Інститут
біоорганічної
хімії та нафтохімії
ім. В.П. Кухаря
НАН України

1. T.V. Tkachenko, D.S. Kamenskyh, Y.V. Sheludko, V.O. Yevdokymenko . Structural and morphological features of nanoсellulose from soybean straw. Nanoobjects & Nanostructuring. Volume I / Edited by Lidiya M. Boichyshyn and Oleksandr. V. Reshetnyak. ‒ Mississauga, Ontario: Nova Printing Inc. 2022. Р. 145-160.

2. Bondar M.V., Faryadras S., Munera N., Chang H.-T., Uddin M., Beldield K.D., Kachkovsky O.D., Van Stryland E.W., Hagan D.J.. New two-photon absorbing Squaraine derivative with efficient near-infrared fluorescence, superluminescence, and high photostability. J. Phys. Chem. B. 2022. V.126, N 21. P. 3897-3907. https://doi.org/10.1021/acs.jpcb.2c01288

3. V.A. Tsygankova, Ya.V. Andrusevich, O.I. Shtompel, R.M. Solomyanny, A.O. Hurenko, M.S. Frasinyuk, G.P. Mrug, O.V. Shablykin, S.G. Pilyo, A.M. Kornienko, V.S. Brovarets. New Auxin and Cytokinin Related Compounds Based on Synthetic Low Molecular Weight Heterocycles. Auxins, Cytokinins and Gibberellins Signaling in Plants. Signaling and Communication in Plants. Aftab, T. (Eds). Springer Nature. Switzerland AG. 2022. 377 p. Pp. 353-377. http://dx.doi.org/10.1007/978-3-031-05427-3_16

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

5. D. Hodyna, V. Kovalishyn, I. Semenyuta, S. Rogalsky, O. Trokhimenko, A. Gryniukova, L. Metelytsia. Ester-Functionalized Imidazolium- and Pyridinium-Based Ionic Liquids: Design, Synthesis and Cytotoxicity Evaluation. Biointerface Research in Applied Chemistry. 2022. V. 12, N 3. P. 2905-2957. https://doi.org/10.33263/BRIAC123.29052957

6. L.O. Metelytsia,D.M. Hodyna, I.V. Semenyuta,V.V. Kovalishyn,S.P. RogalskyY.K. Derevianko, V.S. Brovarets,I.V. Tetko. Theoretical and Experimental Studies of Phosphonium Ionic Liquids as Potential Antibacterials of MDR Acinetobacter baumannii. Journal of Antibiotics. 2022. V. 11. P. 491. https://doi.org/10.3390/antibiotics11040491.

7. Vydzhak R.N., Panchishin S.Y.,Kachaeva M.V.,Pilyo S.G., Moskvina V.S., Shablykina O.V., Kozytskiy A.V.,Brovarets V.S. Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones. Molecular diversity. 2022. Vol. 26, N 2. Р. 1115-1128. https://doi.org/10.1007/s11030-021-10234-2

8. O.V. Moshynets,T.P. Baranovskyi,O.S. Iungin, N.P. Kysil, L.O. Metelytsia,I. Pokholenko, V.V. Potochilova,G. Potters, K.L. Rudnieva,S.Y. Rymar, I.V. Semenyuta, A.J. Spiers, O.P. Tarasyuk,S.P. Rogalsky eDNA inactivation and biofilm inhibition by the polymeric biocide polyhexamethylene guanidine hydrochloride (PHMG-Cl). International Journal of Molecular Sciences. 2022. V. 23. Р. 731. https://doi.org/10.3390/ijms23020731

9. Obernikhina N.V.,Kachaeva M.V., Kachkovsky O.D.,Brovarets V.S. In silico Study of Conjugated Nitrogen Heterocycles Affinity in their Biological Complexes. Chemistry of Heterocyclic Compounds 2022. V. 58, N 8. Р. 412-420. DOI 10.1007/s10593-022-03107-5

10. D.S. Kamenskyh, T.V. Tkachenko, V.A. Yevdokymenko, Y.V. Sheludko, M.M. Filonenko, V.A. Povazhny, M.M. Baran, O.V. Pavluik, V.I. Kashkovsky Synthesis, characterization and optimization of the aluminum–nickel–molybdenum catalyst for hydrogenation Applied Nanoscience. 2022. P. 1-13. https://doi.org/10.1007/s13204-022-02644-x

