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Інститут органічної хімії НАН України

Публікації

 Публікації співробітників Інституту за 2021 рік

  1. Bratenko, M.; Perepelytsya, O.; Yaremii, I.; Kupchanko, K.; Panasenko, N.; Vovk, M. Synthesis and Hypoglycemic Activity of the Derivatives of 4-(1,3-Thiazolidine-5-Ylidene)Pyrazole-3-Carbonic Acid and Its Esters. Biointerface Res. Appl. Chem. 2021, 11 (6), 14403–14412. https://doi.org/10.33263/BRIAC116.1440314412.
  2. Barus, M.; Rotar, D.; Bratenko, M.; Panasenko, N.; Zvarych, V.; Stasevych, M.; Vovk, M. Synthesis and Evaluation of Antimicrobial Activities of New Functional Derivatives of 3-[5-(4-Nitrophenyl)-2-Furyl]-4-Pyrazole-Carbaldehydes. Biointerface Res. Appl. Chem. 2021, 11 (4), 12159–12169. https://doi.org/10.33263/BRIAC114.1215912169.
  3. Seliverstova, E.; Ibrayev, N.; Omarova, G.; Ishchenko, A.; Kucherenko, M. Competitive Influence of the Plasmon Effect and Energy Transfer between Chromophores and Ag Nanoparticles on the Fluorescent Properties of Indopolycarbocyanine Dyes. J. Lumin. 2021, 235. https://doi.org/10.1016/j.jlumin.2021.118000.
  4. Grozav, A.; Fedoriv, M.; Chornous, V.; Yakovychuk, N.; Kemskyi, S.; Vovk, M. Synthesis and Bioevaluation of 5-Chloro-4-(1,3-Oxazol-5-Yl)-1Н-Pyrrole-3-Carboxyamides as Antimicrobial Agents. Biointerface Res. Appl. Chem. 2021, 11 (3), 10595–10606. https://doi.org/10.33263/BRIAC113.1059510606.
  5. Zasukha, S.; Khairulin, A.; Shermolovich, Y. The Reactions of N-Trimethylsilyl Substituted Ethers of α- and β-Amino Acids with Sulfur Tetrafluoride and Morpholinosulfur Trifluoride. J. Sulfur Chem. 2021, 1–13. https://doi.org/10.1080/17415993.2021.1912045.
  6. Radchenko, D. S.; Naumchyk, V. S.; Dziuba, I.; Kyrylchuk, A. A.; Gubina, K. E.; Moroz, Y. S.; Grygorenko, O. O. One-Pot Parallel Synthesis of 1,3,5-Trisubstituted 1,2,4-Triazoles. Mol. Divers. 2021. https://doi.org/10.1007/s11030-021-10218-2.
  7. Shishkina, S. V.; Ishchenko, A. A.; Kulinich, A. V. Structure and Intermolecular Interactions of the Fully Negative Solvatochromic Merocyanine in the Crystal Phase. Struct. Chem. 2021, 32 (3), 1341–1345. https://doi.org/10.1007/s11224-021-01774-2.
  8. Markitanov, Y. N.; Timoshenko, V. M.; Rusanov, E. B.; Shermolovich, Y. G. [3+2] Cycloaddition Reactions of 1-Substituted 3,3,3-Trifluoropropenes with Isonitriles – Synthesis of Pyrroles and Pyrrolines. Chem. Heterocycl. Compd. 2021, 57 (3), 253–260. https://doi.org/10.1007/s10593-021-02901-x.
  9. Kobzar, L. L.; Shulha, Y. V.; Buldenko, V. M.; Mrug, G. P.; Kolotylo, M. V.; Stanko, O. V.; Onysko, P. P.; Vovk, I. I. Alkyl and Aryl α-Ketophosphonate Derivatives as Photoactive Compounds Targeting Glutathione S-Transferases. Phosphorus, Sulfur Silicon Relat. Elem. 2021. https://doi.org/10.1080/10426507.2021.1901703.
  10. Yakovenko, G. G.; Yagodkina-Yakovenko, M. S.; Suykov, S. Y.; Vovk, M. V. A Beckmann Rearrangement Initiated by Trifluoromethanesulfonic Anhydride in the Synthesis of Compounds Containing a New Pyrazolo[3’,4’:5,6]Pyrido[3,2-b]Azepine Heterocyclic System. Chem. Heterocycl. Compd. 2021, 57 (2), 199–206. https://doi.org/10.1007/s10593-021-02893-8.
  11. Biffis, A.; Baron, M.; Tubaro, C.; Rancan, M.; Armelao, L.; Marchenko, A.; Koidan, G.; Hurieva, A. N.; Kostyuk, A. Gold(I) Complexes with Multifunctional Phosphane Ligands: Synthesis and Catalysis. Inorganica Chim. Acta 2021, 517. https://doi.org/10.1016/j.ica.2020.120218.
  12. Belous, A. G.; Ishchenko, A. A.; V’yunov, O. I.; Torchyniuk, P. V. Preparation and Properties of Films of Organic-Inorganic Perovskites MAPbX3 (MA = CH3NH3; X = Cl, Br, I) for Solar Cells: A Review. Theor. Exp. Chem. 2021, 56 (6), 359–386. https://doi.org/10.1007/s11237-021-09666-6.
  13. Rayevsky, A.; Sharifi, M.; Demianenko, E.; Volochnyuk, D.; Tukalo, M. Effect of Charge Distribution in a Modified TRNA Substrate on Pre-Reaction Protein-TRNA Complex Geometry. ACS Omega 2021, 6 (6), 4227–4235. https://doi.org/10.1021/acsomega.0c05143.
  14. Zvarych, V.; Stasevych, M.; Novikov, V.; Vovk, M. Synthesis and Study of Antimicrobial Activity of 2-Dithiocarbamate-n-(9,10-Dioxo-9,10-Dihydroanthracenyl)Acetamides. Biointerface Res. Appl. Chem. 2021, 11 (1), 7725–7734. https://doi.org/10.33263/BRIAC111.77257734.
  15. Herasymchuk, M.; Melnykov, K. P.; Yarmoliuk, D. V.; Serhiichuk, D.; Rotar, V.; Pukhovoi, T.; Kuchkovska, Y. O.; Holovach, S.; Volochnyuk, D. M.; Ryabukhin, S. V.; Grygorenko, O. O. Last of the Gem-Difluorocycloalkanes 2: Synthesis of Fluorinated Cycloheptane Building Blocks. European J. Org. Chem. 2021. https://doi.org/10.1002/ejoc.202001530.
  16. Borodkin, Y. S.; Shermolovich, Y. G. Synthesis of Novel 1,4-Oxathiine Derivatives Containing Polyfluoroalkyl Substituents at Positions 2 and 6. Chem. Heterocycl. Compd. 2021, 57 (1), 69–74. https://doi.org/10.1007/s10593-021-02869-8.
  17. Palamar, A. A.; Yaremii, I. N.; Chornous, V. A.; Grozav, A. N.; Vovk, M. V. Effects of [(1-Phenyl-5-Formyl-1H-Imidazol-4-Yl)Thio]Acetic Acid on the Antioxidant Status of the Liver and Kidney in Rats with Tetrachloromethane Poisoning. Pharm. Chem. J. 2021, 54 (11), 1101–1105. https://doi.org/10.1007/s11094-021-02328-w.
  18. Utecht-Jarzyńska, G.; Mykhaylychenko, S. S.; Rusanov, E. B.; Shermolovich, Y. G.; Jasiński, M.; Mlostoń, G. Highly Fluorinated 2,3-Dihydro-1,3,4-Thiadiazole Derivatives via [3+2]-Cycloadditions of Tertiary Thioamides with Nitrile Imines Derived from Trifluoroacetonitrile. J. Fluor. Chem. 2021, 242. https://doi.org/10.1016/j.jfluchem.2020.109702.
  19. Yesypenko, O. A.; Osipova, A. O.; Tribrat, O. O.; Kravchenko, S. O.; Usachov, O. M.; Dyakonenko, V. V.; Ryabitskii, A. B.; Pirozhenko, V. V.; Shishkina, S. V.; Rozhenko, A. B.; Kalchenko, V. I. Synthesis and Enantiorecognition Properties of Stereoisomeres of Inherently Chiral Propyloxy-Octyloxy-Calix[4]Arene Acetic Acids. Tetrahedron 2021, 80. https://doi.org/10.1016/j.tet.2020.131894.
  20. Zabolotna, Y.; Lin, A.; Horvath, D.; Marcou, G.; Volochnyuk, D. M.; Varnek, A. Chemography: Searching for Hidden Treasures. J. Chem. Inf. Model. 2021, 61 (1), 179–188. https://doi.org/10.1021/acs.jcim.0c00936.
  21. Mityuk, A. P.; Hrebonkin, A.; Lebed, P. S.; Grabchuk, G. P.; Volochnyuk, D. M.; Ryabukhin, S. V. Efficient Route for the Synthesis of Diverse Heteroannelated 5-Cyanopyridines. Synth. 2021. https://doi.org/10.1055/a-1360-9852.
  22. Kulinich, A. V.; Ishchenko, A. A.; Bondarev, S. L.; Knyukshto, V. N. Effect of Donor and Acceptor End-Groups on Electronic Structure and Spectral-Fluorescent Properties of Merocyanines in Frozen Ethanol. J. Photochem. Photobiol. A Chem. 2021, 405. https://doi.org/10.1016/j.jphotochem.2020.112932.
  23. Golembiovska, О.; Voskoboinik, O.; Berest, G.; Kovalenko, S.; Logoyda, L. Method Development and Validation for the Determination of Residual Solvents in Quinabut API by Using Gas Chromatography. Message 2. Pharmacia 2021, 68 (1), 53–59. https://doi.org/10.3897/pharmacia.68.e52119.
  24. Golembiovska, O.; Voskoboinik, O.; Berest, G.; Kovalenko, S.; Logoyda, L. Quality by Design Approach for Simultaneous Determination of Original Active Pharmaceutical Ingredient Quinabut and Its Impurities by Using HPLC. Message. Pharmacia 2021, 68 (1), 79–87. https://doi.org/10.3897/pharmacia.68.e50704.
  25. Demchuk, O. P.; Hryshchuk, O. V.; Vashchenko, B. V.; Trofymchuk, S. A.; Melnykov, K. P.; Skreminskiy, A.; Volochnyuk, D. M.; Grygorenko, O. O. Fluoroalkyl-Containing 1,2-Disubstituted Cyclobutanes: Advanced Building Blocks for Medicinal Chemistry. European J. Org. Chem. 2021, 2021 (1), 87–95. https://doi.org/10.1002/ejoc.202001345.

