RAS Chemistry & Material ScienceЖурнал органической химии Russian Journal of Organic Chemistry

  • ISSN (Print) 0514-7492
  • ISSN (Online) 3034-6304

Interaction of Cyanoselenoacetamide with 1-Aryl-2-Bromoethanones

PII
S3034630425110104-1
DOI
10.7868/S3034630425110104
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 61 / Issue number 11
Pages
1611-1615
Abstract
When cyanoselenoacetamide was reacted with 1-aryl-2-bromoethanones in ethanol or DMF, 4,6-diamino-2-[(2-aryl-2-oxoethyl)seleno]nicotinonitriles were obtained with yields of 68–93%.
Keywords
цианоселеноацетамид 1-арил-2-бромэтаноны 2-алкилселеноникотинонитрилы
Date of publication
08.08.2025
Year of publication
2025
Number of purchasers
0
Views
29

References

  1. 1. Iwaoka M., Arai K. Curr. Chem. Biol. 2013, 7, 2–24. https://doi.org//10.2174/2212796811307010002
  2. 2. Refaay D.A., Ahmed D.M., Mowafy A.M., Shaaban S. Med. Chem. Res. 2022, 31, 894–904. https://doi.org//10.1007/s00044-022-02879-x
  3. 3. Obieziurska-Fabisiak M., Pacuła-Miszewska A.J., Laskowska A., Scianowski J. Arkivoc. 2022, 2023 (5), 69–92. https://doi.org//10.24820/ark.5550190.p011.908
  4. 4. Makhaeva N.A., Amosova S.V., Filippov A.S., Potapov V.A., Musalov M.V. Biomolecules. 2024, 14, 1546. https://doi.org//10.3390/biom14121546
  5. 5. Mugesh G., du Mont W.-W., Sies H. Chem. Rev. 2001, 101, 2125–2179. https://doi.org//10.1021/cr000426w
  6. 6. Nogueira C.W., Zeni G., Rocha J.B.T. Chem. Rev. 2004, 104, 6255–6285. https://doi.org//10.1021/cr0406559
  7. 7. Hatfield D.L. (Ed.), Selenium. Its Molecular Biology and Role in Human Health, Springer, New York, 2012, I– XIX. https://doi.org//10.1007/978-1-4615-1609-5
  8. 8. Dotsenko V.V., Frolov K.A., Krivokolysko S.G. Chem. Heterocycl. Compd. 2013, 49, 657–675. https://doi.org//10.1007/s10593-013-1296-z
  9. 9. Frolov K.A., Krivokolysko B.S., Aksenov N.A., Krivokolysko S.G. Russ. J. Org. Chem. 2025, 61 (4), 621–624. https://doi.org//10.1134/S1070428025600366
  10. 10. Abramenko V.L., Krivokolysko S.G., Pakholka N.A., Krivokolysko B.S., Dotsenko V.V., Bespalov A.V., Aksenov N.A., Aksenova I.V. Russ. J. Gen. Chem. 2024, 94 (7), 1645–1658. https://doi.org//10.1134/S1070363224070065
  11. 11. Pakholka N.A., Abramenko V.L., Dotsenko V.V., Aksenov N.A., Aksenova I.V., Krivokolysko S.G. Russ. J. Gen. Chem. 2021, 91 (3), 357–368. https://doi.org//10.1134/S1070363221030038
  12. 12. Pakholka N.A., Dotsenko V.V., Aksenov N.A., Aksenova I.V., Krivokolysko S.G. Russ. J. Gen. Chem. 2024, 94 (10), 2578–2585. https://doi.org//10.1134/S1070363224100025
  13. 13. Dyachenko V.D., Dyachenko I.V., Nenajdenko V.G. Russ. Chem. Rev. 2018, 87 (1), 1–27. https://doi.org//10.1070/rcr4760
  14. 14. Магеррамов А.М, Шихалиев Н.Г., Дяченко В.Д., Дяченко И.В., Ненайденко В.Г. α-Цианотиоацетамид. Москва: Техносфера, 2018, ISBN 978-5-94836-510-7.
  15. 15. Pizzo C., Mahler S.G. J. Org. Chem. 2014, 79, 1856–1860. https://doi.org//10.1021/jo402661b
  16. 16. Hussein B.R.M., El
  17. 17. Funakoshi Y., Takido T., Itabashi K. Synth. Commun. 1985, 15 (14), 1299–1303. https://doi.org//10.1080/00397918508077278
  18. 18. Онлайн-калькулятор Scientific Instrument Services (Adaptas Solutions). https://www.sisweb.com/referenc/tools/exactmass.htm
  19. 19. Litvinov V.P., Dyachenko V.D. Zh. Org. Khim. 1999, 35, 1406–1412.
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