.1109/SENSORS56945.2023.10325230
20. I.P. Matushko, Yu.V. Noskov,V.A. Moiseienko,V.Y. Malyshev,L.M. Grishchenko. Electromagnetic Microwave Absorption Performances of PVC/AC Composites. Materials Proceedings. 2023. V. 14, N.1. Р. 15.https://doi.org/10.3390/IOCN2023-14537
21. D.О. Zhytnyk, I.P. Matushko, Yu.V. Noskov, V.A. Moiseienko, V.Yu. Malyshev, O.О. Barsukov, N.A. Atamas, L.M. Grishchenko. Microwave properties of composite materials based on PVC and oxidized activated carbon. Proceedings of the III International Scientific and Practical Conference “Science in the environment of rapid changes”, 2023, Brussels, Belgium. P. 237-244.
22. Kobzar O.L.,Tatarchuk, A.V.,Mrug G.P.,Bondarenko S.P., Demydchuk B.A., Frasinyuk M.S.,Vovk A.I.. Carboxylated chalcones and related flavonoids as inhibitors of xanthine oxidase. Medicinal Chemistry Research. 2023. V. 32, N 8. Р. 1804-1815
23. Velihina Y.,Gesese R.,Zhirnov V.,Kobzar O.,Bui B.,Pilyo S.,Vovk A.,Shen H.Brovarets V.. Design, synthesis and evaluation of the anti-breast cancer activity of 1,3-oxazolo[4, 5-d] pyrimidine and 1, 3-oxazolo[5, 4-d] pyrimidine derivatives. RSC Medicinal Chemistry. 2023. V. 14, N 4.Р. 692-699
24. Kovalishyn V.,Severin O.,Kachaeva M.,Kobzar O.,Keith K.A.,Harden E.A.,Hartline C.B.,James S.H.,Vovk A.,Brovarets V.. In Silico Design and Experimental Validation of Novel Oxazole Derivatives Against Varicella zoster virus. Molecular Biotechnology. 2023. Р. 1-11
25. Los O.V.,Sinenko V.O.,Kobzar O.L.,Zhirnov V.V.,Vovk A.I.,Brovarets V.S.. Synthesis and in vitro anticancer potential of new thiazole-containing derivatives of rhodanine. Chemistry of Heterocyclic Compounds. 2023. V. 59, N 6-7. Р. 484-493
26. Zhirnov V.,Shablykin O., Chumachenko S.,Kornii Y.,Keith K. A.,Harden E. A.,Hartline C.B.,James S.H.,Kobzar O.,Kovalishyn V.,Vovk A.Brovarets V.. In vitro activity of novel 4-iminohydantoin sulfamide derivatives against human cytomegalovirus. Chemical Papers. 2023. Р. 1-8
27. Hodyna D.,Kovalishyn V., Kachaeva M.,Shulha Y.,Klipkov A.,Shaitanova E.,Kobzar O.,Shablykin O.,Metelytsia L.. In Silico, In Vitro and In Vivo Study of Substituted Imidazolidinone Sulfonamides as Antibacterial Agents. Chemistry & Biodiversity. 2023. Р. e202301267
28. Derevyanchuk M.Kretynin S., Bukhonska Y., Pokotylo I., Khripach V., Ruelland E., Filepova R., Dobrev P.I., Martinec, J., Kravets V.. Influence of Exogenous 24-Epicasterone on the Hormonal Status of Soybean. Plants. 2023. V.12. N 20. Р. 3586
29. Kretynin S.V., Kolesnikov Y.S.. The role of calcium in implementation of the effect of brassinosteroids during the induction of oxidative stress in tobacco. Cytology and Genetics. 2023. V. 57. Р. 312-319
30. Rogalsky S., Tarasyuk O., Vashchuk A., Dzhuzha O., Cherniavska T., Makhno S.. Thermophysical properties and ionic conductivity of new imidazolium based protic ionic liquids. Journal of Molecular Liquids. 2023. V. 382. Р. 121942
31. Lishchuk P., Vashchuk A., Rogalsky S., Chepela L., Borovyi M., Lacroix D., Isaiev M.. Thermal transport properties of porous silicon filled by ionic liquid nanocomposite system. Scientific Reports. 2023. V.13. Р. 5889
32. Rogalsky S., Tarasyuk O., Babkina N., Makhno S., Pertko O., Povazhnyi V., Cherniavska T., Fatyeyeva K.. Fabrication of new proton conducting membrane for fuel cell applications based on porous polyimide Matrimid® and hydrophobic protic ionic liquid. Journal of Applied Polymer Science. 2023. V. 140, N 15. Р. e53731
33. Talaniuk V., Godzierz M., Vashchuk A., Iurhenko M., Chaber P., Sikorska W., Kobyliukh A., Demchenko V., Rogalsky S., Szeluga U., Adamus G.. Development of Polyhydroxybutyrate – Based Packaging Films and Methods to Their Ultrasonic. Materials. 2023. V.16, N 20. Р. 6617
34. Rogalsky S., Hodyna D., Semenyuta I., Frasinyuk M., Tarasyuk O., Riabov S., Kobrina L., Tetko I., Metelytsia L.. Antibacterial activity of 1-dodecylpyridinium tetrafluoroborate and its inclusion complex with sulfobutyl ether-b-cyclodextrin against MDR Acinetobacter baumannii strains. Innovative Biosystems and Bioengineering. 2023. V.7, N 4.Р. 25-35
35. Vortman M.Ya., Berezhnytska O.S., Aksenovska O.A., Kobylinskyi S.M., Kobrina L.V., Lemeshko V.N., Shevchenko V.V.. Guanidinium-containing oligoether as a complexing agent of transition metal ions. Functional Materials. 2023. V.30, N 1. Р. 120-127
36. Patrylak L.,Konovalov S.,Yakovenko A.,Pertko O.,Povazhnyi V.. Polycationic Nanostructured Faujasite Zeolite Catalysts for Glucose Transformation into 5-Hydroxymethylfurfural. Applied Nanoscience. 2023,V. 13. Р. 5743–5754https://doi.org/10.1007/s13204-023-02820-7
37. Shvets O.V.,Kurmach M.M., Yaremov P.S., Voloshyna Yu.G., Shcherban N.D.. Zeolite nanocomposites with variable acid and basic properties: effective catalysts for fine chemical synthesis and industrial reaction. Applied Nanoscience. 2023. https://doi.org/10.1007/s13204-023-02955-7
38. Muzychka L.,Boiko I.,Vrynchanu N., Smolii O.. Synthesis, antibacterial, and antibiofilm activities of pulmonarin B analogues. Curr. Chem. Lett. 2024. V. 24. doi:10.5267/j.ccl.2023.11.005
39. I. Semenyuta, D. Hodyna, V. Kovalishyn, B. Demydchuk, M. Kachaeva,S. Pilyo, V. Brovarets, L. Metelytsia. Development and application of in silico models to design new antibacterial5-amino-4-cyano-1,3-oxazoles against colistin-resistant E. coli strains. Artificial Intelligence Chemistry. 2023. V. 1, N 2. Р. 100024.https://doi.org/10.1016/j.aichem.2023.100024
40. D. Hodyna, V. Kovalishyn, Y. Romanenko, I. Semenyuta,V. Blagodatny, M. Kachaeva, O. Brazhko L. Metelytsia. Quinoline Hydrazone Derivatives as New Antibacterialsagainst Multidrug Resistant Strains. Chem. Biodiversity 2023. V. 20, N 10. Р. e202300839doi.org/10.1002/cbdv.2023008
41. D. Hodyna,V. Kovalishyn,I. Semenyuta,M. Kachaeva,Y. Shulha,M. Bugera, V. Blagodatny, O. Shablykin,L. Metelytsia. Design and Biological Evaluation of 4-Iminohydantoin Sulfamides as New Anti-Acinetobacter baumannii Agents. Biointerface Res. Appl. Chem. 2023. V. 13, N 6. P. 511-524.DOI: https://doi.org/1.33263/BRIAC136.511
42. G. Mrug,D. Hodyna,L. Metelytsia,V. Kovalishyn,O. Trokhimenko, S. Bondarenko,K. Kondratyuk,A. Kozitskiy, M. Frasinyuk. Structure-Activity Relationship Prediction-Based Synthesis and Cytotoxicity Evaluation against the HEp-2 Laryngeal Carcinoma Cell of Isoflavone–Cytisine Mannich Bases. Chemistry & Biodiversity. 2023. V. 20, N 8. Р. e202300560.https://doi.org/10.1002/cbdv.202300560
43. Pilyo S.G., Demydchuk B.A., Moskvina V.S., Shablykina O.V., Brovarets V.S.. A combinatorial library of substituted 3-sulfonyl-2-imino-1,2-dihydro-5H-dipyrido[1,2-a:2′,3′-d]pyrimidin-5-ones and their anticancer activities. Biopolym. Cell. 2022. V. 38, N 4. Р. 242-256. http://dx.doi.org/10.7124/bc.000A7B
44. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M.. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension. Adv. Pharm. Bull. 2023. V.13, N 2. С. 399-407. https://doi.org/10.34172/apb.2023.044
45. Zyabrev V., Demydchuk B., Zhirnov V., Brovarets V.. Synthesis, characterization, and in vitro anticancer evaluation of 2-aryl-4-arylsulfonyl-5-RS-1,3-oxazoles. Biointerface Res. Appl. Chem. 2023. V.13, N 3. P. 300. DOI: 10.33263/BRIAC133.300
46. Kovalishyn V., Severin O., Kachaeva M., Semenyuta I., Keith K.A., Harden E.A., Hartline C.B., James S.H., Metelytsia L., Brovarets V.. Design and experimental validation of the oxazole and thiazole derivatives as potential antivirals against of human cytomegalovirus. SAR and QSAR in Environmental Res. 2023. V.34, N 7. P. 523-541
47. Bondar D., Bragina O., Lee Ji Y., Semenyuta I., Jӓrving I., Brovarets V., Wipf P., Bahar I., Karpichev Y.. Hydroxamic Acids as PARP-1 Inhibitors: Molecular Design and Anticancer Activity of Novel Phenanthridinones. Helv. Chim. Acta. 2023. https://doi.org/10.1002/hlca.202300133
48. Zyabrev V., Pilyo S., Demydchuk B., Kachaeva M., Semenyuta I., Zhirnov V., Velihina Ye., Brovarets V.. Synthesis, characterization and in vitro anticancer evaluation of 5-sulfinyl(sulfonyl)-4-arylsulfonyl substituted 1,3-thiazoles. Chem. Med. Chem. 2023. V.18, N 14. Р. E202300161
49. Shablykin O.V., Merzhievskyi D.O., Brovarets V.S., Shishkina S.V.. New oxazole to oxazole recyclization. Chem. Het. Compd. 2023. V. 59, N 6. P. 521-524
50. Konovalenko A.S., Shablykin O.V., Shablykina O.V., Moskvina V.S., Shishkina S.V., Kozytskyi A.V., Brovarets V.S.. Distinctive features of 3-acetyl- and 3-benzoylisocoumarins’ interaction with active primery amines. Chem. Select. 2023. V.8, N 37. Р. e202301380. https://doi.org/10.1002/slct.202301380
51. Golovchenko O.V., Brusnakov M.V., Shabelko Yu.O., Brovarets V.S., Vydzhak R.M., Bahrieieva O.S., Potikha L.M., Shishkina S.V.. Synthesis and properties of methanesulfonyl derivatives of diethyl esters of 5-(hydroxyalkylamino)-1,3-oxazol-4-yl-phosphonic acids. Phosphorus, Sulfur, and Silicon and the Related Elements. 2023. DOI: 10.1080/10426507.2023.2251639
52. Shaydyuk Ye.O., Bashmacova N.V., Klishevich G.V., Dmytruk A.M., Kachkovsky O.D., Kuziv Ya.B., Dubey I.Ya., Befield K.D., Bondar M.V.. Nature of linear spectra; properties and fast relaxations in the excited states and two-photon absorption efficiency of 3-thiazolyl and 3-phenylthiazolyl coumarin derivatives.. ACS Publications. 2023. V.18, N 12. P. 11564-11573