Публікації співробітників Інституту за 2020 рік

  1. Quandt, A.; Kyrylchuk, A.; Seifert, G.; Tománek, D. Liquid Flow through Defective Layered Membranes: A Phenomenological Description. Phys. Rev. Appl. 2020, 14 (4), 44038. https://doi.org/10.1103/PhysRevApplied.14.044038.
  2. Litvinchuk, M. B.; Bentya, A. V.; Saliyeva, L. N.; Rusanov, E. B.; Vovk, M. V. Characteristic Features of Interaction between (5-Methyl-1,3-Thiazolidin-2-Ylidene) Ketones and Tosyl Azide. Chem. Heterocycl. Compd. 2020, 56 (9), 1230–1233. https://doi.org/10.1007/s10593-020-02804-3.
  3. Kozachkova, O. M.; Tsaryk, N. V.; Shtokvish, O. O.; Pekhnyo, V. I.; Trachevskii, V. V.; Rozhenko, A. B.; Dyakonenko, V. V. Interaction between 2-Pyrrolidine-1-Hydroxymethane-1,1-Diphosphonic Acid and Palladium(II) in Aqueous Solutions. Inorganica Chim. Acta 2020, 505, 119503. https://doi.org/10.1016/j.ica.2020.119503.
  4. Litvinchuk, M. B.; Bentya, A. V.; Slyvka, N. Y.; Rusanov, E. B.; Vovk, M. V. A Convenient Method of Synthesis of 8-Acyl-2,3,6,7-Tetrahydro-5Н-[1,3]Thiazolo[3,2-c]Pyrimidin-5-Ones. Chem. Heterocycl. Compd. 2020, 56 (1), 101–107. https://doi.org/10.1007/s10593-020-02629-0.
  5. Mechchate, H.; Es-Safi, I.; Bourhia, M.; Kyrylchuk, A.; El Moussaoui, A.; Conte, R.; Ullah, R.; Ezzeldin, E.; Mostafa, G. A.; Grafov, A.; Bekkari, H.; Bousta, D. In-Vivo Antidiabetic Activity and In-Silico Mode of Action of LC/MS-MS Identified Flavonoids in Oleaster Leaves. Molecules 2020, 25 (21), 5073. https://doi.org/10.3390/molecules25215073.
  6. Tereshchenko, O. D.; Perebiynis, M. Y.; Knysh, I. V.; Vasylets, O. V.; Sorochenko, A. A.; Slobodyanyuk, E. Y.; Rusanov, E. B.; Borysov, O. V.; Kolotilov, S. V.; Ryabukhin, S. V.; Volochnyuk, D. M. Electrochemical Scaled-up Synthesis of Cyclic Enecarbamates as Starting Materials for Medicinal Chemistry Relevant Building Bocks. Adv. Synth. Catal. 2020, 362 (15), 3229–3242. https://doi.org/10.1002/adsc.202000450.
  7. Khlebnikova, T. S.; Piven’, Y. A.; Zinovich, V. G.; Baranovskii, A. V.; Rusanov, B.; Panibrat, O. V.; Ogurtsova, S.; Lakhvich, F. A. Synthesis and Cytotoxic Activity of Fluorine-Containing 6,7-Dihydroindazolone and 6,7-Dihydrobenzisoxazolone Derivatives. Pharm. Chem. J. 2020, 54 (7), 700–706. https://doi.org/10.1007/s11094-020-02258-z.
  8. Tsizorik, N. M.; Hrynyshyn, Y. V.; Musiychuk, A. R.; Bol’but, A. V.; Nechayev, M.; Vovk, M. V. Synthesis of 4-Heteryl-Substituted Derivatives of Methylpyrazolo[1,5-a]Pyrazine-4-Carboxylates. Chem. Heterocycl. Compd. 2020, 56 (12), 1554–1559. https://doi.org/10.1007/s10593-020-02849-4.
  9. Cheipesh, T. A.; Kharchenko, D. V.; Taranets, Y. V.; Rodik, R. V.; Mchedlov-Petrossyan, N. O.; Poberezhnyk, M. M.; Kalchenko, V. I. Reaction Rates in Aqueous Solutions of Cationic Colloidal Surfactants and Calixarenes: Acceleration and Resolution of Two Steps of Fluorescein Diesters Hydrolysis. Colloids Surfaces A Physicochem. Eng. Asp. 2020, 606. https://doi.org/10.1016/j.colsurfa.2020.125479.
  10. Danyliuk, I. Y.; Vaskevych, A. I.; Vaskevych, R. I.; Rusanov, E. B.; Vovk, M. V. Cyclosulfenylation of N-(1(2)-Naphthyl) Styrylacetamides as a Synthetic Route to 4(2)-Arylthio Naphtho[1,2-b]([2,1-b])Azepin-2(4)-Ones. J. Sulfur Chem. 2020, 42 (3), 264–280. https://doi.org/10.1080/17415993.2020.1855431.
  11. Ivanytsya, M. O.; Ryabukhin, S. V.; Volochnyuk, D. M.; Kolotilov, S. V. Modern Approaches to the Creation of Immobilized Metal-Complex Catalysts for Hydrogenation, Alkene Metathesis, and Cross-Coupling Processes: A Review. Theor. Exp. Chem. 2020, 56 (5), 283–308. https://doi.org/10.1007/s11237-020-09660-4.
  12. Marchenko, A.; Koidan, G.; Hurieva, A. N.; Shishkina, S.; Rusanov, E.; Kostyuk, A. Ring Enlargement of N-Phosphanyl-1,2,3,4-Tetrahydroquinazolines. J. Org. Chem. 2020, 85 (22), 14467–14472. https://doi.org/10.1021/acs.joc.0c00750.
  13. Blahun, O. P.; Rozhenko, A. B.; Rusanov, E.; Zhersh, S.; Tolmachev, A. A.; Volochnyuk, D. M.; Grygorenko, O. O. Twisting and Turning the Sulfonamide Bond: A Synthetic, Quantum Chemical, and Crystallographic Study. J. Org. Chem. 2020, 85 (8), 5288–5299. https://doi.org/10.1021/acs.joc.9b03394.
  14. Tairov, M. A.; Levchenko, V.; Stadniy, I. A.; Dmytriv, Y. V.; Dehtiarov, S. O.; Kibalnyi, M. O.; Melnyk, A. V.; Veselovych, S. Y.; Borodulin, Y. V.; Kolotilov, S. V.; Ryabukhin, S. V.; Volochnyuk, D. M. Practical Synthetic Method for Functionalized 1-Methyl-3/5-(Trifluoromethyl)-1H-Pyrazoles. Org. Process Res. Dev. 2020, 24 (11), 2619–2632. https://doi.org/10.1021/acs.oprd.0c00300.
  15. Cherednichenko, A. S.; Bezgubenko, L. V.; Rusanov, E. B.; Onys’ko, P. P.; Rassukana, Y. V. Enantiomeric N-Tert-Butylsulfinyl Imines of Methyl Trifluoropyruvate: Promising Building Blocks in Asymmetric Synthesis of α-Trifluoromethylated Amino Acids and Derivatives. ChemistrySelect 2020, 5 (43), 13569–13574. https://doi.org/10.1002/slct.202003500.
  16. Shermolovich, Y. G.; Khyzhan, A. I.; Rusanov, E. B.; Mazepa, A. V.; Rakipov, I. M.; Mykhaylychenko, S. S. Reaction of N,N-Disubstituted Polyfluoroalkanethioamides with Diazomethane: Entry to New Thiirane Derivatives. European J. Org. Chem. 2020. https://doi.org/10.1002/ejoc.202001104.
  17. Saliyeva, L. N.; Diachenko, I. V.; Vas’kevich, R. I.; Slyvka, N. Y.; Vovk, M. V. Imidazothiazoles and Their Hydrogenated Analogs: Methods of Synthesis and Biomedical Potential. Chem. Heterocycl. Compd. 2020, 56 (11), 1394–1407. https://doi.org/10.1007/s10593-020-02827-w.
  18. Asaula, V. M.; Lytvynenko, A. S.; Mishura, A. M.; Kurmach, M. M.; Buryanov, V. V.; Gavrilenko, K. S.; Ryabukhin, S. V.; Volochnyuk, D. M.; Kolotilov, S. V. In-Situ Formation of NixB/MIL-101(Cr) and Pd/MIL-101(Cr) Composites for Catalytic Hydrogenation of Quinoline. Inorg. Chem. Commun. 2020, 121. https://doi.org/10.1016/j.inoche.2020.108203.
  19. Litvinchuk, M. B.; Bentya, A. V.; Slyvka, N. Y.; Vovk, M. V. 2-Ylidene-1,3-Thiazolidines and Their Nonhydrogenated Analogs: Methods of Synthesis and Chemical Properties. Chem. Heterocycl. Compd. 2020, 56 (9), 1130–1145. https://doi.org/10.1007/s10593-020-02787-1.
  20. Yesypenko, O. A.; Boiko, Y. S.; Belikov, K. N.; Bryleva, K. Y.; Bunina, Z. Y.; Rozhenko, A. B.; Shishkina, S. V.; Drapailo, A. B.; Rodik, R. V.; Atamas, L. I.; Golub, A. A.; Kalchenko, V. I. Surface Modification of Aminopropylated Silica Gel with Tetraphosphorylated Bis-Methoxycarbonylmethoxycalix[4]Arenes for Effective Europium(Iii) Sorption. Theor. Exp. Chem. 2020, 56 (4), 252–260. https://doi.org/10.1007/s11237-020-09656-0.
  21. Asaula, V. M.; Shvets, O. V.; Pariiska, O. O.; Bur’yanov, V. V.; Ryabukhin, S. V.; Volochnyuk, D. M.; Kolotilov, S. V. Composites Based on Nanodispersed Nickel, Graphene-Like Carbon, and Aerosil for Catalytic Hydrogenation of Furfural and Quinoline. Theor. Exp. Chem. 2020, 56 (4), 261–267. https://doi.org/10.1007/s11237-020-09657-z.
  22. Grygorenko, O. O.; Chernykh, A. V.; Olifir, O. S.; Kuchkovska, Y. O.; Volochnyuk, D. M.; Yarmolchuk, V. S. Fluoroalkyl-Substituted Cyclopropane Derivatives: Synthesis and Physicochemical Properties. J. Org. Chem. 2020, 85 (19), 12692–12702. https://doi.org/10.1021/acs.joc.0c01848.
  23. da Silva Mesquita, R.; Kyrylchuk, A.; Costa de Oliveira, R.; Costa Sá, I. S.; Coutinho Borges Camargo, G.; Soares Pontes, G.; Araújo da Silva, F. M.; Nunomura, R. de C. S.; Grafov, A. Alkaloids of Abuta Panurensis Eichler: In Silico and in Vitro Study of Acetylcholinesterase Inhibition, Cytotoxic and Immunomodulatory Activities. PLoS One 2020, 15 (9 September). https://doi.org/10.1371/journal.pone.0239364.
  24. Ivonin, S. P.; Yurchenko, A. A.; Voloshchuk, V. V.; Yurchenko, S. A.; Rusanov, E. B.; Pirozhenko, V. V.; Volochnyuk, D. M.; Kostyuk, A. N. A Convenient Approach to 3-Trifluoromethyl-6-Azaindoles. J. Fluor. Chem. 2020, 233. https://doi.org/10.1016/j.jfluchem.2020.109509.
  25. Syrota, N.; Kemskiy, S. V.; Bol’but, A. V.; Chernobaev, I. I.; Vovk, M. V. An Efficient Method for Accessing Carboannulated and Functionalized [1,2,3]Triazolo[4,5-b]Pyridines. Chem. Heterocycl. Compd. 2020, 56 (8), 1048–1053. https://doi.org/10.1007/s10593-020-02771-9.
  26. Tkachuk, V. M.; Lukianov, O. O.; Vovk, M. V.; Gillaizeau, I.; Sukach, V. A. Chan-Evans-Lam N1-(Het)Arylation and N1-Alkenylation of 4-Fluoroalkylpyrimidin-2(1H)-Ones. Beilstein J. Org. Chem. 2020, 16, 2304–2313. https://doi.org/10.3762/BJOC.16.191.
  27. Kleban, I.; Krokhmaliuk, Y.; Reut, S.; Shuvakin, S.; Pendyukh, V. V.; Khyzhan, O. I.; Yarmoliuk, D. S.; Tymtsunik, A. V.; Rassukana, Y. V.; Grygorenko, O. O. Multigram Synthesis of Heterabicyclo[n.1.0]Alkan-1-Yl Trifluoroborates. European J. Org. Chem. 2020. https://doi.org/10.1002/ejoc.202000977.
  28. Adamovskyi, M. I.; Avramenko, M. M.; Volochnyuk, D. M.; Ryabukhin, S. V. Fluoral Hydrate: A Perspective Substrate for the Castagnoli-Cushman Reaction. ACS Omega 2020, 5 (33), 20932–20942. https://doi.org/10.1021/acsomega.0c02394.
  29. Sierov, D.; Nazarenko, K.; Shvydenko, K.; Shvydenko, T.; Kostyuk, A. Synthetic Approaches to Tetrahydro-2,7- and -1,6-Naphthyridines. Tetrahedron Lett. 2020, 61 (33). https://doi.org/10.1016/j.tetlet.2020.152194.
  30. Pavlenko, N. V.; Peng, S.; Petrov, V.; Jackson, A.; Sun, X.; Sprague, L.; Yagupolskii, Y. L. Catalytic Hydrosilylation of Hydrofluoroolefins (HFOs): Synthesis of New Fluorinated Silanes and Diversity of Their Synthetic Character. European J. Org. Chem. 2020, 2020 (33), 5425–5435. https://doi.org/10.1002/ejoc.202000853.
  31. Hys, V. Y.; Shevchuk, O. I.; Vashchenko, B. V.; Karpenko, O. V.; Gorlova, A. O.; Grygorenko, O. O. Functionalization of 2-Trifluoromethyl-1H-Pyrrole: A Convenient Entry into Advanced Fluorinated Building Blocks Including All Isomeric 2-(Trifluoromethyl)Prolines. European J. Org. Chem. 2020, 2020 (25), 3896–3905. https://doi.org/10.1002/ejoc.202000519.
  32. Pikun, N. V.; Sobolev, A.; Plotniece, A.; Rucins, M.; Vigante, B.; Petrova, M.; Muhamadejev, R.; Pajuste, K.; Shermolovich, Y. G. Synthesis of Fluorinated 3,6-Dihydropyridines and 2-(Fluoromethyl)Pyridines by Electrophilic Fluorination of 1,2-Dihydropyridines with Selectfluor®. Molecules 2020, 25 (14). https://doi.org/10.3390/molecules25143143.
  33. Aristova, D.; Volynets, G.; Chernii, S.; Losytskyy, M.; Balanda, A.; Slominskii, Y.; Mokhir, A.; Yarmoluk, S.; Kovalska, V. Far-Red Pentamethine Cyanine Dyes as Fluorescent Probes for the Detection of Serum Albumins. R. Soc. Open Sci. 2020, 7 (7), 200453. https://doi.org/10.1098/rsos.200453.
  34. Vaskevych, R. I.; Vaskevych, A. I.; Rusanov, E. B.; Mel’nyk, O. Y.; Vovk, M. V. Synthesis of New-Type 1,3,6-Triazocine via Intramolecular Reactions of Iodocyclization and [3+2] Azido Cycloaddition. J. Heterocycl. Chem. 2020, 57 (8), 3202–3212. https://doi.org/10.1002/jhet.4028.
  35. Guzyr, O. I.; Kozel, V. N.; Rusanov, E. B.; Rozhenko, O. B.; Fetyukhin, V. N.; Shermolovich, Y. G. Enhanced Preparation of Aryl and Heteryl Sulfur Pentafluorides Using Mercury (II) Oxide – Hydrogen Fluoride Media as a Fluorinating Reagent. J. Fluor. Chem. 2020, 239, 109635. https://doi.org/10.1016/j.jfluchem.2020.109635.
  36. Bondareva, J.; Kolotylo, M.; Rozhkov, V.; Burilov, V.; Lukin, O. A Convergent Approach to Sulfonimide-Based Dendrimers and Dendrons. Tetrahedron Lett. 2020, 61 (25). https://doi.org/10.1016/j.tetlet.2020.152011.
  37. Sedykh, A. E.; Sotnik, S. A.; Kurth, D. G.; Volochnyuk, D. M.; Kolotilov, S. V.; Müller-Buschbaum, K. Similarities of Coordination Polymer and Dimeric Complex of Europium(III) with Joint and Separate Terpyridine and Benzoate. Zeitschrift fur Anorg. und Allg. Chemie 2020, 646 (20), 1710–1714. https://doi.org/10.1002/zaac.201900319.
  38. Kleban, I.; Radchenko, D. S.; Tymtsunik, A. V.; Shuvakin, S.; Konovets, A. I.; Rassukana, Y.; Grygorenko, O. O. Cyclopropyl Boronic Derivatives in Parallel Synthesis of Sp 3-Enriched Compound Libraries. Monatshefte fur Chemie 2020, 151 (6), 953–962. https://doi.org/10.1007/s00706-020-02619-0.
  39. Kulinich, A. V.; Ishchenko, A. A. Structural Background of Fast Nonradiative Deexcitation of Benzo[Cd]Indole Polymethine Dyes. Comput. Theor. Chem. 2020, 1178. https://doi.org/10.1016/j.comptc.2020.112782.
  40. Orysyk, S. I.; Borovyk, P. V.; Repich, H. H.; Severynovska, O. V.; Zborovskii, Y. L.; Mishchenko, A. M.; Orysyk, V. V.; Pekhnyo, V. I.; Vovk, M. V. Synthesis, Spectral Characterization and DFT Calculations of Novel Ag(I) π-Coordination Polymeric Complexes Based on N-Allylmorpholine-4-Carbothioamide. J. Mol. Struct. 2020, 1208. https://doi.org/10.1016/j.molstruc.2020.127866.
  41. Pang, Y.; Fan, S.; Wang, Q.; Oprych, D.; Feilen, A.; Reiner, K.; Keil, D.; Slominsky, Y. L.; Popov, S.; Zou, Y.; Strehmel, B. NIR-Sensitized Activated Photoreaction between Cyanines and Oxime Esters: Free-Radical Photopolymerization. Angew. Chemie – Int. Ed. 2020, 59 (28), 11440–11447. https://doi.org/10.1002/anie.202004413.
  42. 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. Phosphorus, Sulfur Silicon Relat. Elem. 2020, 195 (10), 848–857. https://doi.org/10.1080/10426507.2020.1759062.
  43. De Oliveira, R. C.; Pontes, G. S.; Kostyuk, A.; Camargo, G. B. C.; Dhyani, A.; Shvydenko, T.; Shvydenko, K.; Grafov, A. Anticancer and Immunomodulatory Activities of a Novel Water-Soluble Derivative of Ellipticine. Molecules 2020, 25 (9). https://doi.org/10.3390/molecules25092130.
  44. Sokolenko, T. M.; Yagupolskii, Y. L. Trifluoromethoxypyrazines: Preparation and Properties. Molecules 2020, 25 (9). https://doi.org/10.3390/molecules25092226.
  45. Ostos, F. J.; Lebrón, J. A.; López-Cornejo, P.; López-López, M.; García-Calderón, M.; García-Calderón, C. B.; Rosado, I. V.; Kalchenko, V. I.; Rodik, R. V.; Moyá, M. L. Self-Aggregation in Aqueous Solution of Amphiphilic Cationic Calix[4]Arenes. Potential Use as Vectors and Nanocarriers. J. Mol. Liq. 2020, 304. https://doi.org/10.1016/j.molliq.2020.112724.
  46. Ivonin, S. P.; Rusanov, E. B.; Volochnyuk, D. M. Synthesis and Oxidation of All Isomeric 2-(Pyrazolyl)Ethanols. Chem. Heterocycl. Compd. 2020, 56 (3), 320–325. https://doi.org/10.1007/s10593-020-02662-z.
  47. Humbert, N.; Kovalenko, L.; Saladini, F.; Giannini, A.; Pires, M.; Botzanowski, T.; Cherenok, S.; Boudier, C.; Sharma, K. K.; Real, E.; Zaporozhets, O. A.; Cianférani, S.; Seguin-Devaux, C.; Poggialini, F.; Botta, M.; Zazzi, M.; Kalchenko, V. I.; Mori, M.; Mély, Y. (Thia)Calixarenephosphonic Acids as Potent Inhibitors of the Nucleic Acid Chaperone Activity of the HIV-1 Nucleocapsid Protein with a New Binding Mode and Multitarget Antiviral Activity. ACS Infect. Dis. 2020, 6 (4), 687–702. https://doi.org/10.1021/acsinfecdis.9b00290.
  48. Kremlev, M. M.; Mushta, O. I.; Yagupolskii, Y. L.; Rusanova, J. A.; Peng, S.; Petrov, V. Synthesis of 9,10-Bis(Trifluoromethyl)Benzobarrelenes through Reaction of Hexafluorobut-2-Yne and Substituted Naphthalenes. J. Fluor. Chem. 2020, 232. https://doi.org/10.1016/j.jfluchem.2020.109450.
  49. Mushta, O.; Kremlev, M. M.; Filatov, A. A.; Yagupolskii, Y. L. Reaction of Substituted Phenols and Alcohols with (E)-1-Chloro-3,3,3-Trifluoropropene (HFCO-1233zd). J. Fluor. Chem. 2020, 232. https://doi.org/10.1016/j.jfluchem.2020.109456.
  50. 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 SF 4: Safety vs Efficacy. Synlett 2020, 31 (6), 565–574. https://doi.org/10.1055/s-0037-1610744.
  51. Gerasov, A.; Dolgonos, G. A.; Mandzhulo, A. Y.; Ryabitsky, A.; Fetyukhin, V.; Lukin, O.; Shivanyuk, A. Selective Synthesis of Exo -Spiro[2′,2′-Difluorocyclopropane-3′,2′-Tropanes]. Synth. 2020, 52 (7), 1015–1024. https://doi.org/10.1055/s-0039-1691560.
  52. Ivaniuk, K.; Pidluzhna; Stakhira, P.; Baryshnikov, G. V.; Kovtun, Y. P.; Hotra, Z.; Minaev, B. F.; Ågren, H. BODIPY-Core 1,7-Diphenyl-Substituted Derivatives for Photovoltaics and OLED Applications. Dye. Pigment. 2020, 175. https://doi.org/10.1016/j.dyepig.2019.108123.
  53. Trofymchuk, S.; Bugera, M. Y.; Klipkov, A. A.; Razhyk, B.; Semenov, S.; Tarasenko, K.; Starova, V. S.; Zaporozhets, O. A.; Tananaiko, O. Y.; Alekseenko, A. N.; Pustovit, Y.; Kiriakov, O.; Gerus, I. I.; Tolmachev, A. A.; Mykhailiuk, P. K. Deoxofluorination of (Hetero)Aromatic Acids. J. Org. Chem. 2020, 85 (5), 3110–3124. https://doi.org/10.1021/acs.joc.9b03011.
  54. Ikim, M. I.; Dekhtyar’, M. L.; Rozenbaum, V. M.; Bugaev, A. S.; Trakhtenberg, L. I. Symmetry of Brownian Photomotors. Russ. J. Phys. Chem. B 2020, 14 (2), 332–335. https://doi.org/10.1134/S1990793120020074.
  55. Yakovenko, G. G.; Lukianov, O.; Yagodkina-Yakovenko, M. S.; Bol’but, A. V.; Vovk, M. V. Synthesis of 5-Amino-1H-Pyrazolo[4,3-b]Pyridine Derivatives and Annulation of Imidazole and Pyrimidine Rings Thereto. Chem. Heterocycl. Compd. 2020, 56 (3), 347–354. https://doi.org/10.1007/s10593-020-02666-9.
  56. Derevyanko, N. A.; Ishchenko, A. A.; Kulinich, A. V. Deeply Coloured and Highly Fluorescent Dipolar Merocyanines Based on Tricyanofuran. Phys. Chem. Chem. Phys. 2020, 22 (5), 2748–2762. https://doi.org/10.1039/c9cp05827c.
  57. Demchuk, O. P.; Hryshchuk, O. V.; Vashchenko, B. V.; Kozytskiy, A. V.; Tymtsunik, A. V.; Komarov, I. V.; Grygorenko, O. O. Photochemical [2 + 2] Cycloaddition of Alkenyl Boronic Derivatives: An Entry into 3-Azabicyclo[3.2.0]Heptane Scaffold. J. Org. Chem. 2020, 85 (9), 5927–5940. https://doi.org/10.1021/acs.joc.0c00265.
  58. da Silva Mesquita, R.; Kyrylchuk, A.; Grafova, I.; Kliukovskyi, D.; Bezdudnyy, A.; Rozhenko, A.; Tadei, W. P.; Leskelä, M.; Grafov, A. Synthesis, Molecular Docking Studies, and Larvicidal Activity Evaluation of New Fluorinated Neonicotinoids against Anopheles Darlingi Larvae. PLoS One 2020, 15 (2). https://doi.org/10.1371/journal.pone.0227811.
  59. Menon, A.; Slominskii, Y. L.; Joseph, J.; Dimitriev, O. P.; Guldi, D. M. Reversible Charge Transfer with Single-Walled Carbon Nanotubes Upon Harvesting the Low Energy Part of the Solar Spectrum. Small 2020, 16 (8). https://doi.org/10.1002/smll.201906745.
  60. Chepurna, O. M.; Yakovliev, A.; Ziniuk, R.; Nikolaeva, O. A.; Levchenko, S. M.; Xu, H.; Losytskyy, M. Y.; Bricks, J. L.; Slominskii, Y. L.; Vretik, L. O.; Qu, J.; Ohulchanskyy, T. Y. Core-Shell Polymeric Nanoparticles Co-Loaded with Photosensitizer and Organic Dye for Photodynamic Therapy Guided by Fluorescence Imaging in near and Short-Wave Infrared Spectral Regions. J. Nanobiotechnology 2020, 18 (1). https://doi.org/10.1186/s12951-020-0572-1.
  61. Davydenko, I. G.; Slominskiy, Y. L.; Obernikhina, N. V.; Kachkovsky, A. D.; Tolmachev, A. I. Near Infrared Polyene Radical-Cation Derived from 7,8-Dihydrobenzo[c,d]Furo[2,3-f]Indole: Synthesis, Spectra and Nature of Electron Transitions. ChemistrySelect 2020, 5 (2), 674–681. https://doi.org/10.1002/slct.201904086.
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Публікації співробітників Інституту за 2019 рік

  1. Maksym Bugera, Serhii Trofymchuk, Karen Tarasenko, Olga Zaporozhets, Yurii Pustovit, and Pavel K. Mykhailiuk, “Deoxofluorination of aliphatic carboxylic acids: A route to trifluoromethyl-substituted derivatives,” JOURNAL OF ORGANIC CHEMISTRY 84, 16105–16115 (2019).
  2. Bohdan A. Chalyk, Andrii Khutorianskyi, Andrii Lysenko, Yulia Fil, Yuliya O. Kuchkovska, Konstantin S. Gavrilenko, Iulia Bakanovych, Yurii S. Moroz, Alina O. Gorlova, and Oleksandr O. Grygorenko, “Regioselective synthesis of functionalized 3-or 5-fluoroalkyl isoxazoles and pyrazoles from fluoroalkyl ynones and binucleophiles,” JOURNAL OF ORGANIC CHEMISTRY 84, 15212–15225 (2019).
  3. O. P. Dimitriev, Yu. P. Piryatinski, and Yu. L. Slominskii, “Abnormal emission in the heterogeneous j-aggregate system,” JOURNAL OF PHYSICAL CHEMISTRY C 123, 28611–28619 (2019).
  4. Oleksandr P. Boiko, Bohdan Ya Lenyk, Oleg Yu Posudievskiy, Yurii L. Slominskiy, Sergii A. Tsybulia, Yuriy A. Nastishin, and Vassili G. Nazarenko, “Electronic energy levels in lyotropic chromonic liquid crystals formed by ionic perylene diimide derivatives,” SYNTHETIC METALS 257, 116147 (2019).
  5. Ye. O. Shaydyuk, O. P. Boyko, O. D. Kachkovsky, Yu. L. Slominsky, J. L. Bricks, K. D. Belfield, and M. V. Bondar, “Electronic nature of new styryl dye bases: Linear photophysical, photochemical, and transient absorption spectroscopy studies,” DYES AND PIGMENTS 170 (2019), 10.1016/j.dyepig.2019.107582.
  6. A. Yakovliev, R. Ziniuk, D. Wang, B. Xue, L. O. Vretik, O. A. Nikolaeva, M. Tan, G. Chen, Yu L. Slominskii, J. Qu, and T. Y. Ohulchanskyy, “Hyperspectral multiplexed biological imaging of nanoprobes emitting in the short-wave infrared region,” NANOSCALE RESEARCH LETTERS 14, 243 (2019).
  7. Nadiia Pikun, V, Natalya P. Kolesnyk, Eduard B. Rusanov, Aiva Plotniece, Arkadij Sobolev, Ilona Domracheva, and Yuriy G. Shermolovich, “Contrasting reactivity of fluorinated 2,6-heptanediones towards amines and ammonia, leading to cyclohexanediones or 2-oxa-6-azabicyclo[2.2.2]octanes and evaluation of their cytotoxicity,” NEW JOURNAL OF CHEMISTRY 43, 10537–10544 (2019).
  8. Andrii I. Subota and Dmitriy M. Volochnyuk, “Piperidines decorated by small (cyclo)alkyl substituents (microreview),”CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 601–603 (2019).
  9. Ganna A. Senchyk, Andrey B. Lysenko, Eduard B. Rusanov, and Kostiantyn V. Domasevitch, “Crystal structure of tetrakis[mu-3-carboxy-1-(1,2,4-triazol-4-yl)adamantane-kappa n-2(1):n-2]tetrafluoridodi-mu(2)-oxido-dioxidodisilver(i)divanadium(v) tetrahydrate,” ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS 75, 808+ (2019).
  10. Kostyantyn Grytsenko, Peter Lytvyn, and Yurii Slominskii, “Toward deposition of organic solid with controlled morphology on selected surfaces,” APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING 125 (2019), 10.1007/s00339-019-2699-1.
  11. Oleg V. Stanko, Yuliya V. Rassukana, and Petro P. Onys’ko, “Fluorinated iminophosphonates bearing stereodirecting phenylethyl group in synthesis of biorelevant scalemic aminophosphonates,” PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS 194, 331–332 (2019) , 22nd International Conference on Phosphorus Chemistry (ICPC), Budapest, HUNGARY, JUL 08-13, 2018.
  12. Sergiy Cherenok, Olexander Soldatkin, Svetlana Marchenko, Olga Soldatkina, Olga Kalchenko, Olena Prineva, Oleg Silenko, Sergiy Dzyadevych, and Vitaly Kalchenko, “3-methylsulfidopropoxycalixarene methylenebisphosphonic acid for aminoacids chemosensor,” PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS 194, 382–383(2019), 22nd International Conference on Phosphorus Chemistry (ICPC), Budapest, HUNGARY, JUL 08-13, 2018.
  13. Andrii Karpus, Oleksandr Yesypenko, Sergii Cherenok, Vyacheslav Boiko, Olga Kalchenko, Zoia Voitenko, Oleksandr Trybrat, Rinaldo Poli, Jean-Claude Daran, Eric Manoury, and Vitaly Kalchenko, “Chiral phosphorus-containing calixarenes,” PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS 194, 471–475 (2019), 22nd International Conference on Phosphorus Chemistry (ICPC), Budapest, HUNGARY, JUL 08-13, 2018.
  14. Volodymyr Sukach, Serhii Melnykov, Sylvain Bertho, Iryna Diachenko, Pascal Retailleau, Mykhailo Vovk, and Isabelle Gillaizeau, “Access to unprotected beta-fluoroalkyl beta-amino acids and their alpha-hydroxy derivatives,” ORGANIC LETTERS 21, 2340–2345 (2019).
  15. Evgeniy Yu. Slobodyanyuk and Dmitriy M. Volochnyuk, “Decoration of 1,3-oxazole by alkyl substituents via ch activation (microreview),”CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 202–204 (2019).
  16. Alessandra Forni, Davide Franchini, Federico Dapiaggi, Stefano Pieraccini, Maurizio Sironi, Patrick Scilabra, Tullio Pilati, Kirill Petko, I, Giuseppe Resnati,and Yurii L. Yagupolkii, “Featuring i···n halogen bond and weaker interactions in iodoperfluoroalkylimidazoles: An experimental and theoretical charge density study published as part of the crystal growth and design israel goldberg memorial virtual special,” CRYSTAL GROWTH & DESIGN 19, 1621–1631 (2019).
  17. Olena Paiuk, Nataliya Mitina, Miroslav Slouf, Ewa Pavlova, Nataliya Finiuk, Nataliya Kinash, Andriy Karkhut, Nazar Manko, Taras Gromovoy, Orest Hevus, Yuriy Shermolovich, Rostyslav Stoika, and Alexander Zaichenko, “Fluorine-containing block/branched polyamphiphiles forming bioinspired complexes with biopolymers,” COLLOIDS AND SURFACES B-BIOINTERFACES 174, 393–400 (2019).
  18. Mykola Kolotylo, Volodymyr Holovatiuk, Julia Bondareva, Oleg Lukin, and Vladimir Rozhkov, “Synthesis of sulfonimide-based dendrimers and dendrons possessing mixed 1 -¿ 2 and 1 -¿ 4 branching motifs,”TETRAHEDRON LETTERS 60, 352–354 (2019).
  19. Olga Kalchenko, Andrew Solovyov, and Vitaly Kalchenko, “Recognition and binding of aliphatic dicarboxylic acids c4 -c10 by diiminocalix[4]arene,” FRENCH-UKRAINIAN JOURNAL OF CHEMISTRY 7, 61–67 (2019).
  20. V. Shchodryi, N. Obernikhina, Ye. Shaydyk, O. Kachkovsky, Yu. Slominskiy, and Z. Tkachuk, “Fluorescent probe for investigation of influence of ribonucleosides with d-mannitol,” in 2019 IEEE 39TH INTERNATIONAL CONFERENCE ON ELECTRONICS AND NANOTECHNOLOGY (ELNANO), IEEE; Igor Sikorsky Kyiv Polytechn Inst; IEEE Ukraine Sect; IEEE Commun Soc; IEEE MTT S; IEEE Cent Ukraine Chapter; IEEE Elect Packaging Soc; IEEE Electron DevicesSoc; IEEE Solid State Circuits Soc; IEEE EMB Ukraine Chapter; IEEE AP MTT ED AES GRS NPS EMB SocE Ukraine Joint Chapter; IEEE Ukraine Sect IE IA PE Soc Joint Chapter; IEEE Ukraine Sect PE IE PEL Soc Joint Chapter; IEEE KPI Student Branch; IEEE Ukraine AES SP Joint Chapter; Natl Acad Sci Ukraine, V Ye Lashkaryov Inst Semiconductor Phys; U S Army Int Technol Ctr; Natl Acad Sci Ukraine, Inst Microdevices (IEEE, 345 E 47TH ST, NEW YORK, NY 10017 USA, 2019) pp. 385–389, 39th IEEE International Conference on Electronics and Nanotechnology (ELNANO), Kyiv, UKRAINE, APR 16-18, 2019.
  21. Olena Golembiovska, I, Alexander Yu Galkin, and Alexander B. Besarab, “Development and validation of a dissolution test for ursodeoxycholic acid and taurine from combined formulation,” SCIENTIFIC STUDY AND RESEARCH-CHEMISTRY AND CHEMICAL ENGINEERING BIOTECHNOLOGY FOOD INDUSTRY 20, 377–394 (2019).
  22. Maysoon Saleh, I, Ihor D. Panas, Florian Frenze, Christian Wuerth, Bastian Ruehle, Yuri L. Slominskii, Aleksander Demchenko, and Ute Resch-Genger, “Sensitization of upconverting nanoparticles with a nir-emissive cyanine dye using a micellar encapsulation approach,” METHODS AND APPLICATIONS IN FLUORESCENCE 7 (2019), 10.1088/2050-6120/aafe1f.
  23. V. Zvarych, M. Stasevych, V. Novikov, E. Rusanov, M. Vovk, P. Szweda, K. Grecka, and S. Milewski, “Anthra[1,2-d][1,2,3]triazine-4,7,12(3h)-triones as a new class of antistaphylococcal agents: Synthesis and biological evaluation,” Molecules 24 (2019), 10.3390/molecules24244581 ..
  24. N.O. Mchedlov-Petrossyan, N.N. Kriklya, A.P. Kryshtal, A.A. Ishchenko, M.L. Malysheva, V.V. Tkachenko, A.Y. Ermolenko, and E. Osawa, “Corrigendum to “the interaction of the colloidal species in hydrosols of nanodiamond with inorganic and organic electrolytes” (journal of molecular liquids (2019) 283 (849–859), (s0167732219302132),(10.1016/j.molliq.2019.03.095)),” Journal of Molecular Liquids 295 (2019), 10.1016/j.molliq.2019.111654 ..
  25. Y.S. Borodkin, E.B. Rusanov, A.I. Khizhan, and Y.G. Shermolovich, “Synthesis of fluorinated dipyrazolyl sulfones from bis(2-fluoro-2-polyfluoroalkylalkenyl) sulfones and diazomethane,” Chemistry of Heterocyclic Compounds 55, 1065–1069 (2019).
  26. N.. Syrota, S.V. Kemskiy, A.V. Bol’but, and M.V. Vovk, “4-(boc-amino)-1-1,2,3-triazole-5-carboxylic acids –convenient reagents for the synthesis of 1,4,6,7-tetrahydro[1,2,3]- triazolo[4,5-][1,4]diazepine-5,8-diones,” Chemistry of Heterocyclic Compounds 55, 1092–1097 (2019).
  27. Y.V. Hrynyshyn, A.R. Musiychuk, N.M. Tsizorik, A.V. Bol’but, and M.V. Vovk, “Synthesis of 4-aryl(hetaryl)pyrazolo[1,5-a]pyrazines by palladium-catalyzed suzuki–miyaura cross coupling,” Chemistry of Heterocyclic Compounds 55, 1070–1074 (2019) ..
  28. M. Kovalenko, D.V. Yarmoliuk, D. Serhiichuk, D. Chernenko, V. Smyrnov, A. Breslavskyi, O.V. Hryshchuk, I. Kleban, Y. Rassukana, A.V. Tymtsunik, A.A. Tolmachev, Y.O. Kuchkovska, and O.O. Grygorenko, “The boron-wittig olefination of aldehydes and ketones with bis[(pinacolato)boryl]methane: an extended reaction scope,” European Journal of Organic Chemistry 2019, 5624–5635 (2019) ..
  29. I.Y. Danyliuk, R.I. Vas’kevich, A.I. Vas’kevich, and M.V. Vovk, “Hydrogenated benzazepines: recent advances in the synthesis and study of biological activity,” Chemistry of Heterocyclic Compounds 55, 802–814 (2019) ..
  30. N.M. Tsizorik, Y.V. Hrynyshyn, A.R. Musiychuk, A.V. Bol’but, and M.V. Vovk, “Synthesis of pyrazolo[1,5-a]pyrazin-4-ylacetonitriles and their annulation with pyridine ring,” Chemistry of Heterocyclic Compounds 55, 893–896 (2019) ..
  31. A.I. Subota and D.M. Volochnyuk, “Piperidines decorated by small (cyclo)alkyl substituents (microreview),”Chemistry of Heterocyclic Compounds 55, 601–603 (2019) ..
  32. S.G. Shlykov, A.M. Kushnarova-Vakal, A.V. Sylenko, L.G. Babich, O.Y. Chunikhin, O.A. Yesypenko, V.I. Kalchenko, and S.O. Kosterin, “Calix[4]arene chalcone amides effects on myometrium mitochondria,” Ukrainian Biochemical Journal 91, 46–55 (2019) ..
  33. E.Y. Slobodyanyuk and D.M. Volochnyuk, “Decoration of 1,3-oxazole by alkyl substituents via ch activation (microreview),” Chemistry of Heterocyclic Compounds 55, 202–204 (2019) ..
  34. G.G. Yakovenko, O.. Lukianov, A.V. Bol’but, and M.V. Vovk, “A convenient synthesis method of 5-oxopyrazolo[4,3-b]pyridine-6-carboxylic acids and their nitriles,” Chemistry of Heterocyclic Compounds (2019), 10.1007/s10593-019-02603-5 ..
  35. E.Y. Slobodyanyuk, Y.L. Berezowska, V.V. Solomin, D.M. Volochnyuk, A.B. Rozhenko, S.V. Ryabukhin, and O.O. Grygorenko, “Formation of 10/12/14-membered rings is favored over 5/6/7-membered. an unexpected result from oxazole chemistry,” European Journal of Organic Chemistry 2019, 4962–4967 (2019) ..
  36. O.O. Grygorenko, D.M. Volochnyuk, S.V. Ryabukhin, and D.B. Judd, “The symbiotic relationship between drug discovery and organic chemistry,” Chemistry – A European Journal (2019), 10.1002/chem.201903232 ..
  37. I.Y. Danyliuk, R.I. Vaskevych, A.I. Vaskevych, S.Y. Suikov, E.B. Rusanov, V.O. Chornous, and M.V. Vovk, “Synthesis of naphtho[1,2-b]-, naphtho[2,1-b]-, and naphtho[2,3-b]azepinones via proton-induced cyclization of n-1(2)-naphthyl styrylacetamides,” Journal of Heterocyclic Chemistry (2019), 10.1002/jhet.3779 ..
  38. Bohdan A. Chalyk, Kateryna V. Hrebeniuk, Yulia V. Fil, Konstantin S. Gavrilenko, Alexander B. Rozhenko, Bohdan V. Vashchenko, Oleksandr V. Borysov, Angelina V. Biitseva, Pavlo S. Lebed, Iulia Bakanovych, Yurii S. Moroz, and Oleksandr O. Grygorenko, “Synthesis of 5-(fluoroalkyl)isoxazole building blocks by regioselective reactions of functionalized halogenoximes,” JOURNAL OF ORGANIC CHEMISTRY 84, 15877–15899 (2019) ..
  39. Heorhii Humeniuk, V, Nadezhda A. Derevyanko, Alexander A. Ishchenko, and Andrii Kulinich, V, “Merocyanines based on 1,2-diphenyl-3,5-pyrazolidinedione,” NEW JOURNAL OF CHEMISTRY 43, 13954–13966 (2019) ..
  40. N. A. Davidenko, I. I. Davidenko, A. A. Ishchenko, L. Kurdyukova, V, E. Mokrinskaya, V, L. S. Tonkopieva, and N. G. Chuprina, “Photoelectric properties of composite films based on poly(n-epoxypropyl carbazole) and merocyanine dyes,” JOURNAL OF APPLIED SPECTROSCOPY 86, 578–583 (2019) ..
  41. David Tomanek and Andrii Kyrylchuk, “Designing an all-carbon membrane for water desalination,” PHYSICAL REVIEW APPLIED 12 (2019), 10.1103/PhysRevApplied.12.024054 ..
  42. Tetiana Shvydenko, Kostiantyn Nazarenko, Kostiantyn Shvydenko, Eduard Rusanov, Andrei Tolmachev, and Aleksandr Kostyuk, “Annelated aminoimidazoles in synthesis of imidazo[4,5-b]pyridines,” CHEMISTRYSELECT 4, 8450–8452 (2019) ..
  43. Oleg A. Yeshchenko, Anastasiya V. Tomchuk, Viktor V. Kozachenko, Antonina P. Naumenko, Yuri L. Slominskii, Randall J. Knize, Michael Haftel, and Anatoliy O. Pinchuk, “Planar plasmonic nanocavity for efficient enhancement of photoluminescence of molecular emitters,” OPTICAL MATERIALS 94, 348–355 (2019) ..
  44. Andrii I. Subota, Sergey V. Ryabukhin, Alina O. Gorlova, Oleksandr O. Grygorenko, and Dmitriy M. Volochnyuk, “An approach to the synthesis of 3-substituted piperidines bearing partially fluorinated alkyl groups,” JOURNAL OF FLUORINE CHEMISTRY 224, 61–66 (2019) ..
  45. Pavel S. Nosik, Andrii S. Poturai, Mykola O. Pashko, Kostiantyn P. Melnykov, Sergey V. Ryabukhin, Dmitriy M. Volochnyuk, and Oleksandr O. Grygorenko, “N-difluorocyclopropyl-substituted pyrazoles: Synthesis and reactivity,” EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2019, 4311–4319 (2019) ..
  46. Yuriy V. Zatsikha, Natalia O. Didukh, Rachel K. Swedin, Viktor P. Yakubovskyi, Tanner S. Blesener, Andrew T. Healy, David E. Herbert, David A. Blank, Victor N. Nemykin, and Yuriy P. Kovtun, “Preparation of viscosity-sensitive isoxazoline/isoxazolyl-based molecular rotors and directly linked bodipy-fulleroisoxazoline from the stable meso-(nitrile oxide)-substituted bodipy,” ORGANIC LETTERS 21, 5713–5718 (2019) ..
  47. Anton V. Chernykh, Kostiantyn P. Melnykov, Nataliya A. Tolmacheva, Ivan S. Kondratov, Dmytro S. Radchenko, Constantin G. Daniliuc, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, Yuliya O. Kuchkovska, and Oleksandr O. Grygorenko, “Last of the gem-difluorocycloalkanes: Synthesis and characterization of 2,2-difluorocyclobutyl-substituted building blocks,” JOURNAL OF ORGANIC CHEMISTRY 84, 8487–8496 (2019) ..
  48. Andrii I. Subota, Anton O. Lutsenko, Bohdan V. Vashchenko, Dmitriy M. Volochnyuk, Vitalina Levchenko, Yurii V. Dmytriv, Eduard B. Rusanov, Alina O. Gorlova, Sergey V. Ryabukhin, and Oleksandr O. Grygorenko, “Scalable and straightforward synthesis of all isomeric (cyclo)alkylpiperidines,” EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2019, 3636–3648 (2019) ..
  49. N. A. Davidenko, I. I. Davidenko, A. A. Ishchenko, I. V. Kurdiukova, E. V. Mokrinskaya, L. S. Tonkopieva, and N. G. Chuprina, “Photoelectric properties of film composites derived from poly-n-epoxypropylcarbazole and zwitter-ionic dyes,” THEORETICAL AND EXPERIMENTAL CHEMISTRY 55, 103–109 (2019) ..
  50. E. V. Seliverstova, D. A. Temirbayeva, N. Kh. Ibrayev, and A. A. Ishchenko, “Plasmon effect of ag nanoparticles on forster resonance energy transfer in a series of cationic polymethine dyes,” THEORETICAL AND EXPERIMENTAL CHEMISTRY 55, 115–124 (2019) ..
  51. Nikolay O. Mchedlov-Petrossyan, Nika N. Kriklya, Alexander P. Kryshtal, Alexander A. Ishchenko, Maria L. Malysheva, Vitalii V. Tkachenko, Anna Yu. Ermolenko, and Eiji Osawa, “The interaction of the colloidal species in hydrosols of nanodiamond with inorganic and organic electrolytes,” JOURNAL OF MOLECULAR LIQUIDS 283, 849–859 (2019) ..
  52. Andrii Kulinich, V, Vladimir V. Kurdyukov, and Alexander A. Ishchenko, “Effect of bulky substituents in the donor and acceptor terminal groups on solvatochromism of brooker’s merocyanine,” NEW JOURNAL OF CHEMISTRY 43, 7379–7385 (2019) ..
  53. Anila Hoskere Ashoka, Pichandi Ashokkumar, Yuriy P. Kovtun, and Andrey S. Klymchenko, “Solvatochromic near-infrared probe for polarity mapping of biomembranes and lipid droplets in cells under stress,” JOURNAL OF PHYSICAL CHEMISTRY LETTERS 10, 2414–2421 (2019) ..
  54. Vitalii V. Solomin, Dmytro S. Radchenko, Evgeniy Y. Slobodyanyuk, Oleksandr V. Geraschenko, Bohdan V. Vashchenko, and Oleksandr O. Grygorenko, “Widely exploited, yet unreported: Regiocontrolled synthesis and the suzuki-miyaura reactions of bromooxazole building blocks,” EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2019, 2884–2898 (2019) ..
  55. Kirill I. Petko, Taras M. Sokolenko, Andrey A. Filatov, Vitaliy V. Polovinko, Eduard B. Rusanov, Vadim A. Dudko, and Yurii L. Yagupolskii, “N-difluoromethylation of monosubstituted polydentate azoles,” CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 359–366 (2019) ..
  56. Georgiy G. Yakovenko, Oleh A. Lukianov, Andriy V. Bol’but, and Mykhailo V. Vovk, “N-boc-4-aminopyrazole-5-carbaldehydes in friendlander synthesis of pyrazolo[4,3-b]pyridines,” CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 379–385 (2019) ..
  57. Alina N. Grozav, Mariana Z. Fedoriv, Vitaliy A. Chornous, Alina A. Palamar, Mykhailo K. Bratenko, and Mykhailo V. Vovk, “Synthesis of thieno[2,3-b]pyrrole-2(4)-carboxylic and 2,4-dicarboxylic acids,” CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 435–441 (2019) ..
  58. Alex J. King, Yuriy V. Zatsikha, Tanner Blessener, Forrest Dalbec, Philip C. Goff, Mathew Kayser, David A. Blank, Yuriy P. Kovtun, and Victor N. Nemykin, “Ultrafast electron-transfer in a fully conjugated coumarin-ferrocene donor-acceptor dyads,” JOURNAL OF ORGANOMETALLIC CHEMISTRY 887, 86–97 (2019) ..
  59. Yurii L. Yagupolskii, Natalia Pavlenko, V, Igor I. Gerus, Sheng Peng, and Mario Nappa, “1,1,1,4,4,4-hexafluorobut-2-yne (hfb) as a versatile dipolarophile for [3+2] cycloaddition with 1,3-dipoles toward azoles with adjacent cf3 groups,” CHEMISTRYSELECT 4, 4604–4610 (2019) ..
  60. Alexander A. Ishchenko, Nikolay O. Mchedlov-Petrossyan, Nika N. Kriklya, Aleksandr P. Kryshtal, Eiji Osawa, and Andrii V. Kulinich, “Interaction of polymethine dyes with detonation nanodiamonds,” CHEMPHYSCHEM 20, 1028–1035 (2019) ..
  61. Andrii V. Kulinich and Alexander A. Ishchenko, “Electronic structure of merocyanine dyes derived from 3h-indole and malononitrile in the ground and excited states: Dft/td-dft analysis,” COMPUTATIONAL AND THEORETICAL CHEMISTRY 1154, 50–56 (2019) ..
  62. Kostiantyn P. Melnykov, Artem N. Artemenko, Bohdan O. Ivanenko, Yevhenii M. Sokolenko, Pavel S. Nosik, Eugeniy N. Ostapchuk, Oleksandr O. Grygorenko, Dmitriy M. Volochnyuk, and Sergey Ryabukhin, V, “Scalable synthesis of biologically relevant spirocyclic pyrrolidines,” ACS OMEGA 4, 7498–7515 (2019) ..
  63. Liubov V. Sokolenko, Raisa K. Orlova, Andrey A. Filatov, Yurii L. Yagupolskii, Emmanuel Magnier, Bruce Pegot, and Patrick Diter, “General, practical and selective oxidation protocol for cf3s into cf3s(o) group,” MOLECULES 24 (2019), 10.3390/molecules24071249 ..
  64. R. I. Gurtovyi, A. A. Ishchenko, and Ya. D. Lampeka, “Effect of aromatic and aliphatic hydrocarbons on the spectral and luminescent properties of composites derived from a zinc-containing coordination polymer and dyes,”THEORETICALAND EXPERIMENTAL CHEMISTRY 55, 29–35 (2019) ..
  65. A. V. Kulinich and A. A. Ishchenko, “Structures and fluorescence spectra of merocyanine dyes in polymer films,” JOURNAL OF APPLIED SPECTROSCOPY 86, 35–42 (2019) ..
  66. Yuliya Rassukana, V, Oleg Stanko, V, and Petro P. Onys’ko, “Enantiomeric o,o-dimenthyl alpha-iminotrifluoroethylphosphonates: Novel chiral building blocks in asymmetric synthesis of alpha-trifluoromethylated alpha-aminophosphonic acid derivatives,” JOURNAL OF FLUORINE CHEMISTRY 219, 123–128 (2019) ..
  67. Natalia O. Didukh, Viktor P. Yakuboyskyi, Yuriy Zatsikha, V, Gregory T. Rohde, Victor N. Nemykin, and Yuriy P. Kovtun, “Flexible bodipy platform that offers an unexpected regioselective heterocyclization reaction toward preparation of 2-pyridone[a]-fused bodipys,”JOURNAL OF ORGANIC CHEMISTRY 84, 2133–2147 (2019) ..
  68. Sergiy S. Mykhaylychenko, Yuriy N. Markitanov, Timofii V. Rudenko, Eduard B. Rusanov, and Yuriy G. Shermolovich, “Synthesis of 4-polyfluoroalkyl-1,3-dithiolanes via [3+2] cycloaddition of thiocarbonyl ylide to polyfluoroalkanethioamides,” CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 189–192 (2019) ..
  69. Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, Yurii S. Moroz, Olena Savych, Alexander Chuprina, Dragos Horvath, Yuliana Zabolotna, Alexandre Varnek, and Duncan B. Judd, “Evolution of commercially available compounds for hts,” DRUG DISCOVERY TODAY 24, 390–402 (2019) ..
  70. Kostiantyn P. Melnykov, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, Eduard B. Rusanov, and Oleksandr O. Grygorenko, “A conformationally restricted gaba analogue based on octahydro-1h-cyclopenta[b]pyridine scaffold,” AMINO ACIDS 51, 255–261 (2019) ..
  71. Andrii Kulinich, V, Nadezhda A. Derevyanko, Alexander A. Ishchenko, Nataliia B. Gusyak, Igor M. Kobasa, Piotr P. Romanczyk, and Stefan S. Kurek, “Structure and redox properties of polymethine dyes: Electrochemical and dft/td-dft study,”DYES AND PIGMENTS 161, 24–33 (2019) ..
  72. Ivanna Yu. Danyliuk, Ruslan I. Vas’kevich, Alla I. Vas’kevich, Eduard B. Rusanov, and Mykhailo V. Vovk, “Sulfanyl chloride induced heterocyclization of n-(pyrazolyl)styrylacetamides,” PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS 194, 156–162 (2019) ..
  73. V. V. Kurdyukov and I. V. Kurdyukova, “Unsymmetrical 2,6-di-tert-butyl-substituted pyrylo-4-squaraines,” RUSSIAN JOURNAL OF ORGANIC CHEMISTRY 55, 93–100 (2019) ..
  74. Viktor M. Tkachuk, Serhii V. Melnykov, Anastasiia V. Vorobei, Volodymyr A. Sukach, and Mykhailo V. Vovk, “Study of regioselectivity in cyanomethylation of 4-(trifluoromethyl)pyrimidin-2(1h)-ones,”CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 66–71 (2019) ..
  75. A. K. Aimukhanov, N. Kh. Ibrayev, A. A. Ishchenko, and A. V. Kulinich, “Effect of silver and gold nanoparticles on the spectral and luminescent properties of a merocyanine dye,”THEORETICAL AND EXPERIMENTAL CHEMISTRY 54,369–374 (2019) ..
  76. Pavel S. Nosik, Sergey V. Ryabukhin, Mykola O. Pashko, Galyna P. Grabchuk, Oleksandr O. Grygorenko, and Dmitriy M. Volochnyuk, “Synthesis of 1-hetary1-2,2-difluorocyclopropane-derived building blocks: The case of pyrazoles,” JOURNAL OF FLUORINE CHEMISTRY 217, 80–89 (2019) .
  77. Alexander A. Sikalov, Vladimir V. Pavlovskiy, and Andrey A. Kirilchuk, “Ruthenium(ii) p-cymene complexes bearing 2-(1,2,4-triazol-3-yl)pyridines: Linkage isomerism and related nmr/dft studies,” INORGANIC CHEMISTRY COMMUNICATIONS 99, 156–159 (2019) ..
  78. Y.M. Markitanov, V.M. Timoshenko, T.V. Rudenko, E.B. Rusanov, and Y.G. Shermolovich, “3-functional substituted 4-trifluoromethyl tetrahydrothiophenes via [3 + 2]-cycloaddition reactions,” Journal of Sulfur Chemistry 40, 629–640 (2019),cited By 0.
  79. Roman N. Solomyannyi, Olga V. Shablykina, Viktoriia S. Moskvina, Volodymir P. Khilya, Eduard B. Rusanov, and Vladimir S. Brovarets, “8-(methyl(phenyl)sulfonyl)-2,6-dihydroimidazo[1,2-c]- pyrimidin-5(3h)-ones and 9-(methyl(phenyl)sulfonyl)-2,3,4,7-dihydro-6h-pyrimido[1,6-a]pyrimidin -6-ones: synthesis and antiviral activity,” CHEMISTRY OF HETEROCYCLIC COMPOUNDS 55, 401–407 (2019) ..
  80. Niazbek Ibrayev, Alexander Ishchenko, Dmitriy Afanasyev, and Nazerke Zhumabay, “Active laser medium for near-infrared spectral range based on electron-unsymmetrical polymethine dye and silver nanoparticles,”APPLIED PHYSICS B-LASERS AND OPTICS 125 (2019), 10.1007/s00340-019-7292-y ..
  81. Maryna Stasevych, Viktor Zvarych, Volodymyr Novikov, and Mykhailo Vovk, “Amidoxime-functionalized (9,10-dioxoantracen-1-yl)hydrazones,” CHEMISTRY & CHEMICAL TECHNOLOGY 13, 417–423 (2019) ..
  82. Vladyslav M. Buldenko, Viacheslav V. Trush, Oleksandr L. Kobzar, Andriy B. Drapailo, Vitaly Kalchenko, I, and Andriy Vovk, I, “Calixarene-based phosphinic acids as inhibitors of protein tyrosine phosphatases,” BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 29, 797–801 (2019) ..
  83. E.Y. Slobodyanyuk, A.A. Andriienko, B.V. Vashchenko, D.M. Volochnyuk, S.V. Ryabukhin, and O.O. Grygorenko, “Expanding the chemical space of sp 3-enriched 4,5-disubstituted oxazoles via synthesis of novel building blocks,” Chemistryof Heterocyclic Compounds 55, 421–434 (2019) ..
  84. V.V. Kurdyukov and Y.G. Vlasenko, “Isomeric bisdicyanomethylene-substituted 1,3- and 1,2-pyrilo-4-squaraines: Synthesis, molecular, and crystal structure,” Russian Journal of General Chemistry 89, 212–218 (2019) ..
  85. Aleksandr Mandzhulo, Iryna Vashchenko, Andrii Gerasov, Mykhaylo Vovk, Eduard Rusanov, Volodymyr Fetyukhin, Oleg Lukin, and Alexander Shivanyuk, “Selective synthesis of n-protected exo-spiro[oxirane-3,2 ‘-tropanes],”ORGANIC CHEMISTRY FRONTIERS 6, 1692–1697 (2019) ..
  86. Petro Lutsyk, Yuri Piryatinski, Mykola Shandura, Mohammed AlAraimi, Maria Tesa, Georgios E. Arnaoutakis, Ambrose Ashwin Melvin, Oleksiy Kachkovsky, Anatoly Verbitsky, and Aleksey Rozhin, “Self-assembly for two types of j-aggregates: cis-isomers of dye on the carbon nanotube surface and free aggregates of dye trans-isomers,” JOURNAL OF PHYSICAL CHEMISTRY C 123, 19903–19911 (2019) ..
  87. S.V. Zasukha, V.M. Timoshenko, A.A. Tolmachev, V.O. Pivnytska, O. Gavrylenko, S. Zhersh, Y. Shermolovich, and O.O. Grygorenko, “Sulfonimidamides and imidosulfuric diamides: Compounds from an underexplored part of biologically relevant chemical space,” Chemistry – A European Journal 25, 6852 (2019) ..
  88. Yuriy V. Zatsikha, Rachel K. Swedin, Andrew T. Healy, Philip C. Goff, Natalia O. Didukh, Tanner S. Blesener, Mathew Kayser, Yuriy P. Kovtun, David A. Blank, and Victor N. Nemykin, “Synthesis, characterization, and electron-transfer properties of ferrocene-bodipy-fullerene near-infrared-absorbing triads: Are catecholopyrrolidine-linked fullerenes a good architecture to facilitate electron-transfer?” CHEMISTRY-A EUROPEAN JOURNAL 25, 8401–8414 (2019) ..
  89. A. Marchenko, G. Koidan, A. Hurieva, Y. Vlasenko, A.B. Rozhenko, J.-M. Sotiropoulos, and A. Kostyuk, “Transformation routes of p v – and p iii -n-substituted acyclic diaminocarbenes,”European Journal of Inorganic Chemistry 2019, 1621–1632 (2019) ..
  90. M. Dekhtyar, W. Rettig, A. Rothe, V. Kurdyukov, and A. Tolmachev, “Variation of donor and acceptor strength in analogues of brooker’s merocyanine and generalization to various classes of charge transfer compounds,”JOURNAL OF PHYSICAL CHEMISTRY A 123, 2694–2708 (2019) ..

