Zobrazeno 1 - 8
of 8
pro vyhledávání: '"I. A. Senyushkina"'
Autor:
G. I. Kurochkina, K. A. Lysenko, M. K. Grachev, I. A. Senyushkina, Larisa K. Vasyanina, E. E. Nifant'ev
Publikováno v:
Russian Journal of Organic Chemistry. 46:1506-1510
Stable host-guest complexes of a-cyclodextrin and its silyl derivative with some aromatic monocarboxylic acids of pharmacological interest were prepared. The structure of the a-cyclodextrin complex with nicotinic acid was studied by X-ray diffraction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1bde4586d898621cb4eb47bc7394505
https://doi.org/10.1134/s1070428010100118
https://doi.org/10.1134/s1070428010100118
Publikováno v:
Russian Journal of General Chemistry. 79:1831-1834
The ways for the practical preparation of stable inclusion complexes of β-cyclodextrin with dihydroxyphenols of various nature are developed. Mutual orientation of hydroxy groups and the nature of the bridge in the bisphenols are shown to affect con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aca3bc5519bfe452f64d8c7f4ea5b24
https://doi.org/10.1134/s1070363209090102
https://doi.org/10.1134/s1070363209090102
Autor:
Vitali A. Grinberg, T. A. Batalova, G. I. Kurochkina, I. A. Senyushkina, E. E. Nifant'ev, M. K. Grachev
Publikováno v:
Russian Journal of General Chemistry. 79:1167-1170
The practical pathways are proposed for the synthesis of cyclodextrins and some of their derivatives inclusion compounds with the “Ibuprofen“ remedy substrate. The effect of the cavity size, nature of the solvent and character and number of subst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46869d5628820b14562e297efde16899
https://doi.org/10.1134/s1070363209060231
https://doi.org/10.1134/s1070363209060231
Publikováno v:
Russian Journal of General Chemistry. 78:57-60
Inclusion compounds of β-cyclodextrin with hexane-1-ol and 1-(4-isobutylphenyl)propanoic acid were subjected to competitive phosphorylation with phosphorous diamidoester derived from 1,2-O-isopropylideneglycerol to show that the reactions occur unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62ad1ab9c721513d18a2effa1378841f
https://doi.org/10.1134/s1070363208010106
https://doi.org/10.1134/s1070363208010106
Publikováno v:
Russian Journal of General Chemistry. 78:61-64
Phosphorylation of secondary hydroxy groups in per-6-O-(tert-butyldimethylsilyl)-β-cyclodextrin with a phosphorous diamidoester is found to proceed, unlike phosphorylation of free β-cyclodextrin, at an elevated temperature and is accompanied by sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16b4ca8ac95aa47cd5a6d368cfd1682f
https://doi.org/10.1134/s1070363208010118
https://doi.org/10.1134/s1070363208010118
Publikováno v:
Russian Journal of General Chemistry. 76:1533-1536
Phosphorylation of β-cyclodextrin with trivalent phosphorus acid diamides in pyridine is found to proceed selectively at primary hydroxy groups under mild conditions (20°C) due to the supramolecular effect of the cyclodextrin cavity. The compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::297a180f22afaa8f5ce885d148c86ff4
https://doi.org/10.1134/s1070363206100045
https://doi.org/10.1134/s1070363206100045
Publikováno v:
Russian Journal of General Chemistry. 78:880-882
Phosphorylation of β-cyclodextin with substituted secondary hydroxy groups using 1,2-O,O′-isopropylideneglyceryl phosphorous diamide as a phosphorylating agent, in contrast to phosphorylation with trivalent phosphorus acid chlorides, is found to p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57a82628746f34c443a4d40747d72b17
https://doi.org/10.1134/s1070363208050071
https://doi.org/10.1134/s1070363208050071
Publikováno v:
Russian Journal of General Chemistry. 76:1679-1680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3b0566023fd66e6427a21c27cf0faf0
https://doi.org/10.1134/s107036320610032x
https://doi.org/10.1134/s107036320610032x