Zobrazeno 1 - 10
of 16
pro vyhledávání: '"A. V. Zuraev"'
Autor:
Vladislav A. Budevich, Sergei V. Voitekhovich, Alexander V. Zuraev, Vadim E. Matulis, Vitaly E. Matulis, Alexander S. Lyakhov, Ludmila S. Ivashkevich, Oleg A. Ivashkevich
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 385-395 (2021)
Tetrazolium-5-aminides have been prepared by the tert-butylation of 5-aminotetrazole and its N-methyl derivatives by the t-BuOH/HClO4 system followed by the treatment of the tetrazolium salts by alkali. The mesoionic compounds have been found to show
Externí odkaz:
https://doaj.org/article/4aaefbff75a74d36af0b57beed206cbc
Autor:
Vitaly E. Matulis, Ekaterina G. Ragoyja, Alexander V. Zuraev, Yuri V. Grigoriev, Oleg A. Ivashkevich
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 19-31 (2020)
The structure of copper(II) poly-5-vinyltetrazolate and the products of its thermolysis has been studied by means of density functional theory and infrared spectroscopy. Copper(II) poly-5-vinyltetrazolate has been obtained and subsequently subjected
Externí odkaz:
https://doaj.org/article/2166afd42c9f4b46b78bfc28e8b664a9
Autor:
Cyril M. Verbilo, Alexander V. Zuraev, Yuri V. Grigoriev, Vladislav A. Budevich, Oleg A. Ivashkevich
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 48-63 (2020)
The target for antibacterial action of 1,4-di- and 1,4,5-trisubstituted 1H-1,2,3-triazoles against E. coli ATCC 25922 and S. aureus ATCC 6538 was proposed. Structures of target proteins and investigated triazoles were built using molecular modeling.
Externí odkaz:
https://doaj.org/article/502ba7fb953941ccaf6bf1db912bb88a
Autor:
Olga S. Scherbakova, Yuri V. Grigoriev, Alexander V. Zuraev, Inna M. Grigorieva, Oleg A. Ivashkevich
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 45-50 (2019)
Optimization of the method for the synthesis of methylated poly-5-vinyltetrazole was carried out and it was shown that the process of its preparation, both with the homopolymer acrylonitrile and the commercially available copolymer with methyl acryla
Externí odkaz:
https://doaj.org/article/de6f96b1867845d4ab9afde090d9224b
Autor:
Alexander V. Zuraev, Yuri V. Grigoriev, Inna M. Grigorieva, Lyubov I. Pan’ko, Ludmila S. Ivashkevich, Alexander S. Lyakhov, Oleg A. Ivashkevich
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 67-75 (2018)
The method for synthesis of copper poly-5-vinyltetrazole salt (Cu-PVT) which based on interaction between the aqueous solutions of sodium poly-5-vinyltetrazolate and Сu(NO3)2 was developed. By using of the solutions of Сu(NO3)2 with a concentration
Externí odkaz:
https://doaj.org/article/1455876082d74e9696bd30abdde7d998
Autor:
A. V. Blokhin, Ya. N. Yurkshtovich, E. N. Stepurko, D. I. Shiman, A. V. Zuraev, S. V. Voitekhovich
Publikováno v:
Russian Journal of Physical Chemistry A. 96:1849-1855
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cffe05a06740429376af332963cfff7
https://doi.org/10.1134/s0036024422090059
https://doi.org/10.1134/s0036024422090059
Autor:
Alexander V. Zuraev, Vladislav A. Budevich, Oleg A. Ivashkevich, Vadim E. Matulis, Sergei V. Voitekhovich, Vitaly E. Matulis, Ludmila S. Ivashkevich, Alexander S. Lyakhov
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 385-395 (2021)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Tetrazolium-5-aminides have been prepared by the tert-butylation of 5-aminotetrazole and its N-methyl derivatives by the t-BuOH/HClO4 system followed by the treatment of the tetrazolium salts by alkali. The mesoionic compounds have been found to show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b15757b5e3394ef8c2d42b0e6d45eb9
https://doaj.org/article/4aaefbff75a74d36af0b57beed206cbc
https://doaj.org/article/4aaefbff75a74d36af0b57beed206cbc
Autor:
Yuri V. Grigoriev, Alexander V. Zuraev, Vladislav A. Budevich, Cyril M. Verbilo, Oleg A. Ivashkevich
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 48-63 (2020)
The target for antibacterial action of 1,4-di- and 1,4,5-trisubstituted 1H-1,2,3-triazoles against E. coli ATCC 25922 and S. aureus ATCC 6538 was proposed. Structures of target proteins and investigated triazoles were built using molecular modeling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2799831dfc150530929382bc7392a34
https://doi.org/10.33581/2520-257x-2020-1-48-63
https://doi.org/10.33581/2520-257x-2020-1-48-63
Autor:
Yuri V. Grigoriev, Vitaly E. Matulis, Oleg A. Ivashkevich, Ekaterina G. Ragoyja, Alexander V. Zuraev
Publikováno v:
Журнал Белорусского государственного университета: Химия, Iss 1, Pp 19-31 (2020)
The structure of copper(II) poly-5-vinyltetrazolate and the products of its thermolysis has been studied by means of density functional theory and infrared spectroscopy. Copper(II) poly-5-vinyltetrazolate has been obtained and subsequently subjected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59bdf2f53f04c886c277d6936f76d302
https://journals.bsu.by/index.php/chemistry/article/view/1276
https://journals.bsu.by/index.php/chemistry/article/view/1276
Autor:
Alexander S. Bunev, Pavel V. Gushchin, Aleksandra V. Protas, Cyril M. Verbilo, Vadim P. Boyarskiy, Vladimir Bakulev, Mikhail A. Kinzhalov, Tatiyana V. Serebryanskaya, Nina A. Kasyanenko, Ingo Ott, Alexander V. Zuraev, Georgii V. Alekseev, Andrey S. Smirnov, Petra Lippmann, Anastasiya Andreeva, Taras L. Panikorovskii
Publikováno v:
New Journal of Chemistry. 44:5762-5773
Bis-ADC complexes cis-[Pd{C(NHC6H4NH2)N(H)R}2]Cl2 (R = Xyl 4a, Cy 4b, C6H4-4-F 4c) and cis-[Pt{C(NHC6H4NH2)N(H)R}2]Cl2 (R = Xyl 5a, Cy 5b, C6H4-4-F 5c) were synthesized via the metal-mediated coupling of two isocyanide ligands in cis-[MCl2(CNR)2] (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::839cc2e230aa6e9d9bd510ebfd047718
https://doi.org/10.1039/d0nj00060d
https://doi.org/10.1039/d0nj00060d