Zobrazeno 1 - 10
of 14
pro vyhledávání: '"N. O. Soboleva"'
Autor:
Yu. B. Evdokimenkova, N. O. Soboleva
Publikováno v:
Russian Chemical Bulletin. 67:1936-1941
The bibliometric analysis of scientific works on medicinal chemistry published over the last ten years is performed. The data obtained from the Web of Science Core Collection citation database suggest a decrease in the number of studies in the Europe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d94b1224ed7a5305192cd1366dd1172
https://doi.org/10.1007/s11172-018-2312-3
https://doi.org/10.1007/s11172-018-2312-3
Autor:
N. O. Soboleva, Yu. B. Evdokimenkova
Publikováno v:
Bibliotekovedenie [Library and Information Science (Russia)]. 67:291-298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a447d17526016839f5bf9c1df4da5e3
https://doi.org/10.25281/0869-608x-2018-67-3-291-298
https://doi.org/10.25281/0869-608x-2018-67-3-291-298
Autor:
Yu. B. Evdokimenkova, N. O. Soboleva
Publikováno v:
Russian Chemical Bulletin. 65:1648-1652
Bibliometric analysis of the journal Izvestiya Akademii Nauk. Seriya Khimicheskaya (Russian Chemical Bulletin) was carried out using international databases of scientific citation Web of Science and Scopus. It is shown that the publication has stable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbd7a89b130d5752181e52295d1b2619
https://doi.org/10.1007/s11172-016-1494-9
https://doi.org/10.1007/s11172-016-1494-9
Autor:
M. K. Grachev, Larisa K. Vasyanina, D. A. Shipilov, Elena N. Rasadkina, G. I. Kurochkina, N. O. Soboleva
Publikováno v:
Russian Journal of General Chemistry. 85:2605-2608
A possibility of the direct monoesterification of β-cyclodextrin with benzoic, p-aminobenzoic, 2-(4-isobutylphenyl)propionic, nicotinic, and isonicotinic acids was shown. Regioselectivity of substitution on the primary hydroxyl groups was confirmed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2e118f6810bc1083f0d7931aa9b7d7c
https://doi.org/10.1134/s107036321511016x
https://doi.org/10.1134/s107036321511016x
Autor:
M. K. Grachev, N. O. Soboleva, A. V. Edunov, G. I. Kurochkina, Larisa K. Vasyanina, E. E. Nifant'ev
Publikováno v:
Russian Chemical Bulletin. 61:181-187
New representatives of amphiphilic α-cyclodextrin derivatives containing residues of pharmacologically important acids both at the primary and secondary hydroxyl groups were synthesized using acyl chlorides of palmitic acid and a series of aromatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c01ba56842d58e4745f55ea5c65e79d
https://doi.org/10.1007/s11172-012-0025-6
https://doi.org/10.1007/s11172-012-0025-6
Autor:
Larisa K. Vasyanina, G. I. Kurochkina, N. O. Soboleva, M. K. Grachev, T. A. Batalova, A. A. Charaev, E. E. Nifant'ev
Publikováno v:
Russian Journal of General Chemistry. 81:2129-2135
Stable monomeric and dimeric inclusion compounds of β-cyclodextrin with binuclear guests containing the residues of some pharmacologically important aromatic monocarboxylic acids were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8e3b7be30ee9e9018a72a2e5ee80c0e
https://doi.org/10.1134/s1070363211100161
https://doi.org/10.1134/s1070363211100161
Publikováno v:
Russian Journal of General Chemistry. 75:1204-1207
Phosphorylation of β-cyclodextrin with protected primary hydroxy groups with tetraethylphosphorodiamidochloridite, contrary to phosphorylation with hexaethylphosphorous triamide, proceeds irregularly and leads to compounds with mixed functions, whos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d1778ef4ecc1ac4b50e0afaf6ed59ad
https://doi.org/10.1007/s11176-005-0396-6
https://doi.org/10.1007/s11176-005-0396-6
Publikováno v:
Russian Journal of General Chemistry. 75:49-52
Phosphorylation of 1,4:3,6-dianhydro-D-mannitol with diphenylphosphinous chloride provided a bisphosphinite derivative that, unlike what is observed in the phosphorylation with phosphorous chlorides and amides, undergoes fast phosphinite-phosphine ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b5d44d44646adaff3a5f610886cb70c
https://doi.org/10.1007/s11176-005-0171-8
https://doi.org/10.1007/s11176-005-0171-8
Autor:
Larisa K. Vasyanina, M. K. Grachev, G. I. Kurochkina, N. O. Soboleva, G. S. Bratash, E. E. Nifant'ev
Publikováno v:
Russian Journal of General Chemistry. 74:1616-1619
Controlled tosylation of 1,4:3,6-dianhydro-D-mannitol and -D-sobitol is studied. The nature of amines that act both as reaction activators and hydrogen chloride acceptors exerts a considerable effect on the ratio and structure of the resulting produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8d3b8315b719c6d932ffaae2d886a5b
https://doi.org/10.1007/s11176-005-0067-7
https://doi.org/10.1007/s11176-005-0067-7
Autor:
G. I. Kurochkina, V. K. Bel'skii, M. K. Grachev, Larisa K. Vasyanina, N. O. Soboleva, E. E. Nifant'ev
Publikováno v:
Russian Journal of General Chemistry. 73:903-908
A number of bis-phosphorylated 1,4:3,6-dianhydro-D-mannitol derivatives were synthesized. The increased steric loading of the phosphorus-containing residues in the compounds prepared gives rise to complicated 1H and 31P NMR spectra and magnetic noneq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52da9996785dfa6281563387f72b6f53
https://doi.org/10.1023/a:1026348701071
https://doi.org/10.1023/a:1026348701071