RAS Chemistry & Material ScienceЖурнал общей химии Russian Journal of General Chemistry

  • ISSN (Print) 0044-460X
  • ISSN (Online) 3034-5596

Synthesis of aromatic bishydrazones: new facets of a known reaction

PII
10.31857/S0044460X2311001X-1
DOI
10.31857/S0044460X2311001X
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 93 / Issue number 11
Pages
1643-1649
Abstract
This work reconsiders the known condensation reaction of 1,2-diketones with arylhydrazines in the synthesis of the corresponding bishydrazones. It was shown that the reaction outcome significantly depends on the nature of the substituent of the aromatic ring of arylhydrazine. In addition, representatives of unsymmetrically substituted bishydrazones, rarely found in the literature, were obtained. The proposed approach is easy to carry out and isolate target bishydrazones, which opens the way to the preparation of various nitrogen-containing molecular systems based on them.
Keywords
конденсация бисгидразоны дикетоны арилгидразины
Date of publication
15.11.2023
Year of publication
2023
Number of purchasers
0
Views
33

References

  1. 1. Popiolek L. // Med. Chem. Res. 2017. Vol. 26. P. 287. doi 10.1007/s00044-016-1756-y
  2. 2. Popiolek L. // Biomed. Pharmacother. 2023. Vol. 163. P. 114853. doi 10.1016/j.biopha.2023.114853
  3. 3. K�lmel D.K., Kool E.T. // Chem. Rev. 2017. Vol. 117. P. 10358. doi 10.1021/acs.chemrev.7b00090
  4. 4. Bystrov D.M., Ananyev I.V., Fershtat L.L., Makhova N.N. // J. Org. Chem. 2020. Vol. 85. P. 15466. doi 10.1021/acs.joc.0c02243
  5. 5. Kulikov A.S., Epishina M.A., Churakov A.I., Anikina L.V., Fershtat L.L., Makhova N.N. // Mendeleev Commun. 2018. Vol. 28. P. 623. doi 10.1016/j.mencom.2018.11.020
  6. 6. Butler R.N., Cunningham D., McArdle P., O'Halloran G.A. // J. Chem. Soc. Chem. Commun. 1988. Vol. 3. P. 232. doi 10.1039/C39880000232
  7. 7. Butler R.N., Evans A.M., McNeela E.M., O'Halloran G.A., O'Shea P.D., Cunningham D., McArdle P. // J. Chem. Soc. Perkin Trans. 1 1990. P. 2527. doi 10.1039/P19900002527
  8. 8. Wu Z.-C., Boger D.L. // J. Am. Chem. Soc. 2019. Vol. 141. P. 16388. doi 10.1021/jacs.9b07744
  9. 9. Wu Z.-C., Boger D.L. // J. Org. Chem. 2022. Vol. 87. P. 16829. doi 10.1021/acs.joc.2c02687
  10. 10. Japp F.R., Klingemann F. // Lieb. Ann. Chem. 1888. Vol. 247. P. 190. doi 10.1002/jlac.18882470208
  11. 11. Butler R.N., O'Shea D.F. // Heterocycles. 1994. Vol. 37. P. 571. doi 10.3987/REV-93-SR1
  12. 12. Tabbiche A., Bouchama A., Chafai N., Zaidi F., Chiter C., Yahiaoui M., Abiza A. // J. Mol. Struct. 2022. Vol. 1261. P. 132865. doi 10.1016/j.molstruc.2022.132865
  13. 13. Butler R.N., Hanniffy J.M., Stephens J.C., Burke L.A. // J. Org. Chem. 2008. Vol. 73. P. 1354. doi 10.1021/jo702423z
  14. 14. Nagaraj K., Singh A., Shetty A.N., Trivedi D.R. // Supramol. Chem. 2021. Vol. 33. P. 534. doi 10.1080/10610278.2022.2087524
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