Reaction of 2-alkylthio-substituted 2-penten-4-ynals with N,N- and N,O-binucleophiles

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Abstract

The condensation of 2-alkylthiosubstituted 2-en-4-ynals with N , N - and N , O -binucleophiles gives the corresponding 1,3-perhydrodiazines, 1,3-imidazolidines, and 1,3-oxazolidines with an original combination of substituents.

About the authors

V. G Fedoseeva

Favorskii Irkutsk Institute of Chemistry SB RAS

Email: vchislo@irioch.irk.ru

E. A Verochkina

Favorskii Irkutsk Institute of Chemistry SB RAS

Email: vchislo@irioch.irk.ru

L. I Larina

Favorskii Irkutsk Institute of Chemistry SB RAS

Email: vchislo@irioch.irk.ru

N. V Vchislo

Favorskii Irkutsk Institute of Chemistry SB RAS

Email: vchislo@irioch.irk.ru

References

  1. Голованов А.А., Один И.С., Злотский С.С. Усп. хим. 2019, 88, 280-318.
  2. Golovanov A.A., Odin I.S., Zlotskii S.S. Russ. Chem. Rev. 2019, 88, 280-318. doi: 10.1070/RCR4808
  3. Голованов А.А., Гусев Д.М., Один И.С., Злотский С.С. ХГС. 2019, 55, 333-348.
  4. Golovanov A.A., Gusev D.M., Odin I.S., Zlotskii S.S. Chem. Heterocycl. Compd. 2019, 55, 333-348.
  5. Igushkina A.V., Golovanov A.A., Boyarskaya I.A., Kolesnikov I.E., Vasilyev A.V. Molecules. 2020, 25, 5920. doi: 10.3390/molecules25245920
  6. Shechter H., Hoffman R.V. J. Am. Chem. Soc. 1978, 100, 7934. doi: 10.1021/ja00493a024
  7. Shechter H. J. Am. Chem. Soc. 1978, 100, 7927-7933. doi: 10.1021/ja00493a023
  8. Shechter H., Hoffman R.V. J. Org. Chem. 1974, 39, 2939-2940. doi: 10.1021/jo00933a031
  9. Shechter H., Hoffman R.V. J. Am. Chem. Soc. 1971, 93, 5940-5941. doi: 10.1021/ja00751a082
  10. Bonrath W., Buser D., Pauling H., Thum A. Molecules. 2002, 7, 341. doi: 10.3390/70300341
  11. Li Y., Sun J., Zheng G., Fu Y., Wang L., Zhang Q. Org. Lett. 2018, 20, 5597-5600. doi: 10.1021/acs.orglett.8b02272
  12. Fedoseeva V.G., Verochkina E.A., Larina L.I., Kondrashov E.V., Rozentsveig I.B., Vchislo N.V. Mendeleev Commun. 2021, 31, 856-858. doi: 10.1016/j.mencom.2021.11.029
  13. Vchislo N.V., Fedoseeva V.G., Verochkina E.A., Larina L.I. Polycycl. Arom. Compd. 2022, 42, 7407-7413. doi: 10.1080/10406638.2021.2002375
  14. Кейко Н.А., Фунтикова Е.А., Вчисло Н.В., Ларина Л.И., Фролов Ю.Л. ЖОрХ. 2011, 47, 1794-1802.
  15. Keiko N.A., Funtikova E.A., Vchislo N.V., Larina N.V., Frolov Yu.L. Russ. J. Org. Chem. 2011, 47, 1832-1840. doi: 10.1134/S1070428011120098
  16. Паперная Л.К., Шатрова А.А., Албанов А.И., Левковская Г.Г. ЖОрХ. 2018, 54, 731-737.
  17. Papernaya L.K., Shatrova А.А., Albanov А.I., Levkovskaya G.G. Russ. J. Org. Chem. 2018, 54, 734-741. doi: 10.1134/S107042801805010X
  18. Манькова П.А., Резников А.Н., Ширяев В.А., Баймуров М.Р., Рыбаков В.Б., Климочкин Ю.Н. ЖОрХ. 2021, 57, 268-279.
  19. Man'kova P.A., Reznikov A.N., Shiryaev V.A., Baimuratov M.R., Rybakov V.B., Klimochkin Yu.N. Russ. J. Org. Chem. 2021, 57, 226-236. doi: 10.1134/S1070428021020135
  20. Husain A., Ahmad A., Khan S.A., Asif M., Bhutani R., Al-Abbasi F.A. Saudi Pharm. J. 2016, 24, 104-114. doi: 10.1016/j.jsps.2015.02.008

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