Synthesis of new derivatives of 2-oxo-2,5-dihydrofurans containing а 4-oxothiazolidine ring
- Autores: Karapeyan L.V.1, Tokmajyan G.G.1
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Afiliações:
- Yerevan State University
- Edição: Volume 60, Nº 4 (2024)
- Páginas: 527-532
- Seção: Articles
- URL: https://archivog.com/0514-7492/article/view/672186
- DOI: https://doi.org/10.31857/S0514749224040159
- EDN: https://elibrary.ru/RXRWHI
- ID: 672186
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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.
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
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