Semicarbazones of acetyldihydropyrans: diastereoselective acetylene-based two-step synthesis
- Authors: Tatarinova I.V1, Lobanova N.A1, Ushakov I.A1, Schmidt E.Y.1,2, Trofimov B.A1
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Affiliations:
- A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
- Angarsk State Technical University
- Issue: Vol 59, No 3 (2023)
- Pages: 405-410
- Section: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/144744
- DOI: https://doi.org/10.31857/S0514749223030126
- EDN: https://elibrary.ru/TMBRLV
- ID: 144744
Cite item
Abstract
About the authors
I. V Tatarinova
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: boris_trofimov@irioch.irk.ru
N. A Lobanova
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: boris_trofimov@irioch.irk.ru
I. A Ushakov
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: boris_trofimov@irioch.irk.ru
E. Yu. Schmidt
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences;Angarsk State Technical University
Email: boris_trofimov@irioch.irk.ru
B. A Trofimov
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences
Email: boris_trofimov@irioch.irk.ru
References
- Rodygin K.S., Werner G., Kucherov F.A., Ananikov V.P. Chem. Asian J. 2016, 11, 965-976. doi: 10.1002/asia.201501323
- Voronin V.V., Ledovskaya M.S., Bogachenkov A.S., Rodygin K.S., Ananikov V.P. Molecules. 2018, 23, 2442. doi: 10.3390/molecules23102442
- Trofimov B.A., Schmidt E.Yu. Acc. Chem. Res. 2018, 51, 1117-1130. doi: 10.1021/acs.accounts.7b00618
- Шмидт Е.Ю., Трофимов Б.А. Докл. РАН. Химия, науки о материалах. 2022, 505, 5-24. doi: 10.31857/S268695352270008X
- Schmidt E.Yu., Trofimov B.A., Zorina N.V., Mikhaleva A.I., Ushakov I.A., Skital'tseva E.V., Kazheva O.N., Alexandrov G.G., Dyachenko O.A. Eur. J. Org. Chem. 2010, 75, 6727-6730. doi: 10.1002/ejoc.201001229
- Афонин А.В., Ушаков И.А., Тарасова О.А., Шмидт Е.Ю., Михалева А.И., Воронов В.К. ЖОрХ. 2000, 36, 1831-1837.
- Afonin A.V., Ushakov I.A., Tarasova O.A., Schmidt E.Yu., Mikhaleva A.I., Voronov V.K. Russ. J. Org. Chem. 2000, 36, 1777-1783.
- Venkatachalam T.K., Bernhardt P.V., Noble Ch.J., Fletcher N., Pierens G.K., Thurecht K.J., Reutens D.C. J. Inorg. Biochem. 2016, 162, 295-308. doi: 10.1016/j.jinorgbio.2016.04.006.
- Jaiswal Sh., Akhilesh, Uniyal A., Tiwari V., Ayyannan S.R. Bioorg. Med. Chem. 2022, 60, 116698. doi: 10.1016/j.bmc.2022.116874
- Rajmohan G., Shanmugam R., Elangovan A., Ravindran G., Sangeetha T., Arivazhagan G. Mater. Today Proc. 2022, 60, 1310-1319. doi: 10.1016/j.matpr.2021.09.305
- Cocco M.T., Cogiv C., Onnis V., Pellerano M.L., de Logu A. Bioorg. Med. Chem. 2002, 10, 501-506. doi: 10.1016/S0968-0896(01)00310-8
- Jia X., Liu Q., Wang Sh., Zeng B., Du G., Zhang Ch., Li Y. Bioorg Med. Chem. 2020, 28, 115557. doi: 10.1016/j.bmc.2020.115557
- Pósa V., Hajdu B., Tóth G., Dömötör O., Kowol Ch.R., Keppler B.K., Spengler G., Gyurcsik B., Enyedy É.A. J. Inorg. Biochem. 2022, 231, 111786. doi: 10.1016/j.jinorgbio.2022.111786
- Kumar S., Malachowski W.P., DuHadaway J.B., LaLonde J.M., Carroll P.J., Jaller D., Metz R., Prendergast G.C., Muller A.J. J. Med. Chem. 2008, 51, 1706-1718. doi: 10.1021/jm7014155
- Yoo N.H., Jang D.S., Yoo J.L., Lee Y.M., Kim Y.S., Cho J.-H., Kim J.S. J. Nat. Prod. 2008, 71, 713-716. doi: 10.1021/np070489a
- Cao J., Yu H., Wu Y., Wang X. Mini-Rev. Med. Chem. 2019, 19, 292-309. doi: 10.2174/1389557518666181026091449
- Desimoni G., Faita G., Quadrelli P. Chem. Rev. 2018, 118, 2080-2248. doi: 10.1021/acs.chemrev.7b00322