Публікації співробітників Інституту за 2018 рік

  1. A. Marchenko, G. Koidan, A. Hurieva, A. Kostyuk,D .Franco, M. Baron, A. Biffis. PdII Complexes with N-(Diadamantylphosphanyl)diaminocarbene and Related Ligands: Synthesis and Catalytic Applications in Intermolecular Alkyne Hydroaminations// Eur.J.Inorg.Chem-2018, P.652-658.
  2. N.O. Didukh,V.P. Yakubovskyi, Yu.V. Zatsikha,V.N. Nemykin,Yu.P. Kovtun. meso-Nitromethyl-substituted BODIPYs – a new type of water switchable fluorogenic dyes useful for further core modifications// Dyes and Pigments, 2018, Vol. 149, P. 774–782.
  3. V. Polishchuk, M. Stanko, A. Kulinich, M. Shandura. D–π–A–π–D Dyes with a 1,3,2-dioxaborine cycle in the polymethine chain: efficient long-wavelength fluorophores// Eur. J. Org. Chem., 2018, P. 240–246.
  4. A.V.Kulinich, A. A. Ishchenko, I. N. Kukhta, L. K. Mitryukhin, S. M. Kazakov, A.V. Kukhta. Electron impact excitation of the merocyanine molecule in the gas phase// Chem. Phys., 2018, V. 503, P. 20–24.
  5. A. A. Ishchenko, A. V. Kulinich, S. L. Bondarev,T. F. Raichenok. UV–Vis absorption spectra and electronic structure of merocyanines in the gas phase// Spectrochim. Acta A., 2018, V. 190,P. 332–335.
  6. A.V.Kulinich, N. A. Derevyanko, A. A. Ishchenko, N. B. Gusyak, I. M. Kobasa, P. P. Romańczyk, S. S. Kurek. Structure and redox properties of polymethine dyes: Electrochemical and DFT/TD-DFT study// Dyes and Pigments, 2019, Vol. 161, P. 24–33.
  7. A. V. Kulinich, A. A. Ishchenko, G. V. Bulavko, N. A. Davidenko. Effect of structure on the photovoltaic properties of merocyanine dyes in polymer films// Theor. Exp. Chem., 2018, Т. 54, № 3, С. 178–188.
  8. A. V. Kulinich, A. A. Ishchenko, L. F. Sharanda, S. V. Shulga,V. M. Ogenko. Sorption of Polymethine Dyes on Nanographites and Carbon Nanotubes// Ukr. J. Phys. – 2018. – V. 63, N 5. – P. 379–385.
  9. A. G. Belous, O. I. V’yunov, S. D. Kobylyanskaya, A. A. Ishchenko, A.V.Kulinich. Influence of synthesis conditions on the morphology and spectral-luminescent properties of films of organic-inorganic perovskite CH3NH3PbI2.98Cl0.02// Russ. J. Gen. Chem., 2018, V. 88, N 1, P. 114–119.
  10. A. V. Kulinich. Comments on “Novel fluorene-based supramolecular sensor for selective detection of amoxicillin in water and blood”// Ecotoxicol. Environ. Saf., 2018, V. 152, P. 139.
  11. O.P. Dimitriev, Yu.P. Piryatinski,Yu.L. Slominskii. Excimer emission in J-aggregates// J. Phys. Chem. Lett., Vol. 9, P. 2138–2143.
  12. O.V. Stanko, Y.V. Rassukana, K.A. Zamulko, V. Dyakonenko, S.V. Shyishkina, P.P. Onys’ko. Diastereoselective synthesis of polyfluoroalkylated α-aminophosphonic acid derivatives// J. Fluor. Chem. 2018. Vol. 216. P. 47-56.
  13. O.V. Stanko, Yu.V. Rassukana, P.P. Onys’ko. Fluorinated Iminophosphonates Bearing Stereodirecting Phenylethyl Group in Synthesis of Biorelevant Scalemic Aminophosphonates// Phosphorus Sulfur Silicon Relat. Elem. 2018, DOI: 10.1080/10426507.2018.154048.
  14. O. Kalchenko, S. Cherenok, S. Suikov, V. Kalchenko. Study of Calixarene Complexation with Biologically Active Carboxylic Acids by RP HPLC Method// French- Ukrainian Journal of Chemistry. – 2017. – Vol. 05, issue 02. – P. 49-55.
  15. V.M. Buldenko, O.L. Kobzar, V.V. Trush,A.B. Drapailo,V.I. Kalchenko, A.I.Vovk. Sulfonyl-bridged calix[4]arene as an inhibitor of protein tyrosine phosphatases// French- Ukrainian Journal of Chemistry. – 2017. – Vol. 05, issue 02. – P. 144-151.
  16. A. Karpus, A.Yesipenko,V. Boiko, D. Jean-Claude, Z. Voitenko, V. Kalchenko, E. Manoury. Synthesis of a new enantiomerically pure inherently chiral calix[4]arene phosphonic acid and its first evaluation as organocatalyst// Journal of Organic Chemistry. – 2018. – Vol. 83, No. 3. – P. 1146-1153. (DOI:10.1021/acs.joc.7b02312).
  17. R. Rodik, M. Poberezhnyk, V.Kalchenko. Calixarene Derivatives for (Nano)Biotechnologies (огляд)// Макрогетероциклы / Macroheterocycles. – 2017. – Т. 10, № 4-5. – С. 421-431. (Росія).
  18. V. M. Buldenko, L. A. Kononets, O. L. Kobzar, A. B. Drapailo, S. G.Vyshnevsky, V. I.Kalchenko, A. I.Vovk. The inhibitory potential of calixarenes against nucleotide pyrophosphatase/-phosphodiesterase 1// Ж. Органічної та Фармацевтичної Хімії. – 2017. – Т. 15, вип. 4(60). – С. 41-47.
  19. Iu.Iu. Mazur, T.O. Veklich,O.A. Shkrabak, N.A. Mohart, A.M. Demchenko, I.V.Gerashchenko, R.V. Rodik,V.I. Kalchenko, S.O. Kosterin. Selective inhibition of smooth muscle plasma membrane transport Са2+,Mg2+-АТРase by calixarene C-90 and its activation by IPT-35 compound. General Physiology and Biophysics. – 2018. – Vol. 37. – P. 223-231.
  20. O. O. Soldatkin, S. V. Marchenko, O. V. Soldatkina, S. O. Cherenok, O.I.Kalchenko, O. S. Prynova, O. M. Sylenko, V. I. Kalchenko, S. V. Dzyadevych. Conductometric sensor with calixarene‑based chemosensitive element for the arginine detection// Chemical Papers. – 2018. – Vol. 72, Issue 11. – P. 2687-2697.
  21. D. Ternova, A. Ouadi, V. Mazan, S. Georg, M. Boltoeva, V. Kalchenko, S.Miroshnichenko, I. Billard, C. Gaillar. New Ionic Liquid Based on the CMPO Pattern for the Sequential Extraction of U(VI), Am(III) and Eu(III)// J. Solution Chem. – 2018. – doi.org/10.1007/s10953-018-0730-3. – Published online 16 March 2018.
  22. R.D. Labyntseva, V.I.Yavorovska, O.V.Bevza, V.I,Kalchenko, S.O.Kosterin. Calix[4]arenes as the Effectors of Smooth Muscle Myosin ATPase// In book: David Broadbent (ed.) / Myosin. Biosynthesis, Classes and Function. – New York: Nova science publishers, Inc. – 2018. – P. 89-134.
  23. R Rodik, S.Cherenok, O.Kalchenko, O.Yesypenko, J.Lipkowski, V.Kalchenko. Functional Сalixarenes for material and life science (огляд)// Current Organic Chemistry. – 2018. – Vol. 22. – P. 2196-2218 (DOI:10.2174/1385272822666181015141327).
  24. Т.O.Veklich, O.A.Skrabak, Yu.V.Nikonishyna, R.V. Rodik, V.I.Kalchenko, S.O.Kosterin. Calix[4]arene С-956 selectively inhibits plasma membrane Са2+,Mg2+-АТРase in myometrial cells// Ukr. Biochem. J. – 2018. – Vol. 90, Nо. 5. – З. 34-42.
  25. A. Karpus, O. Yesypenko, S. Cherenok, V. Boiko, O. Kalchenko, Z. Voitenko, O.Tribrat, R. Poli, J.-C. Daran, E.Manoury, V. Kalchenko. Chiral phosphorus-containing calixarenes// Phosphorus, Sulfur and Silicon. – 2018. – V. 193. – P. ?? (DOI: 10.1080/10426507.2018.1539994).
  26. Z.I. Kazantseva., I.A.Koshets, Yu.M Shirshov, V.I Kalchenko. The role of shear module and viscosity of thin organic films in the adsorption response of QCM sensors// Semiconductor Physics, Quantum Electronics and Optoelectronics (укр.). – 2018. – Vol. 21, № 3. – Р. 307-314.
  27. E.Y. Slobodyanyuk, O.S. Artamonov, I.B. Kulik, E. Rusanov, D.M. Volochnyuk, O.O. Grygorenko. A bio-inspired approach to proline-derived 2,4-disubstituted oxazoles// Heterocyclic Communications.2018. 24(1), pp.11-17.
  28. P.S. Nosik, S.V. Ryabukhin, O.O. Grygorenko, D.M. Volochnyuk. Transition Metal-free gem-difluorocyclopropanation of Alkenes with CF3SiMe3−NaI System: a Recipe for Electron-deficient Substrates// Advanced Synthesis and Catalysis2018 360(21), pp. 4104-4114.
  29. B.A. Chalyk, K.V Hrebeniuk., K.S Gavrilenko, I.B. Kulik, A.B. Rozhenko, D.M.Volochnyuk, O.S. Liashuk, O.O. Grygorenko. Synthesis of 4-hetarylisoxazoles from amino acid-derived halogenoximes and push-pull enamines// European Journal of Organic Chemistry.2018, (40), pp. 5585-5595.
  30. O.O. Grygorenko, D. Demenko, D.M. Volochnyuk, I.V. Komarov. Following Ramachandran 2: Exit vector plot (EVP) analysis of disubstituted saturated rings// New Journal of Chemistry.2018, 42(11), pp. 8355-8365.
  31. K.P. Melnykov, D.M. Volochnyuk, S.V. Ryabukhin, E.B. Rusanov, O.O.Grygorenko. A conformationally restricted GABA analogue based on octahydro-1H-cyclopenta­[b]pyridine scaffold// Amino Acids. 2018, pp1-7DOI 10.1007/s00726-018-2660-1.
  32. O.M.Kozachkova, N.V.Tsaryk, V.I.Pekhnyo, V.V.Trachevskyi, A.B.Rozhenko,V.V.Dyakonenko. Complexation of dichloro(ethylene­diamine)­palladium(II) with 1-hydroxyethylidene-1,1-diphosphonic acid// Inorg. Chim. Acta, 2018, 474, p. 96-103.
  33. A. V. Pulya, I. I. Seifullina, L. S. Skorokhod, V. I. Pavlovskii,V. Kh. Kravtsov, S.L. Bogza, S. Yu. Suikov. Molecular and Crystal Structure of the Condensation Product of 2-(7-Bromo-2-Oxo-5-Phenyl-3H-1,4-Benzdiazepin-1-Yl)Acetohydrazide (Gidazepam) with Salicylic Aldehyde// J. Struct. Chem. 2018, 59, p. 497-501.
  34. K.P. Melnikov, D.M. Volochnyuk, S.V. Ryabukhin, E.B. Rusanov, O.O.Grygorenko. A Conformationally restricted GABA analogue based on actahydro-1H-cyclopenta[b]pyridine scaffold// Amino Acids, 2018, published on-line, https://doi.org/10.1007/s00726-018-2660-1.
  35. L.M. Saliyeva, N.Y. Slyvka, R.I. Vas’kevich, E.B. Rusanov, M.V.Vovk. Unexpected aminolysis reaction of 2-methyl-2,3-dihydroimidazo[2,1-b][1,3]thiazole-5(6H)-one// Chem. Het. Comp. 2018, 54, p. 902–904.
  36. M. Kachaeva, S. Pilyo, S. Popilnichenko, A. Kornienko, E. Rusanov, V.Prokopenko, V. Zyabrev, V. Brovarets. Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)-1,3-oxazole-4-carboxylates and α-aminoazoles involving the Smiles rearrangement// Curr. Chem. Lett., 2018, 7, p. 101-110.
  37. N.V. Pikun, N.P. Kolesnyk, E.B. Rusanov, A. Plotniece, M. Rucins, A. Sobolev, Y.G. Shermolovich. Synthesis of fluorinated 2,6-heptanediones and 2-oxa-6-azabicyclo[2.2.2]octanes from 1,4-dihydropyridines// Tetrahedron, 2018, 18, p. 2884-2890.
  38. A.B. Lysenko, O.A. Bondar, G.A. Senchyk, E.B. Rusanov, M. Srebro-Hooper, J.Hooper, K. Prsa, K.W. Kramer, S. Decurtins, O. Waldmann, S.-X. Liu. On the border between low-nuclearity and one-dimensional Solids: A Unique interplay of 1,2,4-triazolyl-based[CuS(OH)2] Clusters and Mo-oxide matrix// Inorg. Chem. 2018, 57, p. 6076-6083.
  39. V.S. Brovarets, O.V. Golovchenko, E.B. Rusanov, J.A. Rusanova. Crystal structure of diethyl{2,2,2-trichlioro-1-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-methylpentanamido]ethyl}phosphonate// Acta Cryst. 2018, E74, p. 915-917.
  40. L.M. Saliyeva, N.Y. Slyvka, D.A. Mel’nyk, E.B. Rusanov, R.I. Vas’kevich, M.V.Vovk. Synthesis of spiro-[imidazo-[2,1-b][1,3]thiazole-6,3′-pyrrolidine] derivatives// Chem. Heterocyc. Comp. 2018, 54, p. 130–137.
  41. O.O. Soldatkin, S.V. Marchenko, O.V. Soldatkina, S.O. Cherenok, О.I.Kalchenko, O. S. Prynova, O. M. Sylenko, V. I. Kalchenko, S.V. Dzyadevych. Conductometric sensor with calixarene‑based chemosensitive element for the arginine detection// Сhemical Paper, 2018, р. 1-11. DOI: 10.1007/s11696-018-0515-6.
  42. Z. Wu, Jian Xu, G. Deng, X. Chu, L. Sokolenko, T. Trabelsi, J.S. Francisco, A.K.Eckhardt, P.R. Schreiner, X. Zeng. The trifluoromethyl sulfinyl and oxathiyl radicals// Chemistry – A European Journal, 2018, V. 24 (7), P. 1505-1508.
  43. K.I. Petko. Difluoromethylation of parent azoles// J. Fluor. Chem., 2018, V. 205, P. 5-7.
  44. K.I. Petko, A.A. Filatov. New N-difluoromethylindoles: features of N-difluoromethylation of indoles with electron-donor or electron-withdrawing substituents// French-Ukrainian Journal of Chemistry, 2018, V. 06 (01), P. 101-108.
  45. N.V.Pikun, S.S. Mykhaylychenko, Yu. G. Shermolovich. The synthesis of fluorine-containing endothiopeptide analogs by the reaction of perfluorinated dithiocarboxylic acid amides with esters of α-amino acids and dipeptides// Arkivoc. 2018, part iii, 36−44.
  46. L. Biliavska, Y. Pankivska, O. Povnitsa, N. Pikun, Y. Shermolovich, S.Zagorodnya. Effect of fluorinated N-alkylthioamides on HSV-1 multiplicity// Biopolymers and Cell.- 2018.- V. 34 (1).- P. 49–58.
  47. S. Siryi, Yu. G. Shermolovich, V. V. Kinzhybalo, T. J Bednarchuk, V.M.Timoshenko. Trifluoromethylated Thiopyranoid Glycals: Synthesis and Ferrier (I) Type Reactions// Eur. J. Org. Chem. – 2018. – P. xxx. https://doi.org/10.1002/ejoc.201800643.
  48. K. Naumenko, A. Golovan, L. Zelena, Yu. Shermolovych, G. Gudz, S.Zagorodnya. Antiviral and apoptosis modulating potential of fluorinated derivatives of uracil// ScienceRise:Biological Science. – 2018. – № 10. – P. 31–38.
  49. B. Vigante, A. Plotniece, M. Rucins, M. Petrova, R. Muhamadejev, K. Pajuste, S.Belyakov, Yu. G. Shermolovich, A. Sobolevs. An efficient synthesis of multisubstituted nitrodienamines and application in cyclization reaction// Tetrahedron.-2018. v.74.-N.1.-P.2596-2607.
  50. O. Paink, N. Mitina, O. Miahkota, K. Volanime, N.Musat, G.Stryganyak, O.Resethyak, N. Kinash, O. Hevus, Yu. Shermolovsch, O. Zaichenko. Fluorine-containing polyamphiphiles of block structure constructed from synthetic and biopolumer blocks// Biopolymers and Cell.- 2018.- V. 34 (1).- P. 49–58.
  51. S.V. Melnykov, A.S. Pataman, Yu.V. Dmytriv, S.V. Shishkinа, M.V. Vovk, V.A.Sukach. Regioselective decarboxylative addition of malonic acid and its mono(thio)esters to 4-trifluoro-methylpyridin-2(1H)-ones// Beilst. J. Org. Chem. 2017, 13, 2617-2625.
  52. M. Stasevych, V. Zvarych, V. Lunin, N. Kopak, Omarovska-Porokhnyavets, N.Deniz, C. Sayil, M. Ozyurek, K. Guclu, M. Vovk, V. Novikov. Synthesis and investigation of antimicrobial and antioxidant activity of antraquinonylhydrazones// Monatsh. Chem., 2018, vol. 149, N 6, p. 1111-1119.
  53. M. Stasevych, V. Zvarych, S. Khomyak, V Lunin, N. Kopak, V. Novikov, M.V.Vovk. Proton-initiated conversion of dithiocarbamates of 9,10-antracendione// Chemistry and Chemical Technology, 2018, vol. 12, N3, p.300-304.
  54. M.S. ahodkina-Yakovenko, A.V. Bol’but, M.V. Vovk. Synthesis of benzofuro[3,2-b]furo [2,3-d]pyridin-4(5H)-ones, derivatives of a novel heterocyclic system// Heterocyclic Commun., 2018, vol.24, N 4, p.177-181.
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Публікації співробітників Інституту за 2017 рік