11. T.V. Tkachenko, M.M. Baran, V.O. Yevdokymenko, D.S. Kamenskyh, V.I. Kashkovsky Optimization of Ether Production by Proton Current Materials Today: Proceedings. 2022. V. 62, N 15. P. 7643-7649. https://doi.org/10.1016/j.matpr.2022.02.004

12. L.K. Patrylak, S.V. Konovalov, A.V. Yakovenko, O.P. Pertko, V.A. Povazhnyi, Yu.G. Voloshyna, O.V. Melnychuk, M.M. Filonenko Micro–mesoporous kaolin-based zeolites as catalysts for glucose transformation into 5-hydroxymethylfurfural Applied Nanoscience. 2022. P.1-14. https://doi.org/10.1007/s13204-022-02620-5

13. L. Patrylak, S. Zubenko, S. Konovalov, A. Yakovenko, V. Povazhnyi, O. Pertko, Y. Voloshyna, O. Melnychuk Mykhailo Filonenko Іsomerization of limonene on zeolite-containing catalysts based on Кaolin Chemistry Journal of Moldova. 2022. P. 1857-1727. http://dx.doi.org/10.19261/cjm.2022.980

14. V. Pidlisnyuk, A. Mamirova, R.A. Newton, T. Stefanovska, O. Zhukov, V. Tsygankova, P. Shapoval The role of plant growth regulators in Miscanthus × giganteus utilisation on soils contaminated with trace elements Agronomy. 2022. V. 12, N 12. Р. 2999. https://doi.org/10.3390/agronomy12122999

15. Vasetska O., Zhminko P., Prodanchuk M., Galkin A., Tsygankova V. Perspective for using2,6-dimethylpyridine-N-oxide to reduce the toxic effect of xenobiotics in mammals. J. Adv. Pharm. Educ. Res. 2022. V. 12, N 1. P. 21 – 29. https://doi.org/10.51847/TXCxI0PsO1

16. Tsygankova V.A., Voloshchuk I.V., Klyuchko S.V., Pilyo S.G., Brovarets V.S., Kovalenko O.A. The effect of pyrimidine and pyridine derivatives on the growth and productivity of sorghum International Journal of Botany Studies. 2022. V. 7, N 5. P. 19-31. https://www.botanyjournals.com/archives/2022/vol7/issue5/7-4-28

17. Tsygankova V.A., Voloshchuk I.V., Andrusevich Ya.V., Kopich V.M., Pilyo S.G., Klyuchko S.V., Kachaeva M.V., Brovarets V.S. Pyrimidine derivatives as analogues of plant hormones for intensification of wheat growth during the vegetation period Journal of Advances in Biology. 2022. V. 15. P. 1-10. DOI: https://doi.org/10.24297/jab.v15i.9237

18. Tsygankova V.A., Oliynyk O.O., Kvasko O.Yu., Pilyo S.G., Klyuchko S.V., Brovarets V.S. Effect of Plant Growth Regulators Ivin, Methyur and Kamethur on the Organogenesis of Miniature Rose (Rosa mini L.) in Vitro Int. J. Med. Biotechnol. Genetics. 2022. S1: V. 2, N 1. P.1-8. https://scidoc.org/IJMBG-2379-1020-S1-02-001.php

19. Y. Kolesnikov, S. Kretynin, Y. Bukhonska, I. Pokotylo, E. Ruelland, J. Martinec, V. Kravets Phosphatidic Acid in Plant Hormonal Signaling: From Target Proteins to Membrane Conformations Int. J. Mol. Sci. 2022, V. 23, N 6. Р. 3227; https://doi.org/10.3390/ijms23063227

20. Kobzar O.,Shulha Yu.,Buldenko V.,Cherenok S.,Silenko O.,Kalchenko V.,Vovk A. Inhibition of glutathione S-transferases by photoactive calix[4]arene α-ketophosphonic acids. Bioorganic and Medicinal Chemistry Letters. 2022. V. 77. Р. 129019. https://doi.org/10.1016/j.bmcl.2022.129019

21. Silenko O.,Cherenok S.,Shulha Yu.,Kobzar O.,Rusanov E.,Karpichev E.,Vovk A.Kalchenko V. Thiacalix [4] arene phosphoric acids. Synthesis, structure, and inhibition of glutathione S-transferases. Phosphorus, Sulfur, and Silicon and the Related Elements. 2022. V.197 (5-6). Р. 538-541. https://doi.org/10.1080/10426507.2021.2011877

22. Velihina Y.,Pilʹo S.,Kobzar O.,Zaliavska O.,Prichard M. N.,James S. H.Keith K.,Hartline C.,Zhirnov V.,Vovk A.,Brovarets V. Synthesis of some oxazolo [4, 5-d] pyrimidine derivatives and evaluation of their antiviral activity and cytotoxicity. Arkivok. 2022. Р. 108-117. 

