Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rusalia M. Vafina"'
Autor:
Nikita V. Shtyrlin, Mikhail V. Pugachev, Sergey V. Sapozhnikov, Marsel R. Garipov, Rusalia M. Vafina, Denis Y. Grishaev, Roman S. Pavelyev, Renata R. Kazakova, Mariya N. Agafonova, Alfiya G. Iksanova, Svetlana A. Lisovskaya, Marina I. Zeldi, Elena S. Krylova, Elena V. Nikitina, Alina E. Sabirova, Airat R. Kayumov, Yurii G. Shtyrlin
Publikováno v:
Molecules, Vol 25, Iss 18, p 4341 (2020)
A series of 108 novel quaternary bis-ammonium pyridoxine derivatives carrying various substituents at the quaternary nitrogen’s and acetal carbon was synthesized. Thirteen compounds exhibited antibacterial and antifungal activity (minimum inhibitor
Externí odkaz:
https://doaj.org/article/3173c442871045d0a08a8fd0266eb676
Autor:
Roman S. Pavelyev, Rusalia M. Vafina, Konstantin V. Balakin, Oleg I. Gnezdilov, Aleksey B. Dobrynin, Olga A. Lodochnikova, Rashid Z. Musin, Galina A. Chmutova, Svetlana A. Lisovskaya, Liliya E. Nikitina
Publikováno v:
Journal of Chemistry, Vol 2018 (2018)
Synthesis of β-hydroxysulfides of 1,3-dioxepane series and their further functionalization were performed. Chiral β-hydroxysulfides were separated into enantiomers using enzymatic acylation by lipase PS. Study of antifungal activity of the obtained
Externí odkaz:
https://doaj.org/article/e8d01ec389d74868938a8c8626f57210
Autor:
E. N. Klimovitskii, Svetlana A. Lisovskaya, Rusalia M. Vafina, Roman S. Pavelyev, S. G. Gnevashev, Alexey B. Dobrynin, Liliya E. Nikitina, O. I. Gnezdilov
Publikováno v:
ChemInform. 43
Both the endo- and exo-isomers of epoxy acetals (II)/(III) are reacted with thiophenol to afford corresponding hydroxy sulfides, which are further transformed in search for new antimycotic substances.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8fe11aa22b9ddc6ad2799df6fa821f5
https://doi.org/10.1002/chin.201242184
https://doi.org/10.1002/chin.201242184
Autor:
Alexey B. Dobrynin, Rusalia M. Vafina, E. N. Klimovitskii, Svetlana A. Lisovskaya, O. I. Gnezdilov, S. G. Gnevashev, Liliya E. Nikitina, Roman S. Pavelyev
Publikováno v:
Mendeleev Communications. 22:127-128
Both exo- and endo-isomers of 4-phenyl-3,5,8-trioxabicyclo[5.1.0]octane were reacted with thiophenol to afford individual diastereomers of hydroxy sulfides which were further processed in search for new antimycotic substances.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4f4bf857aa3ce5e6058c386feb14f6f
https://doi.org/10.1016/j.mencom.2012.05.003
https://doi.org/10.1016/j.mencom.2012.05.003
Autor:
Vitaly Yu. Fedorenko, Rusalia M. Vafina, Rustam N. Baryshnikov, Yurii G. Shtyrlin, E. N. Klimovitskii
Publikováno v:
Mendeleev Communications. 17:170-171
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d8e1aad452312b8b1b69937996ae5f2
https://doi.org/10.1016/j.mencom.2007.05.013
https://doi.org/10.1016/j.mencom.2007.05.013