Mannich reaction in the synthesis of azaperoxides

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Resumo

The applicability of the Mannich reaction in the synthesis of new tetraoxazodispiroalkanes by a three-component reaction of primary arylamines with gem-dihydroperoxides and cyclohexanone with the participation of Sm(NO3)3 6H2O as a catalyst has been established.

Sobre autores

N. Makhmudiyarova

Institute of Petrochemistry and Catalysis UFIC RAS

Email: natali-mnn@mail.ru

I. Ishmukhametova

Institute of Petrochemistry and Catalysis UFIC RAS

Email: natali-mnn@mail.ru

Bibliografia

  1. Amewu R.K., Chadwick J., Hussain A., Panda S., Rinki R., Janneh O., Ward S.A., Miguel C., Burrell-Saward H., Vivas L., O'Neill P.M. Bioorg. Med. Chem. 2013, 21, 7392-7397. doi: 10.1016/j.bmc.2013.09.047
  2. Tang Y., Dong Y., Karle J.M., DiTusa C.A., Vennerstrom J.L. J. Org. Chem. 2004, 69, 6470-6473. doi: 10.1021/jo040171c
  3. Dong Y., Chollet J., Matile H., Charman S.A., Chiu F.C.K., Charman W.N., Scorneaux B., Urwyler H., Tomas J.S., Scheurer C., Snyder C., Dorn A., Wang X., Karle J.M., Tang Y., Wittlin S., Brun R., Vennerstrom J.L. J. Med. Chem. 2005, 48, 4953-4961. doi: 10.1021/jm049040u
  4. Dong Y., Tang Y., Chollet J., Matile H., Wittlin S., Charman S.A., Charman W.N., Tomas J.S., Scheurer C., Snyder C., Scorneaux B., Bajpai S., Alexander S.A., Wang X., Padmanilayam M., Cheruku S.R., Brun R., Vennerstrom J.L. Bioorg. Med. Chem. 2006, 14, 6368-6382. doi: 10.1016/j.bmc.2006.05.041
  5. Tang Y., Dong Y., Wittlin S., Charman S.A., Chollet J., Chiu F.C.K., Charman W.N., Matile H., Urwyler H., Dorn A., Bajpai S., Wang X., Padmanilayam M., Karle J.M., Brun R., Vennerstrom J.L. Bioorg. Med. Chem. Lett. 2007, 17, 1260-1265. doi: 10.1016/j.bmcl.2006.12.007
  6. Slack R., Jacobine A., Posner G. Med. Chem. Comm. 2012, 3, 281-297. doi: 10.1039/C2MD00277A
  7. Vil' V., Yaremenko I., Ilovaisky A., Terent'ev A. Molecules. 2017, 22, 1881. doi: 10.3390/molecules22111881
  8. Liu D.-Z., Liu J.-K. Nat. Prod. Bioprospect. 2013, 3, 161-206. doi: 10.1007/s13659-013-0042-7
  9. Kawamura Y., Takayama R., Nishiuchi M., Tsukayama M. Tetrahedron Lett. 2000, 41, 8101-8106. doi: 10.1016/S0040-4039(00)01412-X
  10. White E.H., Li M., Roswell D.F. Photochem. Photobiol. 1991, 53, 125-130. doi: 10.1111/j.1751-1097.1991.tb08477.x
  11. Kraljic I., El Mohsni S. Photochem. Photobiol. 1978, 28, 577-581. doi: 10.1111/j.1751-1097.1978.tb06972.x
  12. Vennerstrom J.L. J. Med. Chem. 1989, 32, 64-67. doi: 10.1021/jm00121a013
  13. Sundar N., Jacob V.T., Bhat S.V., Valecha N., Biswas S. Bioorg. Med. Chem. Lett. 2001, 11, 2269-2272. doi: 10.1016/S0960-894X(01)00396-1
  14. Махмудиярова Н.Н., Рахимов Р.Ш., Тюмкина Т.В., Мещерякова Е.С., Ибрагимов А.Г., Джемилев У.М. ЖОрХ. 2019, 55, 713-727. doi: 10.1134/s1070428019050075
  15. Makhmudiyarova N.N., Ishmukhametova I.R., Dzhemileva L.U., Tyumkina T.V., D'yakonov V.A., Ibragimov A.G., Dzhemilev U.M. RSC Adv. 2019, 9, 18923-18929. doi: 10.1039/c9ra02950h
  16. Makhmudiyarova N.N., Ishmukhametova I.R., Dzhemileva L.U., D'yakonov V.A., Ibragimov A.G., Dzhemilev U.M. Molecules. 2020, 25, 1874. doi: 10.3390/molecules25081874
  17. Махмудиярова Н.Н., Ишмухаметова И.Р., Джемилева Л.У., Дьяконов В.А., Ибрагимов А.Г., Джемилев У.М. ЖОрХ. 2020, 56, 746-752. doi: 10.1134/s1070428020050115
  18. Makhmudiyarova N.N., Ishmukhametova I.R., Shangaraev K.R., Dzhemileva L.U., D'yakonov V.A., Ibragimov A.G., Dzhemilev U.M. New J. Chem. 2021, 45, 2069-2077. doi: 10.1039/d0nj05511e
  19. Terent'ev A.O., Platonov M.M., Ogibin Y.N., Nikishin G.I. Synth. Commun. 2007, 37, 1281-1287. doi: 10.1080/00397910701226384

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