Zobrazeno 1 - 10
of 17
pro vyhledávání: '"L. Z. Latypova"'
Autor:
A. M. Khabibrakhmanova, E. S. Rabbanieva, D. P. Gerasimova, O. A. Lodochnikova, L. Z. Latypova, A. R. Kurbangalieva
Publikováno v:
Učënye Zapiski Kazanskogo Universiteta. Seriâ Estestvennye Nauki, Vol 165, Iss 1 (2023)
Novel disulfinyl derivatives based on 3,4-dichloro-2(5H)-furanone, aliphatic dithiols, and monoterpene alcohols were synthesized. Chiral bis-thioethers in the molecules of which the dithiol fragment links two five-membered cycles at C4 atoms were obt
Externí odkaz:
https://doaj.org/article/b60ef11e40d74d8abbbd259e93bfc2b8
Autor:
Katsunori Tanaka, Ivan S. Smirnov, Kseniya S. Bulygina, Konstantin S. Usachev, Almira Kurbangalieva, Dilyara Chulakova, L. Z. Latypova, Ambara R. Pradipta, Danil R. Kuznetsov, Olga A. Lodochnikova
Publikováno v:
Chemistry – An Asian Journal. 14:4048-4054
The chiral substituted 1,5-diazacyclooctane (1,5-DACO) is of considerable importance and has attracted attention from a wide range of fields due to their unique chemical and biological properties. Despite the application potential, further study has
Publikováno v:
Russian Chemical Bulletin. 68:313-327
The anionoid elimination of the substituent from position 5 of the lactone ring is the predominant pathway of electrochemical reduction of 5-arylsulfanyl- and 5-arylsulfonyl-3,4-dichloro-2(5H)-furanones in acetonitrile. The contribution of the compet
Autor:
Aidar T. Gubaidullin, Almira Kurbangalieva, G. A. Chmutova, Olga A. Lodochnikova, Timur I. Madzhidov, L. Z. Latypova, Julia K. Voronina
Publikováno v:
CrystEngComm. 21:1499-1511
An original supramolecular motif has been found in one of two polymorphic modifications of (3,4-dichloro-2-oxo-2,5-dihydrofuran-5-ylsulfonyl)ethanoic acid: above and below the center of the classical carboxyl H-bonded dimer, the sulfonyl groups of tw
Autor:
Almira Kurbangalieva, Katsunori Tanaka, Ayumi Tsutsui, Dilyara Chulakova, L. Z. Latypova, Ivan V. Smirnov, Ambara R. Pradipta
Publikováno v:
BioNanoScience. 6(No. 4):364-367
Despite being fundamentally ubiquitous and important species in organic and bioorganic chemistry, the reactivities of N-alkyl-α,β-unsaturated imines have not been thoroughly explored due to their instability. Here, we describe novel reactivities of
Publikováno v:
BioNanoScience. 7:189-193
In order to optimize the study of the anti-inflammatory activity of novel drugs, in the current study, we used simple in vitro test system, which included osmotic and free radical hemolysis of human erythrocytes and human platelets aggregation, to sc
Autor:
I. Kh. Rizvanov, A. A. Kalinin, D. M. Rakov, L. Z. Latypova, Vladimir I. Morozov, Vakhid A. Mamedov, V. V. Yanilkin
Publikováno v:
Macroheterocycles. 9:34-45
Publikováno v:
Russian Chemical Bulletin. 64:2444-2453
The crystal structure of the known triclinic modification of mucochloric acid (MCA) was refined significantly, as well as its earlier unknown orthorhombic modification was discovered. In both forms, the compound is represented by two independent mole
Autor:
Timur I. Madzhidov, V. V. Yanilkin, Natalya V. Nastapova, V. A. Milyukov, R. P. Shekurov, Vladimir I. Morozov, G. R. Nasybullin, L. Z. Latypova
Publikováno v:
Russian Journal of Electrochemistry. 51:645-664
Based on ferrocene-1,1'-diyl-bisphosphinic acids Fc[P(R)(O)OH]2 (R = H, Me, Et, Ph) in methanol, two types of electrochemically driven molecular rotors are developed. Monoanions of acids are fixed in the cis-conformation due to the presence of an int
Autor:
Airat R. Kayumov, Mareike Klinger-Strobel, Mathias W. Pletz, Rawil Fakhrullin, Mikhail I. Bogachev, Oliwia Makarewicz, Elvira Rozhina, Diana R. Baidamshina, Maria N. Ryzhikova, Regina Sibgatullina, Irshad S. Sharafutdinov, L. Z. Latypova, Elena Y. Trizna, Almira Kurbangalieva, Alsu M Khabibrakhmanova
Publikováno v:
Frontiers in Microbiology, Vol 8 (2017)
The gram-positive opportunistic bacterium Staphylococcus aureus is one of the most common causatives of a variety of diseases including skin and skin structure infection or nosocomial catheter-associated infections. The biofilm formation that is an i