23. Obernikhina N.V., Kobzar O.L.,Kachaeva M.V., Kachkovsky O.D. , Brovarets V.S. In silico and in vitro estimation of structure and biological affinity of 1, 3-oxazoles: fragment-to-fragment approach. Curr. Comput.-Aided Drug Des. 2022. V. 18. P. 95-109. https://doi.org/10.2174/1573409918666220404100022

24. Ivanenko I.,Ruda A.,Povazhnyi V. Cobalt-nitrogen-doped activated carbons for hydrogen generation. Materials Today: Proceedings.2022. V. 62 ( P15). Р. 7691-7697. https://doi.org/10.1016/j.matpr.2022.03.170

25. Yu.G. Voloshyna,O.P. Pertko,V.A. Povazhnyi,L.K. Patrylak Peculiarities of products’ distribution in n-hexane hydroisomerization on modified mordenite-containing rock Appl. Nanosci. 2022. https://doi.org/10.1007/s13204-022-02632-1

26. Yu. Kholodko, A. Bondarieva, V. Tobilko, V. Pavlenko, O. Melnychuk, V. Glukhovskyi. Synthesis and characterization of kaolinite-based granular adsorbents for the removal of Cu(II), Cd(II), Co(II), Zn(II), and Cr(VI) from contaminated water. Eastern-European Journal of Enterprise Technologies.2022. V. 4 N. 10. Р. 118. https://doi.org/10.15587/1729-4061.2022.262994

27. Rogalsky S., Tarasyuk O., Vashchuk A., Davydenko V., Dzhuzha O., Motrunich S., Cherniavska T., Papeikin O., Bodachivska L., Bardeau J.-F. Synthesis and evaluation of N,N-dibutylundecenamide as new eco-friendly plasticizer for polyvinyl chloride. Journal of Materials Science. 2022. V. 57. Р. 6102-6114. https://doi.org/10.1007/s10853-022-07006-0

28. Rogalsky S., Tarasyuk O., Dzhuzha O., Hodyna D., Cherniavska T., Hubina A., Filonenko M., Metelytsia L. Evaluation of N,N-dibutylolelamide as a bifunctional additive for poly(vinyl chloride). Colloid and Polymer Science. 2022. V. 300 (12). Р. 1-8. http://dx.doi.org/10.1007/s00396-022-05038-1

29. S.I. Vdovenko,I.I. Gerus,M. Pagacz-Kostrzewa,M. Wierzejewska. Influence of the features of the spatial and electronic structure of α-substituted β-ethoxyvinyl trifluoromethyl ketones and secondary amines on their reactivity. Journal of Molecular Structure. 2022. V. 1255. Р. 132417. https://doi.org/10.1016/j.molstruc.2022.132417

30. J. Liu, W. Lin,A.E. Sorochinsky,G. Butler,A. Landa, J. Han,V.A. Soloshonok. Successful trifluoromethoxy-containing pharmaceuticals and agrochemicals. Journal of Fluorine Chemistry. 2022. V. 257-258. Р. 109978. https://doi.org/10.1016/j.jfluchem.2022.109978

31. J. Han,J. Escorihuela,S. Fustero,A. Landa,V.A. Soloshonok, A. Sorochinsky. Asymmetric Michael addition in synthesis of β-substituted GABA derivatives. Molecules. 2022. V. 27. Р. 3797. https://doi.org/10.3390/molecules27123797

32. Q. Wang, J. Han, A. Sorochinsky, A. Landa, G. Butler, V. A. Soloshonok. The latest FDA-approved pharmaceuticals containing fragments of tailor-made amino acids and fluorine. Pharmaceuticals. 2022. V. 15. Р. 999. https://doi.org/10.3390/ph15080999

33. V.D. Romanenko. From elusive monomeric metaphosphates to oligomeric metaphosphate reagents:New avenue to halogen-free phosphorylation of biomolecules. Current Organic Chemistry. 2022. V. 26, Р. 432-437. https://doi.org/10.2174/1385272826666220330111824

34. Chernykh A.V.,Aloshyn D.,Kuchkovska Yu.O.,Daniliuc C.G.,Tolmachova N.A.,Kondratov I.S.,Zozulya S.,Grygorenko O.O., Haufe G. Impact of β-perfluoroalkyl substitution of proline on the proteolytic stability of its peptide derivatives Org. Biomol. Chem. 2022. V. 20. Р. 9337-9350. https://doi.org/10.1039/D2OB01430K

