Urea and thiourea derivatives in the synthesis of hexaoxazadispiroalkane carboxamides
- Autores: Makhmudiyarova N.1, Ishmukhametova I.1
-
Afiliações:
- Institute of Petrochemistry and Catalysis UFIC RAS
- Edição: Volume 59, Nº 6 (2023)
- Páginas: 802-806
- Seção: 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
Citar
Resumo
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.
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
Bibliografia
- 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