53. Brusnakov M.Yu., Golovchenko O.V., Potikha L.M., Brovarets V.S.. Condenced azole-based organophosphorus heterocycles. Chem. Het. Compd. 2023. V.59, N 4/5. P. 217-236. Doi:10.1007/s10593-023-03184-0
54. Konovalenko A., Shablykin O., Shablykina O., Kozytskyi A., Brovares V.. Convenient and versatile method of 8-amino-6-(2-R-thiazol-4-yl)1,7-naphthyridines. Curr. Chem. Lett. 2024. V.13, N 1. P. 163-172. Doi: 10.5267/j.ccl.2023.7.004
55. Nallaparaju J.V., Nikonovich T., Jarg T., Merzhyievskyi D., Aav R., Kananovich D.G.. Mechanochemistry – amended barbier reaction as an expedient alternative to Grignar synthesis. Angew. Chem. Int. Edd. 2023. E202305775.
56. Dibchak D., Snisarenko M., Mishuk A., Shablykin O., Bortnichuk L., Klymenko-Ulianov O., Kheylik Yu., Sadkova I., Rzepa H.S., Mykhailiuk P.K.. General synthesis of 3‐azabicyclo [3.1.1]heptanes and evaluation of their properties as saturated isosteres. Angewandte Chemie. 2023. V.135, N 39. Р. e202304246. https://doi.org/10.1002/ange.202304246
57. Kirichok A.,Tkachuk H., Kozyriev Ye., Shablykin O., Datsenko O., Granat D., Yegorova T., Bas Yu., Semirenko V., Pishel I., Kubyshkin V., Lesyk D., Klymenko-Ulianov O., Mykhailiuk P.K.. 1‐Azaspiro[3.3]heptane as a bioisostere of piperidine. Angewandte Chemie. 2023. e202311583. https://doi.org/10.1002/ange.202311583
58. Krasylov I.V., Moskvina V.S., Khilya V.P.. Unexpected but prominent imines formation in Beckmann rearrangement of (spiro)pyranocoumarin oximes. Tetrahedron Lett. 2023. V. 129. P. 154747. https://doi.org/10.1016/j.tetlet.2023.154747
59. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S. V., Brovarets V.S.. Use of pyridine and pyrimidine derivatives as new wheat growth regulators. Global Meet on Food Science and Technology”. March 23, 2023. Webinar GMFST 2023, LAS VEGAS, USA. P. 19-20
60. Chernykh A.V., Kudryk O.V., Olifir O.S., Dobrydnev A.V., Rusanov E., Moskvina V.S., Volochnyuk D.M., Grygorenko O.O.. Expanding the chemical space of 1,2-difunctionalized cyclobutanes. J. Org. Chem. 2023. V. 88, N 5. P. 3109-3131. https://doi.org/10.1021/acs.joc.2c02892
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63. Myshko N.V., Mrug G.P., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S.. Coumarin-based homoisoflavonoids as precursors in the synthesis of 8-heteroarylmethylcoumarins. Chem. Heterocycl. Compd. 2023. V. 59, N 6/7. P. 456-464. https://doi.org/10.1007/s10593-023-03216-9
64. Levterov V., Panasyuk Ya., Sahun K., Stashkevich O., Badlo V., Shablykin O., Sadkova I., Bortnichuk L., Klymenko-Ulianov O., Holota Yu., Lachmann L., Borysko P., Horbatok K., Bodenchuk I., Bas Yu., Dudenko D., Mykhailiuk P.K.. 2-Oxabicyclo [2.2.2]octane as a new bioisostere of the phenyl ring. Nature Commun. 2023. V.14, N 1. P. 5608. https://doi.org/10.1038/s41467-023-41298-3
65. Goulden T., Bodachivskyi Iu., Padula M.P., Williams D.B.G.. Concentrated ionic liquids for proteomics: Caveat emptor. International Journal of Biological Macromolecules. 2023. V. 253, № 7. Р. 127438. https://doi.org/10.1016/j.ijbiomac.2023.127438.
66. Kornii Yu., Shablykin O., Tarasiuk T., Stepaniuk O., Matvienko V., Aloshyn D., Zahorodniuk N., Sadkova I.V., Mykhailiuk P.K.. Fluorinatedaliphatic diazirines: preparation, characterization, and model photolabeling studies. J. Org. Chem. 2023. V. 88, N 1. P. 1-17. Doi:10.1021/acs.joc.2c02262
67. Malets Ye. S., Vashchenko B. V., Moskvina V.S., Golovchenko O.V., Brovarets V.S., Grygorenko O.O.. Parent 5(7)-azachromones and their partially hydrogenated derivatives: synthesis and physiochemical properties. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 494-499
68. Kukushkina K.V., Moskvina V.S., Shablykina O.V., Khilya V.P.. Expanding the isoflavone, pyrazole, and oxazole chemical space through 2′-carboxamido-2-hydroxy-deoxybenzoin precursors.. Chem. Heterocycl. Comp. 2023. V.59, N 6/7. P. 479-483. https://doi.org/10.1007/s10593-023-03219-6
69. Lyutenko N.V., Sorochinsky A.E., Soloshonok V.A.. Asymmetric synthesis of pyroglutamic acids via Ni(II) complex methodology. Chem. Heterocycl. Comp. 2023. Р. 332-340. https://doi.org/10.1007/s10593-023-03203-0
70. Shablykin O.V., Brovarets V.S., Shablykina O.V.. Recyclization of 5-aminooxazoles as a route to new functionalized heterocycles (developments of V.P. Kukhar institute of bioorganic chemistry and petrochemistry of the NAS of Ukraine). Chem. Record. 2023. e202300264. https://doi.org/10.1002/tcr.202300264
71. Gaponov A.M., Pavlenko O.L., Dmytrenko O.P., Kulish M.P., Ryzhkova A.S., Lesiuk A.I., Obernikhina N.V., Łuszczyńska B., Kachkovsky O.D.. Molecular heteroassociation in films of thiochrome and tryptophan. Mol. Cryst. Liquid Cryst. 2023. https://doi.org/10.1080/15421406.2023.2257515
72. Tsygankova V.A., Andrusevich Ya.V., Pilyo S.G., Brovarets V.S.. Effect of plant growth regulators and fertilizers of the vegetative growth of sunflowers (Helianthus annuus L). The scientific heritage. 2023.N 116. P. 3-9. DOI: 10.5281/zenodo.8129039
73. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Use of synthetic plant growth regulators in combination with fertilizers to improve wheat growth. Int J Med Biotechnol Genetics. 2023. S1:02:002:9-14. URL: http://scidoc.org/IJMBGS1V2.php
74. Tsygankova V.A., Voloshchuk I.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Studying the effect of plant growth regulators Ivin, Methyur and Kamethur on growth and productivity of sunflower. J. Advanc. Agricult. 2023. V.14. P. 17-24. DOI: https://doi.org/10.24297/jaa.v14i.9453
75. Tsygankova V.A., Andrusevich Ya.V., Kopich V.M., Voloshchuk I.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Application of pyrimidine and pyridine derivatives for regulation of chickpea (Cicer arietinum L.) growth. Int. J. Innovat. Sci. Res. Techn. (IJISRT). 2023. V.8, N 6. P. 19-28. DOI: https://doi.org/10.5281/zenodo.8020671
76. Tsygankova V.A., Kopich V.M., Voloshchuk I.V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. New growth regulators of barley based on pyrimidine and pyridine derivatives. Sciences of Europe. 2023. N. 124. P. 13-23. https://doi.org/10.5281/zenodo.8327852.
77. Tsygankova V.A., Andrusevich Ya.V., Kopich V.M., Voloshchuk I.V., Bondarenko O.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Effect of pyrimidine and pyridine derivatives on the growth and photosynthesis of pea microgreens. Int. J. Med. Biotechnol. Genetics. 2023. S1:02:003:15-22. https://UBAscidoc.org/IJMBGS1V2.php
78. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Klyuchko S.V., Pilyo S.G., Brovarets V.S.. Use of Ivin, Methyur, Kamethur and microfertilizers to improve the growth of oilseed flax (Linum usitatissimum L.). Annali d’Italia. 2023. N. 48. P. 3-10. https://doi.org/10.5281/zenodo.10034698.
79. Hodyna D.M., Kovalishyn V.V., Derevianko K.Yu., Pilyo S.G., Metelytsia L.O.. 1,3-Oxazole derivatives as antibacterials against colistin-resistants acinetobacter baumanni strains. IV Intern. Scient. Theoret. Conf. 16 june 2023. Athens: Hellenic Rep. P. 83-85
80. Semenyuta I.V., Hodyna D.M., Kovalishyn V.V., Demydchuk B. A., Pilyo S.G., Metelytsia L.O.. 5-Amino-4-cyano-1,3-oxazoles as new antibacterials against antibiotic-resistants Escherichia coli strains. IV Intern. Scient. Practical. Conf. 16 may 2023. Boston: USA. P. 117-121
81. Tsygankova V.A., Andreev A.M., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Synergistic effect of synthetic plant growth regulators and microfertilizers on the growth of canola (Brassica napus L.). Danish Scient. J. (DSJ). 2023. V.1, N. 77. P. 8-12. https://doi.org/10.5281/zenodo.10053315
82. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Oliynyk O.O., Stefanovska T.R., Pidlisnyuk V., Pilyo S.G., Klyuchko S.V., Brovarets V.S.. Use of synthetic plant growth regulators in agriculture and biotechnology.. Polish J. Sci. 2023. V. 1, N. 68. P. 12-17. https://doi.org/10.5281/zenodo.10131991.
83. Bondar M.V., Faryadras S., Munera N., Chang H.-T., Uddin M., Beldield K.D., Kachkovsky O.D., Van Stryland E.W., Hagan D.J.. New two-photon absorbing Squaraine derivative with efficient near-infrared fluorescence, superluminescence, and high photostability. J. Phys. Chem. B. 2022. V.126, N 21. P. 3897-3907
84. 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-4-carbonitrile and 4-sulfonylamide-5-phenyl-1,3-thiazole derivatives in vitro. Letters in Applied Nanobioscience. 2023. https://doi.org/10.33263/LIANBS120.000
85. Denisenko A., Garbuz P., Makovetska Ye., Shablykin O., Lesyk D., Al-Maali G., Korzh R., Sadkova I., Mykhailiuk P.. 1,2-Disubstituted bicyclo[2.1.1]hexanes as bioisosteres of the ortho-substituted benzene. Chem. Sci. 2023. 10.1039/D3SC05121H
86. E. Shaitanova, V. Matoušek, T. Herentin, M. Adamec, R. Matyáš, B. Klepetářová, P. Beier. Synthesis and Cycloaddition Reactions of 1-Azido-1,1,2,2-tetrafluoroethane. J. Org. Chem. 2023. V. 88, N 21. Р. 14969-14977
87. J. He, Z. Li, G. Dhawan, W. Zhang, A. E. Sorochinsky, G. Butler, V. A. Soloshonok, J. Han. Fluorine-containing drugs approved by the FDA in 2021. Chinese Chemical Letters. 2023. V. 34. Р. 107578
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2022 р.