35. Logvinenko I.G.,Kondratov I.S.,Pridma S.O.,Tolmachova N.A.,Morev R.N.,Dolovanyuk V.G.,Boretsky A.L.,Stepaniuk R.O.,Trofymchuk S.A.,Mück-Lichtenfeld C., Daniliuc C.G.,Haufe G. Synthesis and physical chemical properties of CF3O-containg secondary amines – Perspective building blocks for drug discovery Journal of Fluorine Chemistry.2022. V. 257–258. Р. 109990. https://doi.org/10.1016/j.jfluchem.2022.109990

36. Homon A.A.,Shynder L.V.,Demchuk O.P.,Hryshchuk O.V.,Kondratov I.S.,Gerus I.I.,Grygorenko O.O. Synthesis of 1,3-bifunctional cyclobutane derivatives with α-CHF2/CF3 group – advanced building blocks for medicinal chemistry Journal of Fluorine Chemistry. 2022. V. 263. Р. 110041. https://doi.org/10.1016/j.jfluchem.2022.110041

37. Kondratov I.S.,Moroz Yu.S.,Irwin J.J.,Shoichet B.K. Drug building blocks and libraries at risk in Ukraine Science. 2022. V. 376(6596). Р. 929. https://doi.org/10.1126/science.abq7841

38. Kondratov I.S.,Moroz Yu.S.,Grygorenko O.O.,Tolmachev A.A. The Ukrainian Factor in Early-Stage Drug Discovery in the Context of Russian Invasion: The Case of Enamine Ltd ACS Med. Chem. Lett. 2022. V. 13. N 7. Р. 992-996. https://doi.org/10.1021/acsmedchemlett.2c00211

39. M. Aksylenko, E. Sheludko, N. Himach, V. Yevdokimenko. Polygalacturonates of biogenic metals – prospective components of new composite preparations for wheat. J. Annual Research & Review in Biology. 2022. V. 37 (12). P. 17-28. https://doi.org/10.9734/arrb/2022/v37i1294273

40. A.O. Kolodiazhna,O.I. Kolodiazhnyi Сatalytic asymmetric synthesis of C-chiral phosphonate Symmetry. 2022. V. 14. P. 1758-1825. https://doi.org/10.3390/sym14091758

41. D. Prysiazhnuk, A. Kolodiazhna, O. Kolodiazhnyi Сonvergent method for the determination of halo-2,3-dihydro-1H-inden-1-ol absolute configuration Arkivoc. 2022. V. IX. P. 23-32. https://doi.org/10.24820/ark.5550190.p011.835

42. N.A. Ogurtsov,A.V. Mamykin,O.L. Kukla,A.S. Pavluchenko,M.V. Borysenko,Yu.P. Piryatinski,J.-L. Wojkiewicz,A.A. Pud. The impact of interfacial interactions on structural, electronic and sensing properties of poly(3-methylthiophene) in the core-shell nanocomposites. Application to the CWA simulants detection. Macromolecular Materials and Engineering. 2022. V. 307(4). P. 2100762. http://dx.doi.org/10.1002/mame.202100762

43. T. Feng, Y. Yuan, X. Chen,S. Zhao, M. Cao, L. Feng,S. Shi, H. Wang,T. Liu, A. Pud,L. Han, R. Scaffaro, B. He, N. Wang. Ultrasensitive and highly specific detection of iodine ions using zirconium (IV)-enhanced oxidation Cell. Reports Physical Science. 2022. V. 3 (11). P. 101143 (10 pages). https://doi.org/10.1016/j.xcrp.2022.101143

44. Potikha L.M., Brovarets V.S., Zhirnov V.V. Anticancer evaluation of difunctional substituted 1,2-dihydrophthalazines Chem. Data Collect. 2022. V. 37. P. 100817. https://doi.org/10.1016/j.cdc.2021.100817

45. Demydchuk B.A., Mykhalchenko O.A., Rusanov E.B., Moskvina V.S., Brovarets V.S. Concise and regioselective synthesis of 5H-imidazo[1,2-e][1,3,5]triazepines. Arkivoc. 2022. V. ІІ. P. 204-214. http://dx.doi.org/10.24820/ark.5550190.p011.689

