Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Dmitriy Yu. Vandyshev"'
Autor:
Dmitriy Yu. Vandyshev, Olga V. Sleptsova, Vladislav Yu. Gazin, Stanislav A. Malyutin, Naum R. Malkin, Khidmet S. Shikhaliev
Publikováno v:
Конденсированные среды и межфазные границы, Vol 25, Iss 3 (2023)
Among the available technologies for treating natural and wastewater from clay materials, coagulation/flocculation is the most common method due to its high efficiency, simplicity, and cost-effectiveness. Inorganic coagulants such as aluminum sulfate
Externí odkaz:
https://doaj.org/article/1a047177012d4e0e9c77acd007cb5cbc
Publikováno v:
Molecules, Vol 27, Iss 16, p 5268 (2022)
The building of heterocyclic systems containing hydrogenated fragments is an important step towards the creation of biologically-active compounds with a wide spectrum of pharmacological activity. Among the numerous methods for creating such systems,
Externí odkaz:
https://doaj.org/article/59fb348c64564458b3e17e3a319ef245
Autor:
Dmitriy Yu. Vandyshev, Khidmet S. Shikhaliev, Mikhail Yu. Krysin, Tatiana N. Ilyinova, Daria A. Mangusheva, Oleg E. Sidorenko, Renata R. Iminova
Publikováno v:
Mendeleev Communications. 32:637-639
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28fcfbe53317ce1963b7dd03b06261e3
https://doi.org/10.1016/j.mencom.2022.09.023
https://doi.org/10.1016/j.mencom.2022.09.023
Autor:
Alexey A. Kruzhilin, Gleb L. Denisov, E. A. Kosheleva, Dmitriy Yu. Vandyshev, Khidmet S. Shikhaliev
Publikováno v:
ChemistrySelect. 6:5801-5806
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d8f6e4aa4db0572a864bcbf2df75409
https://doi.org/10.1002/slct.202101372
https://doi.org/10.1002/slct.202101372
Autor:
Dmitriy Yu. Vandyshev, Khidmet S. Shikhaliev, Mikhail A. Prezent, Oleg A. Kozaderov, Oleg V. Ovchinnikov, Mikhail S. Smirnov, Tatiana N. Ilyinova, Daria A. Mangusheva, Renata R. Iminova, Prabhakar Chetti
Publikováno v:
Luminescence : the journal of biological and chemical luminescenceREFERENCES. 37(10)
The article presents a method for the construction of a new tricyclic system of imidazo[1,2-b]pyrido[4,3-e][1,2,4]triazin-6(7Н)-ones based on subsequent reactions of the obtained 1,2-diamino-4-phenylimidazole ethyl ether of 3-methyl-6-phenylimidazo[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::700e476285f572391e04a7f0938023e8
https://pubmed.ncbi.nlm.nih.gov/35863912
https://pubmed.ncbi.nlm.nih.gov/35863912
Autor:
Dmitriy Yu. Vandyshev, Evgeniya A. Kosheleva, Vladimir A. Polikarchuk, Daria A. Mangusheva, Gleb L. Denisov, Khidmet S. Shikhaliev
Publikováno v:
Mendeleev Communications. 31:821-823
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b89d2c0390f45b7969eb9ef09a62027
https://doi.org/10.1016/j.mencom.2021.11.017
https://doi.org/10.1016/j.mencom.2021.11.017
Autor:
Mikhail Yu. Krysin, Khidmet S. Shikhaliev, Oleg А. Kozadyorov, Yuliya V. Chertova, Dmitriy Yu. Vandyshev, Andrei Yu. Potapov, Chetti Prabhakar, Irina V. Ledenyova, Yevgeniya А. Kosheleva, G. V. Shatalov, Vladimir А. Polikarchuk
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1054-1061
A new multicomponent reaction for regioselective synthesis of substituted 1,2,4-triazolo[1,5-a]pyrimidines using aminotriazoles, β-ketoglutaric acid dimethyl ester, and dimethylformamide dimethyl acetal was implemented. The selective reduction of 1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d08a51877ba2c9cb29d9bb874d87927
https://doi.org/10.1007/s10593-020-02773-7
https://doi.org/10.1007/s10593-020-02773-7
Autor:
Mohammad N. Mawlood, Andrei Yu. Potapov, Dmitriy Yu. Vandyshev, Irina V. Ledenyova, Khidmet S. Shikhaliev, Evgeniya А. Kosheleva, Mikhail А. Potapov
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:1075-1079
Condensation of 1H-1,2,4-triazolo-5-diazonium salts with 1,3-cyclohexanedione, accompanied by cascade processes of cyclization and oxidative aromatization, brought about the synthesis of novel derivatives of [1,2,4]triazolo[5,1-c][1,2,4]benzotriazin-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82fe4b1fca7ee088dcf1829340698214
https://doi.org/10.1007/s10593-019-02580-9
https://doi.org/10.1007/s10593-019-02580-9
Autor:
Mikhail Yu. Krysin, Yevgeniya A. Kosheleva, Khidmet S. Shikhaliev, Andrei Yu. Potapov, Yurii A. Kovygin, Dmitriy Yu. Vandyshev, Irina V. Ledenyova
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:748-754
A new variant of Hantzsch reaction was developed for the synthesis of 1,2,3,4,5,6,7,8-octahydroquinolines on the basis of regioselective cascade recyclization of N-arylitaconimides in reactions with 3-aminocyclohex-2-enones. The mechanism of this dom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcb6c776ca7448bd05e3732dd7d58af8
https://doi.org/10.1007/s10593-019-02530-5
https://doi.org/10.1007/s10593-019-02530-5
Autor:
Dmitriy Yu. Vandyshev, Yevgeniya A. Kosheleva, Mikhail A. Potapov, Vladimir A. Polikarchuk, Khidmet S. Shikhaliev, Andrei Yu. Potapov
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:207-212
A method has been developed for the preparation of new pyrazolo[3,4-b]pyridines and tetrahydropyrazolo[3,4-b]quinolinones by the reactions of 5-amino-1-aryl-1H-pyrazole-4-carbonitriles with aliphatic and cyclic 1,3-dicarbonyl compounds in the presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35fc55d0097f6676b489a73f3aea5345
https://doi.org/10.1007/s10593-017-2041-9
https://doi.org/10.1007/s10593-017-2041-9