Synthesis of new derivatives of 2-imino-2,5-dihydrofurans containing 4-oxothiazolidine ring

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

The reactions of 5,5-dialkyl- N -alkyl-2-imino-2,5-dihydrofuran-3-carboxamide thiosemicarbazones with diethyl acetylenedicarboxylate and maleic anhydride in absolute ethanol gave rise to potentially bioactive compounds containing iminodihydrofuran and 4-oxothiazolidine rings. The synthesized compounds were characterized by 1H and 13C NMR spectroscopy and elemental analysis data.

作者简介

L. Karapetyan

Yerevan State University

Email: lkarapetyan@ysu.am

G. Tokmajyan

Yerevan State University

参考

  1. 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. Vol. 5. N 4. P. 598. doi: 10.1021/acsinfecdis.8b00345
  2. Sahiba N., Sethiya A., Soni J., Agarwal D.K., Agarwal Sh. // Top. Curr. Chem. 2020. Vol. 378. N 2. P. 34. doi: 10.1007/s41061-020-0298-4
  3. Agrawal N. // Curr. Chem. Lett. 2021. Vol. 10. N 2. P. 119. doi: 10.5267/j.ccl.2020.11.002
  4. Trotsko N. // Eur. J. Med. Chem. 2021. Vol. 215. P. 113266. doi: 10.1016/j.ejmech.2021.113266
  5. Mishchenko M., Shtrygol S., Kaminskyy D., Lesyk R. // Sci. Pharm. 2020. Vol. 88. N 1. P. 16. doi: 10.3390/scipharm88010016
  6. Popiołek Ł., Piątkowska-Chmiel I., Gawrónska-Grzywacz M., Biernasiuk A., Izdebska M., Herbet M., Sysa M., Malm A., Dudka J., Wujec M. // Biomed. Pharmacother. 2018. Vol. 103. P. 1337. doi: 10.1016/j.biopha.2018.04.163
  7. Masoud G.N., Youssef A.M., Abdel Khaled M.M., Abdel Wahab A.E., Labouta I.M., Hazzaa A.A.B. // Med. Chem. Res. 2013. Vol. 22. P. 707. doi: 10.1007/s00044-012-0057-3
  8. Pejović A., Mini'c A., Jovanovi'c J., Pešić M., Komatina D.I., Damljanović I., Stevanović D., Mihailović V., Katanić J., Bogdanović G.A. // J. Organomet. Chem. 2018. Vol. 869. P. 1. doi: 10.1016/j.jorganchem.2018.05.014
  9. Аветисян А.А., Токмаджян Г.Г. // Хим. ж. Арм. 2007. Т. 60. С. 698.
  10. Ramshid P.K., Jagadeeshan S., Krishnan A., Mathew M., Asha Nair S., Radhakrishna P. M. // Med. Chem. 2010. Vol. 6. P. 306. doi: 10.2174/157340610793358909
  11. Карапетян Л.В., Токмаджян Г.Г., Макарян Г.М. // ЖOрХ. 2019. Т. 55. Вып. 11. С. 1796
  12. Karapetyan L.V., Tokmajyan G.G., Makaryan G.M. // Russ. J. Org. Chem. 2019. Vol. 55. N 11. P. 1806. doi: 10.1134/S1070428019110265
  13. Карапетян Л.В., Токмаджян Г.Г., Пароникян Р.В. // ЖOрХ. 2021. T. 57. Вып. 1. C. 133
  14. Karapetyan L.V., Tokmajyan G.G., Paronikyan R.V. // Russ. J. Org. Chem. 2021. Vol. 57. N 1. P. 131. doi: 10.1134/S1070428021010206
  15. Benmohammed A., Khoumeri O., Djafri A., Terme T., Vanelle P. // Molecules. 2014. Vol. 19. N 3. P. 3068. doi: 10.3390/molecules19033068
  16. Jangale A.D., Dalal D.S. // ChemistrySelect. 2019. Vol. 4. P. 1323. doi: 10.1002/slct.201802366
  17. Asghari S., Pourshab M., Mohseni M. // Chem. Monthly. 2018. Vol. 149. P. 2327. doi: 10.1007/s00706-018-2292-x
  18. Ramadan S.K., El-Helwa E.A.E. // Russ. J. Org. Chem. 2019. Vol. 55. N 10. P. 1626. doi: 10.1134/S1070428019100282
  19. Porshamsian K., Montazeri N., Rad-Moghadam K., Ali-Asgari S. // J. Heterocycl. Chem. 2010. Vol. 47. N 6. P. 1439. doi: 10.1002/jhet.458

版权所有 © Russian Academy of Sciences, 2023

##common.cookie##