Розділи в зарубіжних монографіях

• V.A. Tsygankova, Ya.V. Andrusevich, O.I. Shtompel, R.M. Solomyanny, A.O. Hurenko, M.S. Frasinyuk, G.P. Mrug, O.V. Shablykin, S.G. Pilyo, A.M. Kornienko, V.S. Brovarets. New Auxin and Cytokinin Related Compounds Based on Synthetic Low Molecular Weight Heterocycles. Auxins, Cytokinins and Gibberellins Signaling in Plants. Signaling and Communication in Plants. Aftab, T. (Eds). Springer Nature. Switzerland AG. 2022. 377 p. Pp. 353-377.

• S. Konovalov,S. Zubenko,L. Patrylak, A. Yakovenko, V. Povazhnyi, K. Burlachenko. Revisiting the Synthesis of Fatty Acid Alkyl Esters of Lower Monohydric Alcohols by Homogeneous Base-Catalyzed Transesterification of Vegetable Oils. Chemmotological Aspects of Sustainable Development of Transport. Sustainable Aviation. 2022, Springer, Cham.Р. 49-80 https://doi.org/10.1007/978-3-031-06577-4_4

Публікації в зарубіжних виданнях

1. D. Hodyna, V. Kovalishyn, I. Semenyuta, S. Rogalsky, O. Trokhimenko, A. Gryniukova, L. Metelytsia. Ester-Functionalized Imidazolium- and Pyridinium-Based Ionic Liquids: Design, Synthesis and Cytotoxicity Evaluation. Biointerface Research in Applied Chemistry. 2022. V. 12, N 3. P. 2905-2957. doi.org/10.33263/BRIAC123.29052957
2. L.O. Metelytsia,D.M. Hodyna, I.V. Semenyuta,V.V. Kovalishyn,S.P. RogalskyY.K. Derevianko, V.S. Brovarets,I.V. Tetko. Theoretical and Experimental Studies of Phosphonium Ionic Liquids as Potential Antibacterials of MDR Acinetobacter baumannii. Journal of Antibiotics. 2022. V. 11. P. 491. https://doi.org/10.3390/antibiotics11040491.
3. Vydzhak R.N., Panchishin S.Y.,Kachaeva M.V.,Pilyo S.G., Moskvina V.S., Shablykina O.V., Kozytskiy A.V.,Brovarets V.S. Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones. Molecular diversity. 2022. Vol. 26, N 2. Р. 1115-1128.DOI: 10.1007/s11030-021-10234-2
4. O.V. Moshynets,T.P. Baranovskyi,O.S. Iungin, N.P. Kysil, L.O. Metelytsia,I. Pokholenko, V.V. Potochilova,G. Potters, K.L. Rudnieva,S.Y. Rymar, I.V. Semenyuta, A.J. Spiers, O.P. Tarasyuk,S.P. Rogalsky eDNA inactivation and biofilm inhibition by the polymeric biocide polyhexamethylene guanidine hydrochloride (PHMG-Cl). International Journal of Molecular Sciences. 2022. V. 23. Р. 731.DOI: 10.3390/ijms23020731.
5. Obernikhina N.V.,Kachaeva M.V., Kachkovsky O.D.,Brovarets V.S. In silico Study of Conjugated Nitrogen Heterocycles Affinity in their Biological Complexes Chemistry of Heterocyclic Compounds 2022. V. 58, N 8. Р. 412-420.DOI 10.1007/s10593-022-03107-5
6. D.S. Kamenskyh, T.V. Tkachenko, V.A. Yevdokymenko, Y.V. Sheludko, M.M. Filonenko, V.A. Povazhny, M.M. Baran, O.V. Pavluik, V.I. Kashkovsky Synthesis, characterization and optimization of the aluminum–nickel–molybdenum catalyst for hydrogenation Applied Nanoscience. 2022. P. 1-13. https://doi.org/10.1007/s13204-022-02644-x
7. T.V. Tkachenko, M.M. Baran, V.O. Yevdokymenko, D.S. Kamenskyh, V.I. Kashkovsky Optimization of Ether Production by Proton Current Materials Today: Proceedings. 2022. V. 62, N 15. P. 7643-7649. https://doi.org/10.1016/j.matpr.2022.02.004
8. L.K. Patrylak, S.V. Konovalov, A.V. Yakovenko, O.P. Pertko, V.A. Povazhnyi, Yu.G. Voloshyna, O.V. Melnychuk, M.M. Filonenko Micro–mesoporous kaolin-based zeolites as catalysts for glucose transformation into 5-hydroxymethylfurfural Applied Nanoscience. 2022. P.1-14. https://doi.org/10.1007/s13204-022-02620-5
9. L. Patrylak, S. Zubenko, S. Konovalov, A. Yakovenko, V. Povazhnyi, O. Pertko, Y. Voloshyna, O. Melnychuk Mykhailo Filonenko Іsomerization of limonene on zeolite-containing catalysts based on Кaolin Chemistry Journal of Moldova. 2022. P. 1857-1727. DOI: dx.doi.org/10.19261/cjm.2022.980
10. V. Pidlisnyuk, A. Mamirova, R.A. Newton, T. Stefanovska, O. Zhukov, V. Tsygankova, P. Shapoval The role of plant growth regulators in Miscanthus × giganteus utilisation on soils contaminated with trace elements Agronomy. 2022. V. 12, N 12. Р. 2999. https://doi.org/10.3390/agronomy12122999
11. Vasetska O., Zhminko P., Prodanchuk M., Galkin A., Tsygankova V. Perspective for using2,6-dimethylpyridine-N-oxide to reduce the toxic effect of xenobiotics in mammals J. Adv. Pharm. Educ. Res. 2022. V. 12, N 1. P. 21 – 29.
12. Tsygankova V.A., Voloshchuk I.V., Klyuchko S.V., Pilyo S.G., Brovarets V.S., Kovalenko O.A. The effect of pyrimidine and pyridine derivatives on the growth and productivity of sorghum International Journal of Botany Studies. 2022. V. 7, N 5. P. 19-31.https://www.botanyjournals.com/archives/2022/vol7/issue5/7-4-28
13. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Kachaeva M.V., Brovarets V.S. Pyrimidine derivatives as analogues of plant hormones for intensification of wheat growth during the vegetation period Journal of Advances in Biology. 2022. V. 15. P. 1-10. DOI: https://doi.org/10.24297/jab.v15i.9237
14. Tsygankova V.A., Oliynyk O.O., Kvasko O.Yu., Pilyo S.G., Klyuchko S.V., Brovarets V.S. Effect of Plant Growth Regulators Ivin, Methyur and Kamethur on the Organogenesis of Miniature Rose (Rosa mini L.) in Vitro Int. J. Med. Biotechnol. Genetics. 2022. S1: V. 2, N 1. P.1-8.https://scidoc.org/IJMBG-2379-1020-S1-02-001.php
15. Y. Kolesnikov, S. Kretynin, Y. Bukhonska, I. Pokotylo, E. Ruelland, J. Martinec, V. Kravets Phosphatidic Acid in Plant Hormonal Signaling: From Target Proteins to Membrane Conformations Int. J. Mol. Sci. 2022, V. 23, N 6. Р. 3227; https://doi.org/10.3390/ijms23063227
16. Kobzar O.,Shulha Yu.,Buldenko V.,Cherenok S.,Silenko O.,Kalchenko V.,Vovk A. Inhibition of glutathione S-transferases by photoactive calix[4]arene α-ketophosphonic acids Bioorganic and Medicinal Chemistry Letters. 2022. V. 77. Р. 129019
17. Silenko O.,Cherenok S.,Shulha Yu.,Kobzar O.,Rusanov E.,Karpichev E.,Vovk A.Kalchenko V. Thiacalix [4] arene phosphoric acids. Synthesis, structure, and inhibition of glutathione S-transferases Phosphorus, Sulfur, and Silicon and the Related Elements. 2022. V.197 (5-6). Р. 538-541
18. Velihina Y.,Pilʹo S.,Kobzar O.,Zaliavska O.,Prichard M. N.,James S. H.Keith K.,Hartline C.,Zhirnov V.,Vovk A.,Brovarets V. Synthesis of some oxazolo [4, 5-d] pyrimidine derivatives and evaluation of their antiviral activity and cytotoxicity Arkivok. 2022. Р. 108-117
19. Obernikhina N.V., Kobzar O.L.,Kachaeva M.V., Kachkovsky O.D. , Brovarets V.S. In silico and in vitro estimation of structure and biological affinity of 1, 3-oxazoles: fragment-to-fragment approach Curr. Comput.-Aided Drug Des. 2022. V. 18. P. 95-109
20. Ivanenko I.,Ruda A.,Povazhnyi V. Cobalt-nitrogen-doped activated carbons for hydrogen generation Materials Today: Proceedings.2022. V. 62 ( P15). Р. 7691-7697
21. Yu.G. Voloshyna,O.P. Pertko,V.A. Povazhnyi,L.K. Patrylak Peculiarities of products’ distribution in n-hexane hydroisomerization on modified mordenite-containing rock Appl. Nanosci. 2022.https://doi.org/10.1007/s13204-022-02632-1
22. Yu. Kholodko, A. Bondarieva, V. Tobilko, V. Pavlenko, O. Melnychuk, V. Glukhovskyi Synthesis and characterization of kaolinite-based granular adsorbents for the removal of Cu(II), Cd(II), Co(II), Zn(II), and Cr(VI) from contaminated water Eastern-European Journal of Enterprise Technologies.2022. V. 4 N. 10. Р. 118
23. Rogalsky S., Tarasyuk O., Vashchuk A., Davydenko V., Dzhuzha O., Motrunich S., Cherniavska T., Papeikin O., Bodachivska L., Bardeau J.-F. Synthesis and evaluation of N,N-dibutylundecenamide as new eco-friendly plasticizer for polyvinyl chloride Journal of Materials Science. 2022. V. 57. Р. 6102-6114
24. Rogalsky S., Tarasyuk O., Dzhuzha O., Hodyna D., Cherniavska T., Hubina A., Filonenko M., Metelytsia L. Evaluation of N,N-dibutylolelamide as a bifunctional additive for poly(vinyl chloride) Colloid and Polymer Science. 2022. V. 300 (12). Р. 1-8
25. S.I. Vdovenko,I.I. Gerus,M. Pagacz-Kostrzewa,M. Wierzejewska Influence of the features of the spatial and electronic structure of α-substituted β-ethoxyvinyl trifluoromethyl ketones and secondary amines on their reactivity Journal of Molecular Structure. 2022. V. 1255. Р. 132417
26. J. Liu, W. Lin,A.E. Sorochinsky,G. Butler,A. Landa, J. Han,V.A. Soloshonok Successful trifluoromethoxy-containing pharmaceuticals and agrochemicals Journal of Fluorine Chemistry. 2022. V. 257-258. Р. 109978
27. J. Han,J. Escorihuela,S. Fustero,A. Landa,V.A. Soloshonok,A. Sorochinsky Asymmetric Michael addition in synthesis of β-substituted GABA derivatives Molecules. 2022. V. 27. Р. 3797
28. Q. Wang, J. Han, A. Sorochinsky, A. Landa, G. Butler, V. A. Soloshonok The latest FDA-approved pharmaceuticals containing fragments of tailor-made amino acids and fluorine Pharmaceuticals. 2022. V. 15. Р. 999
29. V.D. Romanenko From elusive monomeric metaphosphates to oligomeric metaphosphate reagents:New avenue to halogen-free phosphorylation of biomolecules Current Organic Chemistry. 2022. V. 26, Р. 432-437.DOI: 10.2174/1385272826666220330111824
30. Chernykh A.V.,Aloshyn D.,Kuchkovska Yu.O.,Daniliuc C.G.,Tolmachova N.A.,Kondratov I.S.,Zozulya S.,Grygorenko O.O., Haufe G. Impact of β-perfluoroalkyl substitution of proline on the proteolytic stability of its peptide derivatives Org. Biomol. Chem. 2022. V. 20. Р. 9337-9350. https://doi.org/10.1039/D2OB01430K
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32. Homon A.A.,Shynder L.V.,Demchuk O.P.,Hryshchuk O.V.,Kondratov I.S.,Gerus I.I.,Grygorenko O.O. Synthesis of 1,3-bifunctional cyclobutane derivatives with α-CHF2/CF3 group – advanced building blocks for medicinal chemistry Journal of Fluorine Chemistry. 2022. V. 263. Р. 110041. https://doi.org/10.1016/j.jfluchem.2022.110041
33. Kondratov I.S.,Moroz Yu.S.,Irwin J.J.,Shoichet B.K. Drug building blocks and libraries at risk in Ukraine Science. 2022. V. 376(6596). Р. 929https://doi.org/10.1126/science.abq7841
34. Kondratov I.S.,Moroz Yu.S.,Grygorenko O.O.,Tolmachev A.A. The Ukrainian Factor in Early-Stage Drug Discovery in the Context of Russian Invasion: The Case of Enamine Ltd ACS Med. Chem. Lett. 2022. V. 13. N 7. Р. 992-996. https://doi.org/10.1021/acsmedchemlett.2c00211
35. M. Aksylenko, E. Sheludko, N. Himach, V. Yevdokimenko Polygalacturonates of biogenic metals – prospective components of new composite preparations for wheat J. Annual Research & Review in Biology. 2022. V. 37 (12). P. 17-28 https://doi.org/10.9734/arrb/2022/v37i1294273
36. A.O. Kolodiazhna,O.I. Kolodiazhnyi Сatalytic asymmetric synthesis of C-chiral phosphonate Symmetry. 2022. V. 14. P. 1758-1825https://doi.org/10.3390/sym14091758
37. D. Prysiazhnuk, A. Kolodiazhna, O. Kolodiazhnyi Сonvergent method for the determination of halo-2,3-dihydro-1H-inden-1-ol absolute configuration Arkivoc. 2022. V. IX. P. 23-32.https://doi.org/10.24820/ark.5550190.p011.835
38. N.A. Ogurtsov,A.V. Mamykin,O.L. Kukla,A.S. Pavluchenko,M.V. Borysenko,Yu.P. Piryatinski,J.-L. Wojkiewicz,A.A. Pud The impact of interfacial interactions on structural, electronic and sensing properties of poly(3-methylthiophene) in the core-shell nanocomposites. Application to the CWA simulants detection Macromolecular Materials and Engineering. 2022. V. 307(4). P. 2100762
39. T. Feng, Y. Yuan, X. Chen,S. Zhao, M. Cao, L. Feng,S. Shi, H. Wang,T. Liu, A. Pud,L. Han, R. Scaffaro, B. He, N. Wang Ultrasensitive and highly specific detection of iodine ions using zirconium (IV)-enhanced oxidation Cell Reports Physical Science. 2022. V. 3 (11). P. 101143 (10 pages)
40. Potikha L.M., Brovarets V.S., Zhirnov V.V. Anticancer evaluation of difunctional substituted 1,2-dihydrophthalazines Chem. Data Collect. 2022. V. 37. P. 100817. https://doi.org/10.1016/j.cdc.2021.100817
41. Demydchuk B.A., Mykhalchenko O.A., Rusanov E.B., Moskvina V.S., Brovarets V.S. Regioselective synthesis of 5H-imidazolo[1,2-e][1,3,5]triazepines Arkivoc. 2022. V. ІІ. P. 204-214
42. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension Adv. Pharm. Bull., 2022. DOI: 10.34172/apb.2023.044
43. Brusnakov M., Golovchenko O., Velihina Ye., Liavynets O., Zhirnov V., Brovarets V. Evaluation of anticancer activity of 1,3-oxazol-4-ylphosphonium salts in vitro Chem. Med. Chem. 2022. V. 17, № 20. P. e202200319. DOI: 10.1002/cmdc.202200319
44. Biletska I.M., Mrug G.P., Prostota Ya.O., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S. Synthesis of 2-trifluoroacetonyl-3-alkyl/alkoxy-chromones and their reactions with 1,2-bidentate nucleophiles Heterocycles. 2022. V. 104, N 7. P. 1229-1244
45. Frasinyuk M., Chhabria D., Kartsev V., Dilip H., Sirakanyan S.N., Kirubakaran S., Petrou A., Geronikaki A., Spinelli D. Benzothiazole and chromone derivatives as potential ATR kinase inhibitors and anticancer agents Molecules. 2022. V.27, N 14. P. 4637
46. Waszkowska K., Krupka A., Smokal V., Kharchenko O., Migalska-Zalas A., Frasinyuk M., Wielgosz R., Andrushchak A., Sahraoui B. Correlation between nonlinear optical effects and structural features of aurone-based methacrylic polymeric thin films Materials. 2022. V.15, N 17. P. 6076
47. Obernikhina N.V., Kachaeva M.V., Kachkovsky O.D., Brovarets V.S. In silico study of conjugated nitrogen heterocycles affinity in their biological complexes Chem. Heterocycl. Comp. 2022. V. 58, N8/9. P. 412-420
48. Kornii Yu., Shablykin O., Tarasiuk T., Stepaniuk O., Matvienko V., Aloshyn D., Zahorodniuk N., Sadkova I.V., Mykhailiuk P.K. Fluorinatedaliphatic diazirines: preparation, characterization, and model photolabeling studies J. Org. Chem. 2022. Doi:10.1021/acs.joc.2c02262
49. Glibov E.K., Gorbulenko N.V., Moskvina V.S., Suprun A.V., Shablykina O.V. Shokol T.V., Khilya V.P. Synthesis and recyclization of methylenbisflavonoids based on heterocyclic analogues of umbelliferon and formononetin Chem. Nat. Compd. 2022. V. 58, N 4. P. 617-622. https://doi.org/10.1007/s10600-022-03755-1
50. Konovalenko A.S., Shablykina O.V., Shablykin O.V., Moskvina V.S., Brovarets V.S. 1H-isochromene-1-ones and isoquinoline-1(2H)-ones with carbonyl group in position 3: Features of synthetic approaches and transformation Arkivoc. 2022. V. VІІІ. P. 79-112. https://doi.org/10.24820/ark.5550190.p011.861
51. Potikha L.M., Brovarets V.S., Zhirnov V.V. Biological evaluation of 3-aminoisoquinolin-1(2H)-one derivatives as potential anticancer agents French-Ukr. J. Chem. 2021. V.9, №2. P. 52-63
52. A.V. Mamykin, O.L. Kukla, A.S. Pavluchenko, Z.I. Kazantseva, I.A. Koshets, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, V.I. Kalchenko Electronic nose-type chemosensory systems for detection of gaseous poisonous substances Semiconductor Physics, Quantum Electronics & Optoelectronics. 2022. V.25, No.4. Р. 429-440https://doi.org/10.15407/spqeo25.04.429

2021 р.

Розділи в зарубіжних монографіях

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

Publications в зарубіжних виданнях

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

Publications 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.
55. Adejuwon A.O., Odeleye O.D., Odewale O.A., Obayemi O.S., Tsygankova V.A., Thonda O.,Donova M.V.. Effective medicinal plants’ extract on ability to properly empty bladder in patients with benign prostatic hyperplasia and Escherichia coli infection. Stem Cell. 2020. V.11, № 3. P. 42-44.

2019 р.

