Email this article 
Synthesis New 1,2,3-Triazole Derivatives of Methyl 4-Propargylthieno[3,2-b]Pyrrolcarboxylate
- Authors: Nuriakhmetova Z.F.1, Torosyan S.A.1, Gimalova F.A.1, Miftakhov M.S.1
-
Affiliations:
- Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
- Issue: Vol 61, No 9 (2025)
- Pages: 1328-1331
- Section: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/380402
- DOI: https://doi.org/10.7868/S3034630425090051
- ID: 380402
Cite item
Open Access
Access granted
Subscription Access
Abstract
About the authors
Z. F. Nuriakhmetova
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Email: fangim@anrb.ru
ORCID iD: 0000-0002-7628-3452
prosp. Oktyabrya, 69, Ufa, 450054 Russia
S. A. Torosyan
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Email: fangim@anrb.ru
ORCID iD: 0000-0002-9555-7228
prosp. Oktyabrya, 69, Ufa, 450054 Russia
F. A. Gimalova
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Email: fangim@anrb.ru
ORCID iD: 0000-0002-5176-1227
prosp. Oktyabrya, 69, Ufa, 450054 Russia
M. S. Miftakhov
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Email: fangim@anrb.ru
ORCID iD: 0000-0002-0269-7484
prosp. Oktyabrya, 69, Ufa, 450054 Russia
References
- Sall C., Ayé M., Bottzeck O., Praud A., Blache Y. Bioorg. Med. Chem. Lett. 2018, 28, 155–159. http://doi.org/10.1016/j.bmcl.2017.11.039
- Todorov L., Kostova I. Front. Chem. 2023, 11, 1247805. http://doi.org/10.3389/fchem.2023.1247805
- Wang Z.-J., Gao Y., Hou Y.-L., Zhang C., Yu S.-J., Bian Q., Li Z.-M., Zhao W.-G. Eur. J. Med. Chem. 2014, 86, 8794. http://doi.org/10.1016/j.ejmech.2014.08.029
- Krajczyk A., Kulinska K., Kulinski T., Hurst B.L., Day C.W., Smee D.F., Ostrowski T., Januszczyk P., Zeidler J. Antivir. Chem. Chemother. 2014, 23, 161–171. http://doi.org/10.3851/IMP2564
- Elamari H., Slimi R., Chabot G.G., Quentin L., Scherman D., Girard C. Eur. J. Med. Chem. 2013, 60, 360–364. http://doi.org/10.1016/j.ejmech.2012.12.025
- Reddy V.G., Bonam S.R., Reddy T.S., Akunuri R., Naidu V.G.M., Nayak V.L., Bhargava S.K., Kumar H.S., Srihari P., Kamal A. Eur. J. Med. Chem. 2018, 144, 595–611. http://doi.org/10.1016/j.ejmech.2017.12.050
- Jadhav R.P., Raundal H.N., Patil A.A., Bobade V.D. J. Saudi Chem. Soc. 2017, 21, 152–159. http://doi.org/10.1016/j.jscs.2015.03.003
- Kuntala N., Mareddy J., Telu J.R., Banothu V., Pal S., Anireddy J.S. J. Heterocycl. Chem. 2021, 58 (10), 2018–2032. http://doi.org/10.1002/jhet.4328 АЗОЛЬНЫХ ПРОИЗВОДНЫХ 1331
- Pokhodylo N., Manko N., Finiuk N., Klyuchivska O., Matiychuk V., Obushak M., Stoika R. J. Mol. Struct. 2021, 1246, 131146. http://doi.org/10.1016/j.molstruc.2021.131146
- Wheless J.W., Vazquez B. Epilepsy Curr. 2010, 10, 1–6. http://doi.org/10.1111/j.1535-7511.2009.01336.x
- Corrado C., Flugy A.M., Taverna S., Raimondo S., Guggino G., Karmali R., De Leo G., Alessandro R. PLoS One. 2012, 7, e42310. http://doi.org/10.1371/journal.pone.00 42310
- Tornoe C.W., Christensen C., Meldal M. J. Org. Chem. 2002, 67, 3057–3062. http://doi.org/10.1021/jo011148j
- Zheng Zh.-J., Wang D., Xu Zh., Xu L.-W. Beilstein J. Org. Chem. 2015, 11, 2557–2576. http://doi.org/10.3762/bjoc.11.276
- Торосян С.А., Загитов В.В., Гималова Ф.А., Ерастов А.С., Мифтахов М.С. ЖОрХ. 2018, 54 (6), 909–913. [Torosyan S.A., Zagitov V.V., Gimalova F.A., Erastov A.S., Miftakhov M.S. Russ. J. Org. Chem. 2018, 54, 6, 912–917.] http://doi.org/10.1134/S1070 428018060131
- Торосян С.А., Нуриахметова З.Ф., Гималова Ф.А., Мифтахов М.С. ЖОрХ. 2023, 59, 266–270. [Torosyan S.A., Nuriakhmetova Z.F., Gimalova F.A., Miftakhov M.S. Russ. J. Org. Chem. 2023, 59, 328–331.] http://doi.org/10.1134/S1070 42802302015X
Supplementary files
