Email this article Key Blocks for Constructing π-Conjugated Systems Based on Thieno[3,2-b]pyrroles
- Authors: Torosyan S.A.1, Nuriakhmetova Z.F.1, Lobov A.N.1, Gimalova F.A.1
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Affiliations:
- Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
- Issue: Vol 94, No 2 (2024)
- Pages: 203-208
- Section: Articles
- URL: https://journals.rcsi.science/0044-460X/article/view/260301
- DOI: https://doi.org/10.31857/S0044460X24020058
- EDN: https://elibrary.ru/GVKDJN
- ID: 260301
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Abstract
Cross-coupling products with isobutyl acrylate were obtained by the Heck reaction based on dibromides of methyl esters of 4-methyl- and 4-benzyl-4H-thieno[3,2-b]pyrrole-5-carboxylic acids.
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About the authors
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
Russian Federation, Ufa, 450054
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
Russian Federation, Ufa, 450054
A. N. Lobov
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Email: fangim@anrb.ru
ORCID iD: 0000-0002-9223-508X
Russian Federation, Ufa, 450054
F. A. Gimalova
Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences
Author for correspondence.
Email: fangim@anrb.ru
ORCID iD: 0000-0002-5176-1227
Russian Federation, Ufa, 450054
References
- Ching K.-Ch., Kam Y.-W., Merits A., Ng L.F.P., Chai C.L.L. // J. Med. Chem. 2015. Vol. 58. P. 9196. doi: 10.1021/acs.jmedchem.5b01047
- Hernando M.J.I., Ontoria J.M., Malancona S., Attenni B., Fiore F., Bonelli F., Koch U., Di Marco S., Colarusso S., Ponzi S., Gennari N., Vignetti S.E., Rico Ferreira M.d.R., Habermann J., Rowley M., Narjes F. // ChemMedChem. 2009. Vol. 4. N 10. P. 1695. doi: 10.1002/cmdc.200900184
- Jones C., Boudinet D., Xia Y., Denti M., Das A., Facchetti A. Driver T.G. // Chem. Eur. J. 2014. Vol. 20. N 20. P. 5938. doi: 10.1002/chem.201304914
- Gunawardhana R., Bulumulla C., Gamage P.L., Timmerman A.J., Udamulle Gedara C.M., Biewer M.C., Stefan M.C. // ACS Omega. 2019. Vol. 4. N 22. P. 19676. doi: 10.1021/acsomega.9b02274
- Arias A.C., MacKenzie J.D., McCulloch I., Rivnay J., Salleo A. // Chem. Rev. 2010. Vol. 110. P. 3. doi: 10.1021/cr900150b
- Gamage P.L., Udamulle Gedara C.M., Gunawardhana R., Bulumulla C., Ma Z., Shrivastava A., Biewer M.C., Stefan M.C. // Appl. Sci. 2022. Vol. 12. 3150. doi: 10.3390/app12063150
- Honsho Y., Saeki A., Seki Sh. // Int. J. Spectrosc. 2012. Vol. 2012. 983523. doi: 10.1155/2012/983523
- Beletskaya I.P., Cheprakov A.V. // Chem. Rev. 2000. Vol. 100. P. 3009. doi: 10.1021/cr9903048
- Biffis A., Centomo P., Del Zotto A., Zecca M. // Chem. Rev. 2018. Vol. 118. P. 2249. doi: 10.1021/acs.chemrev.7b00443
- Corbet J.P., Mignani G. // Chem. Rev. 2006. Vol. 106. P. 2651. doi: 10.1021/cr0505268
- Miftakhov M.S., Torosyan S.A., Gimalova F.A., Khursan S.L., Nuriakhmetova Z.F., Shchurik E.V., Kraevaya O.A., Shestakov A.F., Troshin P.A. // Polymer Chem. 2023. Vol. 14. P. 4986. doi: 10.1039/d3py00893b.
- Торосян С.А., Загитов В.В., Гималова Ф.А., Ерастов А.С., Мифтахов М.С. // ЖОрХ. 2018. Т. 54. С. 909; Torosyan S.A., Gimalova F.A., Zagitov V.V., Erastov A.S., Miftakhov M.S. // Russ. J. Org. Chem. 2018. Vol. 54. P. 912. doi: 10.1134/S1070428018060131
- Spencer A. // J. Organometal. Chem. 1984. Vol. 265. P. 323. doi: 10.1016/0022-328X(84)80097-2
- Stephan M.S., Teunissen A.J.J.M., Verzijl G.K.M., De Vries J.G. // Angew. Chem. Int. Ed. 1998. Vol. 37. P. 662. doi: 10.1002/(SICI)1521-3773(19980316)37:5<662::AID-ANIE662>3.0.CO;2-0
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