1. Pluhařová K., Leontovyčová H., Stoudková V., Pospíchalová R., Maršík P., Klouček P., Starodubtseva A., Iakovenko O., Krčková Z., Valentová O., Burketová L., Janda M., Kalachova T. “Salicylic Acid Mutant Collection” as a Tool to Explore the Role of Salicylic Acid in Regulation of Plant Growth under a Changing Environment. International journal of molecular sciences. 2019. Vol. 20 (24). P. 6365. DOI: 10.3390/ijms20246365.
   https://www.mdpi.com/1422-0067/20/24/6365
2. Xie Y., Kril L.M., Yu T., Zhang W., Frasinyuk M.S., Bondarenko S.P., Kondratyuk K.M., Hausman E., Martin Z.M., Wyrebek P.P., Liu X., Deaciuc A., Dwoskin L.P., Chen J., Zhu H., Zhan C.-G., Sviripa V.M., Blackburn J., Watt D.S., Liu C. Semisynthetic aurones inhibit tubulin polymerization at the colchicine-binding site and repress PC-3 tumor xenografts in nude mice and myc-induced T-ALL in zebrafish. Scientific Reports. 2019. Vol. 9 (1). P. 6439. DOI: 10.1038/s41598-019-42917-0.
   https://www.nature.com/articles/s41598-019-42917-0
3. Kachaeva M.V., Hodyna D.M., Obernikhina N.V., Pilyo S.G., Kovalenko Y.S., Prokopenko V.M., Kachkovsky O.D., Brovarets V.S. Dependence of the anticancer activity of 1,3-oxazole derivatives on the donor/acceptor nature of his substitues. Journal of Heterocyclic Chemistry. 2019. Vol. 56 (11). P. 3122-3134. DOI: 10.1002/jhet.3711.
   https://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.3711
4. Shaydyuk Y.O., Boyko O.P., Kachkovsky O.D., Slominsky Y.L., Bricks J.L., Belfield K.D., Bondar M.V. Electronic nature of new styryl dye bases: Linear photophysical, photochemical, and transient absorption spectroscopy studies. Dyes and Pigments. 2019. Vol. 170. DOI: 10.1016/j.dyepig.2019.107582.
   https://www.sciencedirect.com/science/article/abs/pii/S0143720819306011
5. Kalachova T., Leontovyčová H., Iakovenko O., Pospíchalová R., Maršík P., Klouček P., Janda M., Valentová O., Kocourková D., Martinec J., Burketová L., Ruelland E. Interplay between phosphoinositides and actin cytoskeleton in the regulation of immunity related responses in Arabidopsis thaliana seedlings. Environmental and Experimental Botany. 2019. Vol. 167. DOI: 10.1016/j.envexpbot.2019.103867.
   https://www.sciencedirect.com/science/article/abs/pii/S009884721930454X
6. Mrug G.P., Biletska I.M., Bondarenko S.P. Sviripa V.M., Frasinyuk M.S. Trifluoroacetylation of 2-Methyl- and 2-Ethylchromones: A Convenient Access to 2-Trifluoroacetonyl Chromones. ChemistrySelect. 2019. Vol. 4 (39). P. 11506-11510. DOI: 10.1002/slct.201903629.
   https://onlinelibrary.wiley.com/doi/abs/10.1002/slct.201903629
7. Kovalchuk V., Voronkina A, Binnewerg B., Schubert M., Muzychka L., Wysokowski M., Tsurkan M.V., Bechmann N., Petrenko I., Fursov A., Martinovic R., Ivanenko V.N., Fromont J., Smolii O.B., Joseph Y., Giovine M., Erpenbeck D., Gelinsky M., Springer A., Guan K., Bornstein S.R., Ehrlich H. Naturally drug-loaded chitin: Isolation and applications. Marine Drugs. 2019. Vol. 17 (10). Р. 574. DOI: 10.3390/md17100574.
   https://www.mdpi.com/1660-3397/17/10/574
8. Kartsev V., Geronikaki A., Bua S., Nocentini A, Petrou A., Lichitsky B., Frasinyuk M., Leitans J., Kazaks A., Tars K., Supuran C.T. Extending the inhibition profiles of coumarin-based compounds against human carbonic anhydrases: Synthesis, biological, and in silico evaluation. Molecules. 2019. Vol. 24 (19). Р. 3580. DOI: 10.3390/molecules24193580.
   https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804193/
9. Schubert M., Binnewerg B., Voronkina A., Muzychka L., Wysokowski M., Petrenko I., Kovalchuk V., Tsurkan M., Martinovic R., Bechmann N., Ivanenko V.N., Fursov A., Smolii O.B., Fromont J., Joseph Y., Bornstein S.R., Giovine M., Erpenbeck D., Guan K., Ehrlich H. Naturally prefabricated marine biomaterials: Isolation and applications of flat chitinous 3D scaffolds from Ianthella labyrinthus (demospongiae: Verongiida). International Journal of Molecular Sciences. 2019. Vol.20 (20). Р. 5105. DOI: 10.3390/ijms20205105.
   https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829448/
10. Kornii Y., Chumachenko S., Shablykin O., Prichard M.N., James S.H., Hartline C., Zhirnov V., Brovarets V. New 2-Oxoimidazolidine Derivatives: Design, Synthesis and Evaluation of Anti-BK Virus Activities in Vitro. Chemistry and Biodiversity. 2019. Vol. 16 (10). e1900391. DOI: 10.1002/cbdv.201900391.
    https://www.ncbi.nlm.nih.gov/pubmed/31479201
11. Savych O., Kuchkovska Y.O., Bogolyubsky A.V., Konovets A.I., Gubina K.E., Pipko S.E., Zhemera A.V., Grishchenko A.V., Khomenko D.N., Brovarets V.S., Doroschuk R., Moroz Y.S., Grygorenko O.O. One-Pot Parallel Synthesis of 5-(Dialkylamino)tetrazoles. ACS Combinatorial Science. 2019. Vol. 21 (9). P. 635-642. DOI: 10.1021/acscombsci.9b00120.
    https://www.ncbi.nlm.nih.gov/pubmed/31437394
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71. Kretynin S.V., Kolesnikov Y.S., Derevyanchuk M.V., Kalachova T.A., Blume Y.B., Khripach V.A., Kravets V.S. Brassinosteroids application induces phosphatidic acid production and modify antioxidant enzymes activity in tobacco in calcium-dependent manner. Steroids. 2019. Стаття № 108444. DOI: 10.1016/j.steroids.2019.108444.
    https://www.ncbi.nlm.nih.gov/pubmed/31295460
72. Pavluik O., Bezugly Y., Kashkovsky V. Ring closing metathesis strategies to isoxazole containing thiadiazepines. French-Ukrainian Journal of Chemistry. 2019. Vol. 7 (1). P. 104-112.
    https://doi.org/10.17721/fujcV7I1P104-112
73. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Kopich V.M., Solomyanny R.M., Brovarets V.S. Study of regulating activity of synthetic low molecular weight heterocyclic compounds, derivatives of pyrimidine on growth of tomato (Solanum lycopersicum L.) seedlings. International Journal of ChemTech Research, 2019, Vol.12 No.05, pp 26-38.
    (CODEN (USA): IJCRGG, ISSN: 0974-4290, ICV: 112.85, Source Normalized Impact Per Paper (SNIP) 2014 = 0.598, Impact per Publication (IPP) = 0.515, H index = 23)
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.
76. Adejuwon A.O. and Tsygankova V.A. Phyto-Chemical Screening and Ethno-Botanical Properties of Selected Plants of the Obafemi Awolowo University, Ile-Ife, Nigeria. J Complement Med Alt Healthcare. 2019; 9(3): 555761. http://dx.doi.org/10.19080/JCMAH.2019.09.555761
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.
    
