Mannich reaction in the synthesis of azaperoxides
- Autores: Makhmudiyarova N.N1, Ishmukhametova I.R1
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Afiliações:
- Institute of Petrochemistry and Catalysis UFIC RAS
- Edição: Volume 59, Nº 2 (2023)
- Páginas: 256-260
- Seção: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/666412
- DOI: https://doi.org/10.31857/S051474922302012X
- EDN: https://elibrary.ru/QKDABL
- ID: 666412
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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.
Palavras-chave
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
- 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
- Tang Y., Dong Y., Karle J.M., DiTusa C.A., Vennerstrom J.L. J. Org. Chem. 2004, 69, 6470-6473. doi: 10.1021/jo040171c
- 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
- 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
- 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
- Slack R., Jacobine A., Posner G. Med. Chem. Comm. 2012, 3, 281-297. doi: 10.1039/C2MD00277A
- Vil' V., Yaremenko I., Ilovaisky A., Terent'ev A. Molecules. 2017, 22, 1881. doi: 10.3390/molecules22111881
- Liu D.-Z., Liu J.-K. Nat. Prod. Bioprospect. 2013, 3, 161-206. doi: 10.1007/s13659-013-0042-7
- Kawamura Y., Takayama R., Nishiuchi M., Tsukayama M. Tetrahedron Lett. 2000, 41, 8101-8106. doi: 10.1016/S0040-4039(00)01412-X
- White E.H., Li M., Roswell D.F. Photochem. Photobiol. 1991, 53, 125-130. doi: 10.1111/j.1751-1097.1991.tb08477.x
- Kraljic I., El Mohsni S. Photochem. Photobiol. 1978, 28, 577-581. doi: 10.1111/j.1751-1097.1978.tb06972.x
- Vennerstrom J.L. J. Med. Chem. 1989, 32, 64-67. doi: 10.1021/jm00121a013
- 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
- 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
- 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
- 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
- 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
- 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
- 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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