Везде

RAS PresidiumДоклады Российской академии наук. Химия, науки о материалах Doklady Chemistry

  • ISSN (Print) 2686-9535
  • ISSN (Online) 3034-5111

Stabilizing Influence of Electron-Deficient Triazole Fragment on the Furan Heterocycle in Renewable Platform Chemicals

You can
PII
10.31857/S2686953524040029-1
DOI
10.31857/S2686953524040029
Publication type
Article
Status
Published
Authors
D. A. Kolykhalov
  • Affiliation:
    Tula State University
    N.D. Zelinsky Institute of Organic Chemistry of Russian Academy of Sciences
Volume/ Edition
Volume 517 / Issue number 1
Pages
13-23
Abstract
The effect of an aromatic triazole ring conjugated with a furan heterocycle on the stability of furan under various reaction conditions was studied, and a significant reduction in the degree of degradation of the electron-rich furan core and hydrolysis of the ester group under the action of a model acid and base in various organic solvents was shown. The lowest degree of degradation and hydrolysis of the triazole-substituted 2-furoic acid ester was achieved in dioxane, as well as in polar aprotic solvents (DMSO and DMF). It was shown that under the same conditions, a significant tarring and hydrolysis of the furan ester, which does not contain a conjugated triazole fragment, occurs.
Keywords
клик-реакция конверсия биомассы соединение-платформа триазол устойчивое развитие фуран фурфурол
Date of publication
18.09.2025
Year of publication
2025
Number of purchasers
0
Views
5

