Výsledky vyhledávání - "L. G Stolyarova"

The etiology of agents of infectious complications after transplantation of liver and kidneys and their resistance to antibiotics

Autor: D. G Akhaladze, T. S Spirina, T. B Safonova, M. N. Kornilov, L. G Stolyarova, O. A Savostyanova, N. I. Gabrielyan, E. M Gorskaya, I. E Tsirulnikova

Publikováno v: Medical Journal of the Russian Federation. 22:232-237

The study was carried out to investigate etiology and rate of prevalence of nosocomial strains of microbes in biosubstrates of patients in case of development of infectious complications and level of their resistance to various groups of antibiotics.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e2d793e9080884d10b842fa3ac6c1c1c
https://doi.org/10.18821/0869-2106-2016-22-5-232-237

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[THE SPECIES COMPOSITION OF AGENTS OF COMMUNITY-ACQUIRED INFECTIONS OF URINARY TRACTS AND SENSITIVITY OF MAIN UROPATHOGENS TO ANTIBACTERIAL PREPARATIONS IN MOSCOW IN 2013]

Autor: O Yu, Filimonova, L G, Stolyarova, S V, Sidorenko, I M, Rott, T I, Lysenko, T V, Narkhova, V A, Dmitrieva, G I, Golovenko, I V, Vlasova, T B, Safonova, L A, Taranenko

Publikováno v: Klinicheskaia laboratornaia diagnostika. 60(10)

The article presents the results of analysis of spectrum of agents of community-acquired infections of urinary tracts in Moscow The prevalence of resistance these infections to antibiotics applied in treatment of the mentioned pathology are considere

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4daab6320de96d9d8a4c5a0e22d9a46a
https://pubmed.ncbi.nlm.nih.gov/26841676

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ChemInform Abstract: O,N-Dimethylation of 5,6-Dihydroxynicotinic Acid

Autor: L. V. Gol'tsova, L. G. Stolyarova, A. I. Chernyshev, O. G. Kesarev, L. D. Smirnov

Publikováno v: ChemInform. 27

AnO,N-dialkylation product, 1-methyl-5-metlioxy-6-oxo-1,6-diliydropyridine-3 carboxylic acid, is formed in the reaction of 5,6-dihydroxynicotinic acid with dimethylsulfate.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::242b24fddb9397ebed3c732ea04219d6
https://doi.org/10.1002/chin.199649158

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Spectroscopic and quantum chemical study of the properties and structure of 5-hydroxy-benzimidazole

Autor: L. G. Stolyarova, S. L. Kuznetsov, B. E. Zaitsev, A. V. Gaevskaya, Yu. V. Kuznetsov, L. D. Smirnov

Publikováno v: Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:1200-1206

The MNDO method has been used to calculate the heats of formation of six tautomeric forms of 5-hydroxybenzimidazole (1), their anionic and cationic forms, as well as the energetic, electronic, and structural characteristics of neutral, protonated, an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1d67aefa8854e0d5c98a8460f9bea8da
https://doi.org/10.1007/bf00864182

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Basicity and structure of 5-hydroxybenzimidazoles in nitromethane

Autor: B. A. Korolev, L. A. Osmolovskaya, Yu. V. Kuznetsov, L. D. Smirnov, L. G. Stolyarova

Publikováno v: Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:333-336

Examination of the acid-base properties of 5-hydroxybenzimidazoles has shown them to exist in nitromethane as the 5-hydroxy-tautomers. Substituents in the 2-position have a predominantly inductive effect on the basicity of the 3-nitrogen, rationalize

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3fc015975ba9c039b6ad3c09c169fe90
https://doi.org/10.1007/bf00869526

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Study of the electrophilic substitution of alkyl-, aryl-, and aralkyl-5(6)-hydroxybenzimidazoles

Autor: Yu. V. Kuznetsov, L. G. Stolyarova, L. D. Smirnov, V. P. Lezina

Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:1716-1720

A series of new 4-sulfo-5(6)-hydroxybenzimidazoles was obtained including mono-, di-, and trinitro derivatives of 2-phenyl- and 2-benzyl-5-hydroxybenzimidazoles. Aromatic groups at C2, in contrast to alkyl groups, enhance the reactivity of the benzim

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ba132c887cf7653da61b9c5ad4b5a799
https://doi.org/10.1007/bf00961508

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Friedel-Crafts acylation of 5-hydroxybenzimidazole derivatives

Autor: Yu. V. Kuznetsov, L. D. Smirnov, M. M. Kazanskii, V. P. Lezina, L. G. Stolyarova

Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:1715-1717

The Friedel-Crafts acylation of 5-hydroxybenzimidazole and its 2-methyl and 1-ethyl-2-methyl derivatives proceeds exclusively at C4 and only with aliphatic acid derivatives.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aa662a65b388eef779749e56c8dc376a
https://doi.org/10.1007/bf01172282

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