  1. Onys’ko, P.P., Zamulko, K.A., Kyselyova, O.I., Syzonenko, Y.A. Novel 2H-1,3-benzoxazine ring formation by intramolecular heterocyclization of N-(α-aryloxyalkyl)imidoyl chlorides (2017) Heterocyclic Communications, 23 (6), pp. 421-428.
  2. Subota, A.I., Volochnyuk, D.M., Gorlova, A.O., Grygorenko, O.O. Scalable synthesis and properties of 7-methyl-4-azaindole (2017) Heterocyclic Communications, 23 (6), pp. 449-453.
  3. Kleban, I., Tymtsunik, A.V., Rassukana, Y.V., Grygorenko, O.O. O-(α-Phenylethyl)hydroxylamine as a ‘chiral ammonia equivalent’: synthesis and resolution of 5-oxopyrrolidine- and 6-oxopiperidine-3-carboxylic acids (2017) Tetrahedron Asymmetry, 28 (12), pp. 1817-1822.
  4. Shvydenko, T., Nazarenko, K., Shvydenko, K., Boron, S., Gutov, O., Tolmachev, A., Kostyuk, A. Reduction of imidazolium salts – An approach to diazocines and diazocanes (2017) Tetrahedron, 73 (49), pp. 6942-6953.
  5. Melnykov, S.V., Pataman, A.S., Dmytriv, Y.V., Shishkina, S.V., Vovk, M.V., Sukach, V.A. Regioselective decarboxylative addition of malonic acid and its mono(thio)esters to 4-trifluoromethylpyrimidin-2(1H)-ones (2017) Beilstein Journal of Organic Chemistry, 13, pp. 2617-2625.
  6. Grozav, A.N., Chornous, V.A., Vovk, M.V. Synthesis of 2,5-dihydroimidazo[4,5-e][1,2,3]thiadiazine 1,1-dioxides—Derivatives of a novel heterocyclic system (2017) Russian Journal of Organic Chemistry, 53 (12), pp. 1890-1892.
  7. 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 (2017) Journal of Organic Chemistry, 82 (23), pp. 12863-12868.
  8. Paschos, G.G., Somaschi, N., Tsintzos, S.I., Coles, D., Bricks, J.L., Hatzopoulos, Z., Lidzey, D.G., Lagoudakis, P.G., Savvidis, P.G. Hybrid organic-inorganic polariton laser (2017) Scientific Reports, 7 (1), art. no. 11377, .
  9. Pikun, N.V., Mykhaylychenko, S.S., Shermolovich, Y.G. The synthesis of fluorine-containing endothiopeptide analogs by the reaction of perfluorinated dithiocarboxylic acid amides with esters of α-amino acids and dipeptides (2017) Arkivoc, 2018 (3), pp. 36-44.
  10. Wu, Z., Xu, J., Sokolenko, L., Yagupolskii, Y.L., Feng, R., Liu, Q., Lu, Y., Zhao, L., Fernández, I., Frenking, G., Trabelsi, T., Francisco, J.S., Zeng, X. Parent Thioketene S-Oxide H2CCSO: Gas-Phase Generation, Structure, and Bonding Analysis (2017) Chemistry – A European Journal, 23 (65), pp. 16566-16573.
  11. Senchyk, G.A., Lysenko, A.B., Domasevitch, K.V., Erhart, O., Henfling, S., Krautscheid, H., Rusanov, E.B., Krämer, K.W., Decurtins, S., Liu, S.-X. Exploration of a Variety of Copper Molybdate Coordination Hybrids Based on a Flexible Bis(1,2,4-triazole) Ligand: A Look through the Composition-Space Diagram (2017) Inorganic Chemistry, 56 (21), pp. 12952-12966.
  12. Repich, H.H., Orysyk, S.I., Orysyk, V.V., Zborovskii, Y.L., Melnyk, A.K., Trachevskyi, V.V., Pekhnyo, V.I., Vovk, M.V. Influence of synthesis conditions on complexation of Cu (II) with O,N,O tridentate hydrazone ligand. X-ray diffraction and spectroscopic investigations (2017) Journal of Molecular Structure, 1146, pp. 222-232.
  13. Chumachenko, S.A., Shablykin, O.V., Rusanov, E.B., Sukhoveev, V.V., Brovarets, V.S. Synthesis of new substituted 5-amino-1H-imidazole-4-carbonitriles (2017) Russian Journal of General Chemistry, 87 (10), pp. 2481-2485.
  14. Grozav, A.N., Chornous, V.A., Dorokhov, V.I., Vovk, M.V. Polyfunctional imidazoles: XIV. 4-sulfonyl-5-formyl-1H-imidazoles (2017) Russian Journal of Organic Chemistry, 53 (10), pp. 1548-1555. Cited 1 time.
  15. Eften’eva, R.I., Kushnir, O.V., Lyavinets, O.S., Mangalagiu, I.I., Vovk, M.V. Catalyzed synthesis of functionalized pyrrolo[3,4-b]quinolines via one-pot three-component reactions under conventional and nonconventional conditions (2017) Monatshefte fur Chemie, 148 (10), pp. 1745-1752.
  16. Tkachuk, V.M., Mel’nikov, S.V., Sukach, V.A., Vovk, M.V. The addition of β-ketoacids to 4-(trifluoromethyl)pyrimidin- 2(1Н)-ones with decarboxylation: an effective method for the synthesis of 4-(2-oxoalkyl)-6-(trifluoromethyl)-3,4-dihydropyrimidin-2-ones (2017) Chemistry of Heterocyclic Compounds, 53 (10), pp. 1124-1127.
  17. Ishchenko, A.A., Kulinich, A.V., Shishkina, S.V. Effect of donor terminal group and polymethine chain length on structure of merocyanine dyes in the crystal state (2017) Dyes and Pigments, 145, pp. 181-188. Cited 1 time.
  18. Rozenbaum, V.M., Dekhtyar’, M.L., Trakhtenberg, L.I. Effect of electron transition kinetics on the photomotor velocity (2017) Russian Journal of Physical Chemistry A, 91 (10), pp. 1951-1956.
  19. Nosik, P.S., Gerasov, A.O., Boiko, R.O., Rusanov, E., Ryabukhin, S.V., Grygorenko, O.O., Volochnyuk, D.M. Gram-Scale Synthesis of Amines Bearing a gem-Difluorocyclopropane Moiety (2017) Advanced Synthesis and Catalysis, 359 (18), pp. 3126-3136.
  20. Repich, H.H., Orysyk, S.I., Orysyk, V.V., Zborovskii, Y.L., Pekhnyo, V.I., Vovk, M.V. Synthesis, crystal structure and spectral characterization of the first Ag+complex compounds involving O,N,O-coordinated N-acylhydrazones of salicylaldehyde (2017) Journal of Molecular Structure, 1144, pp. 225-236.
  21. Ibrayev, N.K., Seliverstova, E.V., Ishchenko, A.A., Kudinova, M.A. The effect of sulfonate groups on spectral-luminescent and photovoltaic properties of squarylium dyes (2017) Journal of Photochemistry and Photobiology A: Chemistry, 346, pp. 570-575.
  22. Stasevych, M.V., Zvarych, V.I., Lunin, V.V., Khomyak, S.V., Vovk, M.V., Novikov, V.P. Synthesis of pyrazole and tetrazole derivatives of 9,10-anthraquinonylhydrazones (2017) Chemistry of Heterocyclic Compounds, 53 (8), pp. 927-929.
  23. Bratenko, M.K., Barus, M.M., Vovk, M.V. Polyfunctional pyrazoles 11*. Synthesis of 5-aroylpyrano[3,4-c]pyrazol-7(2H)-ones (2017) Chemistry of Heterocyclic Compounds, 53 (8), pp. 905-908.
  24. Melnykov, K.P., Nosik, P.S., Kurpil, B.B., Sibgatulin, D.A., Volochnyuk, D.M., Ryabukhin, S.V., Grygorenko, O.O. Synthesis of gem-difluorocyclopentane/hexane building blocks (2017) Journal of Fluorine Chemistry, 199, pp. 60-66. Cited 1 time.
  25. Kurdyukova, I.V., Ishchenko, A.A., Mysyk, D.D. Synthesis and spectral properties of near-IR polymethine dyes derived from tris(2,2,3,3,4,4,5,5-octafluoropentyl)-9H-fluorene-2,4,7-trisulfonate (2017) Dyes and Pigments, 142, pp. 201-211.
  26. Zriba, R., Desmarchelier, A., Cadoret, F., Bouvet, S., Barthelemy, A.-L., Pégot, B., Diter, P., Dagousset, G., Blazejewski, J.-C., Anselmi, E., Yagupolskii, Y., Magnier, E. Dichlorotrifluoromethoxyacetic acid: Preparation and reactivity (2017) Molecules, 22 (6), art. no. 966, . Cited 1 time.
  27. Yakovenko, G.G., Yagodkina, M.S., Bol’but, A.V., Shishkina, S.V., Vovk, M.V. Synthesis of new triazolo[1,5-b][2,4]benzodiazepines via tandem cyclization of o-(azidomethyl)benzoates with cyanoacetamides (2017) Monatshefte fur Chemie, 148 (6), pp. 1-7.
  28. Chumachenko, S.A., Kachaeva, M.V., Shablykin, O.V., Rusanov, E.B., Brovarets, V.S. Reactions of N-(2,2-dichloro-1-cyanoethenyl)-N′-methyl(phenyl)ureas with aliphatic amines (2017) Russian Journal of General Chemistry, 87 (5), pp. 985-990.
  29. Sokolenko, T.M., Dronkina, M.I., Magnier, E., Yagupolskii, L.M., Yagupolskii, Y.L. Evaluation of efficient and practical methods for the preparation of functionalized aliphatic trifluoromethyl ethers (2017) Molecules, 22 (5), art. no. 804, . Cited 1 time.
  30. Bulavko, G.V., Davidenko, N.A., Shkavro, A.G., Tretyak, O.V., Ishchenko, A.A., Kulinich, A.V. Photovoltaic effect in dye-doped polymer films with free-surface and sandwich structures (2017) Functional Materials Letters, 10 (2), art. no. 1750007, .
  31. Tolkunov, A.S., Mazepa, A.V., Palamarchuk, G.V., Shishkin, O.V., Sujkov, S.Y., Bogza, S.L. Pictet–Spengler reaction in the synthesis of condensed benzodiazepines: synthesis of 11-hetaryl derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-ones (2017) Monatshefte fur Chemie, 148 (4), pp. 695-701.
  32. Kirilchuk, A.A., Rozhenko, A.B., Leszczynski, J. On structure and stability of pyrimidine ylidenes and their homologues (2017) Computational and Theoretical Chemistry, 1103, pp. 83-91.
  33. Stasevych, M.V., Zvarych, V.I., Lunin, V.V., Vovk, M.V., Novikov, V.P. Convenient synthesis of 1-hydrazinylanthracene-9,10-diones (2017) Russian Journal of Organic Chemistry, 53 (3), pp. 468-469.
  34. Chornous, V.A., Grozav, A.N., Vovk, M.V. Convenient synthesis of 3-chloroimidazo[1,5-a]quinoxalines (2017) Russian Journal of Organic Chemistry, 53 (3), pp. 474-476.
  35. Chornous, V.A., Mel’nik, O.Y., Grozav, A.N., Suikov, S.Y., Vovk, M.V. Polyfunctional imidazoles: XIII.1 Addition and cyclization reactions of 1-aryl-4-chloro-5-(2-nitroethenyl)-1H-imidazoles with sulfur and nitrogen nucleophiles (2017) Russian Journal of Organic Chemistry, 53 (3), pp. 407-412. Cited 1 time.
  36. Solomyannii, R.N., Pil’o, S.G., Slivchuk, S.R., Prokopenko, V.M., Rusanov, E.B., Brovarets, V.S. Synthesis of 5-methylsulfonylpyrimidines and their fused derivatives (2017) Russian Journal of General Chemistry, 87 (3), pp. 407-413.
  37. Repich, H.H., Orysyk, V.V., Palchykovska, L.G., Orysyk, S.I., Zborovskii, Y.L., Vasylchenko, O.V., Storozhuk, O.V., Biluk, A.A., Nikulina, V.V., Garmanchuk, L.V., Pekhnyo, V.I., Vovk, M.V. Synthesis, spectral characterization of novel Pd(II), Pt(II) π-coordination compounds based on N-allylthioureas. Cytotoxic properties and DNA binding ability (2017) Journal of Inorganic Biochemistry, 168, pp. 98-106. Cited 1 time.
  38. 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 photophysics, two-photon absorption and femtosecond transient absorption spectroscopy of styryl dye bases (2017) Journal of Luminescence, 183, pp. 360-367. Cited 1 time.
  39. Kulinich, A.V., Mikitenko, E.K., Ishchenko, A.A. Synthesis, electronic structure and spectral fluorescent properties of vinylogous merocyanines derived from 1,3-dialkyl-benzimidazole and malononitrile (2017) Spectrochimica Acta – Part A: Molecular and Biomolecular Spectroscopy, 171, pp. 317-324. Cited 2 times.
  40. Yesypenko, O.A., Klyachina, M.A., Dekhtyarenko, M.V., Pirozhenko, V.V., Shishkina, S.V., Boyko, V.I., Voitenko, Z.V., Kalchenko, V.I. Design, synthesis and structure determination of new inherently chiral para-bromoalkoxycalix[4]arenes (2017) Supramolecular Chemistry, 29 (1), pp. 49-58.
  41. Kulinich, A. Comments on “Novel fluorene-based supramolecular sensor for selective detection of amoxicillin in water and blood” (2017) Ecotoxicology and Environmental Safety, . Article in Press.
  42. Yagodkina, M.S., Yakovenko, G.G., Bol’but, A.V., Vovk, M.V. Cascade cyclization of methyl 2-(azidomethyl)furan-3-carboxylates with 2-cyanoacetamides. Efficient synthesis of a new heterocyclic system, furo[3,2-e][1,2,3]triazolo- [1,5-a][1,3]diazepine (2017) Russian Journal of Organic Chemistry, 53 (4), pp. 634-636.
  43. Onys’ko, P.P., Zamulko, K.A., Kyselyova, O.I., Shalimov, O.O., Rusanov, E.B. Synthesis of α-CF3– and α-CCl3– substituted nitrogen heterocycles by aza Diels-Alder and cyclocondensation reactions(2017) Tetrahedron, 73 (25), pp. 3513-3520.
  44. Kirij, N.V., Filatov, A.A., Khrapach, G.Yu., Yagupolskii, Y.L. The first nucleophilic C-H perfluoroalkylation of aromatic compounds via (arene)tricarbonylchromium complexes (2017) Chemical Communications, 53 (13), pp. 2146-2149. Cited 3 times.
  45. Adamovskyi, M.I., Ryabukhin, S.V., Sibgatulin, D.A., Rusanov, E., Grygorenko, O.O. Beyond the five and six: Evaluation of seven-membered cyclic anhydrides in the castagnoli-cushman reaction (2017) Organic Letters, 19 (1), pp. 130-133. Cited 5 times.
  46. Bulavko, G.V., Davidenko, N.A., Derevyanko, N.A., Ishchenko, A.A. Effect of Isomerism of Polymethine Dyes on Photovoltaic Properties of Carbazole- and Thiophene-Containing Polymeric Composites (2017) Theoretical and Experimental Chemistry, 52 (6), pp. 331-336.
  47. Marchenko, A., Koidan, G., Hurieva, A., Vlasenko, Y., Kostyuk, A., Lenarda, A., Biffis, A., Tubaro, C., Baron, M., Graiff, C., Nestola, F. Neutral dinuclear gold(I) complexes with N-phosphanyl, N-heterocyclic carbenes (NHCPs) (2017) Journal of Organometallic Chemistry, 829, pp. 71-78. Cited 2 times.
  48. Rassukana, Y.V., Bezgubenko, L.V., Stanko, O.V., Rusanov, E.B., Kulik, I.B., Onys’ko, P.P. Diastereoselective cycloaddition of (S)-N-(1-phenylethylimino)trifluoropropionate and trifluoroethylphosphonate with diazomethane (2017) Tetrahedron Asymmetry, 28 (4), pp. 555-560. Cited 1 time.
  49. Bauzá, A., Sharko, A.V., Senchyk, G.A., Rusanov, E.B., Frontera, A., Domasevitch, K.V. π-hole interactions at work: crystal engineering with nitro-derivatives (2017) CrystEngComm, 19 (14), pp. 1933-1937. Cited 4 times.
  50. Zarytska, H.M., Brusentsov, V.A., Pavlenko, O.L., Dmytrenko, O.P., Kulish, M.P., Kachkovskyi, O.D., Briks, Iu.L. Electronic structure of the molecular system of the C60 fullerene with indopentamethinecyanine dye for cases of the stacking and covalent interactions (2017) Nanosistemi, Nanomateriali, Nanotehnologii, 15 (3), pp. 507-516.
  51. Danylovych, Iu.V., Danylovych, V., Kolomiets, O.V., Rodik, R.V., Kalchenko, V.I., Kosterin, S.O. Effect of Calix[4]arenes on Ca2+ transport, electric potential and functioning of the electron transport chain in smooth muscle mitochondria (2017) Nanosistemi, Nanomateriali, Nanotehnologii, 15 (2), pp. 365-371.
  52. Rassukana, Y.V., Stanko, O.V., Yelenich, I.P., Onys’ko, P.P. Silylated iminophosphonates: Novel reactive synthons for the preparation of fluorinated aminophosphonates and aminophosphonic acids (2017) Tetrahedron Letters, 58 (35), pp. 3449-3452.
  53. Zhyhadlo, Y.Y., Gaidai, A.V., Levandovskiy, I.A., Bezdudny, A.V., Rassukana, Y.V. Facile synthesis of 3-(trifluoromethyl)adamantane derivatives (2017) Journal of Fluorine Chemistry, 201, pp. 11-14.
  54. Babich, L.G., Shlykov, S.G., Kushnarova, A.M., Esypenko, O.A., Kosterin, S.O. Calix[4]arene chalcone amides – The nanosize modulators of polarization of mitochondrial membranes and content of the ionized Ca in them (2017) Nanosistemi, Nanomateriali, Nanotehnologii, 15 (1), pp. 193-202.
  55. Veklich, T.O., Shkrabak, O.A., Nikonishina, Iu.V., Rodik, R.V., Kalchenko, V.I., Kosterin, S.O. Calix[4]arene C-90 as a promising supramolecular compound to regulate the activity of plasma membrane Ca2+, Mg2+-ATPase of smooth muscle cells (2017) Nanosistemi, Nanomateriali, Nanotehnologii, 15 (2), pp. 373-380.
  56. Dimitriev, O.P., Bricks, J., Smirnova, A.L., Slominskii, Y.L. Towards white-light generation through upconversion of low-power near-infrared photons (2017) RSC Advances, 7 (26), pp. 16126-16130.
  57. Derevyanko, N.O., Ishchenko, O.O., Kulinich, A.V., Sharanda, L.F., Shulga, S.V., Ogenko, V.M. Interaction of polymethine dyes of different ionicity and carbon nanostructures (2017) Nanosistemi, Nanomateriali, Nanotehnologii, 15 (2), pp. 337-344.
  58. Kazantseva, Z.I., Koshets, I.A., Belyaev, A.E., Ryabitskii, A.B., Kharchenko, S.G., Drapailo, A.B., Kalchenko, V.I., Shishkina, S.V., Shishkin, O.V. Phosphorylated thiacalixarenes as molecular receptors for QCM sensors of volatile compounds (2017) Functional Materials, 24 (4), pp. 599-606.
  59. Litvinchuk, M.B., Bentya, A.V., Slyvka, N.Y., Vovk, M.V. Halocyclization of products of allyl isothiocyanate addition to acyclic methylene active compounds (2017) Russian Journal of Organic Chemistry, 53 (5), pp. 709-716.
  60. Subota, A.I., Artamonov, O.S., Gorlova, A., Volochnyuk, D.M., Grygorenko, O.O. Approach to 5-substituted 6,7,8,9-tetrahydro-5H-pyrido[3,2-c]azepines (2017) Tetrahedron Letters, 58 (20), pp. 1989-1991. Cited 1 time.
  61. Yakovliev, A., Vretik, L.O., Ziniuk, R., Briks, J.L., Slominskii, Y.L., Qu, J., Ohulchanskyy, T.Y. Polymeric nanoparticles loaded with organic dye for optical bioimaging in near-infrared range (2017) Optics InfoBase Conference Papers, Part F70-PIBM 2017, 2 p.
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  65. Kozachkova, O.M., Tsaryk, N.V., Trachevskyi, V.V., Rozhenko, A.B., Shermolovich, Y.H., Guzyr, O.I., Sharykina, N.I., Chekhun, V.F., Pekhnyo, V.I. Complexes of palladium(II) with 1-phenyl-1-hydroxymethylene bisphosphoniс acid and their antitumor activity (2017) Ukrainian Biochemical Journal, 89 (2), pp. 106-115.
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  68. Pavlenko, O.L., Kulish, M.P., Dmytrenko, O.P., Kachkovsky, O.D., Brusentsov, V.A., Ilchenko, O.O., Shlapatska, V.V., Slominski, Y.L. Irradiation-induced changes in vibration structure of films of squaraine dye (2017) Problems of Atomic Science and Technology, 111 (5), pp. 31-34.

