Zobrazeno 1 - 10
of 34
pro vyhledávání: '"E. N. Lysenko"'
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 22, Iss 2(62), Pp 42-48 (2017)
Earlier it was found the structure of the reaction products of 1,4-benzoquinones and N-arylsulfonyl-1,4-benzoquinone monoimines with acetylacetone imines depends on the structure of the reagents and the experimental conditions. The indole derivatives
Externí odkaz:
https://doaj.org/article/f96bf53f59cc4f638fa88200a49cb709
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 22, Iss 1(61), Pp 103-118 (2017)
The hydrohalogenation of N-arylaminocarbonyl-1,4-benzoquinone monoimines is optimal method to obtain the halogenated derivatives. This method allows obtaining the pure products in high yield with a halogen atom in the aminophenol ring. The brominatio
Externí odkaz:
https://doaj.org/article/918850d0747e48c1abf71bec574a2d66
Publikováno v:
Inorganic Materials: Applied Research. 13:494-500
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::747cbebae371562530aef1936052e856
https://doi.org/10.1134/s2075113322020265
https://doi.org/10.1134/s2075113322020265
Publikováno v:
Russian Physics Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fb50291e092f66c902a7142a3b4caec
https://doi.org/10.1007/s11182-023-02847-x
https://doi.org/10.1007/s11182-023-02847-x
Publikováno v:
Perspektivnye Materialy. 7:56-65
The paper considers kinetic studies lithium-zinc ferrite synthesis under heating by high-energy electron beam of mixtures of the initial Fe2O3 – Li2CO3 – ZnO reagents of different prehistory. We used samples of bulk density and compressed in hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5497f0859e101d493cce275121b6a7c
https://doi.org/10.30791/1028-978x-2021-7-56-65
https://doi.org/10.30791/1028-978x-2021-7-56-65
Publikováno v:
Eurasian Physical Technical Journal; 2023, Vol. 20 Issue 1, p12-19, 8p
Publikováno v:
Kontrol'. Diagnostika. :40-45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16a5976f0cca1bab501ce0af703c2c0a
https://doi.org/10.14489/td.2018.06.pp.040-045
https://doi.org/10.14489/td.2018.06.pp.040-045
Publikováno v:
Vìsnik Odesʹkogo Nacìonalʹnogo Unìversitetu: Hìmìâ, Vol 22, Iss 1(61), Pp 103-118 (2017)
The hydrohalogenation of N-arylaminocarbonyl-1,4-benzoquinone monoimines is optimal method to obtain the halogenated derivatives. This method allows obtaining the pure products in high yield with a halogen atom in the aminophenol ring. The brominatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90dce87dd92b0542b7306e7654d56fe8
https://doi.org/10.18524/2304-0947.2017.1(61).94716
https://doi.org/10.18524/2304-0947.2017.1(61).94716
Autor:
A. P. Avdeenko, E. N. Lysenko, Svetlana A. Konovalova, A. A. Santalova, Konstantin S. Burmistrov
Publikováno v:
Russian Journal of Organic Chemistry. 52:1287-1296
N-Chloro-1,4-benzoquinone imines reacted with arenethiols to give different products, depending on the conditions and initial quinone imine structure. N-(Arylsulfanyl)-1,4-benzoquinone imines were obtained as a result of nucleophilic substitution of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fe56c755234f4c3009959c1ad143f3d
https://doi.org/10.1134/s1070428016090062
https://doi.org/10.1134/s1070428016090062
Autor:
Svetlana A. Konovalova, A. P. Avdeenko, Viktoriya V. Dyakonenko, E. N. Lysenko, Svetlana V. Shishkina
Publikováno v:
Russian Journal of Organic Chemistry. 52:516-522
N-Arenesulfonyl-1,4-benzoquinone imines reacted with acetylacetone to afford different products, depending on the isolation procedure. Crystallization from polar protic solvents gave N-[4-hydroxy- 3-(2-hydroxy-4-oxopent-2-en-3-yl)phenyl]arenesulfonam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::507ffbd9be357b5abf251aef5857524a
https://doi.org/10.1134/s1070428016040060
https://doi.org/10.1134/s1070428016040060