References

  1. 1. Halkos G.E., Gkampoura E.-C. // Energies. 2020. V. 13. № 11. P. 2906. https://doi.org/10.3390/en13112906
  2. 2. Seitkalieva M.M., Vavina A.V., Strukova E.N. // Dokl. Chem. 2023. V. 513. № 2. P. 380–388. https://doi.org/10.1134/s0012500823600967
  3. 3. Redina E.A., Vikanova K.V., Tkachenko O.P., Kapustin G.I., Kustov L.M. // Dokl. Chem. 2022. V. 507. № 2. P. 261–269. https://doi.org/10.1134/s0012500822600158
  4. 4. Zlotin S.G., Egorova K.S., Ananikov V.P., Akulov A.A., Varaksin M.V., Chupakhin O.N., Charushin V.N., Bryliakov K.P., Averin A.D., Beletskaya I.P., Dolengovski E.L., Budnikova Y.H., Sinyashin O.G., Gafurov Z.N., Kantyukov A.O., Yakhvarov D.G., Aksenov A.V., Elinson M.N., Nenajdenko V.G., Chibiryaev A.M., Nesterov N.S., Kozlova E.A., Martyanov O.N., Balova I.A., Sorokoumov V.N., Guk D.A., Beloglazkina E.K., Lemenovskii D.A., Chukicheva I.Y., Frolova L.L., Izmest’ev E.S., Dvornikova I.A., Popov A.V., Kutchin A.V., Borisova D.M., Kalinina A.A., Muzafarov A.M., Kuchurov I.V., Maximov A.L., Zolotukhina A.V. // Russ. Chem. Rev. 2023. V. 92. № 12. RCR5104. https://doi.org/10.59761/rcr5104
  5. 5. Bozell J.J., Petersen G.R. // Green Chem. 2010. V. 12. № 4. P. 539–554. https://doi.org/10.1039/b922014c
  6. 6. Bielski R., Grynkiewicz G. // Green Chem. 2021. V. 23. № 19. P. 7458–7487. https://doi.org/10.1039/d1gc02402g
  7. 7. Espro C., Paone E., Mauriello F., Gotti R., Uliassi E., Bolognesi M.L., Rodríguez-Padrón D., Luque R. // Chem. Soc. Rev. 2021. V. 50. № 20. P. 11191–11207. https://doi.org/10.1039/d1cs00524c
  8. 8. Gandini A., Lacerda T.M. // Macromol. Mater. Eng. 2022. V. 307. № 6. P. 2100902. https://doi.org/10.1002/mame.202100902
  9. 9. Karlinskii B.Ya., Ananikov V.P. // Chem. Soc. Rev. 2023. V. 52. № 2. P. 836–862. https://doi.org/10.1039/d2cs00773h
  10. 10. Jaswal A., Singh P.P., Mondal T. // Green Chem. 2022. V. 24. № 2. P. 510–551. https://doi.org/10.1039/d1gc03278j
  11. 11. Najmidin K., Kerim A., Abdirishit P., Kalam H., Tawar T. // J. Mol. Model. 2013. V. 19. № 9. P. 3529–3535. https://doi.org/10.1007/s00894-013-1877-x
  12. 12. Kucherov F.A., Romashov L.V., Galkin K.I., Ananikov V.P. // ACS Sustainable Chem. Eng. 2018. V. 6. № 7. P. 8064–8092. https://doi.org/10.1021/acssuschemeng.8b00971
  13. 13. Rani M.A.A.B.A., Karim N.A., Kamarudin S.K. // Int. J. Energy Res. 2022. V. 46. № 13. P. 18996–19050. https://doi.org/10.1002/er.8545
  14. 14. Averochkin G.M., Gordeev E.G., Skorobogatko M.K., Kucherov F.A., Ananikov V.P. // ChemSusChem 2021. V. 14. № 15. P. 3110–3123. https://doi.org/10.1002/cssc.202100818
  15. 15. Shepelenko K.E., Nikolaeva K.A., Gnatiuk I.G., Garanzha O.G., Alexandrov A.A., Minyaev M.E., Chernyshev V.M. // Mendeleev Commun. 2022. V. 32. № 4. P. 485–487. https://doi.org/10.1016/j.mencom.2022.07.018
  16. 16. Shepelenko K.E., Soliev S.B., Nikolaeva K.A., Minyaev M.E., Chernyshev V.M. // Russ. Chem. Bull. 2023. V. 72. № 8. P. 1746–1752. https://doi.org/10.1007/s11172-023-3956-1
  17. 17. John I.G., Radom L. // J. Am. Chem. Soc. 1978. V. 100. № 13. P. 3981–3991. https://doi.org/10.1021/ja00481a001
  18. 18. Cao H., Rupar P.A. // Chem. Eur. J. 2017. V. 23. № 59. P. 14670–14675. https://doi.org/10.1002/chem.201703355
  19. 19. Karlinskii B.Ya., Romashov L.V., Galkin K.I., Kislitsyn P.G., Ananikov V.P. // Synthesis. 2019. V. 51. № 05. P. 1235–1242. https://doi.org/10.1055/s-0037-1610414
  20. 20. Savelyeva N.Yu., Shpirt A.M., Orlova A.V., Chizhov A.O., Kononov L.O. // Russ. Chem. Bull. 2022. V. 71. № 8. P. 1784–1793. https://doi.org/10.1007/s11172-022-3590-3
  21. 21. Johansson G., Sundquist S., Nordvall G., Nilsson B.M., Brisander M., Nilvebrant L., Hacksell U. // J. Med. Chem. 1997. V. 40. № 23. P. 3804–3819. https://doi.org/10.1021/jm970346t
  22. 22. Hashmi A., Enns E., Frost T., Schäfer S., Frey W., Rominger F. // Synthesis. 2008. V. 2008. № 20. P. 3360–3360. https://doi.org/10.1055/s-0028-1083144
  23. 23. Cui X., Xu X., Wojtas L., Kim M.M., Zhang X.P. // J. Am. Chem. Soc. 2012. V. 134. № 49. P. 19981–19984. https://doi.org/10.1021/ja309446n
  24. 24. Fakhrutdinov A.N., Karlinskii B.Ya., Minyaev M.E., Ananikov V.P. // J. Org. Chem. 2021. V. 86. № 17. P. 11456–11463. https://doi.org/10.1021/acs.joc.1c00943
  25. 25. Stini N.A., Gkizis P.L., Kokotos C.G. // Green Chem. 2022. V. 24. № 17. P. 6435–6449. https://doi.org/10.1039/d2gc02332f
  26. 26. Warlin N., Garcia Gonzalez M.N., Mankar S., Valsange N.G., Sayed M., Pyo S.-H., Rehnberg N., Lundmark S., Hatti-Kaul R., Jannasch P., Zhang B. // Green Chem. 2019. V. 21. № 24. P. 6667–6684. https://doi.org/10.1039/c9gc03055g
  27. 27. Hoang T.M.C., van Eck E.R.H., Bula W.P., Gardeniers J.G.E., Lefferts L., Seshan K. // Green Chem. 2015. V. 17. № 2. P. 959–972. https://doi.org/10.1039/c4gc01324g
  28. 28. Tsilomelekis G., Orella M.J., Lin Z., Cheng Z., Zheng W., Nikolakis V., Vlachos D.G. // Green Chem. 2016. V. 18. № 7. P. 1983–1993. https://doi.org/10.1039/c5gc01938a
  29. 29. Shen H., Shan H., Liu L. // ChemSusChem. 2020. V. 13. № 3. P. 513–519. https://doi.org/10.1002/cssc.201902799
  30. 30. Hu X., Kadarwati S., Wang S., Song Y., Hasan M.D.M., Li C.-Z. // Fuel Process. Technol. 2015. V. 137. P. 212–219. https://doi.org/10.1016/j.fuproc.2015.04.024
  31. 31. Motornov V., Pohl R., Klepetářová B., Beier P. // Chem. Commun. 2023. V. 59. № 61. P. 9364–9367. https://doi.org/10.1039/d3cc00987d
  32. 32. Bauerová I., Ludwig M. // Collect. Czech. Chem. Commun. 2000. V. 65. № 11. P. 1777–1790. https://doi.org/10.1135/cccc20001777
  33. 33. Nummert V., Piirsalu M., Mäemets V., Koppel I. // Collect. Czech. Chem. Commun. 2006. V. 71. № 1. P. 107–128. https://doi.org/10.1135/cccc20060107
  34. 34. Mangione M.I., Spanevello R.A., Anzardi M.B. // RSC Adv. 2017. V. 7. № 75. P. 47681–47688. https://doi.org/10.1039/c7ra09558a
  35. 35. Kozlov K.S., Romashov L.V., Ananikov V.P. // Green Chem. 2019. V. 21. № 12. P. 3464–3468. https://doi.org/10.1039/c9gc00840c
  36. 36. Guan Y., Buivydas T., Lalisse R.F., Ali R., Hadad C.M., Mattson A.E. // Synthesis. 2022. V. 54. № 19. P. 4210–4219. https://doi.org/10.1055/a-1811-8075
QR
Translate

Индексирование

Scopus

Scopus

Scopus

Crossref

Scopus

Higher Attestation Commission

At the Ministry of Education and Science of the Russian Federation

Scopus

Scientific Electronic Library