Zobrazeno 1 - 10
of 17
pro vyhledávání: '"L. P. Shamsutdinova"'
Publikováno v:
RUDN Journal of Ecology and Life Safety, Vol 0, Iss 4, Pp 63-69 (2012)
The article is devoted to the study of the morphological structure of solid waste on the example of Ufa. The problem of solid waste (MSW) of large cities is now urgent. Only if there is reliable information on the number of accumulated waste can effe
Externí odkaz:
https://doaj.org/article/efd765978c0d4d4ba45b05cd1e9d774f
Autor:
Yu. S. Kirillina, Rafail A. Khairullin, Mukattis B. Gazizov, L. P. Shamsutdinova, S. Yu. Ivanova
Publikováno v:
Russian Journal of General Chemistry. 90:84-88
The adduct of O, O-dialkyldithiophosphoric acid and enamine reacts exothermically with an electrophilic reagent. In the case of sulfenyl bromide, the iminium salt reduced at the C-Br bond and bis(dialkoxythiophosphorylthio)-disulfide have been formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f51aea2c4e9fbbad65f9755bfed7fbb4
https://doi.org/10.1134/s1070363220010120
https://doi.org/10.1134/s1070363220010120
Autor:
N. S. Tikhonova, L. P. Shamsutdinova, A. L. Pistsova, R. N. Burangulova, Mukattis B. Gazizov, R. F. Karimova, R. K. Ismagilov
Publikováno v:
Russian Journal of General Chemistry. 87:2891-2894
The addition of thioacetic acid to 2,6-di-tert-butyl-4-(phosphorylmethylidene)cyclohexa-2,5-dien-1-ones has been accomplished for the first time. The resulting adduct is readily hydrolyzed with hydrazine hydrate to give 2,6-di-tert-butyl-4-[phosphory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34671e08896e5256ab3de77a164eae32
https://doi.org/10.1134/s1070363217120246
https://doi.org/10.1134/s1070363217120246
Publikováno v:
Russian Chemical Bulletin. 65:2943-2947
A reaction of PIII acid esters with 2,6-di-tert-butyl-4-chloromethylidenecyclohexa-2,5-dienone leads to the formation of phosphorylated phosphorus ylides, 3,3’,5,5’-tetra-tert-butylstilbenequinone, and diphosphorylated sterically hindered phenols
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cb4323816868fb205ee611854d7dfaf
https://doi.org/10.1007/s11172-016-1682-7
https://doi.org/10.1007/s11172-016-1682-7
Autor:
R. N. Burangulova, R. F. Karimova, L. P. Shamsutdinova, R. K. Ismagilov, A. L. Tarakanova, Mukattis B. Gazizov
Publikováno v:
Russian Journal of General Chemistry. 86:326-330
New method for synthesis of phosphorylated methylene quinones via bromination of the sterically hindered phenol [prepared via benzylation of secondary chlorophosphines with 4-(methoxymethyl)-2,6-di-tert-butylphenol] with N-bromosuccinimide followed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6782f737670dbac26c1b21839843d41
https://doi.org/10.1134/s1070363216020213
https://doi.org/10.1134/s1070363216020213
Autor:
R. K. Ismagilov, L. P. Shamsutdinova, R. F. Karimova, R. N. Burangulova, Mukattis B. Gazizov, A. L. Pistsova
Publikováno v:
Russian Journal of General Chemistry. 87:1101-1103
The addition of alkanethiols, benzenethiol, and hetarenethiols to phosphorylated quinomethanes afforded P,S- and N,P,S-containing polyfunctional organic compounds as potential bactericidal agents.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd22c161cf768fa5a8f98e43c7b82f01
https://doi.org/10.1134/s107036321705036x
https://doi.org/10.1134/s107036321705036x
Autor:
S. Yu. Ivanova, L. P. Shamsutdinova, Mukattis B. Gazizov, R. F. Karimova, R. K. Ismagilov, R. N. Burangulova
Publikováno v:
Russian Journal of General Chemistry. 84:654-657
Reaction of (4-hydroxy-3,5-di-tert-butylphenyl)chloromethanediphenylchlorophosphonium chloride with trimethyl orthoformate affords (4-hydroxy-3,5-di-tert-butylphenyl)chloromethanediphenylphosphine oxide. The latter undergoes dehydrochlorination under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f7f0a276414fdfb979b11743fbb06b2
https://doi.org/10.1134/s1070363214040094
https://doi.org/10.1134/s1070363214040094
Publikováno v:
Russian Journal of General Chemistry. 82:212-216
The main stable products of the reactions 4-chloromethylene-2,6-di-tert-butylcyclohexa-2,5-dien-1-one with triethyl phosphite and ethyl diphenylphosphinite are the phosphorylated phosphorus ylides, 3,3′,5,5′-tetra-tert-butylstilbenequinone, and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8ceb32d4fb3ec2be1029efdee3ce241
https://doi.org/10.1134/s1070363212020089
https://doi.org/10.1134/s1070363212020089
Autor:
K. A. Nikitina, Mukattis B. Gazizov, R. K. Ismagilov, A. A. Bashkirtsev, L. P. Shamsutdinova, Oleg G. Sinyashin, Rashid Z. Musin, R. F. Karimova
Publikováno v:
Russian Journal of General Chemistry. 82:1587-1589
Received March 23, 2012 LETTERS TO THE EDITOR ISSN 1070-3632, Russian Journal of General Chemistry, 2012, Vol. 82, No. 9, pp. 1587–1589. © Pleiades Publishing, Ltd., 2012. Original Russian Text © M.B. Gazizov, R.K. Ismagilov, L.P. Shamsutdinova,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8660a4df32f6659e38ebad864ef357de
https://doi.org/10.1134/s1070363212090241
https://doi.org/10.1134/s1070363212090241
Autor:
R. K. Ismagilov, R. F. Karimova, Rashid Z. Musin, Mukattis B. Gazizov, L. P. Shamsutdinova, Oleg G. Sinyashin, A. A. Bashkirtsev
Publikováno v:
Russian Journal of General Chemistry. 80:533-535
The phosphorylated sterically hindered phenols and methylenequinones are potential inhibitors of oxidation of organic materials like polymers, petrochemical products, and biological systems [1–2]. In extension of studying the reaction of geminal po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2d741c2e966c101cfcb7e6f79f53be
https://doi.org/10.1134/s1070363210030278
https://doi.org/10.1134/s1070363210030278