Synthesis of new derivatives of 2-oxo-2,5-dihydrofurans containing а 4-oxothiazolidine ring
- Autores: Karapeyan L.V.1, Tokmajyan G.G.1
 - 
							Afiliações: 
							
- Yerevan State University
 
 - Edição: Volume 60, Nº 4 (2024)
 - Páginas: 527-532
 - Seção: Articles
 - URL: https://transsyst.ru/0514-7492/article/view/672186
 - DOI: https://doi.org/10.31857/S0514749224040159
 - EDN: https://elibrary.ru/RXRWHI
 - ID: 672186
 
Citar
Texto integral
Resumo
New derivatives of 2-oxo-2,5-dihydrofurans containing 4-oxothiazolidine ring were synthesized by the interaction of 2-oxo-2,5-dihydrofuran thiosemicarbazones with diethylacetylenedicarboxylate in absolute ethanol and with maleic anhydride in chloroform. The synthesized compounds were characterized by NMR spectroscopy and elemental analysis data.
Texto integral
Sobre autores
L. Karapeyan
Yerevan State University
							Autor responsável pela correspondência
							Email: lkarapetyan@ysu.am
				                	ORCID ID: 0000-0002-9765-6131
				                																			                												                	Armênia, 							ul. Aleksa Manukyana, 1, Yerevan, 0025						
G. Tokmajyan
Yerevan State University
														Email: lkarapetyan@ysu.am
				                	ORCID ID: 0000-0002-2561-8494
				                																			                												                	Armênia, 							ul. Aleksa Manukyana, 1, Yerevan, 0025						
Bibliografia
- Bockman M.R., Engelhart C.A., Cramer J.D., Howe M.D., Mishra N.K., Zimmerman M., Larson P., Alvarez-Cabrera N., Park S.W., Boshoff H.I.M., Bean J. M., Young V.G., Ferguson D.M., Dartois V., Jarrett J.T., Schnappinger D., Aldrich C.C. ACS Infect. Dis. 2019, 5, 598–617. doi: 10.1021/acsinfecdis.8b00345
 - Sahiba N., Sethiya A., Soni J., Agarwal D.K., Agarwal Sh. Top. Curr. Chem. 2020, 378, 34124. doi: 10.1007/s41061-020-0298-4
 - Agrawal N. Curr. Chem. Lett. 2021, 10, 119–138. doi: 10.5267/j.ccl.2020.11.002
 - Trotsko N. Eur. J. Med. Chem. 2021, 215, 113266-113288. doi: 10.1016/j.ejmech.2021.113266
 - Mech D., Kurowska A., Trotsko N. Int. J. Mol. Sci. 2021, 22, 11533–11584. doi: 10.3390/ijms222111533.
 - Mishchenko M., Shtrygol S., Kaminskyy D., Lesyk R. Sci. Pharm. 2020, 88, 16–29. doi: 10.3390/scipharm88010016
 - Popiołek Ł., Piątkowska-Chmiel I., Gawrońska-Grzywacz M., Biernasiuk A., Izdebska M., Herbet M., Sysa M., Malm A., Dudka J., Wujec M. Biomed. Pharmacother. 2018, 103, 1337–1347. doi: 10.1016/j.biopha.2018.04.163
 - Masoud G.N., Youssef A.M., Abdel Khaled M.M., Abdel Wahab A.E., Labouta I.M., Hazaa A.A. B. Med. Chem. Res. 2013, 22, 707–725. doi: 10.1007/s00044-012-0057-3
 - Pejović A., Minić A., Jovanović J., Pešić M., Komatina D.I., Damljanović I., Stevanović D., Mihailović V., Katanić J., Bogdanović G.A., J. Organomet. Chem. 2018, 869, 1–10. doi: 10.1016/j.jorganchem.2018.05.014
 - Huber-Villaume S., Revelant G., Sibille E., Philip-pot S., Morabito A., Dunand S., Chaimbault P., Bagrel D., Kirsch G., Hesse S., Schohn H. Bioorg. Med. Chem. 2016, 24, 2920–2928. doi: 10.1016/j.bmc.2016.04.063
 - Аветисян А. А., Токмаджян Г. Г. Хим. ж. Арм. 1993, 46, 219–236.
 - Аветисян А.А., Токмаджян Г.Г. Хим. ж. Арм. 2007, 60, 698–712.
 - Leon-Rojas A.F., Urbina-Gonzalez J.M. Avances en Quimica. 2015, 10, 67–78.
 - Rossi R., Lessi M., Marianetti G., Bellina F. Curr. Org. Chem. 2017, 21, 964–1018. doi: 10.2174/1385272821666170111151917
 - Husain A., Khan S.A., Iram F., Iqbal M.A., Asif M. Eur. J. Med. Chem. 2019, 171, 66–92. doi: 10.1016/j.ejmech.2019.03.021
 - Ramshid P.K., Jagadeeshan S., Krishnan A., Mathew M., Asha Nair S., Radhakrishna P.M. Med. Chem. 2010, 6, 306–312. doi 10.2174/ 157340610793358909
 - Карапетян Л.В., Токмаджян Г.Г., Макарян Г.М. ЖOрХ. 2019, 55, 1796–1799. [Karapetyan L.V., Tokmajyan G. G., Makaryan G. M. Russ. J. Org. Chem. 2019, 55, 1806–1808.] doi: 10.1134/S1070428019110265
 - Карапетян Л.В., Токмаджян Г.Г., Пароникян Р.В. ЖOрХ. 2021, 57, 133–137. [Karapetyan L.V., Tokmajyan G.G., Paronikyan R.V. Russ. J. Org. Chem. 2021, 57, 102–105.] doi: 10.1134/S1070428021010206
 - Benmohammed A., Khoumeri O., Djafri A., Terme T., Vanelle P. Molecules. 2014, 19, 3068–3083. doi: 10.3390/molecules19033068
 - Tokmajyan G.G., Karapetyan L.V., Paronikyan R.V., Stepanyan H.M. Proceedings of the Yerevan State University. 2020, 54, 12–16.
 - Jangale A.D., Dalal D.S. ChemistrySelect. 2019, 4, 1323-1329. doi: 10.1002/slct.201802366
 - Asghari S., Pourshab M., Mohseni M. Chem. Monthly. 2018, 149, 2327–2336. doi: 10.1007/s00706-018-2292-x
 - Ramadan S.K., El-Helwa E.A.E. Russ. J. Org. Chem. 2019, 55, 1626–1628. doi: 10.1134/S1070428019100282
 - Porshamsian K., Montazeri N., Rad-Moghadam K., Ali-Asgari S. J. Heterocycl. Chem. 2010, 47, 1439–1442. doi: 10.1002/jhet.458
 - Karapetyan L.V., Tokmajyan G.G. ChemistrySelect, 2022, 7, e202202745. doi: 10.1002/slct.202202745
 - Карапетян Л.В., Токмаджян Г.Г. ЖОХ, 2023, 93, 385–392. [Karapetyan L.V., Tokmajyan G.G. Russ. J. Gen. Chem. 2023, 93, 506–512.] doi: 10.1134/S1070363223030076
 
Arquivos suplementares
				
			
						
						
					
						
						
									