    Monographs
    
    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.
2. Fatyeyeva K., Rogalsky S., Tarasyuk O., Chappey C., Marais S.. Vapour sorption and permeation behaviour of supported ionic liquid membranes: application for organic solvent/water separation. Reactive and functional polymers. – 2018. – Vol.130. – P.16-28.
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.
4. Hodyna D., Kovalishyn V., Semenyuta I., Blagodatnyi V., Rogalsky S., Metelytsia L.. Imidazolium ionic liquids as effective antiseptics and disinfectants against drug resistant S. aureus: in silico and in vitro studies. Computational Biology and Chemistry. – 2018. – Vol.73. – P.127-138.
5. Kolodiazhnyi O.I., Kolodiazhna A.O.. Stereoselective syntheses of sanshool derivatives. Phosphorus, Sulfur and Silicon and the Related Elements.- 2018.- Vol. 193 doi:10.1080/10426507.2018.1514404.
6. Kolodiazhnyi O.I.. Stereochemistry of electrophilic and nucleophilic substitution at phosphorus. Phosphorus, Sulfur and Silicon and the Related Elements.- 2018, Vol.193 doi:10.1080/10426507.2018.1521409.
7. Trush M.M., Kovalishyn V., Ocheretniuk A.D., Kobzar O.L., Kachaeva M.V., Brovarets V.S., Metelytsia L.O.. QSAR study of some 1,3-oxazolylphosphonium derivatives as new potent anti-Candida agents and their toxicity evaluation. . Curr. Drug Discov. Technol.- 2018. – Vol.15. – P. 1-6 DOI: 10.2174/1570163 815666180418145422.
8. Trush M.M., Kovalishyn V.V., Ocheretniuk A.D., Kalashnikova L.E., Prokopenko V.M., Holovchenko O.V., Kobzar O.L., Brovarets V.S., Metelytsia L.O.. New 1,3-oxazolylphosphonium Salts as Potential Biocides: QSAR Study, Synthesis, Antibacterial Activity and Toxicity Evaluation.. Letters in Drug Design & Discovery. – 2018.- Vol. 15 Issue:12. – P. 1259-1267.
9. I. Pokotylo, V. Kravets, J. Martinec, E. Ruelland. The phosphatidic acid paradox: Too many actions for one molecule class? Lessons from plants. Progress in Lipid Research.- 2018.- V.71.- P. 43-53.
10. Kovalishyn V., Grouleff J., Semenyuta I., Sinenko V.O., Slivchuk S.R., Hodyna D., Brovarets V., Blagodatny V., Poda G., Tetko I.V., Metelytsia L.. Rational design of isonicotinic acid hydrazide derivatives with anti-tubercular activity: Machine learning, molecular docking, synthesis and biological testing.. Chem. Biol. & Drug Des.- 2018.- V.92 (№1).- P. 1272-1278.
11. Kachaeva M.V., Hodyna D.M., Semenyuta I.V., Pilyo S.G., Prokopenko V.M., KovalishynV.V., Metelytsia L.O., Brovarets V.S.. Design, synthesis and evaluation of novel sulfonamides as potential anticancer agents.. Comput. Biol. Chem.- 2018.- V.10 (№74).- P. 294-303.
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.
13. Iu. Little, E. Alorkpa, V. Khan, V. Povazhnyi, A.Vasiliev. Efficient porous adsorbent for removal of cesium from contaminated water. J. Porous Mater.- 2018.- Vol. 244.- Р. 55-63.
14. P.Le. Maout, J.-L. Wojkiewicz, N. Redon, C. Lahuec, F. Seguin, L. Dupont, S. Mikhaylov, Yu. Noskov, N. Ogurtsov, A. Pud. Polyaniline nanocomposites based sensor array for breath ammonia analysis. Portable e-nose approach to non-invasive diagnosis of chronic kidney disease. Sensors and Actuators B.- 2018.- Vol. 274.- Р. 616-626.
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.
17. Trepyadko D., Korzh R, Kremenetskii V, Nasieka Iu., Naseka V., Stanovyi O., Bortyshevskii V.. Graphitic carbon sub-nitride: synthesis, structure, electron and proton transport, phо-toluminescence and thermoelectric proper-ties. Materials Chemistry and Physics. – 2018. – Vol. 209. – P. 95-106.
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.
20. Tarasenko K.V., Romanenko V.D., Sorochinsky A.E.. Condensation of diethyl fluoromethylphosphonate with esters: An alternative synthetic route to diethyl ?-fluoro-?-ketophosphonates. J. Fluorine Chem.- 2018.- Vol. 211.- Р. 124-128.
21. Vdovenko S.I., Gerus I.I., Pagacz M.-Kostrzewa, Wierzejewska M., Zhuk Y.I., Kukhar V.P.. Special feature of kinetics of ZcE isomerization of ?-N-methylaminovinyl trifluoromethyl ketone in Ar matrix exposed to UV radiation and spontaneous E Z isomerization of methyl-N-methylaminovinyl trifluoromethyl ketone. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy.- 2018.- Vol. 199.- Р. 130–140 doi:10.1016/j.saa.2018.03.049.
22. Khlebnicova T.S., Piven Yu.A., Isakova V.G., Baranovsky A.V., Lakhvich F.A., Sorochinsky A.E., Gerus I.I. Regioselective Synthesis of Polyfluoroalkyl Substituted 6,7-Dihydrobenzisoxasolones. Journal of Heterocyclic Chemistry.- 2018.- Vol. 55.- Р. 1791-1797 doi.org/10.1002/jhet.3218.
23. Romanenko V.D., Kukhar V.P.. Phosphonate analogues of nucleoside polyphosphates. Arkivoc.- 2018.- part i.- Р.1-49 https://doi.org/10.24820/ark.5550190.p010.183.
24. Kondratov I.S., Bugera M.Ya., Tolmachova N.A., Daniliuc C.G., Haufe G.. Straightforward synthesis of fluorinated amino acids by Michael addition of ethyl bromodifluoroacetate to ?, ?-unsaturated ?-amino acid derivatives. Journal of Fluorine Chemistry.- 2018.- Vol. 211.- Р. 100-108.
25. Borysko P., Moroz Y.S., Vasylchenko O.V., Hurmach V.V., Starodubtseva A., Stefanishena, N. Nesteruk K., Zozulya S., Kondratov I.S., Grygorenko O.O.. Straightforward hit identification approach in fragment-based discovery of bromodomain-containing protein 4 (BRD4) inhibitors. Bioorganic & medicinal chemistry.- 2018.- Vol. 26, № 12.- Р. 3399-3405.
26. Kondratov I.S., Tolmachova N.A, Haufe G.. Diels–Alder Reaction in the Synthesis of Fluorinated (Hetero) Aromatic Compounds. European Journal of Organic Chemistry.- 2018.- (27-28).- Р. 3618-3647
27. Gerus I.I., Balabon O.A., Pazenok S.V., Lui N., Kondratov I.S., Tarasenko K.V., Shaitanova E.N., Ivasyshyn, V.E. Kukhar V.P. Synthesis and Properties of Polyfunctional Cyclic ?-Alkoxy-Unsaturated Ketones Based on 4-Methylene-1,3-dioxolanes. European Journal of Organic Chemistry.- 2018.- (27-28).- Р. 3853-3861.
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.
30. Frasinyuk M.S., Zhang W., Wyrebek P., Yu T., Xu X., Sviripa V.M., Bondarenko S.P., Xie Y., Ngo H.X., Morris A.J., Mohler J.L., Fiandalo M.V., Watt D.S., Liu C.. Developing antineoplastic agents that target peroxisomal enzymes: cytisine-linked isoflavonoids as inhibitors of hydroxysteroid 17-beta-dehydrogenase-4(HSD17B4). Organic, Biomolecular Chemistry.- 2017. – Vol. 15.- P.7623-7629.
31. Iakovyshen R.S., Kurdyukov V.V., Brusentsov V.A., Pavlenko E.L., Dmytrenko O.P., Kulish M.P., Tolmachev O.I., Kachkovsky O.D.. Spectral and quantum-chemical study of absorption of merocyanines derivatives of cyclohexadienon. J.Advanc.Phys., 2017. – Vol.6. – P. 514-523.
32. Выджак Р.Н., Панчишин С.Я., Броварец В.С.. Алкилирование 1-алкил-3-метил-1,4-дигидропиразоло[3,4-c]-пиразолов эфирами галогенкарбоновых кислот. ЖОХ.- 2018. – Т.88, № 2.- С.242-254.
33. Solomyannyi R., Slivchuk S., Smee D., Choi J., Rusanov E., Zhirnov V., Brovarets V.. In vitro activity of the novel pyrimidines and their condensed derivatives against poliovirus. Current Bioactive Comp. 2018. – Vol.14, № 14. – P. 1-9.
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.
35. Sinenko V.O., Slivchuk S.R., Brovarets V.S.. Lithiation of 2-Bromo-4-(1,3-dioxolan-2- yl)-13-thiazole. Current Chem. Letters.- 2018. – Vol. 8. – P.1-8.
36. Kachaeva M.V., Pilyo S.G., Demydchuk B.A., Prokopenko V.M., Zhirnov V.V., Brovarets V.S.. 4-Cyano-1,3-oxazole-5-sulfonamides as Novel Promising Anticancer Lead Compounds. Intern. J. Curr. Res.- 2018. – Vol. 10, № 5. – P. 69410-69425.
37. Tsygankova V., Andrusevich Y., Shompel O., Kopich V., Solomyanny R., Bondarenko O., Brovarets V.. Phytohormone-like effect of pyrimidine derivatives on regulation of vegetative growth of tomato. International J. of Botany Studies.- 2018. – Vol. 3, № 2. – P. 91-102.
38. Tsygankova V., Andrusevich Y., Kopich V., Shtompel O., Veligina Ye., Pilyo S., Kachaeva M., Kornienko A., Brovarets V.. Application of Oxazole and Oxazolopyrimidine as New Effective Regulatores of Oilseed Rape Growth. Sch. Bull.- 2018. – Vol. 4, № 3. – P. 301-312.
39. Шаблыкин О.В., Волощенюк М.А., Броварец В.С.. Синтез новых 2-(оксиран-2-ил)-1,3-оксазолов. ЖОХ.- 2018. – Т. 88, № 7. – С. 1207-1210.
40. Chalyk B.A., Hrebeniuk K.V., Gavrilenko K.S., Shablykin O.V., Yanshyna O.O., Bash D., Mykhailik P.K., Liashuk O.S., Grygorenko O.O.. Synthesis of Bi- and Polyfunctional Isoxazoles from Amino Acid-Derived Halogenoximes and Active Methylene Nitriles. Eur. J. Org. Chem.- 2018. -Vol. 22. – P. 2753-2761.
