Zobrazeno 1 - 10
of 39
pro vyhledávání: '"R. Kh. Bagautdinova"'
Autor:
M. A. Pudovik, R. Kh. Bagautdinova, Alexander R. Burilov, Anna G. Strelnik, G. N. Aitbay, Lyudmila K. Kibardina
Publikováno v:
Russian Journal of General Chemistry. 90:1756-1759
The reactions of pyridoxal monoimine based on ortho-phenylenediamine with aliphatic aldehydes results in the formation of new C-alkyl-N-pyridoxylmethylbenzimidazoles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87971af98b058b6a9a078b256f51b54f
https://doi.org/10.1134/s1070363220090261
https://doi.org/10.1134/s1070363220090261
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:
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:
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
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
Publikováno v:
Russian Journal of General Chemistry. 85:1204-1206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c053ac8938e8235f6ac16463df7a817
https://doi.org/10.1134/s1070363215050370
https://doi.org/10.1134/s1070363215050370
Publikováno v:
Russian Journal of General Chemistry. 84:2283-2285
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d61a52273c316e7d3aff6c6db830a39
https://doi.org/10.1134/s1070363214110449
https://doi.org/10.1134/s1070363214110449
Autor:
R. M. Kamalov, G. A. Chmutova, N. A. Khailova, S. A. Terent'eva, R. Kh. Bagautdinova, Lyudmila K. Kibardina, A. N. Pudovik, M. A. Pudovik
Publikováno v:
Russian Journal of General Chemistry. 76:376-380
Silicon-containing chloromethylphosphorylated ureas undergo transformation involving evolution of chlorotrimethylsilane and formation of 1,3,4-oxazaphospholes. Their analogs, silicon-containing phosphorylated acylamides, transform in another way, viz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f665f0cb72a8e7c8104476cc8b763bd6
https://doi.org/10.1134/s1070363206030078
https://doi.org/10.1134/s1070363206030078
Autor:
R. Kh. Bagautdinova, Nail M. Azancheev, N. A. Khailova, Igor A. Litvinov, Sh. K. Latypov, Olga N. Kataeva, T. A. Zyablikova, E. A. Evgen’eva, M. A. Pudovik, Rashid Z. Musin, A. N. Pudovik
Publikováno v:
Russian Journal of General Chemistry. 76:381-390
Alcohols and α-hydroxyphosphonates undergo the addition to (chloromethyl)phosphonic(-phosphinic) iso(thio)cyanates, yielding phosphorylated (thio)urethanes. The latter undergo cyclization to form, depending on their structure, saturated or unsaturat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c0f01a4003002279c12d27ad8b9453
https://doi.org/10.1134/s107036320603008x
https://doi.org/10.1134/s107036320603008x
Autor:
A. N. Pudovik, V. V. Zverev, Igor A. Litvinov, Nail M. Azancheev, R. Kh. Bagautdinova, M. A. Pudovik, N. A. Khailova, G. A. Chmutova, Olga N. Kataeva
Publikováno v:
Russian Journal of General Chemistry. 75:359-369
New 1,3,2-thiazaphospholines were prepared, and their steric and electronic structures were examined. The steric and electronic structure of N-[(O-methyl)chloromethylthiophosphoryl]thiourea and the pathways of their intramolecular cyclization and rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dd2e707eb705a478e39aec14b973deb
https://doi.org/10.1007/s11176-005-0232-z
https://doi.org/10.1007/s11176-005-0232-z