46. Nizhenkovska I.V., Matskevych K.V., Golovchenko O.I., Golovchenko O.V., Kustovska A.D., Van M. New prospective phosphodiesterase inhibitors: phosphorylated oxazole derivatives in treatment of hypertension. Adv. Pharm. Bull., 2022. https://doi.org/10.34172/apb.2023.044

47. Brusnakov M., Golovchenko O., Velihina Ye., Liavynets O., Zhirnov V., Brovarets V. Evaluation of anticancer activity of 1,3-oxazol-4-ylphosphonium salts in vitro Chem. Med. Chem. 2022. V. 17, № 20. P. e202200319. https://doi.org/10.1002/cmdc.202200319

48. Biletska I.M., Mrug G.P., Prostota Ya.O., Kondratyuk K.M., Bondarenko S.P., Frasinyuk M.S. Synthesis of 2-trifluoroacetonyl-3-alkyl/alkoxy-chromones and their reactions with 1,2-bidentate nucleophiles. Heterocycles. 2022. V. 104, N 7. P. 1229-1244. http://dx.doi.org/10.3987/COM-22-14659

49. Frasinyuk M., Chhabria D., Kartsev V., Dilip H., Sirakanyan S.N., Kirubakaran S., Petrou A., Geronikaki A., Spinelli D. Benzothiazole and chromone derivatives as potential ATR kinase inhibitors and anticancer agents. Molecules. 2022. V.27, N 14. P. 4637. https://doi.org/10.3390/molecules27144637

50. Waszkowska K., Krupka A., Smokal V., Kharchenko O., Migalska-Zalas A., Frasinyuk M., Wielgosz R., Andrushchak A., Sahraoui B. Correlation between nonlinear optical effects and structural features of aurone-based methacrylic polymeric thin films. Materials. 2022. V.15, N 17. P. 6076. https://doi.org/10.3390/ma15176076

51. Obernikhina N.V., Kachaeva M.V., Kachkovsky O.D., Brovarets V.S. In silico study of conjugated nitrogen heterocycles affinity in their biological complexes. Chem. Heterocycl. Comp. 2022. V. 58, N8/9. P. 412-420. https://doi.org/10.1007/s10593-022-03107-5

52. Kornii Yu., Shablykin O., Tarasiuk T., Stepaniuk O., Matvienko V., Aloshyn D., Zahorodniuk N., Sadkova I.V., Mykhailiuk P.K. Fluorinatedaliphatic diazirines: preparation, characterization, and model photolabeling studies. J. Org. Chem. 2022. https://doi.org/10.1021/acs.joc.2c02262

53. Glibov E.K., Gorbulenko N.V., Moskvina V.S., Suprun A.V., Shablykina O.V. Shokol T.V., Khilya V.P. Synthesis and recyclization of methylenbisflavonoids based on heterocyclic analogues of umbelliferon and formononetin Chem. Nat. Compd. 2022. V. 58, N 4. P. 617-622. https://doi.org/10.1007/s10600-022-03755-1

54. Konovalenko A.S., Shablykina O.V., Shablykin O.V., Moskvina V.S., Brovarets V.S. 1H-isochromene-1-ones and isoquinoline-1(2H)-ones with carbonyl group in position 3: Features of synthetic approaches and transformation. Arkivoc. 2022. V. VІІІ. P. 79-112. https://doi.org/10.24820/ark.5550190.p011.861

55. Potikha L.M., Brovarets V.S., Zhirnov V.V. Biological evaluation of 3-aminoisoquinolin-1(2H)-one derivatives as potential anticancer agents. French-Ukr. J. Chem. 2021. V.9, №2. P. 52-63. http://dx.doi.org/10.17721/fujcV9I2P52-63

56. A.V. Mamykin, O.L. Kukla, A.S. Pavluchenko, Z.I. Kazantseva, I.A. Koshets, A.A. Pud, N.A. Ogurtsov, Yu.V. Noskov, V.I. Kalchenko Electronic nose-type chemosensory systems for detection of gaseous poisonous substances. Semiconductor Physics, Quantum Electronics & Optoelectronics. 2022. V.25, No.4. Р. 429-440. https://doi.org/10.15407/spqeo25.04.429

57. V.D. Romanenko, J.-M. Sotiropoulos. Six-membered rings with two or more heteroatoms with at least one boron. Comprehensive Heterocyclic Chemistry IV, Elsevier. New York. 2022. Р.806-845. http://dx.doi.org/10.1016/B978-0-12-818655-8.00098-6

58. Grygorenko O.O., Hutskalova V., Moskvina V.S. Bicyclic 6-6 system with one bridgehead (ring junction) nitrogen atom: three extra heteroatoms (2:1).Chapter in book: “Comprehensive heterocyclic chemistry IV (Fourth edition)”, 2022. P. 216-278. https://doi.org/10.1016/b978-0-12-409547-2.14958-3.

