电邮这篇文章 Mannich reaction in the synthesis of azaperoxides
- 作者: Makhmudiyarova N.N1, Ishmukhametova I.R1
-
隶属关系:
- Institute of Petrochemistry and Catalysis UFIC RAS
- 期: 卷 59, 编号 2 (2023)
- 页面: 256-260
- 栏目: 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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详细
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.
作者简介
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
参考
- 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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