Zobrazeno 1 - 10
of 14
pro vyhledávání: '"O. A. Zasyadko"'
Autor:
S. I. Remizov, A. V. Andreev, S. A. Gabriel, I. V. Bochkareva, A. N. Perebeynos, O. V. Zasyadko
Publikováno v:
Кубанский научный медицинский вестник, Vol 31, Iss 5, Pp 100-111 (2024)
Background. Acute pancreatitis is recognized as a common disease, occasionally accompanied by the development of local complications that require surgical debridement. Rare complications of pancreatitis may occur in clinical practice, which is one of
Externí odkaz:
https://doaj.org/article/57fe1cb63c674abfa827b920a5e1a84e
Autor:
S. I. Remizov, A. V. Andreev, V. M. Durleshter, S. A. Gabriel, Yu. S. Kuznetsov, O. V. Zasyadko, G. A. Levchenko
Publikováno v:
Вестник хирургии имени И.И. Грекова, Vol 182, Iss 3, Pp 72-76 (2024)
The literature review considers the characteristics of local complications in the classifications of acute pancreatitis, as well as analyzed the effectiveness of modern methods of their diagnosis. Understanding the morphology of changes occurring in
Externí odkaz:
https://doaj.org/article/47eea93181cf4575bc5280ca20da1801
Autor:
A. V. Afonin, S. R. Buzilova, O. A. Zasyadko, A. K. Bogens, Yu. V. Brekhov, L. I. Vereshchagin
Publikováno v:
Chemistry of Heterocyclic Compounds. 25:1385-1389
The 1H- and 13C-NMR spectral parameters of N-vinyltetrazoles have been analyzed. It has been found that rotational isomerism is inherent to 1- and 2-vinyltetrazoles. A quantitative estimate of the ratio of rotational isomers has been made. In the cas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70b0131e01003447fd926a3e9fcf76db
https://doi.org/10.1007/bf00473869
https://doi.org/10.1007/bf00473869
Publikováno v:
Theoretical and Experimental Chemistry. 8:692-695
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e307a2ada893d0c18af8bba84d6a53b
https://doi.org/10.1007/bf00526973
https://doi.org/10.1007/bf00526973
Autor:
E. F. Shibanova, T. N. Vereshchagina, V. V. Makarskii, O. A. Zasyadko, Yu. L. Frolov, M. G. Voronkov, L. V. Sherstyannikova, Nina N. Chipanina, V. A. Lopyrev
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:569-572
3-Chloro- and 3-amino-1,2,4-triazole derivatives were subjected to a theoretical study by means of quantum-chemical calculation by the Pariser-Parr-Pople method. The experimentally observed electron transitions were assigned. The Cl atom and the NH2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81754c32d41952b84bc63dc5d09cda07
https://doi.org/10.1007/bf00473210
https://doi.org/10.1007/bf00473210
Publikováno v:
Journal of Applied Spectroscopy. 15:1377-1381
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3df9e8bd73cc122a024708cf3fbbe4be
https://doi.org/10.1007/bf00606781
https://doi.org/10.1007/bf00606781
Autor:
T. N. Vereshchagina, O. A. Zasyadko, L. V. Sherstyannikova, Nina N. Chipanina, M. G. Voronkov, Yu. L. Frolov, V. V. Makarskii, V. A. Lopyrev, E. F. Shibanova
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:441-443
The manifestation of acid-base interactions in the electronic absorption spectra of 32 1,2,4-triazole derivatives was studied. Ionization of the heteroring does not have a substantial effect on the energies of the electron transitions of 3-chloro-5-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2062458604d3d8f0df329f93358c8e53
https://doi.org/10.1007/bf00482794
https://doi.org/10.1007/bf00482794
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 27:615-617
The previously unknown bromomethyl- and iodomethylacetoxysilanes of general formula (CH3)3−nXCH2-Si(OCOCH3)n (X = Br, I, n = 1-3) were synthesized by reacting the appropriate chloromethylacetoxysilanes with LiBr, NaBr, or NaI in refluxing anhydrous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1012785876aa15c0ac97c5f2685bd04
https://doi.org/10.1007/bf00923958
https://doi.org/10.1007/bf00923958
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 17:2109-2111
1. Aroxyacetylenes, just like other acetylenic compounds, are inclined to form hydrogen bonds through the hydrogen of the acetylene group. 2. It is proposed that in the case of self-association of these molecules, the strength of the hydrogen bonds f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd0725bf09a13cf4f238c083428637ba
https://doi.org/10.1007/bf00904024
https://doi.org/10.1007/bf00904024
Autor:
O. A. Zasyadko, L. P. Ignat'eva, A. A. Stotskii, E. O. Tsetlina, M. G. Voronkov, O. G. Yarosh
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af4cafccb208bdccf650756de1ddd4c
https://doi.org/10.1002/chin.197831262
https://doi.org/10.1002/chin.197831262