Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Arina V. Murashkina"'
Autor:
Arina V. Murashkina, Andrei V. Bogdanov, Alexandra D. Voloshina, Anna P. Lyubina, Alexandr V. Samorodov, Alexander Y. Mitrofanov, Irina P. Beletskaya, Elena A. Smolyarchuk, Kseniya A. Zavadich, Zulfiya A. Valiullina, Kseniya A. Nazmieva, Vladislav I. Korunas, Irina D. Krylova
Publikováno v:
Molecules, Vol 29, Iss 19, p 4764 (2024)
An approach to the synthesis of phosphoryl substituted spiro-1,3-dioxolane oxindoles was developed from the base-catalyzed reaction of various isatins with (3-hydroxyprop-1-yn-1-yl)phosphonates. It was found that various aryl-substituted and N-functi
Externí odkaz:
https://doaj.org/article/75e77c79b7644a14a90cfd1a39000c74
Autor:
Varvara I. Fomenko, Arina V. Murashkina, Alexei D. Averin, Anastasiya A. Shesterkina, Irina P. Beletskaya
Publikováno v:
Catalysts
Volume 13
Issue 2
Pages: 331
Volume 13
Issue 2
Pages: 331
Commercially available copper and copper (II) oxide nanoparticles (CuNPs and CuO NPs) were characterized using TEM and electronography methods to elucidate their true average size and composition. The catalytic amine arylation using unsupported coppe
Autor:
Arina V. Murashkina, Daria S. Kuliukhina, Alexei D. Averin, Anton S. Abel, Evgenii N. Savelyev, Boris S. Orlinson, Ivan A. Novakov, Carlos R.D. Correia, Irina P. Beletskaya
Publikováno v:
Mendeleev Communications. 32:91-93
Autor:
Olga A. Maloshitskaya, Boris S. Orlinson, S. P. Panchenko, M. S. Lyakhovich, A. D. Averin, A. S. Abel, E. N. Savelyev, Ivan A. Novakov, Arina V. Murashkina, Irina P. Beletskaya
Publikováno v:
Russian Journal of Organic Chemistry. 57:768-783
A comparative study of the catalytic efficiency of Pd(0) and Cu(I) complexes in the reactions of adamantanamines with fluoro- and trifluoromethyl-substituted 2-bromopyridines was carried out using previously optimized catalytic systems. It was shown
Autor:
Alexei D. Averin, Svetlana P. Panchenko, Arina V. Murashkina, Varvara I. Fomenko, Daria S. Kuliukhina, Anna S. Malysheva, Alexei A. Yakushev, Anton S. Abel, Irina P. Beletskaya
Publikováno v:
Catalysts. 13:831
Rapid development of the copper-catalyzed amination of aryl halides in the beginning of the 21st century, known as the Renaissance of the Ullmann chemistry, laid foundations for the use of this method as a powerful tool for the construction of the C(
Autor:
Alexander Yu. Mitrofanov, Arina V. Murashkina, Anna I. Barabanova, Alesya V. Vorozheykina, Yan V. Zubavichus, Alexey R. Khokhlov, Irina P. Beletskaya
Publikováno v:
Molecular Catalysis. 541:112915
Publikováno v:
Russian Journal of Organic Chemistry. 56:361-377
The review discusses recently published data on copper-catalyzed arylation of azoles with aryl halides with the formation of new C–N bonds. Ligand-free catalytic systems, recyclable catalysts, and the use of water as solvent are considered.
Autor:
Boris S. Orlinson, A. S. Abel, M. S. Lyakhovich, Olga A. Maloshitskaya, Irina P. Beletskaya, Arina V. Murashkina, E. N. Savelyev, Alexei D. Averin
Publikováno v:
Russian Journal of Organic Chemistry. 55:737-747
The catalytic efficiencies of palladium(0) and copper(I) complexes in the amination of 2-bromopyridine and its fluorine-containing derivatives with (1-adamantyl)methanamine and 2-(1-adamantyloxy)ethanamine were compared. Both types of catalytic syste
Autor:
Yuri K. Grishin, Irina P. Beletskaya, Arina V. Murashkina, Victor B. Rybakov, Alexander Yu. Mitrofanov
Publikováno v:
ChemistrySelect. 3:6810-6813
Autor:
Arina V. Murashkina, Francisco Alonso, Irina P. Beletskaya, Iris Martín-García, Alexander Yu. Mitrofanov
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
Transition-metal catalysed cross-coupling reactions are still dominated by palladium chemistry. Within the recent past, copper has gained ground against palladium by virtue of its cheaper price and equivalent function in certain reactions. Four catal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5689486dc1f3b061ae9ef3d8c942adcb
https://hdl.handle.net/10045/69955
https://hdl.handle.net/10045/69955