 

Публікації співробітників Інституту за 2016 рік

  1. Bliznyuk, V.N., Gasiorowski, J., Ishchenko, A.A., Bulavko, G.V., Rahaman, M., Hingerl, K., Zahn, D.R.T., Sariciftci, N.S. Photovoltaic cells based on ternary P3HT:PCBM:polymethine dye active layer transparent in the visible range of light (2016) Applied Surface Science, 389, pp. 419-427.
  2. Eften’eva, R.I., Kushnir, O.V., Lyavinets, O.S., Mangalagiu, I.I., Vovk, M.V. Synthesis of polyfunctionalized pyrido[1,2-a]pyrazines and pyrazino[1,2-a]quinolines via one-pot multicomponent reactions (2016) Monatshefte fur Chemie, pp. 1-7. Article in Press.
  3. Lutsyk, P., Piryatinski, Y., Alaraimi, M., Arif, R., Shandura, M., Kachkovsky, O., Verbitsky, A., Rozhin, A. Emergence of Additional Visible-Range Photoluminescence Due to Aggregation of Cyanine Dye: Astraphloxin on Carbon Nanotubes Dispersed with Anionic Surfactant (2016) Journal of Physical Chemistry C, 120 (36), pp. 20378-20386.
  4. Ogurok, V.M., Siry, S.A., Rusanov, E.B., Shermolovych, Y.G. Polyfluoroalkyl sulfines derived from 1,1-dihydropolyfluoroalkanesulfinyl chlorides: Decomposition and [4+2]-cycloaddition reactions (2016) Journal of Fluorine Chemistry, 189, pp. 119-126.
  5. Nosik, P.S., Ryabukhin, S.V., Artamonov, O.S., Grygorenko, O.O. Synthesis of trans-disubstituted pyrazolylcyclopropane building blocks (2016) Monatshefte fur Chemie, 147 (9), pp. 1629-1636.
  6. Markitanov, Y.N., Timoshenko, V.M., Shermolovich, Y.G., Mykhalchuk, V.L., Grafova, I.A., Grafov, A.V. Synthesis of 4-(trifluoromethyl)pyrrolidines Containing Sulfonyl, Iminosulfonyl, Sulfamide, or Phosphonyl Substituent (2016) Chemistry of Heterocyclic Compounds, pp. 1-4. Article in Press.
  7. Syza, O.I., Savchenko, O.M., Kvashuk, Y.V., Shtyl’, N.A., Chelyabieva, V.M. New Inhibitors Based on Vegetable Raw Materials and the Regularities of Their Adsorption on the Steel Surface (2016) Materials Science, pp. 1-11. Article in Press.
  8. Rozenbaum, V.M., Dekhtyar, M.L., Lin, S.H., Trakhtenberg, L.I. Photoinduced diffusion molecular transport (2016) Journal of Chemical Physics, 145 (6), art. no. 064110.
  9. Ternova, D., Boltoeva, M., Cointeaux, L., Gaillard, C., Kalchenko, V., Mazan, V., Miroshnichenko, S., Mohapatra, P.K., Ouadi, A., Papaiconomou, N., Petrova, M., Billard, I. Dramatic Changes in the Solubilities of Ions Induced by Ligand Addition in Biphasic System D2O/DNO3//[C1C4im][Tf2N]: A Phenomenological Study (2016) Journal of Physical Chemistry B, 120 (30), pp. 7502-7510.
  10. Zvarych, V.I., Stasevych, M.V., Lunin, V.V., Vovk, M.V., Novikov, V.P. Synthesis of (1H-pyrrol-1-yl)anthracene-9,10-diones (2016) Chemistry of Heterocyclic Compounds, pp. 1-3. Article in Press.
  11. Yelenich, O.V., Lytvyn, R.Z., Skrypska, O.V., Pitkovych, K.Y., Kachkovskii, A.D., Obushak, M.D., Yagodinets, P.I. Synthesis, nature of electronic transitions, and absorption spectra of the dye based on 4-(methyl-1-{2-[4-(1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)phenyl]-2-oxoethyl}pyridinium bromide (2016) Russian Journal of General Chemistry, 86 (8), pp. 1838-1844.
  12. Kemskii, S.V., Bol’but, A.V., Shishkina, S.V., Mel’nik, D.A., Vovk, M.V. Interaction of 1,5,6,8-tetrahydropyrazolo[3,4-е][1,4]diazepine-4,7-diones with some electrophilic reagents (2016) Russian Journal of Organic Chemistry, 52 (8), pp. 1162-1167.
  13. Chernykh, A.V., Tkachenko, A.N., Feskov, I.O., Daniliuc, C.G., Tolmachova, N.A., Volochnyuk, D.M., Radchenko, D.S. Practical Synthesis of Fluorinated Piperidine Analogues Based on the 2-Azaspiro[33]heptane Scaffold (2016) Synlett, 27 (12), art. no. St-2016-b0109-l, pp. 1824-1827.
  14. Kharaneko, O.I., Bogza, S.L. 5,7-Dihydropyrrolo[3,4-d][1,2]diazepin-1(2H)-ones. Synthesis and transformations (2016) Russian Journal of Organic Chemistry, 52 (7), pp. 1043-1049.
  15. Dekhtyar’, M.L., Rozenbaum, V.M., Trakhtenberg, L.I. Near-surface transport of semiconductor nanoclusters upon cyclic photoexcitation (2016) Russian Journal of Physical Chemistry A, 90 (7), pp. 1484-1488.
  16. Danilyuk, I.Y., Vas’kevich, R.I., Vas’kevich, A.I., Vovk, M.V. Electrophilic intramolecular cyclization of functional derivatives of unsaturated compounds: VIII. Cyclization of 4-aryl-N-(thiophen-3-yl)but-3-enamides by the action of polyphosphoric acid and chlorosulfanylarenes (2016) Russian Journal of Organic Chemistry, 52 (7), pp. 987-992.
  17. Karpus, A., Yesypenko, O., Boiko, V., Poli, R., Daran, J.-C., Voitenko, Z., Kalchenko, V., Manoury, E. Chiral Phosphinoferrocenyl-Calixarenes (2016) European Journal of Organic Chemistry, 2016 (20), pp. 3386-3394.
  18. Navozenko, O.M., Naumenko, A.P., Yashchuk, V.M., Bricks, J.L., Slominskii, Yu.L., Ryabitskii, A.B., Kachkovsky, O.D. Nature of the lowest electron transitions in styryl bases benzothiazole derivatives and analogues bearing para-methoxy and -trifluoromethyl substituents in phenylyne moiety (2016) Journal of Molecular Structure, 1113, pp. 32-41.
  19. Grozav, A.N., Chornous, V.A., Vovk, M.V. Polyfunctional imidazoles: XII.1 Synthesis of 1-[(4-chloro-1H-imidazol-5-yl)methyl]-substituted 1,2,3-triazoles and dihydropyrrolo[3,4-d]triazoles from 5-(azidomethyl)-4-chloro-1H-imidazoles (2016) Russian Journal of Organic Chemistry, 52 (6), pp. 873-878.
  20. Bliznyuk, V.N., Seliman, A.А. hchenko, A.A., Derevyanko, N.A., Devol, T.A. New Efficient Organic Scintillators Derived from Pyrazoline (2016) ACS Applied Materials and Interfaces, 8 (20), pp. 12843-12851.
  21. Zasukha, S.V., Novak, O.V., Guzyr, O.I., Shermolovich, Y.G. The first synthesis of chiral dialkylamines with α,α-difluoroethers fragments (2016) Journal of Fluorine Chemistry, 185, pp. 197-200.
  22. Petko, K.I., Vlasenko, Y.G., Kachkovskii, O.D. Unexpected “reverse” cyclization of 2-mercaptobenzimidazole with chlorotrifluoroethylene and hexafluoropropene (2016) Journal of Fluorine Chemistry, 185, pp. 168-172.
  23. Onys’ko, P.P., Zamulko, K.A., Kyselyova, O.I., Yelenich, I.P., Rassukana, Y.V. Synthesis of polyfluoroalkylated α-Aminophosphonic/thiophosphonic acids derivatives (2016) Journal of Fluorine Chemistry, 185, pp. 191-196.
  24. Pikun, N.V., Mykhaylychenko, S.S., Kulik, I.B., Shermolovich, Y.G. Primary polyfluoroalkanethioamides as mild thioacylating reagents for alkyl amines and α-amino acid esters (2016) Journal of Fluorine Chemistry, 185, pp. 86-90.
  25. Serguchev, Y.A., Ponomarenko, M.V., Ignat’Ev, N.V. Aza-fluorocyclization of nitrogen-containing unsaturated compounds (2016) Journal of Fluorine Chemistry, 185, pp. 1-16. Cited 5 times.
  26. Lukashova, M.S., Kharchenko, S.G., Belikov, K.N., Bryleva, K.Y., Kal’chenko, V.I., Shcherbakov, I.B.-K., Slyusarev, A.N., Beda, O.A. Adsorption of Eu(III) ions on silicas with noncovalently immobilized thiacalix[4]arene derivatives (2016) Journal of Analytical Chemistry, 71 (5), pp. 476-481.
  27. Dyachenko, I.V., Vas’kevich, R.I., Vas’kevich, A.I., Shishkina, S.V., Vovk, M.V. Fused pyrimidine systems: XVI. Electrophilic intramolecular cyclization of 2-(alkenylsulfanyl)pteridin-4(3H)-ones (2016) Russian Journal of Organic Chemistry, 52 (5), pp. 745-752.
  28. Shvydenko, T., Nazarenko, K., Shvydenko, K., Filimonchuk, S., Vlasenko, Y., Tolmachev, A., Kostyuk, A. Convenient approach to ω-aminoalkylthiophenes (2016) Tetrahedron Letters, 57 (17), pp. 1909-1911.
  29. Karpenko, I.A., Niko, Y., Yakubovskyi, V.P., Gerasov, A.O., Bonnet, D., Kovtun, Y.P., Klymchenko, A.S. Push-pull dioxaborine as fluorescent molecular rotor: Far-red fluorogenic probe for ligand-receptor interactions (2016) Journal of Materials Chemistry C, 4 (14), pp. 3002-3009. Cited 3 times.
  30. Yesypenko, O.A., Klyachina, M.A., Dekhtyarenko, M.V., Pirozhenko, V.V., Shishkina, S.V., Boyko, V.I., Voitenko, Z.V., Kalchenko, V.I. Design, synthesis and structure determination of new inherently chiral para-bromoalkoxycalix[4]arenes (2016) Supramolecular Chemistry, pp. 1-10. Article in Press.
  31. Shalimov, A.A., Chudakova, T.I., Vlasenko, Y.G., Sinitsa, A.D., Onys’ko, P.P. Heterocyclization of N-(chlorosulfonyl)imidoyl chlorides with anilines, a new method of synthesis of 1,2,4-benzothiadiazine 1,1-dioxides (2016) Chemistry of Heterocyclic Compounds, 52 (4), pp. 267-274.
  32. Ogurok, V.M. 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane in organic synthesis (microreview) (2016) Chemistry of Heterocyclic Compounds, 52 (4), pp. 211-212.
  33. Kemskii, S.V., Hrynyshyn, E.V., Bol’but, A.V., Vovk, M.V. Synthesis of a new heterocyclic system: Pyrazolo[3′,4′: 5,6][1,4]diazepino[7,1-b]quinazoline (2016) Russian Journal of Organic Chemistry, 52 (4), pp. 607-609.
  34. Marchenko, A., Koidan, G., Hurieva, A.N., Vlasenko, Y., Kostyuk, A., Biffis, A. Chelate Palladium(II) Complexes with Saturated N-Phosphanyl-N-Heterocyclic Carbene Ligands: Synthesis and Catalysis (2016) Organometallics, 35 (5), pp. 762-770.
  35. Timoshenko, V.M., Markitanov, Y.M., Shermolovich, Y.G. Reactions of 2-oxo-2-polyfluoroalkyl-sulfones and -sulfamides with nucleophiles (2016) Phosphorus, Sulfur and Silicon and the Related Elements, 191 (3), pp. 347-353.
  36. Povolotskii, M.I., Shablykin, O.V., Rusanov, E.B., Rozhenko, A.B. Molecular and electronic structure of 1,3,2-diazaphosphinine derivatives (2016) Phosphorus, Sulfur and Silicon and the Related Elements, 191 (3), pp. 399-404.
  37. Mishchuk, A., Shtil, N., Poberezhnyk, M., Nazarenko, K., Savchenko, T., Tolmachev, A., Krasavin, M. Keeping it small, polar, and non-flat: diversely functionalized building blocks containing the privileged 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]- and [1,5-a]pyridine cores (2016) Tetrahedron Letters, 57 (9), pp. 1056-1059.
  38. Kolotilo, N.V., Onys’ko, P.P. Cycloaddition and chlorotropic transformations in reactions of dichloromethylenetrifluoroacetamide with phosphites (2016) Russian Journal of General Chemistry, 86 (3), pp. 534-538.
  39. Zakharova, L.Y., Serdyuk, A.A., Mirgorodskaya, A.B., Kapitanov, I.V., Gainanova, G.A., Karpichev, Y., Gavrilova, E.L., Sinyashin, O.G. Amino Acid-Functionalized Calix[4]Resorcinarene Solubilization by Mono- and Dicationic Surfactants (2016) Journal of Surfactants and Detergents, pp. 1-7. Article in Press.
  40. Chernykh, A.V., Feskov, I.O., Chernykh, A.V., Daniliuc, C.G., Tolmachova, N.A., Volochnyuk, D.M., Radchenko, D.S. Synthesis of fluorinated building blocks based on spiro[3.3]heptane scaffold (2016) Tetrahedron, 72 (7), pp. 1036-1041.
  41. Lutsyk, P., Arif, R., Hruby, J., Bukivskyi, A., Vinijchuk, O., Shandura, M., Yakubovskyi, V., Kovtun, Y., Rance, G.A., Fay, M., Piryatinski, Y., Kachkovsky, O., Verbitsky, A., Rozhin, A. A sensing mechanism for the detection of carbon nanotubes using selective photoluminescent probes based on ionic complexes with organic dyes (2016) Light: Science and Applications, 5, art. no. e16028, .
  42. Savateev, A., Vlasenko, Y., Shtil, N., Kostyuk, A. Reduction of λ5-Phosphinines (2016) European Journal of Inorganic Chemistry, 2016 (5), pp. 628-632.
  43. Bentya, A.V., Mel’nichenko, N.V., Vovk, M.V. Synthesis of 2-aryl-2-(trifluoromethyl)-2,5-dihydro-1,3-thiazoles (2016) Russian Journal of Organic Chemistry, 52 (2), pp. 292-293.
  44. Ogurok, V.M., Siry, S.A., Rusanov, E.B., Vlasenko, Y.G., Shermolovich, Y.G. Synthesis of the symmetrical 3,5-bis(difluoromethyl)-1,4-thiazine 1,1-dioxides (2016) Journal of Fluorine Chemistry, 182, pp. 47-52.
  45. Onys’ko, P.P., Zamulko, K.A., Kyselyova, O.I. N-(α;-Hydroxytrihaloethyl)carbamates in synthesis of phosphorus analogs of trihaloalanine derivatives (2016) Phosphorus, Sulfur and Silicon and the Related Elements, 191 (2), pp. 274-278.
  46. Iampolska, A.D., Kharchenko, S.G., Voitenko, Z.V., Shishkin, S.V., Ryabitskii, A.B., Kalchenko, V.I. Synthesis of thiacalix[4]arene task-specific ionic liquids (2016) Phosphorus, Sulfur and Silicon and the Related Elements, 191 (2), pp. 174-179.
  47. Boyko, V.I., Rozhenko, A.B., Pirozhenko, V.V., Shishkina, S.V., Shishkin, O.V., Kalchenko, V.I. Diastereoselective reaction of 1,3-dihydroxy calixarene with acylisocyanates: New and easy approach for preparing inherently chiral calyx[4]arenes (2016) Structural Chemistry, 27 (1), pp. 261-272.
  48. Rozhkov, V.V., Kolotylo, M.V., Onys’Ko, P.P., Lukin, O. Synthesis of sulfonimide-based branched arylsulfonyl chlorides (2016) Tetrahedron Letters, 57 (3), pp. 308-309.
  49. Lysenko, A.B., Senchyk, G.A., Lukashuk, L.V., Domasevitch, K.V., Handke, M., Lincke, J., Krautscheid, H., Rusanov, E.B., Krämer, K.W., Decurtins, S., Liu, S.-X. Composition Space Analysis in the Development of Copper Molybdate Hybrids Decorated by a Bifunctional Pyrazolyl/1,2,4-Triazole Ligand (2016) Inorganic Chemistry, 55 (1), pp. 239-250.
  50. Marchenko, A., Koidan, G., Hurieva, A., Vlasenko, Y., Kostyuk, A. C-Silyl-N,N-dialkyl-N’-arylformamidines: Synthesis and Reactions with Phosphorus(III) Chlorides (2016) European Journal of Inorganic Chemistry, . Article in Press.
  51. Marchenko, A.P., Koidan, G.N., Hurieva, A.N., Rozhenko, A.B., Kostyuk, A.N. Zwitterionic Phosphoranides as Intermediates in the Reaction of Phosphorus Tribromide with N,N-Dimethyl-N′-arylformamidines (2016) Heteroatom Chemistry, 27 (1), pp. 12-22.
  52. Marchenko, A., Koidan, G., Hurieva, A., Vlasenko, Y., Kostyuk, A., Biffis, A. Erratum: Palladium(II) complexes with chelating N-phosphanyl acyclic diaminocarbenes: Synthesis, characterization and catalytic performance in Suzuki couplings (Dalton Transactions (2016) DOI: 10.1039/c5dt02250a) (2016) Dalton Transactions, 45 (4), p. 1779.
  53. Marchenko, A., Koidan, G., Hurieva, A., Vlasenko, Y., Kostyuk, A., Biffis, A. Palladium(ii) complexes with chelating N-phosphanyl acyclic diaminocarbenes: Synthesis, characterization and catalytic performance in Suzuki couplings (2016) Dalton Transactions, 45 (5), pp. 1967-1975.
  54. Mel’nyk, D.B., Yashchuk, V.M., Naumenko, A.P., Gerasyov, A.O., Kachkovski, O.D. Violation of ideal polymethine state in merocyanines with a long chromophore (2016) Ukrainian Journal of Physics, 61 (7), pp. 572-577.
  55. Lukashova, M.S., Belikov, K.N., Bryleva, K.Y., Kharchenko, S.G., Vishnevsky, S.G., Kalchenko, V.I. Merrifield resin modified with thiacalixarene-tetraphosphonates: Synthesis, characterization and europium sorption (2016) Functional Materials, 23 (1), pp. 111-119.
  56. Hodyna, D., Kovalishyn, V., Rogalsky, S., Blagodatnyi, V., Petko, K., Metelytsia, L. Antibacterial Activity of Imidazolium-Based Ionic Liquids Investigated by QSAR Modeling and Experimental Studies (2016) Chemical Biology and Drug Design, pp. 422-433.
  57. Smirnov, I.V., Stepanova, E.S., Drapailo, A.B., Kalchenko, V.I. Extraction of americium and europium with functionalized calixarenes from alkaline solutions (2016) Radiochemistry, 58 (1), pp. 42-51.
  58. Hodyna, D., Kovalishyn, V., Rogalsky, S., Blagodatnyi, V., Petko, K., Metelytsia, L. Antibacterial Activity of Imidazolium-Based Ionic Liquids Investigated by QSAR Modeling and Experimental Studies (2016) Chemical Biology and Drug Design, . Article in Press.
  59. Orysyk, S.I., Repich, G.G., Andrushchenko, O.O., Nikulina, V.V., Orysyk, V.V., Zborovskii, Y.L., Garmanchuk, L.V., Pekhnyo, V.I., Skachkova, O.V., Vovk, M.V. Effect of Pd(II) and Ni(II) coordination compounds with 4-amino-3-mercapto-5-methyl-1,2,4-triazole on the mitochondrial dehydrogenases activity (2016) Ukrainian Biochemical Journal, 87 (1), pp. 64-74.
  60. Didukh, N.O., Zatsikha, Y.V., Rohde, G.T., Blesener, T.S., Yakubovskyi, V.P., Kovtun, Y.P., Nemykin, V.N. NIR absorbing diferrocene-containing: Meso -cyano-BODIPY with a UV-Vis-NIR spectrum remarkably close to that of magnesium tetracyanotetraferrocenyltetraazaporphyrin (2016) Chemical Communications, 52 (77), pp. 11563-11566.
  61. Grygorenko, O.O., Babenko, P., Volochnyuk, D.M., Raievskyi, O., Komarov, I.V. Following Ramachandran: Exit vector plots (EVP) as a tool to navigate chemical space covered by 3D bifunctional scaffolds. The case of cycloalkanes (2016) RSC Advances, 6 (21), pp. 17595-17605.

