Abstract:
Data on furo[2,3-b]pyridines published in the last 15 years are integrated and analyzed for the first time. Information on the methods of synthesis, chemical transformations and biological action of these systems is described systematically. Particular attention is paid to the preparation and study of properties of polycondensed derivatives as the most promising and rapidly developing line of research of furo[2,3-b]pyridine chemistry. The biological properties of this class of compounds are discussed, and examples of furo[2,3-b]pyridines that exhibit high biological activities are given.
The bibliography includes 88 references.
Received: 10.02.2014
Bibliographic databases:
Document Type:
Article
Language: English
Original paper language: Russian
Citation:
S. N. Sirakanyan, A. A. Hovakimyan, A. S. Noravyan, “Synthesis, transformations and biological properties of furo[2,3-b]pyridines”, Russian Chem. Reviews, 84:4 (2015), 441–454
Sumayya Akram, Sana Aslam, Nasir Rasool, Matloob Ahmad, Sami A. Al-Hussain, Magdi E.A. Zaki, Journal of Saudi Chemical Society, 28:5 (2024), 101906
A. A. Bondartseva, L. M. Pevzner, M. L. Petrov, A. V. Stepakov, Russ J Gen Chem, 94:6 (2024), 1257
Hirendra Nath Dhara, Supriya Manna, Bhisma K. Patel, Chemistry A European J, 2024
Pankaj Sharma, Vaishali Suthar, Meenu Aggarwal, Rajeev Singh, K. Poonam Kumar, Recent Developments in the Synthesis and Applications of Pyridines, 2023, 1
Hanan A. Soliman, Ahmed H. Shamroukh, Eman R. Kotb, Khaled. Mahmoud, El Hassane. Anouar, Mohamed I. Hegab, Journal of Molecular Structure, 1263 (2022), 133148
Samvel N. Sirakanyan, Domenico Spinelli, Athina Geronikaki, Luca Zuppiroli, Riccardo Zuppiroli, Victor G. Kartsev, Elmira K. Hakobyan, Hasmik A. Yegoryan, Anush A. Hovakimyan, IJMS, 23:11 (2022), 5904
Amitava Rakshit, Hirendra Nath Dhara, Ashish Kumar Sahoo, Tipu Alam, Bhisma K. Patel, Org. Lett., 24:20 (2022), 3741
Silva D.G., Junker A., de Melo Sh.M.G., Fumagalli F., Gillespie J.R., Molasky N., Buckner F.S., Matheeussen A., Caljon G., Maes L., Emery F.S., ChemMedChem, 16:6 (2021), 966–975
Sirakanyan S.N. Spinelli D. Geronikaki A. Kartsev V.G. Stepanyan H.M. Hakobyan E.K. Hovakimyan A.A., Chem. Heterocycl. Compds., 57:1 (2021), 75–80
S. N. O'Byrne, B. J. Eduful, T. M. Willson, D. H. Drewry, Tetrahedron Lett., 61:38 (2020), 152353
D. Wang, M. Huang, G. Li, Sh. Zheng, P. Yu, Tetrahedron, 76:48 (2020), 131642
S. N. Sirakanyan, V. G. Kartsev, A. Geronikaki, D. Spinelli, A. Petrou, E. K. Hakobyan, J. Glamoclija, M. Ivanov, M. Sokovic, A. A. Hovakimyan, Curr. Top. Med. Chem., 20:24 (2020), 2192–2209
Ch. Fu, G. Li, M. Shen, L. Zhang, P. Yu, D. Wang, Asian J. Org. Chem., 9:5 (2020), 749–752
J. Liu, L. Zhu, W. Wan, X. Huang, Org. Lett., 22:8 (2020), 3279–3285
F. Fumagalli, Sh. M. Gil de Melo, C. M. Ribeiro, M. C. Solcia, F. R. Pavan, Emery Flavio da Silva, Bioorg. Med. Chem. Lett., 29:8 (2019), 974–977
M. M. Ibrahim, M. Al-Refai, M. N. Azmi, H. Osman, M. H. Abu Bakar, A. Geyer, J. Iran Chem. Soc., 16:4 (2019), 715–722
A. A. Golovanov, D. M. Gusev, I. S. Odin, S. S. Zlotskii, Chem. Heterocycl. Compds., 55:4-5 (2019), 333–348
S. N. Sirakanyan, E. K. Hakobyan, A. A. Hovakimyan, Russ. J. Organ. Chem., 55:9 (2019), 1344–1350
Citation in format AMSBIB
Contact us: