Zobrazeno 1 - 10
of 16
pro vyhledávání: '"I. S. Nazarov"'
Autor:
Zh. D. Kobalava, I. S. Nazarov
Publikováno v:
Kardiologiia. 63:66-76
A qualitative change in the risk profile after an episode of decompensated heart failure (HF) calls for an as immediate as possible therapeutic response. In the absence of uniform guidelines for the sequence and timing of administering the background
Autor:
G. F. Sakhautdinova, I. M. Sakhautdinov, I. S. Nazarov, A. G. Mustafin, V. I. Vinogradova, M. S. Yunusov
Publikováno v:
Chemistry of Natural Compounds. 58:903-907
Autor:
E. V. Reznik, N. M. Dubinin, E. Khalatova, I. S. Nazarov, V. A. Kac, L. V. Brilyov, A. S. Dvornikov
Publikováno v:
Kardiologiia. 62:73-76
In cardiological practice, there may be patients with chest pain and heart failure of a specific etiology, including an association with cardiovascular syphilis. This article describes a 49-year patient with chest pain, heart failure, and neurologica
Publikováno v:
Russian Journal of Organic Chemistry. 55:47-73
Publikováno v:
Russian Journal of Organic Chemistry. 54:1122-1126
Reactions were studied of peroxide ozonolysis products obtained from linear and cyclic alkenes with hydroxylamine prepared in situ from NH2OH·HCl by hydrogen chloride neutralization with sodium acetate. A one-pot reactions sequence was performed: al
Publikováno v:
Russian Journal of Organic Chemistry. 54:51-54
A one-pot procedure has been developed for the synthesis of phenylhydrazones by ozonolysis of olefins in methanol at 0°C and subsequent reduction of peroxide intermediate with excess 1: 2 mixture of phenylhydrazine hydrochloride and sodium acetate.
Autor:
I. S. Nazarov, N. M. Ishmuratova, L. R. Garifullina, A. A. Kravchenko, Yu. V. Legostaeva, G. Yu. Ishmuratov
Publikováno v:
Chemistry of Natural Compounds. 53:891-894
Tosylhydrazide was shown to be an effective reductant in protic solvents for the peroxide ozonolysis products of ∆3-carene, (–)-α-pinene, and (S)-limonene. Either α,ω-ditosylhydrazones or α,ω-ketotosylhydrazonoacids were formed depending on
Publikováno v:
Russian Journal of Organic Chemistry. 54:146-148
Optically active isoniazid derivatives containing a cyclopropane or cyclobutane fragment have been synthesized by ozonolysis of (+)-Δ3-carene and (–)-α-pinene, followed by treatment of the ozonolysis products with isonicotinic acid hydrazide.
Autor:
I. S. Nazarov, R. M. Khalikov, Marina P. Yakovleva, L. P. Botsman, Yu. V. Legostaeva, L. R. Garifullina, G. Yu. Ishmuratov
Publikováno v:
Russian Journal of Applied Chemistry. 88:935-940
Transformations of peroxy products formed by ozonolysis of undecylenic acid derivatives (methyl ester and hydride reduction product, 10-undecen-1-ol) in various protic and aprotic solvents (MeOH, PriOH, tetrahydrofuran, 1: 5 AcOH–CH2Cl2 mixture), o
Autor:
G. Yu. Ishmuratov, Marina P. Yakovleva, Yu. V. Legostaeva, D. V. Baidimirov, L. P. Botsman, I. S. Nazarov
Publikováno v:
Russian Journal of Organic Chemistry. 51:610-614
Peroxide products of oleic acid ozonolysis treated with semicarbazide and hydroxylamine hydrochlorides in methanol are predominantly converted into methyl nonanoate and dimethyl nonanedioate, in 2-propanol, into isopropyl nonanoate and monoisopropyl