Synthesis of copper(i) chelates based on heterocyclic thioamides
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[1] Priebbenow, D. L.; Bolm, C. Recent Advances in the Willgerodt-Kindler Reaction. Chem. Soc. Rev. 2013, 42, 7870–7880. https://doi.org/10.1039/C3CS60154D
[2] Zhang, Q.; Soulere, L.; Queneau, Y. Toward More Practical Methods of the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update. Molecules 2023, 28, 3527. https://doi.org/10.3390/molecules28083527
[3] Murai, T. Synthesis of Thioamides. Chemistry of Thioamides; Springer: Singapore, 2019. https://doi.org/10.1007/978-981-13-7828-7_3
[4] Hansen, T. N.; Olsen, Ch. A. Contemporary Application of Thioamides and Methods for Their Synthesis. Chem. Eur. J. 2024, 30, e202303770. https://doi.org/10.1002/chem.202303770
[5] Chojnacki, I.; Monka, M.; Serdiuk, I. E.; Bojarski, P.; Połoński, T., Olszewska, T. Copper(I) Halide Cluster-Based Coordination Polymers Modulated by Chiral Ditopic Dithiodianthranilide Ligands: Synthesis, Crystal Structure and Photoluminescence. CrystEngComm. 2021, 23, 299–307. https://doi.org/10.1039/D0CE01589J
[6] Lobana, T. S.; Sultana, R.; Hundal, G. Heterocyclic Thioamides of Copper(I): Synthesis and Crystal Structures of Copper Complexes with 1,3-Imidazoline-2-thiones in the Presence of Triphenyl Phosphine. Polyhedron 2008, 27, 1008–1016. https://doi.org/10.1016/j.poly.2007.11.036
[7] Long, D. L.; Zeng, D. X.; Xin, X. G.; Huang, X. Y.; Kang, B. Sh. Synthesis and Characterization of Copper(I) and Silver(I) Complexes Containing Thioamide Ligands. Synth. React. Inorg. Met.-Org. Chem. 1996, 26, 723–733. https://doi.org/10.1080/00945719608004331
[8] Gordienko, O.; Titov, T.; Ranskiy, A.; Gumenchuk, O. Synthesis, Structure and Properties of Copper(II) Chelates with Benzimidazole-2-N-arylcarbothioamides. Chem. Chem. Technol. 2018, 12, 176–181. https://doi.org/10.23939/chcht12.02.176
[9] Ranskiy, A.; Didenko, N.; Gordienko, O. Synthesis of Heterocyclic Thioamides and Copper(II) Coordination Compounds Based on Them. Chem. Chem. Technol. 2017, 11, 11–18. https://doi.org/10.23939/chcht11.01.011
[10] Ranskiy, A.; Gordienko, O.; Didenko, N.; Titov, T.; Khutko, M. Synthesis, Structure and Application of Mixed-Ligand Coordination Compounds of Copper(II) with Substituted Thioamides. Chem. Chem. Technol. 2020, 14, 55–61. https://doi.org/10.23939/chcht14.01.055
[11] Orysyk, S.; Pekhnyo, V.; Orysyk, V.; Zborovskii, Y.; Borovyk, P.; Mykhailo, V. Fundamental Aspects of the Coordination Chemistry of Transition Metals with Functionally Substituted Thioamides (Part 1). Ukrainian Chemistry Journal 2022, 88, 85–115. https://doi.org/10.33609/2708-129X.88.02.2022.85-115
[12] Orysyk, S.; Pekhnyo, V.; Orysyk, V.; Zborovskii, Y.; Borovyk, P.; Vovk, M. Fundamental Aspects of Coordination Chemistry of Transition Metals with Functionally Substituted Thioamides (Part 2). Ukrainian Chemistry Journal 2022, 88, 3–27. https://doi.org/10.33609/2708-129X.88.03.2022.3-27
[13] Huang, G.; Cierpicki, T.; Grembecka, J. Unlocking the Potential of the Thioamide Group in Drug Design and Development. Future Med. Chem. 2025, 17, 1–3. https://doi.org/10.1080/17568919.2024.2435245
[14] Huang, G.; Cierpicki, T.; Grembecka, J. Thioamides in medicinal chemistry and as small molecule therapeutic agents. Eur. J. Med. Chem. 2024, 277, 116732. https://doi.org/10.1016/j.ejmech.2024.116732