1. Yakovlieva A., Boichenko S., Zubenko S., Konovalov S. Synthesis and physico-chemical properties of palm kernel oil bioadditives for alternative jet fuel. Systems and means of motor transport. Seleced problems. Seria: Transport. Monografia. Rzeszow (Poland). 2021. Р. 257-264.

2. I.G. Logvinenko, I.S. Kondratov, A.V. Dobrydnev, A.V. Kozytskiy, O.O. Grygorenko. Synthesis and reactions of ω-CF3O-substituted aliphatic sulfonyl chlorides. Journal of Fluorine Chemistry. 2021. V. 246. Р. 109799. https://doi.org/10.1016/j.jfluchem.2021.109799

3. J. Han, N. Lyutenko, A. Sorochinsky, A. Okawara, H. Konno, S. White, V. Soloshonok. Tailor-Made Amino Acids in Pharmaceutical Industry: Synthetic Approaches to aza-tryptophane derivatives. Chem. Eur. J. 2021. https://doi.org/10.1002/chem.202102485

4. E.N. Shaitanova, O.A. Balabon, A.N. Rybakova, T.S. Khlebnicova, F.А. Lakhvich, I.I. Gerus. Synthesis of functionalized fluoroalkyl pyrimidines and pyrazoles from fluoroalkyl enones. Journal of Fluorine Chemistry. 2021. V. 252. Р. 109905 https://doi.org/10.1016/j.jfluchem.2021.109905

5. A.A. Homon, O.V. Hryshchuk, O.V. Mykhailenko, B.V. Vashchenko, K.P. Melnykov, O.M. Michurin, C.G. Daniliuc, I.I. Gerus, V.O. Kovtunenko, I.S. Kondratov, O.O. Grygorenko. 4-(Di‐/Trifluoromethyl)‐2‐heterabicyclo[2.1. 1]- hexanes: advanced fluorinated phenyl isosteres and proline analogues. European Journal of Organic Chemistry. 2021 https://doi.org/10.1002/ejoc.202100414

6. S. Trofymchuk, M. Bugera, A. Klipkov, V. Ahunovych, B. Razhyk, S. Semenov, A. Boretskyi, K. Tarasenko, P. Mykhailiuk. Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4). J. Org. Chem. 2021. V. 86, № 17. Р. 12181-12198 https://doi.org/10.1021/acs.joc.1c01518

7. V.D. Romanenko. New trends in development of P-C bond forming reactions. Current Organic Chemistry. 2021. V.25, № 17. Р. 1937-1976. https://doi.org/10.2174/1385272825666210610153954

8. Noskov Yu., Ogurtsov N., Bliznyuk V., Lvov Yu., Myronyuk I., Pud A. Synthesis and properties of coreshell halloysite–polyaniline nanocomposites. Applied Nanoscience. 2021. V. 12, Р. 1285–1294 https://doi.org/10.1007/s13204-021-01812-9

9. O.I. Kolodiazhnyi. Phosphorus Compounds of Natural Origin: Prebiotic, Stereochemistry, Application. Symmetry. 2021. V. 13(5)., № 889. Р. 1-52. https://doi.org/10.3390/sym13050889

10. D.V. Prysiazhnuk, E.B. Rusanov, O.I. Kolodiazhnyi. The absolute configuration of 2-bromo-2,3-dihydro-1H-inden-1-ols. Synthetic communications. 2021. V. 51, № 19. Р. 3023–3031. https://doi.org/10.1080/00397911.2021.1960378

11. O.O. Kolodiazhna, D.V. Prysiazhnuk, A.O. Kolodiazhna, O.I. Kolodiazhnyi. Synthesis of optically active vicinal fluorocyclopentanols and fluorocyclopentanamines by enzymatic deracemization. Arkivoc 2022, p. iii. Р. 14-26 https://doi.org/10.24820/ark.5550190.p011.634

12. O. Kolodiazhnyi, A. Kolodiazhna, E. Grishkun, D. Prysiazhnuk, O. Kolodiazhna, S. Sheiko. Achievements in developments of stereochemistry. Phosphorus, sulfur, and silicon and the related elements. 2021. Р. 474-479. https://doi.org/10.1080/10426507.2021.2011874

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