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pro vyhledávání: '"Odinokov Viktor N"'
Akademický článek
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Publikováno v:
In Mendeleev Communications 2006 16(2):90-92
Autor:
Rezeda R. Khalitova, Rinat R. Gubaidullin, Darya A. Nedopekina, Yuriy P. Bel’skii, Veniamin A. Khazanov, Anna Yu. Spivak, Odinokov Viktor N, Natalia V. Bel’skaya
Publikováno v:
Medicinal Chemistry Research. 26:518-531
A series of lupane triterpenoid conjugates with the triphenylphosphonium cation, in which the terpenoid molecules are linked to one or two triphenylphosphonium moieties at the С-2, С-28, or С-30 positions by carbon–carbon or ester bonds, have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::596b7c060ebe1f620686aaa7cdba439d
https://doi.org/10.1007/s00044-016-1771-z
https://doi.org/10.1007/s00044-016-1771-z
Autor:
Odinokov Viktor N, Dilyara I. Araslanova, Tatyana V. Tyumkina, Ponedelkina Irina Yu, E. S. Lukina
Publikováno v:
Starch - Stärke. 66:444-449
Partially oxidized starches were obtained by oxidation of water-soluble potato starch with the NaOCl/2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) system in the absence of bromide in aqueous solutions at pH 10.2. Monosaccharide composition of the oxid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63603553d519c1db369237f446e300bf
https://doi.org/10.1002/star.201300130
https://doi.org/10.1002/star.201300130
Publikováno v:
Russian Journal of Organic Chemistry. 47:290-294
Based on the catalyzed by lipase Amano PS kinetic separation of the two-component mixture of diastereomers of (2RS,6R,10R)-6,10,14-trimethylpentadecan-2-ol in the acylation with the succinic anhydride we obtained the (2R,6R,10R)-6,10,14-trimethylpent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8d1b912bacffc51b36f9f32897d6594
https://doi.org/10.1134/s1070428011020217
https://doi.org/10.1134/s1070428011020217
Publikováno v:
Russian Journal of Organic Chemistry. 45:1464-1467
Hydroxycyclopropanation at the ester group in the series of lupane triterpenoids was performed for the first time using 3,3-ethylenedioxybetulonic acid methyl ester and its 20,29-dihydro analog as substrates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b06502a22c763e3408f2630eec9d2c94
https://doi.org/10.1134/s1070428009100078
https://doi.org/10.1134/s1070428009100078
Autor:
Leonard M. Khalilov, M. Yu. Antipin, D. V. Nedopekin, G. F. Krainova, Ivan V. Glukhov, R. G. Savchenko, Aleksander G. Tolstikov, Odinokov Viktor N, Vladimir A. Glushkov
Publikováno v:
Russian Chemical Bulletin. 58:1991-1995
Ozonation of N-acyl-4-phenyl-3a,4,5,9b-tetrahydro-3 H-cyclopenta[ c]quinoline gave stable ozonides: a conformationally mobile isomer with the pseudoequatorial N-acyl group and a conformationally stable isomer with the pseudoaxial N-trifluoroacetyl gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84e2886cef611c1e326665c6c0393198
https://doi.org/10.1007/s11172-009-0272-3
https://doi.org/10.1007/s11172-009-0272-3
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
The modern state of chemical modification of hyaluronic acid, chondroitin sulfates, and heparin is considered, and the possible application of modified glycosaminoglycans as potential drugs is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd0e66354f11203b22cd0d5446e161f1
https://doi.org/10.1134/s1068162008010019
https://doi.org/10.1134/s1068162008010019
Akademický článek
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Autor:
Leonard M. Khalilov, Vadim V. Kachala, A. S. Shashkov, Odinokov Viktor N, S. R. Afon’kina, R. G. Savchenko, R. V. Shafikov
Publikováno v:
Scopus-Elsevier
The 6-oxo group in 2,3:20,22-di-O-isopropylidene derivatives of 20-hydroxyecdysone and its 24,25/25,26-anhydro analog is reduced with NaBH4-CeCl3 in a stereoselective fashion to afford the corresponding 6α-alcohols. In the first case, the reaction i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aa3c146ccb2b903623bdf5673fd55e9
https://doi.org/10.1007/s11178-005-0338-0
https://doi.org/10.1007/s11178-005-0338-0