41. Popova A.V., Bondarenko C.P., Frasinyuk M.S., Wen Zhang, Xie Yanji, Martin Zachary M., Cai Xianfeng, Fiandalo Michael V., Mohler James L., Liu Chunming, Watt David S., Sviripa V.M.. Efficient synthesis of aurone Mannich bases and evaluation of their antineoplastic activity in PC-3 prostate cancer cells. Chemical Papers, 2018. – Vol. 72, № 10. – P. 2443-2456.
42. Kachaeva M., Pilyo S., Popilnichenko S., Kornienko A., Rusanov E., Prokopenko V., Zyabrev V., Brovarets V.. Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)oxazole-4-carboxylates and ?-aminoakoles involving the Smiles rearrangement. Current Chem. Letters.- 2018. – Vol. 7, № 4. – P. 101-110.
43. Brovarets V.S., Golovchenko O.V., Rusanov E.B., Rusanova J.A.. Crystal structure of diethyl {2,2,2-tri¬chloro-1-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-methyl¬pentanamido]¬eth-yl}phospho¬nate. Acta Cryst.- 2018. – Vol. E74. – P. 915-917 https://doi.org/10.1107/S2056989018008277.
44. 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. Chem. Res. J.- 2018. – Vol. 3 (2).- P. 165-173.
45. Velihina Ye., Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S.. Synthesis, Characterization, and Vitro Anticancer Evaluation of 7-Piperazin-substituted [1,3]oxazolo[4,5-d]pyrimidines. Der Pharma Chemica.- 2018. – Vol. 10, № 9. – Р. 1-10.
46. Мруг Г.П., Бондаренко Н.В., Бондаренко С.П., Фрасинюк М.С.. Реакционная способность конденсированных производных изофлавонов по отношению к гидразину. Химия природных соединений.- 2018. – Т.54, №4.- С. 654-659.
47. Бондаренко С.П., Мруг Г.П., Кондратюк К.М., Фрасинюк М.С.. Аминометилирование афроморсина, кладрастина и их 2-метилпроизводных. Химия природных соединений.- 2018. – Т.54, № 4. – С. 660-664.
48. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Acceleration on vegetative growth of wheat (Triticum aestivum L.) using [1,3] oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted 1,3-oxazole. Pharm. Chem. J., 2018. – Vol.5, № 2. – P. 167-175.
49. Bogolyubsky A., Savych O., Zhemera A., Khomenko D., Brovarets V., Moroz Yu., Vybornyi M.. A facile one-pot parallel synthesis of 3-amino-1,2,4-triazoles. ACS Combinatorial Science, 2018. – Vol. 20, № 7.– P. 461-466.
50. Kachaeva M.V., Pilyo S.G., Zhirnov V.V., Brovarets V.S. Synthesis, characterization, and in vitro anticancer evaluation of 2- substituted 5-arylsulfonyl-1,3-oxazole-4-carbonitriles. Med. Chem. Res.- 2018. – Vol. 22, № 12 https://doi.org/10.1007/s00044-018-2265-y.
51. Mrug G.P., Demydchuk B.A., Bondarenko S.P., Sviripa V.M., Wyrebek P., Mohler J. L., Fiandalo M.V., Liu C., Frasinyuk M.S., Watt D.S.. A Direct Synthesis of 2-(?-Carboxyalkyl)-isoflavones from ortho-Hydroxylated Deoxybenzoins. Eur. J. Org. Chem.- 2018. – Vol. 39. – P. 5460- 5463.
52. Bondarenko S.P., Frasinyuk M.S., Mrug G.P., Vinogradova V.I., Khilya V.P.. Synthesis of Isoflavone-Anabasine Conjugates. Chem. Nat. Comp.- 2018.- Vol. 54, № 6. – P. 1068-1071 https://dx.doi.org/10.1007/s10600-018-2557-y.
53. Tsygankova V.A., Andrusevich Ya.V., Shtompel O.I., Solomyanny R.M., Hurenko A.O., Frasinyuk M.S., Mrug G.P., Shablykin O.V., Pilyo S.G., Kornienko A.M., Brovarets V.S.. Study of auxin-like and cytokinin-like activities of derivatives of pyrimidine, pyrazole, isoflavones, pyridine, oxazolopyrimidine and oxazole on haricot bean and pumpkin plants. Intern. J. Chem. Tech. Res.- 2018. -Vol. 11, № 10. – P. 174-190.
54. Nizhenkovska E.V., Sedko K.V., Golovchenko O.I., Golovchenko O.V.. Efficiency of the application of the 1,3-oxazole-4-ylphosphonic acid derivative on the substained arterial hypertension model in rats. Curr. Topics Pharmacology.- 2018. – Vol. 22, № 63. – P. 63-68.
55. Velihina Ye.S., Kachaeva M.V., Pilyo S.G., Mitiukhin O.P., Zhirnov V.V., Brovarets V.S.. Synthesys, characterization and in vitro anticancer evaluation of 7-(1,4-diazepan)substituted [1,3]oxazolo[4,5]pyrimidines. Chem. Res. J.- 2018 Doi:10.1007/s00044-018-2265-y.
56. Pavlenko O.L., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Sendiuk V.A., Kobzar P.Yu., Strelchuk V.V., Slominskyi Yu.L., Kurdiukov B.V., Kachkovskyi O.D., Prostota Ya.O.. Spectral and Quantum-Chemical Study of Interaction Between Fullerenes and Squaraine Dyes. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol.16, № 1. – P. 31–40. https://www.imp.kiev.ua/nanosys/ua/articles/2018/1/nano_vol16_iss1_p0031p0040_2018_abstract.html
57. Pavlenko E.L., Sendiuk V.A., Brusentsov V.A., Dmytrenko O.P., Kulish M.P., Obernihina N.V., Prostota Y.O., Kachkovsky O.D., Brovarets V.S.. Quantum-Chemical Study of Acceptor Properties of Fullerene and Its Bridge Derivatives. Nanosistemi, Nanomateriali, Nanotehnologii.- 2018. – Vol. 16, № 2. – P. 389-401 https://www.imp.kiev.ua/nanosys/ua/articles/2018/2/nano_vol16_iss2_p0389p0401_2018_abstract.html
58. Shokol T.V., Gorbulenko N.V., Frasinyuk M.S., Khilya V.P.. Furo[2,3-h]chromones and pyrano[2’,3’:5,6]chromeno[4,3-b]pyridines based on natural isoflavones. Chem. Nat. Comp.- 2018. – Vol. 54, № 6. – Р. 1065-1067 https://dx.doi.org/10.1007/s10600-018-2556-z.
59. Popova A.V., Bondarenko S.P., Frasinyuk M.S.. Synthesis and aminomethylation of regioisomeric 6-hydroxy-4-methyl- and 4-hydroxy-6-methylaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 9. – P. 832- 839.
60. Bondarenko S.P., Frasinyuk M.S.. Observations from aminomethylation of 7-substituted 6-hydroxyaurones. Chem. Heter. Comp.- 2018. – Vol. 54, № 8. – P. 765-762.
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
12 . Kolodiazhnyi O.I., Kolodiazhna A.O. Stereochemistry of nucleophilic substitution at trivalent phosphorus. // Phosphorus, Sulfur, and Silicon and the Related Elements.- 2017.- V. 192, N 6.- P. 621-633
13 . Ghamrawi S.,Bouchara J.-P.,Tarasyuk O.,Rogalsky S.,Lyoshina L.,Bulko O.,Bardeau J.-F. Promising Silicones Modified with Cationic Biocides for the Development of Antimicrobial Medical Devices // Materials Science and Engineering C. – 2017. – V. 75. – P. 969-979.
14 . McLaughlin K.,Folorunso A.,Deeni Y.,Foster D.,Hapca S.,Immoor C.,Koza A.,Mohammed I.,Moshynets J.,Rogalsky S.,Zawadzki K.,Spiers A. Biofilm formation and cellulose expression by Bordetella avium 197N, the causative agent of bordetellosis in birds and an opportunistic respiratory pathogen in humans. // Research in Microbiology. – 2017. – V. 168(5). – P. 419-430.
15 . Fainleib A.Vashchuk A.Starostenko O.Grigoryeva O.Rogalsky S.Nguyen T.-T., Grande D. Nanoporous Polymer Films of Cyanate Ester Resins Designed by Using Ionic Liquids as Porogens // Nanoscale Research Letters.- 2017.- 12:126 doi: 10.1186/s11671-017-1900-8. Epub 2017 Feb 17.
16 . Kenneth Seaton, Iuliia Little, Cameron Tate, Ray Mohseni, Marina Roginskaya, Volodymyr Povazhniy, Aleksey Vasiliev Adsorption of cesium on silica gel containing embedded phosphotungstic acid // Microporous and Mesoporous Materials.- 2017.- V. 244.- Р. 55-66.
17 . Yu.G. Voloshyna,O.P. Pertko,S.V. Konovalov, L.K. Patrylak Benzene as a by-product of toluene with methanol transformation on the basic zeolite catalysts and its presumable origin // Adsorption Science and Technology.- 2017. – V. 35.- issue 7-8.- P. 700-705.
18 . R. Korzh, V. Bortyshevskii Primary Reactions of Lignite-Water Slurry Gasification under the Supercritical Fluids in the Electric Field // The Journal of Supercritical Fluids. – 2017. – V. 127. – P. 166-175.
19. Nedybaliuk O., Chernyak V., Fedirchyk I.,Popkov V.,Bogaenko M.,Martysh E., Iukhymenko V., Bortyshevskyy V., Korzh R.V.,Dragnev S.,Prysiazhna O., Shapoval V. Plasma-Catalytic Reforming of Bio-Fuels and Diesel Fuel // IEEE Transactions on Plasma Science. Special Issue. – 2017. –V. 45, No. 7. – P. 1803-1811: Print ISSN: 0093-3813, Online ISSN: 1939-9375, DOI: 10.1109/TPS.201.2709348
20 . Muzychka O.V., Kobzar O.L.,Popova A.V., Frasinyuk M.S.,Vovk A.I. Carboxylated aurone derivatives as potent inhibitors of xanthine oxidase // Bioorg. Med. Chem. 2017.– 25.– P. 3606–3613.
21 . Khilya O.V., Milokhov D.S., Kononets L.A., Kobzar O.L.,Vovk A.I.,Volovenko Yu.M.. Synthesis and evaluation of new 2,6-diamino-5-hetarylpyrimidines as inhibitors of dihydrofolate reductase // Monatsh. Chem.-2017,DOI 10.1007/s00706-017-2032-7
22 . Bohdan A. Chalyk, Andrei A.Isakov, Maryna V. Butko, Kateryna V. Hrebeniuk, Olena V. Savych, Olexandr V. Kucher, Konstantin S. Gavrilenko, Tetiana V. Druzherko, Vladimir S. Yarmolchuk, Sergey Zozulya, Pavel K. Mykhailiuk Synthesis of 6-Azaspiro[4.3]alkanes Innovative Scaffolds for Drug Discovery // Eur. J. Org. Chem.- 2017.- № 31.- P.4530-4542.
