Zobrazeno 1 - 7
of 7
pro vyhledávání: '"O. M. Svechnikova"'
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 17, Iss 3, Pp 31-34 (2019)
Aim. To study the acid-base properties of derivatives of 2-(benzoylamino)(1-R-2-oxoindolin-3-ylidene)acetic acid substituted by the location 1 of oxoindolin fragment. Results and discussion. The compounds studied are weak acids, their strength decre
Externí odkaz:
https://doaj.org/article/a3425f52b7914e108c05497d4a8b43bf
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 17, Iss 2, Pp 33-37 (2019)
Aim. To study the reactivity of esters of 2-(benzoylamino)(1-R-2-oxoindoline-3-ylidene) acetic acids. Results and discussion. The reaction rate constants of alkaline hydrolysis of esters of 2-(benzoylamino) (1-R-2-oxoindoline-3-ylidene) acetic acids
Externí odkaz:
https://doaj.org/article/71c8660202974619a077ef7311a19cc6
Publikováno v:
Vìsnik farmacìï. :3-7
The studies in a series of 2-(benzoylamino)(1-R-2-oxoindoline-3-ylidene) acetic acids and their derivatives have shown that compounds of the isostructural series exhibit the nootropic, antihypoxic, anabolic activity. Aim. To study the reactivity of e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::912bf837af720fdf8c739ff9c5795c9f
https://doi.org/10.24959/nphj.18.2209
https://doi.org/10.24959/nphj.18.2209
Publikováno v:
Journal of Organic and Pharmaceutical Chemistry. 16:49-53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecb5c2a58e5c1384583a4072c8e9189f
https://doi.org/10.24959/ophcj.18.937
https://doi.org/10.24959/ophcj.18.937
Publikováno v:
Vìsnik farmacìï. :3-6
The study of the reactivity of substances allows optimizing the conditions of their synthesis and creating mathematical models of the “structure-biological activity” relationship that enable to carry out the targeted search of compounds with a sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5fb1ed98bd3975ca89fcf67db9439ab
https://doi.org/10.24959/nphj.17.2169
https://doi.org/10.24959/nphj.17.2169
Publikováno v:
Vìsnik farmacìï. :3-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b3759d01ab5f19ac1b7e2ddcd0d8f66
https://doi.org/10.24959/nphj.15.2050
https://doi.org/10.24959/nphj.15.2050
Publikováno v:
Vìsnik farmacìï. :12-14
The reactivity of substituted 5,7-dichloro-9-hydrazine acridine that exhibit various pharmacological activity by studying acid-base equilibria in the ethanol-water binary solvent (50 mol % ethanol) at 25 0 С using the method of potentiometric titrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07f36a67936417dc64a855c17fdc37ee
https://doi.org/10.24959/nphj.16.2060
https://doi.org/10.24959/nphj.16.2060