Synthesis, crystal structure and biological activity of hydroxyphosphonates

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 订阅或者付费存取

详细

A series of О,О-dialkyl((aryl(hydroxy)methyl)phosphonates 1-4 with various substituents at the phosphorus atom was obtained by the Abramov reaction. The structure of the isolated products was confirmed by a complex of physical research methods: NMR, IR spectroscopy, mass spectrometry, and X-ray diffraction analysis. All the obtained compounds demonstrated activity against strains of B. cereus and S. aureus bacteria.

作者简介

A. Sedov

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

Email: sedandrey1998@gmail.com

R. Davletshin

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

N. Davletshina

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

Email: kurnosova.nataliya@yandex.ru

K. Ivshin

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

A. Fedonin

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

A. Osogostok

Kazan (Volga region) Federal University, Butlerov Institute of Chemistry

M. Shulaeva

Kazan State Medical Academy

参考

  1. Tezel U., Pavlostathis S.G. Curr. Opin. Biotechnol. 2015, 33, 296-304. doi: 10.1016/j.copbio.2015.03.018
  2. Buffet-Bataillona S., Tattevinc P., Bonnaure-Mallet M., Jolivet-Gougeonb A. Int. J. Antimicrob. Agents. 2012, 39, 381-389. doi: 10.1016/j.ijantimicag.2012.01.011
  3. Pateiro-Moure M., Arias-Estevez M., Simal-Gandara J. Environ. Sci. Technol. 2013, 47, 4984-4998. doi: 10.1021/es400755h
  4. Galkina I.V., Khayarov K.R., Davletshin R.R., Gaynullin A.Z., Gerasimov A.V., Shulaeva M.P., Pozdeev O.K., Egorova S.N., Usupova L.M., Galkin V.I. Phosphorus, Sulfur Silicon Relat. Elem. 2019, 194, 463-466. doi: 10.1080/10426507.2018.1539848
  5. Gayneev A., Davletshin R., Davletshina N., Galkina I., Mirkhuzina M., Sedov A., Kuchaev E., Islamov D. Phosphorus, Sulfur Silicon Relat. Elem. 2022, 197, 1-3. doi: 10.1080/10426507.2021.2021527
  6. Davletshin R., Gayneev A., Ermakova E., Davletshina N., Galkina I., Ivshin K., Shulaeva M., Pozdeev O. Mendeleev Commun. 2022, 32, 180-182. doi: 10.1016/j.mencom.2022.03.009
  7. Lima Y.R., Da Costa G.P., Xavier M.C.D.F., De Moraes M.C., Barcellos T., Alves D., Silva M.S. ChemistrySelect. 2020, 5, 12487-12493. doi: 10.1002/slct.202003761
  8. Kiss N.Z., Radai Z., Keglevich G. Phosphorus, Sulfur Silicon Relat. Elem. 2019, 194, 1-4. doi: 10.1080/10426507.2019.1630407
  9. Sampath S., Raju C.N., Rao C.V. Phosphorus, Sulfur Silicon Relat. Elem. 2016, 191, 95-99. doi: 10.1080/10426507.2015.1032412
  10. Kalla R.M.N., Lee H.R., Cao J., Yoo J.W., Kim I. New J. Chem. 2015, 39, 3916-3922. doi: 10.1039/C4NJ01695E
  11. Колодяжный О.И. Усп. хим. 2006, 75, 254-282. doi: 10.1070/RC2006v075n03ABEH001193
  12. Prechelmacher S., Mereiter K., Hammerschmidt F. Org. Biomol. Chem. 2018, 16, 3672-3680. doi: 10.1039/C8OB00419F
  13. Vincze D.A., Abranyi-Balogh P., Bagi P., Keglevich G. Molecules. 2019, 24, 3859. doi: 10.3390/molecules24213859
  14. Cytlak T., Skibinska M., Kaczmarek P., Kazmierczak M., Rapp M., Kubickia M., Koroniaka H. New J. Chem. 2018, 8, 11957-11974. doi: 10.1039/C8RA01656A
  15. Iorga B., Eymery F., Savignac P. Tetrahedron. 1999, 55, 13109-13150. doi: 10.1016/S0040-4020(99)00822-4
  16. Baccari Z., Sanhoury M.A.K., Crousse B., Barhoumi-Slimi T. Synth. Commun. 2018, 48, 1-7. doi: 10.1080/00397911.2018.1439175
  17. Desai J., Wang Y., Wang K., Malwal S.R., Oldfield E. ChemMedChem. 2016, 11, 1-12. doi: 10.1002/cmdc.201600343
  18. Zengxiang Z., Wanhua X., Yuxing G., Guo T., Yufen Z. Chem. Asian J. 2013, 8, 713-716. doi: 10.1002/asia.201201062
  19. Boobalan R., Chen C. Adv. Synth. Catal. 2013, 355, 3443-3450. doi: 10.1002/adsc.201300653

补充文件

附件文件
动作
1. JATS XML
下载

版权所有 © Russian Academy of Sciences, 2023