23 . Lyubov V. Muzychka, Iryna O. Yaremchuk, Oksana V. Muzychka, Oleg B. Smolii 7-Substituted pyrrolo[2,3-d]-pyrimidines for the synthesis of new 1-deazapyrimido[1,2,3-cd]purines // French-Ukrainian J. Chem. 2017.- V.5, №2.- P.15-23.
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.
25 . Kondratov I.S.,Logvinenko I.G.,Tolmachova N.A.,Morev R.N.,Kliachyna M.A.,Clausen F.,Daniliuc C.,Haufe G. 2-Amino-4-(trifluoromethoxy)butanoic acid – first ?-aminoacid containing a CF3O-group in aliphatic position // Organic and Biomolecular Chemistry.- 2017.-15.- Р.672-679.
26 . Feskov I.O.,Chernykh A.V.,Kondratov I.S.,Klyachina M.,Daniliuc C.G.,Haufe G. Cyclobutyl-Containing Rigid Analogues of Threonine: Synthesis and Physical Chemical Properties // Journal of Organic Chemistry.- 2017.- 82 (23), Р. 12863–12868.
29 . Romanenko V.D.,Kukhar V.P. Phosphonate analogues of nucleoside polyphosphates // Arkivoc.-2017.- (i).- Р. 1-49.
30 . Vdovenko S.I.,Zhuk Yu.I.,Kukhar V.P.,Pagacz-Kostrzewab M.,WierzejewskabM.,Daniliuc C.-G. The conformational analysis of push–pull enaminones using Fourier transform IR and NMR spectroscopy, and quantum chemical calculations. VI. ?-N-Methylaminovinyl trifluoromethyl ketone ?-methyl-?-N-methylaminovinyl trifluoromethyl ketone // Journal of Molecular Structure.- 2017.-1128.- №. 1-3, Р.741–753.
31 . Borisova T.,PozdnyakovaN.,Shaitanova E.,Dudarenko M.,Haufe G.,Kukhar V. Effects of new fluorinated analogues of GABA, pregabalin bioisosters, on the ambient level and exocytotic release of [3H]GABA from rat brain nerve terminals. // Bioorganic & Medicinal Chemistry.- 2017.-25.- Р.759–764.
32 . Соломянный Р.Н.,
Пильо С.Г., Сливчук С.Р., Прокопенко В.М.,
Русанов Э.Б., Броварец В.С. Синтез 5-метил¬сульфонил-пири¬мидинов и их конденсированных производных // ЖОХ.- 2017. –Т.87, №3. – С. 398-404. DOI:10.1134/S1070363217030082.
33 . Выджак Р.Н., Панчишин С.Я., Броварец В.С. Алкилирование 4-(фенилтио)-1Н-пиразол-5-онов метилбромацетатом // ЖОХ.- 2017. – Т.87, №2. – С. 255-262.
34 . Tsygankova V.A., Andrusevich Ya., Shtompel A., Hurenko A.O., Solomyanny R.N., Mrug G., Frasinyuk M.S., Brovarets V.S. Stimulating effect of five and six-membered heterocyclic compounds on seed germination and vege- tative growth of maize (Zea mays L.) // International Journal of Biology Research.- 2016. – V.1, № 4. – P. 1-14.
35 . Demydchuk B.A., Rusanov E.B., Rusanova S.A., Brovarets V.S. Regioselective synthesis of bicyclic by 1,3,5-triazepine system starting from tetrachloro-2-aza-1,3-butadienes // Current Chemistry Letters.- 2017. – 6. – P. 49-54.
36 . Kachaeva M V.,
Kornienko Andriї N., Prokopenko Volodymyr M., Zhirnov Victor V., Prichard Mark N., Keith Kathy A., Yang Guang, Wang Hsu-Kun, Benerjee N.Sanjil, Chow Louise T., Broker Thomas R., Brovarets Volodymyr S. In Vitro Activity of Novel 1,3-Oxazole Derivatives against Human Papilloma-virus // Ibnosina J. of Med. And Biomed. Sciences.- 2017. – V.9, №4. – P.111-118.
37 . Гуренко А.О., Ключко С.В., Шаблыкин О.В., Броварец В.С. Ацилирование пиразоло[3,4-d]¬[1,2,3]триазин-4-онов // ЖОХ, 2017.- Т.87, вып.10. – C.1647-1652.
38 . Tsygankova V., Andrusevich Y., Shtompel O., Myroljubov O., Hurenko A., Solomyuny R., Mrug G., Frasinyuk M., Shablykin O., Brovarets V. Study of auxin, cytokinin and gibberellin – like activity of heterocyclic compounds derivatives of pyrimidin, pyridine, pyrazole and isoflavones // Eur. J. Biotechn. and Biosience.- 2016. – V.4, №12. – P. 29-44.
39 . Чумаченко С.А., Качаева М.В., Шаблыкин О.В., Русанов Э.Б., Броварец В.С. Взаимодействие N-(2,2-дихлор-1-цианоэтенил)-N’-метил(фенил)мочевин с алифатическими аминами // ЖОХ.- 2017. – Т.87, №5. – С.795-800.
Russ. J. Gen. Chem. 2017. – V.87.№5.-P. 985-990. DOI:10.1134/S1070363217050164.
40 . Чумаченко С.А., Шаблыкин О.В., Русанов Э.Б., Суховеев В.В., Броварец В.С. Синтез замещенных 5-амино-1Н-имидазол-4-карбонитрилов // ЖОХ.- 2017. – V.87, вып. 10.- С. 1732-1736.
41 . Holovchenko O., Naumenko A., Vydzhak R., Abdurakhmanova E., Prostota Ya., Kachkovsky O., Brovarets V. Electronik and spectrel properties of phosphonium ylides-betaines, derivatives of 2-oxazoline-5-one // Eur. Chem. Bull., 2017. – V.6, № 9. – Р. 380-392. http://dx.doi.org/10.17628/ecb.2017.6380-392.
42 . Шокол Т.В., Горбуленко Н.В., Фрасинюк М.С., Хиля В.П. Синтез 6-изоксазолилпроизводных 4-метил¬ум¬беллиферона // Химия природных соединений.- 2017.- 4. – С. 547-549.
43 . Popova A.V., Bondarenko S.P., Podobii E.V., Frasinyuk M.S., Vinogradova V.I. Synthesis of flavonoid derivatives of cytisine. 5. Aminomethylation of 6-hydroxyaurones // Chemistry of Natural Compounds.- 2017. – Vol. 53, No.4. – P. 603-607.
44 . Sendiuk V.A., Pavlenko E.L., Dmytrenko O.P.,
Kulish M.P., Viniychuk O.O., Prostota Ya.O., Kachkovsky O.D. Interaction of solitons on 2-dimensional branched ?-electron surface of graphene ribbons // International Journal of Quantum Chemistry.- 2017, electronic “early bird publication”. DOI:10.1002/qua.25454.
45 . Conceicao D.S., Ferreira D.P., Prostota Y., Kachkovsky O.D., Ferreira L.F. Vieira, Santos P.F. Longwavelength absorbing fluorescent polymethine dyes derived from the 6-(N,N-diethylamino)-1,2,3,4-tetrahydroxanthylium system // Journal of photochemistry and Photobiology A: Chemistry.- 2017. – V. 347. – P. 218-226. https://doi.org/1016/j.jphotochem.2017.07.045.
46 . Kobzar P.Y., Pavlenko E.L., Brusentsov V.A., Dmytrenko O.P., Kulish N.P., Bricks J.L., Slominskii Yu.L., Kurdyukov V.V., Tolmachev O.I., Kachkovsky O.D. Comparative Study of Electronic Structure Cyanine Bases versus Parent Cationic Cyanines // J. Advanc. Phys.- 2017. –V.6. – P. 1-12.
47 . Pavlenko O.L., Sendiuk V.A., Dmytrenko O.P., Kulish M.P., Sheludko E.V., Kachkovsky O.D., Ilchenko O.O., Shlapatska V.V. Electron and vibration structure of fluorine – containing polyamides film under high energetic electron irradiation // BAHT (Problems of Atomic Science and Technology).- 2017. – №4 (110). – P. 17-20.
48 . Shaydyuk Y.O., Levchenko S.M., Kurhuzenkau S.A., Anderson D., Masunov A.E., Kachkovsky O.D., Slominsky Y.L., Bricks J.L., Belfield K.D., Bondar M.V. Linear photo-physics, two-photon absorption and femtosecond transient absorption spectroscopy of styryl dye // Journal of Luminescence.- 2017. – V.183. – P. 360-367.
49 . Kachkovsky A., Obernikhina N., Prostota Ya., Naumenko A., Melnyk D., Yashchuk V. Estimation of the basicity of the donor strength of terminal groups in cationic polymethine dyes // Journal of Molecular Structure.- 2018. – 15. – P. 606-618.DOI://doi.org/10.1016/j.molstruc.2017.10.051
50 . Синенко В.О., Сливчук С.Р., Митюхин О.П., Броварец В.С. Синтез новых 1,3-тиазолкарбальде¬гидов. // ЖОХ.- 2017.- Т.87, вып. 2. – С. 1947-1956.
51 . Shablykin O.V., Merzhyievsky D.O.,
Shablykina O.V. The interaction of homophtalic anhydride with (triphenylphosphoranylidene)acetates // French-Ukr. J. Chem. – 2017. – Vol.5, №2. – P. 62-67.
52 . M. Derevyanchuk, S.Kretynin, O. Iakovenko, R. Litvinovskaуа, Y. Blume, J. Martinec, V. Khripach, V. Kravets Effect of 24-epibrassinolide on Brassica napus alternative respiratory pathway, guard cells movements and phospholipid signaling under salt stress // Steroids. – 2017. V. 117. – P. 16–24
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.
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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.
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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.
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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.
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27. Rogalsky S. Structural, thermal and antibacterial properties of polyamide 11/polymeric biocide polyhexamethylene guanidine dodecylbenzenesulfonate composites / S. Rogalsky, J.-F. Bardeau, H. Wu[et al.] // J Mater Sci. — 2016. — 51, №16. — P. 7716–7730.
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29. Sokolyuk P. A. Synthesis of diverse pyrazole-4-sulfonyl chlorides starting from 2-(benzylthio)malonaldehyde / P. A. Sokolyuk, I. S. Kondratov, O. V. Gavrylenko, A. A. Tolmachov // Mol. Divers. — 2016. — 20, №1. — P. 1–7.
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.
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36. Derevyanchuk M. Brassinosteroid-induced de novo protein synthesis in zea mays under salinity and bioinformatic approach for identification of heat shock proteins / M. Derevyanchuk, R. Litvinovskaya, V. Khripach, V. Kravets // Plant Growth Regul. — 2016. — 78, №3. — P. 297–305.
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2015 р.

