Zobrazeno 1 - 10
of 21
pro vyhledávání: '"V P, Gubskaya"'
Autor:
I. T. Khairutdinov, V. P. Gubskaya, R. B. Zaripov, I. A. Nuretdinov, G. M. Fazleeva, Liliya N. Islamova
Publikováno v:
Applied Magnetic Resonance. 53:979-988
Methano[60]fullerenes with two and four nitroxide radicals are studied by EPR spectroscopy. It is shown that nitroxide derivatives of fullerene C60 undergo conformational changes in liquid solution. It is established that transitions between the two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bcabb1fe58f2ddceb2306b2a75863a1
https://doi.org/10.1007/s00723-021-01419-x
https://doi.org/10.1007/s00723-021-01419-x
Autor:
I. A. Nuretdinov, V. P. Gubskaya, Sh. K. Latypov, G. M. Fazleeva, I. E. Ismaev, F. G. Sibgatullina, Yu. Ya. Efremov, K. L. Nodov
Publikováno v:
Russian Chemical Bulletin. 56:1843-1848
Reactions of fullerene C60 with fluorene-2-carbaldehyde or 2,7-diacetylfluorene in toluene gave novel spiromethanofullerenes containing a reactive free formyl group. A novel fluorene-containing fullerenopyrrolidine was obtained by the Prato reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8073b2fc6f688ae3f0fd284aa543c2bf
https://doi.org/10.1007/s11172-007-0286-7
https://doi.org/10.1007/s11172-007-0286-7
Autor:
I. A. Nuretdinov, Vitaliy V. Yanilkin, A. V. Toropchina, V. P. Gubskaya, F. G. Sibgatullina, Vladislav V. Zverev, Nail M. Azancheev, Vladimir I. Morozov
Publikováno v:
Russian Chemical Bulletin. 54:1467-1472
The reactions of fullerene C60 with substituted haloketones, including organophosphorus haloketones, in the presence of bases afforded new methanofullerenes containing carbonyl or carbonyl and acetal groups. The structures of the resulting compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b662e2d1d78f42a8b0ec49751bb545
https://doi.org/10.1007/s11172-005-0428-8
https://doi.org/10.1007/s11172-005-0428-8
Autor:
E. Kh. Kazakova, Igor S. Antipin, A. I. Konovalov, V. P. Gubskaya, V. V. Skripacheva, Margit Gruner, S. E. Solv\\'eva, A. R. Mustafina, W. D. Habicher
Publikováno v:
Russian Chemical Bulletin. 53:1511-1519
The structures and stability of outer-sphere associates of sulfonate derivatives of thiacalix[4]arene and calix[4]resorcinarene with coordinatively saturated cobalt(iii) bis- and tris-chelates ([Co(L-His)2]+, [Co(en)2ox]+, [Co(en)3]3+, and [Co(dipy)3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faca5f55951b7fec1a7257bffa1eb072
https://doi.org/10.1023/b:rucb.0000046249.10018.db
https://doi.org/10.1023/b:rucb.0000046249.10018.db
Autor:
R. G. Gasanov, V. V. Zverev, V. I. Sokolov, Vasily V. Bashilov, L. Sh. Berezhnaya, V. P. Gubskaya, I. A. Nuretdinov, Boris Tumanskii
Publikováno v:
Russian Chemical Bulletin. 52:380-384
The rate constants for the addition of the OP·(OPri)2, Me3C·, and Me(CH2)3·CH2 radicals to the methano[60]fullerenes C60CX1X2 (X1 = X2 = CO2Et; X1 = CO2Me, X2 = OP(OMe)2; X1 = X2 = OP(OEt)2) were determined by ESR spectroscopy. Methanofullerenes a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ced7ebeeb8050bb53a64572cabd53b8
https://doi.org/10.1023/a:1023458816201
https://doi.org/10.1023/a:1023458816201
Autor:
V. P. Gubskaya, F. G. Sibgatullina, G. M. Fazleeva, Nina P. Konovalova, I. P. Karaseva, I. A. Nuretdinov, L. Sh. Berezhnaya
Publikováno v:
Russian Chemical Bulletin. 51:1723-1726
New fullerenopyrrolidines were synthesized by the three-component reactions of fullerene C60, N-methylglycine, and aromatic aldehydes, viz., N,N-bis(2-chloroethyl)-4-aminobenzaldehyde, N-(2-chloroethyl)-N-methyl-4-aminobenzaldehyde, indole-3-carbalde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7766660bcb8a85326cd53017353f1d85
https://doi.org/10.1023/a:1021363808113
https://doi.org/10.1023/a:1021363808113
Autor:
I. A. Nuretdinov, L. Sh. Berezhnaya, F. G. Sibgatullina, V. P. Gubskaya, Vladislav V. Zverev, I. P. Karaseva, G. M. Fazleeva, N. I. Shishikina
Publikováno v:
Russian Chemical Bulletin. 51:337-341
The reactions of carbanions of bis(dialkoxyphosphoryl)bromomethanes with fullerenes C60 and C70 afforded new bis(dialkoxyphosphoryl)methanofullerenes C60 and C70, respectively, whose structures were established by spectroscopic methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::357adbcae726e3ca649a9c95f9176d8c
https://doi.org/10.1023/a:1015472114103
https://doi.org/10.1023/a:1015472114103
Autor:
F. G. Sibgatullina, R. R. Shagidullin, V. P. Gubskaya, A. V. Il'yasov, Vakhid A. Mamedov, R. M. Gainullin
Publikováno v:
Chemistry of Heterocyclic Compounds. 30:1029-1033
Substituted anilides of 1,4-dithiene- and oxathienecarboxylic acids were synthesized. It was shown that the reaction of 3-phenyl-1,4-dithi-2-ene-2-carboxyl chloride with 2-aminopyridines, depending on the base used and the reaction conditions, leads
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee5ee60c4d12c32da97b862a455accaa
https://doi.org/10.1007/bf01171157
https://doi.org/10.1007/bf01171157
Publikováno v:
ChemInform. 32
The reactions of fullerene C60 with bromo(dimethoxyphosphoryl)acetates in the presence of NaH in toluene afforded alkoxycarbonyl(dimethoxyphosphoryl)methanofullerenes whose structures were established by UV, IR, and 1H, 13C, and 31P NMR spectroscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a192af535944f54eb7fd5aa39c2a6027
https://doi.org/10.1002/chin.200128107
https://doi.org/10.1002/chin.200128107
Autor:
L. Sh. Berezhnaya, I. P. Karaseva, F. G. Sibgatullina, N. I. Shishikina, V. P. Gubskaya, Vladislav V. Zverev, I. A. Nuretdinov, G. M. Fazleeva
Publikováno v:
ChemInform. 33
The reactions of carbanions of bis(dialkoxyphosphoryl)bromomethanes with fullerenes C60 and C70 afforded new bis(dialkoxyphosphoryl)methanofullerenes C60 and C70, respectively, whose structures were established by spectroscopic methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67bbad9a6e38158a9444a74ac2e468f5
https://doi.org/10.1002/chin.200237103
https://doi.org/10.1002/chin.200237103