Urea and thiourea derivatives in the synthesis of hexaoxazadispiroalkane carboxamides
- 作者: Makhmudiyarova N.1, Ishmukhametova I.1
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隶属关系:
- Institute of Petrochemistry and Catalysis UFIC RAS
- 期: 卷 59, 编号 6 (2023)
- 页面: 802-806
- 栏目: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/145100
- DOI: https://doi.org/10.31857/S0514749223060095
- EDN: https://elibrary.ru/FBKBVV
- ID: 145100
如何引用文章
详细
An efficient method for the synthesis of di(6,7,13,14,18,19-hexaoxa-16-azadispiro[4.2.48.75]nonadecan-16-yl)methane(thi)ones and N -substituted hexaoxaazadispiroalkanecarboxamides by the reaction of 3,6-di(spiroalkane)substituted heptaoxacycloundecanes with thiourea and urea derivatives (urea, 1,1-dimethylurea, 1-phenylurea, 1-allylurea) with the participation of Sm(NO3)3·6H2O as a catalyst.
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
参考
- Adam W., Forschungsgemeinschaft D. Peroxides Chemistry: Mechanistic and Preparative Aspects of Oxygen Transfer. Weinheim: Wiley-VCH. 2000.
- Ando W. Organic Peroxides. New York: Wiley. 1992.
- Jones C.W. Applications of Hidrogen Peroxides and Derivatives. Cambridge: Royal Society of Chemistry. 1999.
- Chaturvedi D., Goswami A., Saikia P.P., Barua N.C., Rao P.G. Chem. Soc. Rev. 2010, 39, 435-454. doi: 10.1039/b816679j
- O'Brien C., Henrich P.P., Passi N., Fidlock D. Curr. Opin. Infect. Dis. 2011, 24, 570-577. doi 097/QCO.0b013e32834cd3ed
- Slack R.D., Jacobine A.M., Posner G.H. Med. Chem. Commun. 2012, 3, 281-297. doi: 10.1039/C2MD00277A
- Ansari M.T., Saify Z.S., Sultana N., Ahmed I., Saeedul-Hassan S., Tariq I., Khanum M. Mini Rev. Med. Chem. 2013, 13, 1879-1902. doi: 10.2174/13895575113136660097
- Ariey F., Witkowski B., Amaratunga C., Beghain J., Langlois A.-C., Khim N., Kim S., Duru V., Bouchier C., Ma L., Lim P., Leang R., Duong S., Sreng S., Suon S., Chuor C.M., Bout D.M., Menard S., Rogers W.O., Genton B., Fandeur T., Miotto O., Ringwald P., Le Bras J., Berry A., Barale J.-C., Fairhurst R.M., Benoit-Vical F., Mercereau-Puijalon O., Menard D. Nature. 2014, 505, 50-55. doi: 10.1038/nature12876
- Makhmudiyarova N.N., Ishmukhametova I.R., Tyumkina T.V., Ibragimov A.G., Dzhemilev U.M. Tetrahedron Lett. 2018, 59, 3161-3164. doi: 10.1016/j.tetlet.2018.07.010
- 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
- Махмудиярова Н.Н., Ишмухаметова И.Р., Ибрагимов А.Г., Джемилев У.М. Докл. Акад. наук. 2020, 491, 93-100. doi: 10.31857/S2686953520040044
- 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