Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Valentina V. Ilyushenkova"'
Autor:
Andrey V. Stepanov, Vladimir N. Yarovenko, Darina I. Nasyrova, Lyubov G. Dezhenkova, Igor O. Akchurin, Mickhail M. Krayushkin, Valentina V. Ilyushenkova, Andrey E. Shchekotikhin, Evgeny V. Tretyakov
Publikováno v:
Molecules, Vol 29, Iss 20, p 4966 (2024)
Gossypol and its derivatives arouse interest due to their broad spectrum of biological activities. Despite its wide potential application, there is no reported example of gossypol derivatives bearing stable radical functional groups. The first gossyp
Externí odkaz:
https://doaj.org/article/850fdfb4982a4c58bb38beb7163b7f2a
Autor:
Alexey S. Galushko, Valentina V. Ilyushenkova, Julia V. Burykina, Ruslan R. Shaydullin, Evgeniy O. Pentsak, Valentine P. Ananikov
Publikováno v:
Inorganics, Vol 11, Iss 6, p 260 (2023)
Understanding the interface between soluble metal complexes and supported metal particles is important in order to reveal reaction mechanisms in a new generation of highly active homogeneous transition metal catalysts. In this study, we show that, in
Externí odkaz:
https://doaj.org/article/e9b8a09ede844ce69be5270a8f1e6d73
Autor:
Anna D. Zinoveva, Tatiana N. Borisova, Alexander A. Titov, Valentina V. Ilyushenkova, Victor B. Rybakov, Elena A. Sorokina, Alexey V. Varlamov, Leonid G. Voskressensky
Publikováno v:
Synthetic Communications. 52:2311-2321
A convenient approach to the synthesis of 1-aroyl-3,4-dihydro-β-carbolines via Pictet–Spengler reaction has been developed. A variety of reagents, such as unsaturated aldehydes, ketones, maleic anhydride in the construction of functionally diverse
Autor:
Ananikov, Alexey S. Galushko, Valentina V. Ilyushenkova, Julia V. Burykina, Ruslan R. Shaydullin, Evgeniy O. Pentsak, Valentine P.
Publikováno v:
Inorganics; Volume 11; Issue 6; Pages: 260
Understanding the interface between soluble metal complexes and supported metal particles is important in order to reveal reaction mechanisms in a new generation of highly active homogeneous transition metal catalysts. In this study, we show that, in
Autor:
Daniil A. Boiko, Konstantin S. Kozlov, Julia V. Burykina, Valentina V. Ilyushenkova, Valentine P. Ananikov
Publikováno v:
Journal of the American Chemical Society. 144(32)
Mass spectrometry (MS) is a convenient, highly sensitive, and reliable method for the analysis of complex mixtures, which is vital for materials science, life sciences fields such as metabolomics and proteomics, and mechanistic research in chemistry.
Autor:
Valentina V. Ilyushenkova, Marina E. Zimens, Nikolay Yu Polovkov, Artyom P. Topolyan, Roman S. Borisov, Vladimir G. Zaikin
Publikováno v:
Talanta. 253:123922
This work highlights the efficient approach to highly sensitive determination of dipeptides that can present in biological liquids at very low and trace quantities. The approach involves preliminary derivatization of peptides with tris(2,4,6-trimetho
Autor:
Almira R. Miftyakhova, Matvey B. Sidakov, Tatiana N. Borisova, Valentina V. Ilyushenkova, Artem N. Fakhrutdinov, Elena A. Sorokina, Alexey V. Varlamov, Leonid G. Voskressensky
Publikováno v:
Tetrahedron Letters. 103:153991
Autor:
M. S. Slyundina, Valentina V. Ilyushenkova, A. P. Topolyan, Vladimir A. Korshun, Andrey A. Formanovsky, Maria A. Belyaeva, Roman S. Borisov
Publikováno v:
Analytical Methods. 9:6335-6340
The derivatization reagent was prepared in situ by the reaction of tris(2,6-dimethoxyphenyl)methylium hexafluorophosphate with N-(2-aminoethyl)maleimide and used for the modification of a number of low molecular weight thiols. The adducts were analyz
Autor:
Alexander V. Aksenov, Alexey V. Varlamov, Tatiana N. Borisova, Ekaterina A. Sokolova, Leonid G. Voskressensky, Viktor N. Khrustalev, Valentina V. Ilyushenkova, N. I. Guranova
Publikováno v:
Mendeleev Communications. 27:506-508
Cyanomethyl-substituted tetrahydroisoquinolines and tetrahydrothieno[3,2-c]pyridines were synthesized by multicomponent reaction of the dihydro analogues of aforesaid systems with benzyne and acetonitrile. The products obtained relate to alkaloids of
Autor:
Starkova Z; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninskiy Prosp., 119991 Moscow, Russia., Ilyushenkova V; N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prosp., 119991 Moscow, Russia., Polovkov N; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninskiy Prosp., 119991 Moscow, Russia., Voskressenskaya D; Institute of Medicine, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Str., 117198 Moscow, Russia., Pikovskoi I; Core Facility Center 'Arktika', Northern (Arctic) Federal University, 17 nab.Severnoy Dviny, 163002 Arkhangelsk, Russia., Tebenikhin M; Institute of Medicine, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Str., 117198 Moscow, Russia., Vtorushina E; V.I. Shpilman Research and Analytical Center for the Rational Use of the Subsoil, 2 Studencheskaya Str., 628007 Khanty-Mansiysk, Russia., Kanateva A; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninskiy Prosp., 119991 Moscow, Russia., Borisov R; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninskiy Prosp., 119991 Moscow, Russia.; Core Facility Center 'Arktika', Northern (Arctic) Federal University, 17 nab.Severnoy Dviny, 163002 Arkhangelsk, Russia.; Department of Plastics, D. Mendeleev University of Chemical Technology of Russia, 9 Miusskaya Pl., 125047 Moscow, Russia.; Organic Chemistry Department, Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Str., 117198 Moscow, Russia., Zaikin V; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29 Leninskiy Prosp., 119991 Moscow, Russia.
Publikováno v:
Molecules (Basel, Switzerland) [Molecules] 2022 Dec 06; Vol. 27 (23). Date of Electronic Publication: 2022 Dec 06.