 

Публікації співробітників Інституту за 2015 рік

  1. Rozhkov, V.V., Kolotylo, M.V., Onys’Ko, P.P., Lukin, O. Synthesis of sulfonimide-based branched arylsulfonyl chlorides (2016) Tetrahedron Letters, 57 (3), pp. 308-309.
  2. Boyko, V.I., Rozhenko, A.B., Pirozhenko, V.V., Shishkina, S.V., Shishkin, O.V., Kalchenko, V.I. Diastereoselective reaction of 1,3-dihydroxy calixarene with acylisocyanates: new and easy approach for preparing inherently chiral calyx[4]arenes (2016) Structural Chemistry, pp. 1-12. Article in Press. DOI: 10.1007/s11224-015-0706-5
  3. Artamonov, O.S., Bulda, T., Fam, T.K., Slobodyanyuk, E.Y., Volochnyuk, D.M., Grygorenko, O.O. A stereolibrary of conformationally restricted amino acids based on pyrrolidinyl/piperidinyloxazole motifs (2015) Heterocyclic Communications, 21 (6), pp. 391-395.
  4. Smaliy, R.V., Chaykovskaya, A.A., Shtil, N.A., Yurchenko, S.A., Yurchenko, A.A., Lakhtadyr, A.I., Gorlova, A.O., Kostyuk, A.N. Synthesis of CF3-bearing pyrrolidines by hydrogenation of trifluoroacetylated pyrrole derivatives
    (2015) Journal of Fluorine Chemistry, 180, pp. 257-264.
  5. Vakhitova, L.N., Lakhtarenko, N.V., Popov, A.F. Kinetics of the Oxidation of Methyl Phenyl Sulfide by Peroxoborate Anions (2015) Theoretical and Experimental Chemistry, pp. 1-7. Article in Press. DOI: 10.1007/s11237-015-9430-x
  6. Kushnir, O.V., Voloshchuk, O.N., Marchenko, M.M., Vovk, M.V. Synthesis and Antioxidant Activity of Ammonium Salts of 4-(3-Bromophenyl)-5-Methoxycarbonyl-1-(N,N-Dimethylaminopropyl)-3,4-Dihydropyrimidin-2-(1H)-One (2015) Pharmaceutical Chemistry Journal, 4 p. Article in Press. DOI: 10.1007/s11094-015-1318-5
  7. Davidenko, N.A., Davidenko, I.I., Studzinskii, S.L., Kostenko, L.I., Ishchenko, A.A., Mokrinskaya, E.V., Tonkopieva, L.S. Features of the photovoltaic properties of photosemiconductor film composites based on ferrocenyland carbazolyl-containing oligomer doped with a merocyanine dye (2015) High Energy Chemistry, 49 (6), pp. 420-425.
  8. Kremlev, M.M., Mushta, A.I., Tyrra, W., Yagupolskii, Y.L., Naumann, D., Schäfer, M. Approaches to prepare perfluoroalkyl and pentafluorophenyl copper couples for cross-coupling reactions with organohalogen compounds (2015) Dalton Transactions, 44 (45), pp. 19693-19699.
  9. Shvydenko, K., Nazarenko, K., Shvydenko, T., Vlasenko, Y., Tolmachev, A., Kostyuk, A. Ring opening of cyclic thioimidates in reaction with active methylene compounds (2015) Tetrahedron, 71 (40), art. no. 27031, pp. 7567-7574.
  10. Kemskii, S.V., Bol’But, A.V., Vovk, M.V. Synthesis of 4-hydrazinyl-1,6-dihydropyrazolo[3,4-e][1,4]diazepines and their hydrolytic recyclization to 5-amino-4-(1,2,4-triazin-3-yl)-1H-pyrazoles (2015) Russian Journal of Organic Chemistry, 51 (10), pp. 1481-1487.
  11. Kutovaya, I.V., Shmatova, O.I., Tkachuk, V.M., Melnichenko, N.V., Vovk, M.V., Nenajdenko, V.G. Aza-Henry Reaction with CF3-Ketimines: An Efficient Approach to Trifluoromethylated β-Nitroamines, 1,2-Diamines, α-Aminooximes, and Imidazolidinones (2015) European Journal of Organic Chemistry, 2015 (30), pp. 6749-6761.
  12. Kapitanov, I.V., Abakumov, A.A., Serdyuk, A.A. Identification of products in the reaction of 2-[(hydroxyimino)methyl]-1,3-dimethylimidazolium iodide with diethyl 4-nitrophenyl phosphate in alkaline medium (2015) Russian Journal of Organic Chemistry, 51 (10), pp. 1368-1375.
  13. Chornous, V.A., Mel’Nik, O.Ya., Mel’Nik, D.A., Rusanov, E.B., Vovk, M.V. Polyfunctional imidazoles: XI. Reaction of 1-aryl-4-chloro-5-(2-nitrovinyl)-1H-imidazoles with nonstabilized azomethine ylides. Synthesis of (1-aryl-4-chloro-1H-imidazol-5-yl)-substituted nitropyrrolidines and nitropyrrolizines (2015) Russian Journal of Organic Chemistry, 51 (10), pp. 1423-1429.
  14. Varchenko, V.V., Belikov, K.N., Drapailo, A.B. Effect of the p-tert-butylcalix[6]arene modifier on the electrochemical properties of the modified carbon paste electrode (2015) Russian Journal of Electrochemistry, 51 (9), pp. 857-861.
  15. Ivonin, S.P., Kurpil’, B.B., Volochnyuk, D.M., Grygorenko, O.O. Regioselective synthesis of pyrazoles fused with heteroaliphatic amines at the [3,4-c] edges (2015) Tetrahedron Letters, 56 (45), pp. 6248-6250.
  16. Rudakov, E.S., Shul’pin, G.B. Stable organoplatinum complexes as intermediates and models in hydrocarbon functionalization (2015) Journal of Organometallic Chemistry, 793, art. no. 18902, pp. 4-16.
  17. Mitchenko, S.A., Khazipov, O.V., Krasnyakova, T.V. Switching regioselectivity in the sequential iodoplatination of methyl propiolate CC triple bond by PtIV iodo complexes (2015) Journal of Organometallic Chemistry, 793, art. no. 18824, pp. 145-154.
  18. Chernykh, A.V., Radchenko, D.S., Chernykh, A.V., Kondratov, I.S., Tolmachova, N.A., Datsenko, O.P., Kurkunov, M.A., Zozulya, S.X., Kheylik, Y.P., Bartels, K., Daniliuc, C.G., Haufe, G. Synthesis and Physicochemical Properties of 3-Fluorocyclobutylamines (2015) European Journal of Organic Chemistry, 2015 (29), pp. 6466-6471.
  19. Bulavko, G.V., Davidenko, N.A., Derevyanko, N.A., Ishchenko, A.A. Effects of the nature of the anion of cationic polymethine dyes on the photovoltaic properties of polymer photosemiconductor composites (2015) High Energy Chemistry, 49 (5), pp. 331-335.
  20. Onys’Ko, P.P., Klyukovskii, D.V., Bezludnyi, A.V. N-cycloalkyl- and N-arylimidoylphosphonates (2015) Russian Journal of General Chemistry, 85 (9), pp. 2065-2070.
  21. Labyntseva, R.D., Bevza, A.A., Lul’ko, A.O., Cherenok, S.O., Kalchenko, V.I., Kosterin, S.O. Calix[4]arene C-99 inhibits myosin ATPase activity and changes the organization of contractile filaments of myometrium (2015) Ukrainian Biochemical Journal, 87 (6), pp. 95-103.
  22. Bondarenko, N.A., Vas’Kevich, A.I., Bol’But, A.V., Rusanov, E.B., Vovk, M.V. Electrophilic cyclization of N-allyl(propargyl)-5-amino-1H-pyrazole-4-carboxamides. Synthesis of 4-[(dihydro)oxazol-2-yl]-1H-pyrazol-5-amines (2015) Russian Journal of Organic Chemistry, 51 (12), pp. 1774-1783.
  23. Labyntseva, R.D., Bevza, A.A., Lul’ko, A.O., Cherenok, S.O., Kalchenko, V.I., Kosterin, S.O. Calix[4]arene C-99 inhibits myosin ATPase activity and changes the organization of contractile filaments of myometrium (2015) Ukrainian Biochemical Journal, 87 (6), pp. 95-103.
  24. Bondarenko, N.A., Vas’Kevich, A.I., Bol’But, A.V., Rusanov, E.B., Vovk, M.V. Electrophilic cyclization of N-allyl(propargyl)-5-amino-1H-pyrazole-4-carboxamides. Synthesis of 4-[(dihydro)oxazol-2-yl]-1H-pyrazol-5-amines (2015) Russian Journal of Organic Chemistry, 51 (12), pp. 1774-1783.
  25. Vasylevs’Kyy, S.I., Lysenko, A.B., Krautscheid, H., Karbowiak, M., Rusanov, E.B., Domasevitch, K.V. Ag(I)-triazolylcarboxylates: The role of hydrocarbon tails in the formation of “sitting-on-layer” supramolecular bowls (2015) Inorganic Chemistry Communications, 62, pp. 51-54.
  26. Kushnir, O.V., Voloshchuk, O.N., Marchenko, M.M., Vovk, M.V. Synthesis and Antioxidant Activity of Ammonium Salts of 4-(3-Bromophenyl)-5-Methoxycarbonyl-1-(N,N-Dimethylaminopropyl)-3,4-Dihydropyrimidin-2-(1H)-One (2015) Pharmaceutical Chemistry Journal, 49 (8), pp. 515-518.
  27. Sharko, A.V., Senchyk, G.A., Rusanov, E.B., Domasevitch, K.V. Preparative synthesis of 3(5),3′(5′)-dimethyl-4,4′-bipyrazole (2015) Tetrahedron Letters, 56 (44), pp. 6089-6092.
  28. Chornous, V.A., Mel’Nik, O.Ya., Mel’Nik, D.A., Rusanov, E.B., Vovk, M.V. Polyfunctional imidazoles: XI. Reaction of 1-aryl-4-chloro-5-(2-nitrovinyl)-1H-imidazoles with nonstabilized azomethine ylides. Synthesis of (1-aryl-4-chloro-1H-imidazol-5-yl)-substituted nitropyrrolidines and nitropyrrolizines (2015) Russian Journal of Organic Chemistry, 51 (10), pp. 1423-1429.
  29. Mykhaylychenko, S.S., Siryi, S.A., Pikun, N.V., Shermolovich, Y.G. Synthesis of 5-(polyfluoroalkyl)-1,3-thiazolidines from polyfluoroalkanethiocarboxylic acid derivatives (2015) Chemistry of Heterocyclic Compounds, 51 (9), pp. 861-864.
  30. Stasevych, M., Zvarych, V., Lunin, V., Halenova, T., Savchuk, O., Dudchak, O., Vovk, M., Novikov, V. Novel anthraquinone-based derivatives as potent inhibitors for receptor tyrosine kinases (2015) Indian Journal of Pharmaceutical Sciences, 77 (5), pp. 634-637.
  31. Prokop’Eva, T.M., Kapitanov, I.V., Belousova, I.A., Shumeiko, A.E., Kostrikin, M.L., Turovskaya, M.K., Razumova, N.G., Popov, A.F. Supernucleophilic systems based on functionalized surfactants in the decomposition of 4-nitrophenyl esters derived from phosphorus and sulfur acids. III. Reactivity of mixed micellar systems based on tetraalkylammonium and imidazolium surfactants (2015) Russian Journal of Organic Chemistry, 51 (8), pp. 1083-1090.
  32. Zatsikha, Y.V., Maligaspe, E., Purchel, A.A., Didukh, N.O., Wang, Y., Kovtun, Y.P., Blank, D.A., Nemykin, V.N. Tuning Electronic Structure, Redox, and Photophysical Properties in Asymmetric NIR-Absorbing Organometallic BODIPYs (2015) Inorganic Chemistry, 54 (16), pp. 7915-7928.
  33. Chernega, O.I., Levchenko, S.M., Ryabitskii, A.B., Gerasov, A.O., Kachkovskii, O.D., Yagupolskii, Y.L. Nature of the lowest electronic transitions of thia- and quinocyanines with fluorinated polymethine chain (2015) Dyes and Pigments, 123, art. no. 4877, pp. 176-185.
  34. Gaillard, D.C., Boltoeva, M., Billard, I., Georg, S., Mazan, V., Ouadi, A., Ternova, D., Hennig, C. Insights into the Mechanism of Extraction of Uranium (VI) from Nitric Acid Solution into an Ionic Liquid by using Tri-n-butyl phosphate (2015) ChemPhysChem, 16 (12), pp. 2653-2662.
  35. Kulinich, A.V., Mikitenko, E.K., Ishchenko, A.A. Fluorescent properties of merocyanines based on 1,3-indandione (2015) Optics and Spectroscopy (English translation of Optika i Spektroskopiya), 119 (1), pp. 39-48.
  36. Polischuk, K.A., Yesypenko, O.A., Rozhenko, A.B., Pirozhenko, V.V., Salimov, Y.A., Ischenko, V.V., Boyko, V.I., Khilya, V.P., Kalchenko, V.I. Stereoselective synthesis of six stereoisomers of inherently chiral methoxy-propoxy-butoxy-methoxycarbonylmethoxy-tert-butylcalix[4]arene (2015) Tetrahedron Letters, 56 (33), pp. 4788-4791.
  37. Siryi, S.A., Timoshenko, V.M., Vlasenko, Y.G., Rusanov, E.B., Shermolovich, Y.G. The synthesis and properties of 6-trifluoromethyl-substituted thiopyrano[3,4-d]isoxazole derivatives (2015) Chemistry of Heterocyclic Compounds, 51 (7), pp. 630-638.
  38. Kurdyukov, V.V., Tolmachev, A.I., Dekhtyar, M.L., Vlasenko, Y.G., Chernega, A.N. Synthesis, spatial structure and spectral properties of pyrylo-4 (thio) squaraines variously substituted in cyclobutene moiety (2015) Journal of Physical Organic Chemistry, 28 (7), pp. 452-459.
  39. Marchenko, A.P., Koidan, H.N., Kirilchuk, A.A., Rozhenko, A.B., Yurchenko, A.A., Kostyuk, A.N. Investigation of N- and C-Phosphanylation of [1,2,4]Triazolo[4,3-a]pyridines (2015) Heteroatom Chemistry, 26 (4), pp. 277-289.
  40. Marchenko, A., Koidan, G., Hurieva, A., Kurpiieva, O., Vlasenko, Y., Rozhenko, A.B., Kostyuk, A. Stable N-phosphanyl acyclic diaminocarbenes (2015) European Journal of Inorganic Chemistry, 2014 (20), pp. 3259-3270.
  41. Le, T.-N., Diter, P., Pégot, B., Bournaud, C., Toffano, M., Guillot, R., Vo-Thanh, G., Yagupolskii, Y., Magnier, E. Functionalized S-perfluorinated sulfoximines: Preparation and evaluation in catalytic processes (2015) Journal of Fluorine Chemistry, 179, pp. 179-187.
  42. Mel’Nichenko, N.V., Bentya, A.V., Rusanov, E.B., Vovk, M.V. Synthesis of 2-aryl-2-trifluoromethyl-1,3-thiazolidin-4-ones and 2-aryl-2-trifluoromethyltetrahydro-4H-1,3-thiazin-4-ones and their oxidation with hydrogen peroxide (2015) Russian Journal of General Chemistry, 85 (6), pp. 1440-1446.
  43. Ivonin, S.P., Kurpil’, B.B., Bezdudny, A.V., Volochnyuk, D.M., Grygorenko, O.O. An approach to (4-fluoroalkyl-1-alkyl-1H-pyrazol-3-yl)methylamines (2015) Journal of Fluorine Chemistry, 176, pp. 78-81.
  44. Bricks, J.L., Kachkovskii, A.D., Slominskii, Y.L., Gerasov, A.O., Popov, S.V. Molecular design of near infrared polymethine dyes: A review (2015) Dyes and Pigments, 121, pp. 238-255.
  45. Buta, A., Maximyuk, O., Kovalskyy, D., Sukach, V., Vovk, M., Ievglevskyi, O., Isaeva, E., Isaev, D., Savotchenko, A., Krishtal, O. Novel Potent Orthosteric Antagonist of ASIC1a Prevents NMDAR-Dependent LTP Induction (2015) Journal of Medicinal Chemistry, 58 (11), pp. 4449-4461.
  46. Kuperman, M.V., Chernii, S.V., Losytskyy, M.Yu., Kryvorotenko, D.V., Derevyanko, N.O., Slominskii, Y.L., Kovalska, V.B., Yarmoluk, S.M. Trimethine cyanine dyes as fluorescent probes for amyloid fibrils: The effect of N,N′-substituents (2015) Analytical Biochemistry, 484, pp. 9-17.
  47. Onys’ko, P.P., Rassukana, Y.V., Khomutnyk, Y.Y., Yelenich, I.P., Klukovsky, D.V., Synytsya, A.D. A New Strategy for Synthesis of Compounds Bearing Biorelevant α-Aminophosphonate Functionalities (2015) Phosphorus, Sulfur and Silicon and the Related Elements, 190 (5-6), pp. 725-728.
  48. Dimukhametov, M., Belova, N., Mironov, V., Mironova, E., Krivolapov, D., Onys’Ko, P., Rassukanaya, Y. Synthesis and Crystal Structure of 2-Substituted 3-Aryl-2-Oxophenylbenzo[E]-1,4,2-Oxazaphosphinanes (2015) Phosphorus, Sulfur and Silicon and the Related Elements, 190 (5-6), pp. 943-946.
  49. Mironov, V.F., Ivkova, G.A., Bogdanov, A.V., Burnaeva, L.M., Onys’ko, P., Rassukanaya, Y. 2-(5-Methyl-2-Phenyl-2 H -1,2,3-Dizaphosphol-4-YL)-4 H -Benzo[ D ]-1,3,2-Dioxaphosphorin-4-One in the Synthesis of Bis-Heterocyclic 1,4,2-Oxazaphosphepine Derivatives (2015) Phosphorus, Sulfur and Silicon and the Related Elements, 190 (5-6), pp. 932-935.
  50. Petruk, O.M., Kyriukha, Y.A., Bezdudny, A.V., Rozhkov, V.V. Synthesis of 2-methyl-1,5-dinitro-3- and 2-methyl-1,3-dinitro-5-(trifluoromethyl)benzenes and their transformation into 6-nitro-4-(trifluoromethyl)- and 4-nitro-6-(trifluoromethyl)-1H-indoles (2015) Journal of Fluorine Chemistry, 175, pp. 176-179.
  51. Dyachenko, V.D., Ryl’skaya, T.A., Dyachenko, I.V., Kalashnik, I.N., Chernykh, A.V. Three-component synthesis of nicotinamide derivatives based on cross-recyclization of 2,6-diamino-4-aryl-3,5-dicyano-4H-thiopyrans with acetoacetanilide and alkylating reagents (2015) Russian Journal of General Chemistry, 85 (5), pp. 1069-1073.
  52. Fizer, M., Slivka, M., Rusanov, E., Turov, A., Lendel, V. [1,3]Thiazolo[2′,3′:3,4][1,2,4]triazolo[1,5-a]pyrimidines – A new heterocyclic system accessed via bromocyclization (2015) Journal of Heterocyclic Chemistry, 52 (3), pp. 949-952.
  53. Yagupolskii, Y.L., Pavlenko, N.V., Shelyazhenko, S.V., Filatov, A.A., Kremlev, M.M., Mushta, A.I., Gerus, I.I., Peng, S., Petrov, V.A., Nappa, M. Alternative synthetic routes to hydrofluoroolefins (2015) Journal of Fluorine Chemistry, 179, pp. 134-141.
  54. Chernykh, A.V., Radchenko, D.S., Grygorenko, O.O., Daniliuc, C.G., Volochnyuk, D.M., Komarov, I.V. Synthesis and structural analysis of angular monoprotected diamines based on Spiro[3.3]heptane scaffold (2015) Journal of Organic Chemistry, 80 (8), pp. 3974-3981.
  55. Sokolenko, T.M., Davydova, Y.A., Yagupolskii, Y.L. Polyfluoroethoxy derivatives of malonic aldehyde acetal in the synthesis of heterocyclic compounds (2015) Chemistry of Heterocyclic Compounds, 51 (4), pp. 324-326.
  56. Vas’kevich, R.I., Dyachenko, I.V., Vas’kevich, A.I., Rusanov, E.B., Vovk, M.V. Fused pyrimidine systems: XV.∗ Intramolecular electrophilic cyclization of 2-allyl(propargyl, cinnamyl)amino-pyrido[2,3-d]pyrimidin-4(3H)-ones (2015) Russian Journal of Organic Chemistry, 51 (4), art. no. 1015, pp. 556-565.
  57. Chornous, V.A., Grozav, A.N., Mel’nik, O.Y., Pirozhenko, V.V., Vovk, M.V. Polyfunctional imidazoles: X. Synthesis of 4-chloro-5-(2-nitroalkenyl)-1H-imidazoles and their reaction with 5-methyl-2,4-dihydro-3H-pyrazol-3-one (2015) Russian Journal of Organic Chemistry, 51 (4), art. no. 1012, pp. 534-540.
  58. Sokolenko, L.V., Yagupolskii, Y.L., Vlasenko, Y.G., Babichenko, L.N., Lipetskij, V.O., Anselmi, E., Magnier, E. Arylation of perfluoroalkyl vinyl sulfoxides via the Heck reaction (2015) Tetrahedron Letters, 56 (10), pp. 1259-1262.
  59. Bulavko, G.V., Davidenko, N.A., Derevyanko, N.A., Ishchenko, A.A., Kulinich, A.V. Effect of the Structure of Polymethine Dyes on Their Photovoltaic Properties in Polymer Films (2015) Theoretical and Experimental Chemistry, 51 (1), pp. 37-44.
  60. Bratenko, M.K., Barus, M.M., Vovk, M.V. Polyfunctional Pyrazoles. 10∗. Synthesis of 5-OXO-4,5,7,9-Tetrahydropyrazolo[3,4-e][1,2,3]-Triazolo[1,5-a][1,3]Diazepine-3-Carboxamides in a Tandem Reaction of Ethyl 4-(Azido-Methyl)Pyrazole-3-Carboxylates with Cyanoacetamides (2015) Chemistry of Heterocyclic Compounds, 50 (12), pp. 1707-1711.
  61. Torgov, V.G., Kostin, G.A., Us, T.V., Korda, T.M., Drapailo, A.B. Palladium and silver extraction with thiacalix[4]arenes and their acyclic analogs from carbonate and ammonia-carbonate solutions (2015) Russian Journal of Inorganic Chemistry, 60 (3), pp. 372-378.
  62. Tkachuk, V.M., Sukach, V.A., Kovalchuk, K.V., Vovk, M.V., Nenajdenko, V.G. Development of an efficient route to CF3-substituted pyrrolopyrimidines through understanding the competition between Michael and aza-Henry reactions (2015) Organic and Biomolecular Chemistry, 13 (5), pp. 1420-1428.
  63. Shevchenko, I.V., Turcheniuk, K.V., Kirilchuk, A.A., Leszczynski, J., Rozhenko, A.B. On the reaction of diaminocarbenes with aroylimines (2015) Journal of Organic Chemistry, 80 (3), pp. 1387-1394.
  64. Petrenko, V.Y., Dimitriev, O.P., Slominskii, Y.L., Smirnova, A.L. Efficient energy transfer between J-aggregates of thiamonomethinecyanine dyes (2015) Chemical Physics Letters, 621, pp. 22-28.
  65. Onys’ko, P.P., Klyukovskii, D.V., Bezdudnyi, A.V. N-(R-cyclopropyl)fluorobenzimidoyl phosphonates (2015) Russian Journal of General Chemistry, 85 (2), pp. 418-423.
  66. Mykhaylychenko, S.S., Pikun, N.V., Rusanov, E.B., Shermolovich, Y.G. Synthesis of 2-Aryl-4,5-Bis(Polyfluoroalkyl)Imidazoles from Polyfluoroalkanethiocarboxylic Acid Amides (2015) Chemistry of Heterocyclic Compounds, 51 (2), pp. 128-132.
  67. Tsizorik, N.M., Vas’Kevich, A.I., Vas’Kevich, R.I., Vovk, M.V. Electrophilic intramolecular cyclization of functional dervatives of unsaturated compounds: VII. Synthesis of 5-arylsulfanyl-6-phenylpiperidin-2-ones in the absence of salt additives and their selective reduction and oxidation (2015) Russian Journal of Organic Chemistry, 51 (2), pp. 226-230.
  68. Mel’Nik, O.Ya., Chornous, V.A., Vovk, M.V. Polyfunctional imidazoles: IX. Synthesis of 1-aryl-5-(2-aryl-3,4-dihydro-2H-pyrrol-4-yl)-4-chloro-1H-imidazoles (2015) Russian Journal of Organic Chemistry, 51 (2), pp. 240-244.
  69. Lourie, L.F., Serguchev, Y.A., Bentya, A.V., Ponomarenko, M.V., Rusanov, E.B., Vovk, M.V., Fokin, A.A., Ignat’ev, N.V. Metal free electrophilic fluoro-cyclization of unsaturated N-hydroxy- and N-acetoxyamides with N-F reagents (2015) Journal of Fluorine Chemistry, 179, pp. 42-47.
  70. Orysyk, S.I., Zholob, O.O., Bon, V.V., Nikulina, V.V., Orysyk, V.V., Nikolaienko, T.V., Garmanchuk, L.V., Zborovskii, Y.L., Tolstanova, G.M., Khranovska, N.M., Pekhnyo, V.I., Vovk, M.V. Novel chelate complexes of Co(II), Ni(II), Cu(II), Pd(II) derived from anti- and syn-isomers of 2-(2-aminothiazole-4-yl)-2-hydroxyiminoacetic acid with pro-/antiproliferative actions on endothelial cells (2015) Polyhedron, 85, pp. 208-220.
  71. Kirilchuk, A.A., Yurchenko, A.A., Vlasenko, Y.G., Kostyuk, A.N., Rozhenko, A.B. Synthesis and Structure of Phosphanylated Bis-Triazoles as Potential Ligands for Chiral Catalysts (2015) Chemistry of Heterocyclic Compounds, 8 p. Article in Press.
  72. Onys’Ko, P.P., Kyselyova, O.I., Zamulko, K.A., Shalimov, O.O., Kurilchyk, S.M. Synthesis and some transformations of 1-chloro-2,2,2-trifluoroethyl isocyanate (2015) Journal of Fluorine Chemistry, 173, pp. 1-5.
  73. Savateev, A.A., Shtil, N.A., Chaikovskaya, A.A., Smaliy, R.V., Vlasenko, Y.G., Kostyuk, A.N. A simple approach to vicinal pyrrolylphosphane aldehydes (2015) Heteroatom Chemistry, 26 (1), pp. 91-100.
  74. Zatsikha, Y.V., Yakubovskyi, V.P., Shandura, M.P., Kovtun, Y.P. Functionalized bispyridoneannelated BODIPY – Bright long-wavelength fluorophores (2015) Dyes and Pigments, 114 (C), pp. 215-221.
  75. Davydova, Y.A., Sokolenko, T.M., Vlasenko, Y.G., Yagupolskii, Y.L. Chemical properties of 5-(1,1,2,2-tetrafluoroethoxy)-4-phenylthiazole derivatives (2015) Chemistry of Heterocyclic Compounds, 51 (1), pp. 80-87.
  76. Ponomarova, V.V., Rusanova, J.A., Rusanov, E.B., Domasevitch, K.V. Unusual centrosymmetric structure of [M(18-crown-6)]+ (M = Rb, Cs and NH4) complexes stabilized in an environment of hexachloridoantimonate(V) anions (2015) Acta Crystallographica Section C: Structural Chemistry, 71, pp. 867-872.
  77. Dyachenko, V.D., Toropov, A.N., Rusanov, E.B. Revision of 2-(3,8-diaryl-6-oxo-2,7-diazaspiro[4.4]nona-2,8-dien-1-ylidene)malononitrile structure. Molecular and crystal structure of 3-cyano-2-[2-(4-methoxyphenyl)-2-oxoethyl]-2-[5-(4-methoxyphenyl)-1H-pyrrol-2-yl]malononitrile (2015) Chemistry of Heterocyclic Compounds, 51 (1), pp. 31-33.
  78. Subota, A.I., Grygorenko, O.O., Valter, Y.B., Tairov, M.A., Artamonov, O.S., Volochnyuk, D.M., Ryabukhin, S.V. Approach to 3-(Cyclo)alkylpiperidines through ‘sp3-sp3 via sp2-sp3′ Coupling (2015) Synlett, 26 (3), art. no. st-2014-d0832-l, pp. 408-411.
  79. Sukach, V.A., Resetnic, A.A., Tkachuk, V.M., Lin, Z., Kortz, U., Vovk, M.V., Röschenthaler, G.-V. Synthesis of trifluoromethylated analogues of 4,5-dihydroorotic acid (2015) European Journal of Organic Chemistry, 2015 (6), pp. 1290-1301.
  80. Petrenko, V.Yu., Dimitriev, O.P., Slominskii, Yu.L. Interplay of monomers, dimers and J-aggregates of thiamonomethinecyanine dye with PEDOT and PSS in the dye-PEDOT:PSS composite system (2015) Synthetic Metals, 203, pp. 68-73.
  81. Bulavko, G.V., Davidenko, N.A., Ishchenko, A.A., Studzinsky, S.L., Shkavro, A.G. Peculiarities of the photovoltaic properties of films based on photoconducting polymer and organic dye in samples with free surfaces and between electric contacts (2015) Technical Physics Letters, 41 (2), pp. 191-194.
  82. Borysyuk, V.I., Yashchuk, V.M., Naumenko, A.P., Stanova, A.V., Gerasova, V.G., Gerasov, A.O., Kovtun, Y.P., Shandura, M.P., Kachkovsky, O.D. Influence of surplus negative charge on absorption and fluorescence excitation spectra of asymmetric polymethine dyes (2015) Ukrainian Journal of Physics, 60 (7), pp. 593-600.
  83. Melezhyk, I.O., Rodik, R.V., Iavorska, N.V., Klymchenko, A.S., Mely, Y., Shepelevych, V.V., Skivka, L.M., Kalchenko, V.I. Antibacterial properties of tetraalkylammonium and imidazolium tetraalkoxycalix[4]arene derivatives (2015) Anti-Infective Agents, 13 (1), pp. 87-94.
  84. Kibirev, V.K., Osadchuk, T.V., Rodik, R.V., Kalchenko, V.I. Furin inhibitors based on the derivatives of calix[4]arene CX3im (2015) Ukrainian Biochemical Journal, 87 (3), pp. 31-36.
  85. Ibrayev, N., Seliverstova, E., Nuraje, N., Ishchenko, A. FRET-designed dye-sensitized solar cells to enhance light harvesting (2015) Materials Science in Semiconductor Processing, 31 (1), pp. 358-362.
  86. Zvarych, V.I., Stasevych, M.V., Stan’ko, O.V., Komarovskaya-Porokhnyavets, E.Z., Poroikov, V.V., Rudik, A.V., Lagunin, A.A., Vovk, M.V., Novikov, V.P. Erratum to: Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-yl)Acetamide [Pharmaceutical Chemistry Journal, 48-9, 2014, 584-588, DOI 10.1007/s11094-015-1174-3] (2015) Pharmaceutical Chemistry Journal, 48 (10), p. 697.
  87. Kobasa, I., Odosiy, L., Kurdyukova, I., Ishchenko, O., Kurek, S. Electrochemical and energetic characteristics of new dye-sensitizers for photovoltaic cells (2015) Functional Materials Letters, 8 (5), art. no. 1550067, .
  88. Dronova, M., Vrynchanu, N., Varbanets, L., Korotkiy, Y., Brovarska, O. Arylaliphatic aminoalcohol derivative KVM-194 affects E. coli lipopolysaccharide composition (2015) Farmacia, 63 (4), pp. 586-592.
  89. Trofymchuk, S., Bezdudny, A., Pustovit, Y., Mykhailiuk, P.K. Synthesis of isomeric (3,3,3-trifluoropropyl)anilines (2015) Journal of Fluorine Chemistry, 171, pp. 174-176.