[15] Iagodzinski, T. S. Thioamides as Useful Synthons in the Synthesis of Heterocycles. Chem. Rev. 2003, 103, 197–228. https://doi.org/10.1021/cr0200015
[16] Zheng, P.; Zhou, C.; Lu, L.; Liu, B.; Ding, Y. Elesclomol: A Copper Ionophore Targeting Mitochondrial Metabolism for Cancer Therapy. J Exp Clin Cancer Res 2022, 41, 271. https://doi.org/10.1186/s13046-022-02485-0
[17] Okajima, S.; Hamamoto, A.; Asano, M.; Isogawa, K.; Ito, H.; Kato, S.; Hirata, Y.; Furuta, K.; Takemori, H. Azepine Derivative T4FAT, a New Copper Chelator, Inhibits Tyrosinase. Biocem. Biophys. Res. Commun. 2019, 509, 209–215. https://doi.org/10.1016/j.bbrc.2018.12.105
[18] Riaz, Z.; Lee, Y.T.B.; Stjärnhage, J.; Movassaghi, S.; Söhnel, T.; Jamieson, M.F.S.; Shaheen, A.M.; Hanif, M.; Hartinger, G.C. Anticancer Ru and Os Complexes of N-(4-chlorophenyl)pyridine-2-carbothioamide: Substitution of the Labile Chlorido Ligand with Phosphines. J. Inorg. Biochem. 2023, 241, 112115. https://doi.org/10.1016/j.jinorgbio.2022.112115
[19] Borkow, G.; Gabbay, J. Copper as a Biocidal Tool. Curr. Med. Chem. 2005, 12, 2163–2175. http://dx.doi.org/10.2174/0929867054637617
[20] Tarik, A.; Yahia, H.; Lahcen, L. Determination of Ultra Trace Levels of Copper in Whole Blood by Adsorptive Stripping Voltammetry. J. Korean Chem. Soc. 2013, 57, 568–573. https://doi.org/10.5012/jkcs.2013.57.5.568
[21] Boulanouar, M.; Tarik, A.; Naceur, B. DFT Study of Some Copper Complexes and Their Derection Limit. Chem. Chem. Technol. 2022, 16, 185–194. https://doi.org/10.23939/chcht16.02.185
[22] Hassan, Z.M.; Alattar, R.A.; Abass, S.K.; Mihsen H.H.; Abbas, Z.F.; Hussain. K.A. Synthesis, Characterization and Biological Activity of Mixed Ligand (Imine of Benzidine and 1,10-Phenanthroline) Complexes with Fe(II), Co(II), Ni(II) and Cu(II) Ions. Chem. Chem. Technol. 2022, 16, 15–24. https://doi.org/10.23939/chcht16.01.015
[23] Ranskiy, А. P.; Boychenko, S. V.; Gordienko, О. А.; Didenko, N. О.; Voloshynets', V. A. Kompozytsiyni mastyl'ni materialy na osnovi tioamidiv ta yikh kompleksnykh spoluk. Syntez. Doslidzhennya. Vykorystannya; VNTU: Vinnytsia, 2012. https://press.vntu.edu.ua/index.php/vntu/catalog/book/207
[24] Didenko, N. О.; Ranskiy, А. P. Pryamyy syntez koordynatsiynykh spoluk kuprumu(II) iz zamishchenymy tioamidamy; VNTU: Vinnytsia, 2021. https://press.vntu.edu.ua/index.php/vntu/catalog/book/623
[25] Ranskiy, А. P.; Didenko, N. О.; Titov, Т. S.; Bezvozyuk, І. І. Mekhanizm vybirkovoho perenesennya z tochky zoru rezonansnoho potentsialu za Nechayevym [Online]. Scientific Works of Vinnytsia National Technical University. 2010, 4. https://praci.vntu.edu.ua/index.php/praci/article/view/230/228
[26] Bukvić, M.; Gajević, S.; Skulić, A.; Savić, S.; Ašonja, A.; Stojanović, B. Tribological Application of Nanocomposite Additives in Industrial Oils. Lubricants 2024, 12, 21. https://doi.org/10.3390/lubricants12010006
[27] Vahlas, C.; Caussat. B.; Serp, Ph.; Angelopoulos, G.N. Principles and applications of CVD powder technology. Mater. Sci. Eng.: R: Rep.. 2006, 53, 1–72. https://doi.org/10.1016/j.mser.2006.05.001
[28] Izyumskiy, M. S.; Neykovskiy, S. I.; Mel'nik, S. G.; Shtemenko, A. V. Klasternye khlorkarboksilaty direniya(III) kak novye iskhodnye veshchestva dlya khimicheskogo gazofaznogo metoda naneseniya renievykh pokrytiy. Issues of Chemistry and Chemical Technology 2013, 1, 134–136.
[29] Jensen, K. A.; Nielsen, P. H. Infrared Spectra of Thioamides and Selenoamides. Acta Chem. Scand. 1966, 20, 597–629.