Zobrazeno 1 - 9
of 9
pro vyhledávání: '"N. I. Burakov"'
Autor:
T. M. Zubareva, I. V. Kapitanov, T. M. Prokop’eva, V. A. Mikhailov, N. I. Burakov, V. L. Lobachev, B. V. Panchenko, M. K. Turovskaya
Publikováno v:
Russian Journal of Organic Chemistry. 53:351-358
Systems based on organic complexes of tribromide anion generate upon dissolution in water nucleophile–oxidant couple HOBr/BrO– and accelerate hydrolysis of ethyl 4-nitrophenyl ethylphosphonate, diethyl 4-nitrophenyl phosphate, and 4-nitrophenyl p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9c85b97fa24f006e3339ca17a71dd90
https://doi.org/10.1134/s107042801703006x
https://doi.org/10.1134/s107042801703006x
Autor:
A. N. Shendrik, N. I. Burakov, N. M. Khlestov, V. V. Odaryuk, I. D. Odaryuk, L. V. Kanibolotskaya
Publikováno v:
Russian Journal of General Chemistry. 84:268-271
Antiradical activity of 2-substituted 4-(1,3-thiazol-4-yl)-1,2-dihydroxybenzenes in the reaction with 1,1-diphenyl-2-picrylhydrazyl stable radical has been studied. Kinetic parameters of the process have been determined. Energy of homolytic dissosiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8204725d67989608b2cf74d1be4fec38
https://doi.org/10.1134/s1070363214020182
https://doi.org/10.1134/s1070363214020182
Autor:
N. I. Burakov, L. V. Kanibolotskaya, E. N. Poddubnaya, N. Yu. Lebedeva, A. L. Kanibolotskii, A. N. Shendrik, V. V. Odaryuk, I. D. Odaryuk
Publikováno v:
Pharmaceutical Chemistry Journal. 49:96-98
A series of dihydroxyphenylthiazoles were synthesized via the reaction of 4-(chloroacetyl)catechol with thioamide derivatives. Their antiradical activity was studied using the reaction with the cation-radical 2,2′-azinobis(3-ethylbenzothiazoline-6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee3f125ba2923fd354eff7105bf94f96
https://doi.org/10.1007/s11094-015-1229-5
https://doi.org/10.1007/s11094-015-1229-5
Publikováno v:
The journal of physical chemistry. A. 120(24)
The present work describes the structure and binding of adducts of N,N'-diacetylpiperazine with halogens and interhalogens based on combination of different experimental methods and quantum chemical calculations. On the basis of conductometric and sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::187069d3be093f7b2412d524984319dd
https://pubmed.ncbi.nlm.nih.gov/27228362
https://pubmed.ncbi.nlm.nih.gov/27228362
Autor:
N. I. Burakov, T. M. Prokop’eva, Anatolii F. Popov, V. A. Mikhailov, I. V. Kapitanov, V. A. Savelova, E. A. Karpichev, M. K. Turovskaya
Publikováno v:
Russian Journal of Organic Chemistry. 44:637-646
Bis(dialkylamide)hydrogen dibromobromates were synthesized and their reactivity was investigated in decomposition of diethylphosphonic, diethylphosphoric, and 4-toluenesulfonic acids 4-nitrophenyl esters. The nucleophilic reactivity of a typical α-n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af3b83e1a830c2f0199e0bdcd09043a9
https://doi.org/10.1134/s1070428008050011
https://doi.org/10.1134/s1070428008050011
Autor:
N. I. Burakov, E. A. Karpichev, T. M. Prokop’eva, A. L. Kanibolotskii, C. A. Bunton, M. K. Turovskaya, V. A. Savelova, V. A. Mikhailov, Anatolii F. Popov
Publikováno v:
Theoretical and Experimental Chemistry. 40:300-308
We have studied the nucleophilic and oxidative reactivity of the system HOBr/BrO−, in water and in the presence of different types of surfactants, relative to 4-nitrophenyldiethylphosphate, 4-nitrophenyl- 4´-toluenesulfonate (nucleophilic substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b6dc7d84f6a30368ccd6826b78795bf
https://doi.org/10.1023/b:thec.0000049076.85204.82
https://doi.org/10.1023/b:thec.0000049076.85204.82
Autor:
M. Yu. Zubritskii, V. A. Mikhailov, Victor B. Rybakov, Anatolii F. Popov, V. I. Kovalenko, L. G. Boboshko, N. I. Burakov, V. A. Savelova
Publikováno v:
Scopus-Elsevier
The structures of 1-benzoyl-3-(pyridin-2-yl)-thiocarbamide C13H11N3O1S1 (I) and 2-benzoylimino-1,2,4-thiadiazole[2,3-a]pyridine C13H9N3O1S1 (II) are studied by X-ray diffraction. Structures I [a = 5.342(4) A, b = 20.428(5) A, c = 11.784(4) A, β = 90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27f7b728d671056a8aa49ef2639ac554
https://doi.org/10.1134/1.1595182
https://doi.org/10.1134/1.1595182
Autor:
N. I. Burakov, V. A. Savelova, V. V. Kosmynin, V. A. Mikhailov, A. L. Kanibolotskii, G. Yu. Osichenko
Publikováno v:
Russian Journal of Organic Chemistry. 37:1210-1219
N,N-Dialkylcarboxamides react with halogens in the absence of water to form complexes which are likely to have an ionic structure with the Hlg+ ion coordinated at the carbonyl oxygen atom. These products can be isolated as individual compounds. Compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ea9ee17d9551c28a7be84aeca3a7a79
https://doi.org/10.1023/a:1013146630045
https://doi.org/10.1023/a:1013146630045
Autor:
G. Yu. Osichenko, A. L. Kanibolotskii, V. A. Savelova, N. I. Burakov, V. V. Kosmynin, V. A. Mikhailov
Publikováno v:
ChemInform. 33
N,N-Dialkylcarboxamides react with halogens in the absence of water to form complexes which are likely to have an ionic structure with the Hlg+ ion coordinated at the carbonyl oxygen atom. These products can be isolated as individual compounds. Compl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1de5271ea60677733c998daa7969d3e5
https://doi.org/10.1002/chin.200219026
https://doi.org/10.1002/chin.200219026