Urea and thiourea derivatives in the synthesis of hexaoxazadispiroalkane carboxamides

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

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

  1. Adam W., Forschungsgemeinschaft D. Peroxides Chemistry: Mechanistic and Preparative Aspects of Oxygen Transfer. Weinheim: Wiley-VCH. 2000.
  2. Ando W. Organic Peroxides. New York: Wiley. 1992.
  3. Jones C.W. Applications of Hidrogen Peroxides and Derivatives. Cambridge: Royal Society of Chemistry. 1999.
  4. Chaturvedi D., Goswami A., Saikia P.P., Barua N.C., Rao P.G. Chem. Soc. Rev. 2010, 39, 435-454. doi: 10.1039/b816679j
  5. O'Brien C., Henrich P.P., Passi N., Fidlock D. Curr. Opin. Infect. Dis. 2011, 24, 570-577. doi 097/QCO.0b013e32834cd3ed
  6. Slack R.D., Jacobine A.M., Posner G.H. Med. Chem. Commun. 2012, 3, 281-297. doi: 10.1039/C2MD00277A
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. Махмудиярова Н.Н., Ишмухаметова И.Р., Ибрагимов А.Г., Джемилев У.М. Докл. Акад. наук. 2020, 491, 93-100. doi: 10.31857/S2686953520040044
  14. 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

版权所有 © Russian Academy of Sciences, 2023

##common.cookie##