Zobrazeno 1 - 10
of 37
pro vyhledávání: '"A. M. Pudovik"'
Autor:
E. M. Pudovik, R. H. Bagautdinova, M. A. Pudovik, Lyudmila K. Kibardina, Alexander R. Burilov
Publikováno v:
Russian Journal of General Chemistry. 89:2185-2189
The reactions of 4-methylpiperazin-1-amine, 2-amino- and 4-aminomethylpiperidines with pyridoxal afforded the corresponding azomethines. Their reactions with organic and inorganic acids lead to the formation of salt derivatives of pyridoxal azomethin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc1750f5153c8b96320f640435995460
https://doi.org/10.1134/s1070363219110033
https://doi.org/10.1134/s1070363219110033
Autor:
Alexander R. Burilov, E. M. Pudovik, Alexey V. Trifonov, M. A. Pudovik, Lyudmila K. Kibardina
Publikováno v:
Russian Journal of General Chemistry. 88:1918-1921
New nitrogen-containing derivatives of pyridoxal were obtained as a result of its reaction with various amines. The reactions with amines bearing a heterocyclic fragment (pyridine, pyrimidine, quinoline, piperidine) furnished the final products stabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e6d4078a810011aea3fb09aaa6a3892
https://doi.org/10.1134/s1070363218090268
https://doi.org/10.1134/s1070363218090268
Autor:
Lyudmila K. Kibardina, A. V. Trifonov, A. B. Dobrynin, A. R. Burilov, R. Kh. Bagautdinova, E. M. Pudovik, M. A. Pudovik
Publikováno v:
Russian Journal of Organic Chemistry. 54:578-581
New salt structures have been synthesized from pyridoxal and various organic and inorganic acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6c38f17cefac8893eb8c634069858c6
https://doi.org/10.1134/s1070428018040103
https://doi.org/10.1134/s1070428018040103
Autor:
A. V. Trifonov, E. M. Pudovik, M. A. Pudovik, Lyudmila K. Kibardina, Alexander R. Burilov, Yu. I. Ivanova
Publikováno v:
Russian Journal of General Chemistry. 88:41-47
The reaction of pyridoxal with 2,4-dihydroxybenzaldehyde in a hydrochloric acid solution gave 1-(5-formyl-2,4-dihydroxyphenyl)-7-hydroxy-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-5-ium chloride. Treatment of the latter with sodium hydride in ethanol aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::977eef2374963500c40e1158e9ba3a2c
https://doi.org/10.1134/s1070363218010073
https://doi.org/10.1134/s1070363218010073
Autor:
Alexander R. Burilov, S. A. Terent'eva, Alexey B. Dobrynin, E. M. Pudovik, R. Kh. Bagautdinova, Lyudmila K. Kibardina, M. A. Pudovik
Publikováno v:
Russian Journal of General Chemistry. 87:60-65
2-(2-Hydroxyaryl)imidazolidines were synthesized by reaction of aromatic carbonyl compounds with N,N′-dialkylethylenediamines. The title compounds were also prepared using the corresponding Schiff bases instead of carbonyl compounds. Phosphorylatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af15aebbc00748eb2c863a48ac0917ba
https://doi.org/10.1134/s107036321701011x
https://doi.org/10.1134/s107036321701011x
Publikováno v:
Chemistry of nitro compounds and related nitrogen-oxygen systems.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16de85a6217668bc5bb142111bfbf68a
https://doi.org/10.29003/m751.aks-2019/197-198
https://doi.org/10.29003/m751.aks-2019/197-198
Publikováno v:
Russian Journal of Organic Chemistry. 52:922-925
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::107c69881b2a3fb0c475067513a710b7
https://doi.org/10.1134/s1070428016060324
https://doi.org/10.1134/s1070428016060324
Publikováno v:
Russian Journal of General Chemistry. 86:745-748
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1327b50a566f8a126521dae65329b47d
https://doi.org/10.1134/s1070363216030415
https://doi.org/10.1134/s1070363216030415
Autor:
A. V. Trifonov, R. H. Bagautdinova, M. A. Pudovik, Alexander R. Burilov, Alexey B. Dobrynin, E. M. Pudovik, Lyudmila K. Kibardina
Publikováno v:
Russian Journal of General Chemistry. 86:607-612
Interaction of pyridoxal (3-hydroxy-5-hydroxymethyl-2-methylisonicotinaldehyde) with amines, mono- and disubstituted diamines led to the formation of compounds having in their structure imine, imidazolidine, and pyrimidine moieties. Structure of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae976e093f3897da439c2f978d518c10
https://doi.org/10.1134/s1070363216030178
https://doi.org/10.1134/s1070363216030178
Autor:
E. M. Pudovik, Alexander R. Burilov, Alexey V. Trifonov, R. Kh. Bagautdinova, Lyudmila K. Kibardina, M. A. Pudovik
Publikováno v:
Russian Journal of General Chemistry. 87:2097-2099
Reactions of pyridoxal with benzoic acid and its derivatives in alcoholic medium afforded alkoxyfuropyridinium salts with potential biological activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccd81d2b8f0ecb2aa3abe3a5bddfacaf
https://doi.org/10.1134/s1070363217090298
https://doi.org/10.1134/s1070363217090298