Публікації співробітників Інституту за 2014 рік

  1. Shatursky, O.Y., Kasatkina, L.A., Rodik, R.V., Cherenok, S.O., Shkrabak, A.A., Veklich, T.O., Borisova, T.A., Kosterin, S.O., Kalchenko, V.I. Anion carrier formation by calix[4]arene-bis-hydroxymethylphosphonic acid in bilayer membranes
    (2014) Organic and Biomolecular Chemistry, 12 (48), pp. 9811-9821.
  2. Ryabukhin, S.V., Fominova, K.I., Sibgatulin, D.A., Grygorenko, O.O. Synthesis of three-dimensional fused and spirocyclic oxygen-containing cyclobutanone derivatives (2014) Tetrahedron Letters, 55 (52), pp. 7240-7242.
  3. Orysyk, S.I., Repich, G.G., Bon, V.V., Dyakonenko, V.V., Orysyk, V.V., Zborovskii, Y.L., Shishkin, O.V., Pekhnyo, V.I., Vovk, M.V. Novel Fe(III), Co(III), Ni(II), Cu(II) coordination compounds involving 2-[(2-hydroxyphenyl)methylene]hydrazine-N-(2-propenyl)-carbothioamide as ligand: Synthesis, crystal structures and spectral characteristics (2014) Inorganica Chimica Acta, 423 (PA), pp. 496-503.
  4. Zvarich, V.I., Stasevich, M.V., Stan’ko, O.V., Komarovskaya-Porokhnyavets, E.Z., Poroikov, V.V., Rudik, A.V., Lagunin, A.A., Vovk, M.V., Novikov, V.P. Computerized Prediction, Synthesis, and Antimicrobial Activity of New Amino-Acid Derivatives of 2-Chloro-N-(9,10-Dioxo-9,10-Dihydroanthracen-1-Yl)Acetamide (2014) Pharmaceutical Chemistry Journal, 5 p. Article in Press.
  5. Bratenko, M.K., Barus, M.M., Rotar, D.V., Vovk, M.V. Polyfunctional Pyrazoles. 9*. Synthesis of 1-Alkyl(Aryl)-3-[4-(Hydroxymethyl)-1Н-Pyrazol-3-Yl]UReas (2014) Chemistry of Heterocyclic Compounds, 7 p. Article in Press.
  6. Marchenko, A., Koidan, H., Hurieva, A., Kurpiieva, O., Vlasenko, Y., Kostyuk, A., Tubaro, C., Lenarda, A., Biffis, A., Graiff, C. N-phosphanyl-imidazolin-2-ylidenes: Novel stable carbenes as bidentate ligands for late transition metals (2014) Journal of Organometallic Chemistry, 771, pp. 14-23.
  7. Ishchenko, A.Y., Yanik, S., Rusanov, E.B., Komarov, I.V., Kirby, A.J. An expedient and practical approach to functionalized 3-aza-, 3-oxa-, and 3-thiabicyclo[33.1]nonane systems (2014) Synthesis (Germany), 46 (9), art. no. 1379456.
  8. Kurdyukov, V.V., Tolmachev, O.I., Kachkovsky, O.D., Pavlenko, E.L., Dmytrenko, O.P., Kulish, N.P., Iakovyshen, R.S., Brusentsov, V.A., Seryk, M., Momot, A.I.
    Electron structure and nature of electron transitions of squaraine and thiosquaraine as well as their 1,2-isomers (2014) Journal of Molecular Structure, 1076, pp. 583-591.
  9. Adamovskyi, M.I., Artamonov, O.S., Tymtsunik, A.V., Grygorenko, O.O.
    The synthesis of a 2-azabicyclo[3.1.0]hexane by rearrangement of a spirocyclic epoxide (2014) Tetrahedron Letters, 55 (43), pp. 5970-5972.
  10. Shvidenko, K., Nazarenko, K., Shvidenko, T., Vlasenko, Y., Kostyuk, A. Synthesis of thieno[3,4-b]pyrrole derivatives based on the reaction of 1-methyl-2-nitromethylenepyrrolidine with isothiocyanates (2014) Tetrahedron Letters, 55 (41), pp. 5639-5642.
  11. Senchyk, G.A., Lysenko, A.B., Babaryk, A.A., Rusanov, E.B., Krautscheid, H., Neves, P., Valente, A.A., Gonçalves, I.S., Krämer, K.W., Liu, S.-X., Decurtins, S., Domasevitch, K.V. Triazolyl-based copper-molybdate hybrids: From composition space diagram to magnetism and catalytic performance (2014) Inorganic Chemistry, 53 (19), pp. 10112-10121.
  12. Kachkovsky, O.D., Yashchuk, V.M., Navozenko, O.M., Naumenko, A.P., Slominskii, Y.L. On the nature of the lowest electron transitions in the borine dye derivatives benz[cd]indole (2014) Journal of Molecular Structure, 1074, pp. 589-595.
  13. Ivonin, S.P., Kurpil’, B.B., Grygorenko, O.O., Volochnyuk, D.M. Reaction of hydrazones derived from active methylene compounds with Vilsmeier-Haack reagent (2014) Monatshefte für Chemie – Chemical Monthly, . Article in Press.
  14. Maligaspe, E., Hauwiller, M.R., Zatsikha, Y.V., Hinke, J.A., Solntsev, P.V., Blank, D.A., Nemykin, V.N. Redox and photoinduced electron-transfer properties in short distance organoboryl ferrocene-subphthalocyanine dyads (2014) Inorganic Chemistry, 53 (17), pp. 9336-9347.
  15. Rassukana, Y.V., Yelenich, I.P., Vlasenko, Y.G., Onys’ko, P.P. Asymmetric synthesis of phosphonotrifluoroalanine derivatives via proline-catalyzed direct enantioselective C{single bond}C bond formation reactions of N{single bond}H trifluoroacetimidoyl phosphonate (2014) Tetrahedron Asymmetry, . Article in Press.
  16. Kushnir, O.V., Voloshchuk, O.N., Eften’eva, R.I., Marchenko, M.M., Vovk, M.V. Synthesis and Antioxidant Activity of 2-Thioxo-1,2,3,4-Tetrahydropyrimidine-5-Carbamides (2014) Pharmaceutical Chemistry Journal, . Article in Press.
  17. Ponomarenko, M.V., Serguchev, Y.A., Hirschberg, M.E., Röschenthaler, G.-V., Fokin, A.A. Elemental F2 with transannular dienes: Regioselectivities and mechanisms(2014) Chemistry – A European Journal, 20 (33), pp. 10383-10391.
  18. Rassukana, Y.V., Yelenich, I.P., Bezdudny, A.V., Mironov, V.F., Onys’ko, P.P. Chemoselectivity of the reactions of haloacetonitriles with hydrogen phosphonates: the dramatic effect of the nature of the halogen atom(2014) Tetrahedron Letters, . Article in Press.
  19. Trofymchuk, S., Bezdudny, A., Pustovit, Y., Mykhailiuk, P.K.Synthesis of isomeric (3,3,3-trifluoropropyl)anilines(2014) Journal of Fluorine Chemistry, . Article in Press.
  20. Bashmakova, N.V., Shaydyuk, Y.O., Levchenko, S.M., Masunov, A.E., Przhonska, O.V., Bricks, J.L., Kachkovsky, O.D., Slominsky, Y.L., Piryatinski, Y.P., Belfield, K.D., Bondar, M.V. Design and electronic structure of new styryl dye bases: Steady-state and time-resolved spectroscopic studies (2014) Journal of Physical Chemistry A, 118 (25), pp. 4502-4509.
  21. Marchenko, A., Koidan, H., Hurieva, A., Kurpiieva, O., Vlasenko, Y., Kostyuk, A., Tubaro, C., Lenarda, A., Biffis, A., Graiff, C.N-phosphanyl-imidazolin-2-ylidenes: Novel stable carbenes as bidentate ligands for late transition metals (2014) Journal of Organometallic Chemistry, . Article in Press.
  22. Degtyarenko, A.S., Handke, M., Krämer, K.W., Liu, S.-X., Decurtins, S., Rusanov, E.B., Thompson, L.K., Krautscheid, H., Domasevitch, K.V.Mixed-ligand hydroxocopper(II)/pyridazine clusters embedded into 3D framework lattices (2014) Dalton Transactions, 43 (22), pp. 8530-8542.
  23. Shvidenko, K., Nazarenko, K., Shvidenko, T., Vlasenko, Y., Kostyuk, A. Synthesis of thieno[3,4-b]pyrrole derivatives based on the reaction of 1-methyl-2-nitromethylenepyrrolidine with isothiocyanates (2014) Tetrahedron Letters, . Article in Press.
  24. Siry, S.A., Timoshenko, V.M., Vlasenko, Y.G, Baranova, G.V., Zagorodnya, S.D., Nesterova, N.V.Pummerer Reactions of Thiopyran Derivatives as a Method for the Preparation of Trifluoro-Methyl-Substituted Thiolanes with Antiviral Activity (2014) Chemistry of Heterocyclic Compounds .
  25. Kalchenko, O.I., Cherenok, S.O., Solovyov, A.V., Kalchenko, V.I.Study of the complexation of 5,17-bis-(N -tolyliminomethyl)-25,27- dipropoxycalix[4]arene with pyridine carboxylic acids by RP HPLC and molecular modelling (2014) Supramolecular Chemistry, 26 (5-6), pp. 409-413.
  26. Tsymbal, L.V., Lampeka, Y.D., Boyko, V.I., Kalchenko, V.I., Shishkina, S.V., Shishkin, O.V. A ladder-type coordination polymer constructed from two macrocyclic units-calix[4]arene tetracarboxylate and azamacrocyclic nickel(II) complex (2014) CrystEngComm, 16 (18), pp. 3707-3711.
  27. Galyaltdinov, S.F., Ziganshin, M.A., Gubaidullin, A.T., Vyshnevsky, S.G., Kalchenko, O.I., Gorbatchuk, V.V. Anti-sieve effect in guest inclusion by thiacalix[4]arene giving a surge in thermal stability of its clathrates prepared by solid-phase guest exchange (2014) CrystEngComm, 16 (18), pp. 3781-3787.
  28. Rassukana, Y.V., Yelenich, I.P., Synytsya, A.D., Onys’Ko, P.P. Fluorinated NH-iminophosphonates and iminocarboxylates: Novel synthons for the preparation of biorelevant α-aminophosphonates and carboxylates (2014) Tetrahedron, 70 (18), pp. 2928-2937.
  29. Ziegler, C.J., Chanawanno, K., Hasheminsasab, A., Zatsikha, Y.V., Maligaspe, E., Nemykin, V.N. Synthesis, redox properties, and electronic coupling in the diferrocene aza-dipyrromethene and azaBODIPY donor-acceptor dyad with direct ferrocene-α-pyrrole bond (2014) Inorganic Chemistry, 53 (9), pp. 4751-4755.
  30. Cheipesh, T.A., Zagorulko, E.S., McHedlov-Petrossyan, N.O., Rodik, R.V., Kalchenko, V.I. The difference between the aggregates of short-tailed and long-tailed cationic calix[4]arene in water as detected using fluorescein dyes (2014) Journal of Molecular Liquids, 193, pp. 232-238.
  31. Rodik, R.V., Klymchenko, A.S., Mely, Y., Kalchenko, V.I. Calixarenes and related macrocycles as gene delivery vehicles (2014) Journal of Inclusion Phenomena and Macrocyclic Chemistry, . Article in Press.
  32. Dekhtyar, M.L., Rozenbaum, V.M.Symmetry rules for brownian photomotors (2014) Match, 71 (3), pp. 609-626.
  33. Vasylevskyy, S.I., Senchyk, G.A., Lysenko, A.B., Rusanov, E.B., Chernega, A.N., Jezierska, J., Krautscheid, H., Domasevitch, K.V., Ozarowski, A. 1,2,4-triazolyl-carboxylate-based MOFs incorporating triangular Cu(II)-hydroxo clusters: Topological metamorphosis and magnetism (2014) Inorganic Chemistry, 53 (7), pp. 3642-3654.
  34. Ivonin, S.P., Kurpil’, B.B., Rusanov, E.B., Grygorenko, O.O., Volochnyuk, D.M. N-Alkylhydrazones of aliphatic ketones in the synthesis of 1,3,4-trisubstituted non-symmetric pyrazoles (2014) Tetrahedron Letters, 55 (14), pp. 2187-2189.
  35. Kornienko, A.N., Pil’O, S.G., Kozachenko, A.P., Prokopenko, V.M., Rusanov, E.B., Brovarets, V.S. 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 (2014) Chemistry of Heterocyclic Compounds, 50 (1), pp. 76-86.
  36. Kolesnik, N.P., Rozhenko, A.B., Kinzhybalo, V., Lis, T., Shermolovich, Y.G. 1-Oxo-1-fluoro-1,2,4-benzothiadiazines – A new type of cyclic sulfonimidoyl fluorides (2014) Journal of Fluorine Chemistry, 160, pp. 16-19.
  37. Pavlenko, N.V., Oos, T.I., Yagupolskii, Y.L., Gerus, I.I., Doeller, U., Willms, L. Novel Family of (1-aminoalkyl)(trifluoromethyl)- and -(difluoromethyl) phosphinic Acids – Analogues of α-Amino Acids (2014) Beilstein Journal of Organic Chemistry, 10, pp. 722-731.
  38. Nychyporenko, O.S., Melnyk, O.P., Viniychuk, O.O., Pinchuk-Rugal, T.M., Brusentsov, V.A., Pavlenko, E.L., Dmytrenko, O.P., Kulish, N.P., Kachkovsky, O.D. Shape and location of multiple charge carriers in linear π-electron systems (2014) International Journal of Quantum Chemistry, 114 (6), pp. 416-428.
  39. Marchenko, A., Koidan, G., Hurieva, A., Savateev, A., Rozhenko, A.B., Sotiropoulos, J.-M., Shishkina, S.V., Shishkin, O.V., Kostyuk, A. A convenient approach to N-(Di-tert-butylphosphanyl)- and N-(Ditert-butylphosphoroselenoyl)formamidinium Salts: Carbene precursors (2014) European Journal of Inorganic Chemistry, (7), pp. 1192-1203.
  40. Markitanov, Y.M., Timoshenko, V.M., Shermolovich, Y.G. β-Keto sulfones: Preparation and application in organic synthesis (2014) Journal of Sulfur Chemistry, 35 (2), pp. 188-236.
  41. Sukach, V.A., Tkachuk, V.M., Shoba, V.M., Pirozhenko, V.V., Rusanov, E.B., Chekotilo, A.A., Röschenthaler, G.-V., Vovk, M.V. Control of regio- and enantioselectivity in the asymmetric organocatalytic addition of acetone to 4-(trifluoromethyl)pyrimidin-2(1H)-ones (2014) European Journal of Organic Chemistry, 2014 (7), pp. 1452-1460.
  42. Chernykh, A.V., Radchenko, D.S., Grygorenko, O.O., Volochnyuk, D.M., Shishkina, S.V., Shishkin, O.V., Komarov, I.V. Conformationally restricted glutamic acid analogues: Stereoisomers of 1-aminospiro[3.3]heptane-1,6-dicarboxylic acid (2014) RSC Advances, 4 (21), pp. 10894-10902.
  43. Rozhenko, A.B., Schoeller, W.W., Leszczynski, J. On the stability of perfluoroalkyl-substituted singlet carbenes: A coupled-cluster quantum chemical study (2014) Journal of Physical Chemistry A, 118 (8), pp. 1479-1488.
  44. Viniychuk, O.O., Levchenko, S.M., Przhonska, O.V., Kachkovsky, O.D., Bricks, Y.L., Kudinova, M.O., Kovtun, Y.P., Poronik, Y.M., Shandura, M.P., Tolmachev, O.I. Electronic transitions in polymethine dyes involving local and delocalized levels (2014) Journal of Molecular Structure, 1060 (1), pp. 30-37.
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