Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Yulia B. Malysheva"'
Autor:
Yulia L. Kuznetsova, Ksenya S. Gushchina, Karina S. Lobanova, Victoria O. Chasova, Marfa N. Egorikhina, Alexandra O. Grigoreva, Yulia B. Malysheva, Daria A. Kuzmina, Ekaterina A. Farafontova, Daria D. Linkova, Yulia P. Rubtsova, Luydmila L. Semenycheva
Publikováno v:
Polymers, Vol 15, Iss 12, p 2618 (2023)
Polymerization of methyl methacrylate (MMA) in aqueous collagen (Col) dispersion was studied in the presence of tributylborane (TBB) and p-quinone: 2,5-di-tert-butyl-p-benzoquinone (2,5-DTBQ), p-benzoquinone (BQ), duroquinone (DQ), and p-naphthoquino
Externí odkaz:
https://doaj.org/article/c8b1811ba892400a9da306673e74ffc9
Autor:
Ksenia V. Otvagina, Alexey A. Maslov, Diana G. Fukina, Anton N. Petukhov, Yulia B. Malysheva, Andrey V. Vorotyntsev, Tatyana S. Sazanova, Artem A. Atlaskin, Alexander A. Kapinos, Alexandra V. Barysheva, Sergey S. Suvorov, Ivan D. Zanozin, Egor S. Dokin, Ilya V. Vorotyntsev, Olga V. Kazarina
Publikováno v:
Membranes, Vol 13, Iss 6, p 539 (2023)
The current investigation is focused on the development of composite membranes based on polymeric ionic liquids (PILs) containing imidazolium and pyridinium polycations with various counterions, including hexafluorophosphate, tetrafluoroborate, and b
Externí odkaz:
https://doaj.org/article/3176586a916f43448cfe322a9a50cd93
Autor:
Iuliia A. Gracheva, Elena V. Svirshchevskaya, Ekaterina S. Shchegravina, Yulia B. Malysheva, Alsu R. Sitdikova, Alexey Yu. Fedorov
Publikováno v:
Pharmaceutics, Vol 15, Iss 4, p 1034 (2023)
A series of novel heterocyclic colchicine derivatives bearing a C-7 methylene fragment were synthesized via Wittig, Horner–Wadsworth–Emmons and Nenajdenko–Shastin olefination approaches. The in vitro biological activities of the most promising
Externí odkaz:
https://doaj.org/article/b4340d9791064e65afca17c8a9af43a3
Autor:
Anastasiya M. Zimina, Nikolay V. Somov, Yulia B. Malysheva, Nadezhda A. Knyazeva, Alexander V. Piskunov, Ivan D. Grishin
Publikováno v:
Inorganics, Vol 10, Iss 11, p 206 (2022)
A class of so-called POP ligands (Xanthos, NiXantphos, DPEphos) are of a great interest to the coordination chemistry due to their wide P-M-P bite angles and ability to show either κ2- or κ3-binding modes. Such κ2–κ3-rearrangement is valuable f
Externí odkaz:
https://doaj.org/article/7b99a385ec244518a56fbaf7d88a436e
Autor:
Semenycheva, Yulia L. Kuznetsova, Ksenya S. Gushchina, Karina S. Lobanova, Victoria O. Chasova, Marfa N. Egorikhina, Alexandra O. Grigoreva, Yulia B. Malysheva, Daria A. Kuzmina, Ekaterina A. Farafontova, Daria D. Linkova, Yulia P. Rubtsova, Luydmila L.
Publikováno v:
Polymers; Volume 15; Issue 12; Pages: 2618
Polymerization of methyl methacrylate (MMA) in aqueous collagen (Col) dispersion was studied in the presence of tributylborane (TBB) and p-quinone: 2,5-di-tert-butyl-p-benzoquinone (2,5-DTBQ), p-benzoquinone (BQ), duroquinone (DQ), and p-naphthoquino
Autor:
Alexander A. Kaltenberg, Dmitry L. Vorozhtsov, Ivan D. Grishin, Nikolay V. Somov, Yulia B. Malysheva
Publikováno v:
European Journal of Inorganic Chemistry. 2021:4868-4874
Publikováno v:
Journal of Heterocyclic Chemistry. 57:2769-2781
Publikováno v:
European Journal of Organic Chemistry. 2019:6830-6837
Aiming at the development of novel protease-triggered CO-releasing molecules (PT-CORMs) we designed a series of oxycyclohexadiene-Fe(CO)(3) complexes, which are connected through a self-immolative linker with a plasmin-specifying peptide unit. The ch
Autor:
Alexander A. Kaltenberg, Yulia B. Malysheva, Alexander V. Piskunov, Nikolay V. Somov, Ivan D. Grishin, Nadezhda A. Knyazeva
Publikováno v:
Journal of Organometallic Chemistry. 917:121291
Novel complexes of ruthenium with tridentate phosphine ligands: tris(diphenylphosphinomethyl)ethane and bis(2-diphenylphosphinoethyl)phenylphosphine were synthethised starting from the well-known exo-nido-ruthenacarborane [exo-5,6,10-{Ru(Ph3P)2Cl}-5,
Publikováno v:
Synlett. 23:1205-1208
A series of novel combretastatin A-4 analogues was synthesized in 36–64% yields by Negishi cross-coupling reaction under mild conditions. The prepared compounds exhibit good cytotoxicity against HBL100 epithelial cell lines (IC50 = 0.022–10.31 µ