Dibenzoylmethane in the Synthesis of Selenium-Containing Di- and Tetrahydropyridine-3-carbonitriles

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Resumo

Upon the interaction of cyanoselenoacetamide, 2-furan- or 2-thiophenocarbaldehydes and dibenzoylmethane in ethanol in the presence of an excess of piperidine or morpholine under argon, 6-hydroxy-3-cyano-1,4,5,6-tetrahydropyridine-2-ammonium selenolates were obtained, which were used in the synthesis of 2-alkylselenodi- and tetrahydropyridine-3- carbonitriles. The structure of the latter was studied using the method of X-ray diffraction analysis.

Sobre autores

K. Frolov

Chemex Lab, V. Dahl Lugansk State University; St. Luke Lugansk State Medical University

Email: ksg-group-lugansk@mail.ru
ORCID ID: 0000-0002-8045-7582
Lugansk, Russia; Lugansk, Russia

B. Krivokolysko

Chemex Lab, V. Dahl Lugansk State University; St. Luke Lugansk State Medical University

ORCID ID: 0000-0002-3181-7609
Lugansk, Russia; Lugansk, Russia

N. Aksenov

North Caucasus Federal University

ORCID ID: 0000-0002-7125-9066
Stavropol, Russia

S. Krivokolysko

Chemex Lab, V. Dahl Lugansk State University; St. Luke Lugansk State Medical University

ORCID ID: 0000-0001-9879-9217
Lugansk, Russia; Lugansk, Russia

Bibliografia

  1. Iwaoka M., Arai K., Curr. Chem. Biol., 2013, 7, 2–24. doi: 10.2174/2212796811307010002
  2. Refaay D.A., Ahmed D.M., Mowafy A.M., Shaaban S., Med. Chem. Res., 2022, 31, 894–904. doi: 10.1007/s00044-022-02879-x
  3. Obieziruska-Fabisiak M., Pacula-Miszewska A.J., Laskowska A., Scianowski J., Arkivoc, 2022, 2023 (5), 69–92. doi: 10.24820/ark.5550190.p011.908
  4. Makhaeva N.A., Amosova S.V., Filippov A.S., Potapov V.A., Musalov M.V., Biomolecules, 2024, 14, 1546. doi: 10.3390/biom14121546
  5. Mugesh G., du Mont W.-W., Sies H., Chem. Rev., 2001, 101, 2125–2179. doi: 10.1021/cr000426w
  6. Nogueira C.W., Zeni G., Rocha J.B.T., Chem. Rev., 2004, 104, 6255–6285. doi: 10.1021/cr0406559
  7. Hatfield D.L. (Ed.), Selenium. Its Molecular Biology and Role in Human Health, Springer, New York, 2012, I–XIX. doi: 10.1007/978-1-4615-1609-5
  8. Dotsenko V.V., Frolov K.A., Krivokolysko S.G., Chem. Heterocycl. Compd., 2013, 49, 657–675. doi: 10.1007/s10593-013-1296-z
  9. Krivokolysko S.G., Dyachenko V.D., Chernega A.N., Litvinov V.P., Chem. Heterocycl. Compd., 2001, 37, 727–732. doi: 10.1023/A:1011969413764
  10. Krivokolysko S.G., Rusanov E.B., Litvinov V.P., Chem. Heterocycl. Compd., 2002, 38, 1205–1209. doi: 10.1023/A:1021729513180
  11. Litvinov V.P., Dyachenko V.D., Журн. Орг. Хим., 1999, 35, 1406–1412.
  12. Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H., J. Appl. Cryst., 2009, 42, 339–341. doi: 10.1107/S0021889808042726
  13. Sheldrick G.M., Acta Cryst., 2008, A64, 112–122. doi: 10.1107/S0108767307043930
  14. Sheldrick G.M., Acta Cryst., 2015, C71, 3–8. doi: 10.1107/S2053229644024218

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