Zobrazeno 1 - 5
of 5
pro vyhledávání: '"A. S. Galiullina"'
Publikováno v:
European Proceedings of Social and Behavioural Sciences.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2a8469218d68f7413adc830a553c936
https://doi.org/10.15405/epsbs.2021.09.02.60
https://doi.org/10.15405/epsbs.2021.09.02.60
Autor:
A. D. Strel’nik, A. S. Galiullina, Vladimir V. Klochkov, A. A. Balandina, I. Z. Rakhmatullin, L. F. Galiullina, Yu. G. Shtyrlin, Marsel R. Garipov
Publikováno v:
Magnetic Resonance in Chemistry. 55:304-311
The conformational properties of three pyridoxine derivatives were studied by 1 H dynamic NMR spectroscopy. Conformational exchange caused by a rotation of 2-nytrophenyl group around one single C-C bond, of 2,4-dinitrophenyl substituent around two si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::290e359a776c9f45892efcc72f72a67a
https://doi.org/10.1002/mrc.4528
https://doi.org/10.1002/mrc.4528
Autor:
Yurii G. Shtyrlin, Albina S. Galiullina, Ekaterina I. Romanova, Konstantin V. Balakin, Olga A. Lodochnikova, Ruzalia M. Vafina, Roman S. Pavelyev
Publikováno v:
Tetrahedron Letters. 57:3902-3907
Experimental investigation of hexachlorocyclopentadiene [4+2]-cycloaddition to 2-substituted 4,7-dihydro-1,3-dioxepins revealed an atypical stereochemical effect. Clear experimental evidence was obtained that more bulky C2 substituents favour the the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed5dbbc9abcfd1aefc3ce10f465a0906
https://doi.org/10.1016/j.tetlet.2016.07.023
https://doi.org/10.1016/j.tetlet.2016.07.023
Autor:
Airat R. Kayumov, Konstantin V. Balakin, Oksana V. Bondar, Yurii G. Shtyrlin, Elena P. Mirchink, Sergey V. Sapozhnikov, Nikita V. Shtyrlin, Alexander A. Firsov, Elena B. Isakova, Albina S. Galiullina
Publikováno v:
BioMed Research International
ResearcherID
BioMed Research International, Vol 2016 (2016)
ResearcherID
BioMed Research International, Vol 2016 (2016)
A series of novel quaternary ammonium 4-deoxypyridoxine derivatives was synthesized. Two compounds demonstrated excellent activity against a panel of Gram-positive methicillin-resistantS. aureusstrains with MICs in the range of 0.5–2 μg/mL, exceed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2395c046dedbacfdcfec2f66e337835a
http://europepmc.org/articles/PMC5069379
http://europepmc.org/articles/PMC5069379
Autor:
I Z, Rakhmatullin, L F, Galiullina, A A, Balandina, M R, Garipov, A D, Strelnik, A S, Galiullina, Y G, Shtyrlin, V V, Klochkov
Publikováno v:
Magnetic resonance in chemistry : MRC. 55(4)
The conformational properties of three pyridoxine derivatives were studied by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::488df739400207c2d70850a0c43d5b16
https://pubmed.ncbi.nlm.nih.gov/27663994
https://pubmed.ncbi.nlm.nih.gov/27663994