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

2014 р.

1. Acena J. L. Asymmetric synthesis of alpha-amino acids via homologation of Ni(II) complexes of glycine schiff bases. Part 3: michael addition reactions and miscellaneous transformations / J. L. Acena, A. E. Sorochinsky, V. Soloshonok // Amino Acids. – 2014. – 46, №9. – P. 2047-2073.
2. Bondarenko S. P. Synthesis of 4-aryl-3-[2-hydroxy-4-(2-cytisin-12-ylethoxy)phenyl]pyrazoles / S. P. Bondarenko, M. S. Frasinyuk, V. I. Vinogradova, V. P. Khilya // Chem. Nat. Compd. – 2014. – 50, №5. – P. 889-891.
3. Brandmaier S. The qspr-thesaurus: the online platform of the cadaster project / S. Brandmaier, W. Peijnenburg, M. K. Durjava[et al.] // Altern Lab Anim. – 2014. – 42, №1. – P. 13-24.
4. Dahi A. Supported ionic liquid membranes for water and volatile organic compounds separation: sorption and permeation properties / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Journal of Membrane Science. – 2014. – 458. – P. 164-178.
5. Dahi A. Polyimide/ionic liquid composite membranes for fuel cells operating at high temperatures / A. Dahi, K. Fatyeyeva, D. Langevin[et al.] // Electrochimica Acta. – 2014. – 130. – P. 830-840.
6. Derevyanchuk M. V. Influence of brassinosteroids on plant cell alternative respiration pathway and antioxidant systems activity under abiotic stress conditions / M. V. Derevyanchuk, O. I. Grabelnyh, R. P. Litvinovskaya[et al.] // Biopolym. Cell. – 2014. – 30, №6. – P. 436-442.
7. D. Romanenko V. Progress in the development of pyrophosphate bioisosteres: synthesis and biomedical potential of 1-fluoro- and 1,1-difluoromethylene-1,1-bisphosphonates / V. D. Romanenko, V. P. Kukhar // Curr. Org. Chem. – 2014. – 18, №11. – P. 1491-1512.
8. Duboriz I. Polyaniline/poly(ethylene terephthalate) film as a new optical sensing material / I. Duboriz, A. Pud // Sensors and Actuators B: Chemical. – 2014. – 190. – P. 398-407.
9. Frasinyuk M. S. Pentapeptide boronic acid inhibitors of mycobacterium tuberculosis MYCP1 protease / M. S. Frasinyuk, S. Kwiatkowski, J. M. Wagner[et al.] // Bioorg. Med. Chem. Lett. – 2014. – 24, №15. – P. 3546-3548.
10. Goushcha A. O. Self-organization and coherency in biology and medicine / A. O. Goushcha, T. O. Hushcha, L. N. Christophorov, M. Goldsby // Open J. Bioph. – 2014. – 04, №04. – P. 119.
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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.
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16. Kolodiazhnyi O. I. Asymmetric catalysis as a method for the synthesis of chiral organophosphorus compounds / O. I. Kolodiazhnyi, V. P. Kukhar, A. O. Kolodiazhna // Tetrahedron: Asymmetry. – 2014. – 25, №12. – P. 865-922.
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.
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29. Kucher O. V. Enzyme-catalyzed kinetic resolution of 2,2,2-trifluoro-1-(heteroaryl)ethanols: experimental and docking studies / O. V. Kucher, A. O. Kolodiazhnaya, O. B. Smolii[et al.] // Eur. J. Org. Chem. – 2014. – 2014, №34. – P. 7692-7698.
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