Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anastasia A. Borovleva"'
Autor:
Elena K. Avakyan, Anastasia A. Borovleva, Diana Yu. Pobedinskaya, Oleg P. Demidov, Artem P. Ermolenko, Alexander N. Larin, Ivan V. Borovlev
Publikováno v:
Molecules, Vol 27, Iss 22, p 7862 (2022)
For the first time, amides and ureas based on both 5-nitroisoquinoline and 5-nitrosoisoquinoline were obtained by direct nucleophilic substitution of hydrogen in the 5-nitroisoquinoline molecule. In the case of urea and monosubstituted ureas, only 5-
Externí odkaz:
https://doaj.org/article/24cde3a7bcde4f688ec0770fe0239caf
Autor:
Anastasia A. Borovleva, Elena K. Avakyan, Gulminat A. Amangasieva, Oleg P. Demidov, Diana Yu. Pobedinskaya, Artem P. Ermolenko, Alexander N. Larin, Ivan V. Borovlev
Publikováno v:
Chemistry of Heterocyclic Compounds. 58:235-242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e6313b520c6e473b474c0cf539c9dd6
https://doi.org/10.1007/s10593-022-03077-8
https://doi.org/10.1007/s10593-022-03077-8
Autor:
Elena K. Avakyan, Artem P. Ermolenko, Ivan V. Borovlev, Anastasia А. Borovleva, Diana Yu. Pobedinskaya, Oleg P. Demidov, Alexander V. Aksenov
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:166-174
Arylamino derivatives of both the corresponding nitroquinolones and nitrosoquinolones were first obtained by direct nucleophilic substitution of hydrogen in the molecules of 1-methyl-5(6,7,8)-nitroquinolin-2(1Н)-ones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6bc735bce1a4cc7307bb29a4c981c8b
https://doi.org/10.1007/s10593-021-02889-4
https://doi.org/10.1007/s10593-021-02889-4
Autor:
Ivan V. Borovlev, Elena Beketova, Oleg P. Demidov, Elena K. Avakyan, Oksana А. Nechaeva, Gulminat А. Amangasieva, Anastasia А. Borovleva
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:739-747
The stable adducts, N-(1-methyl-5(6,7,8)-nitro-1,2-dihydroquinolin-2-yl)benzamides were synthesized for the first time by the action of amide anions of aromatic acids on the N-methyl salts of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous MeCN. Oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1760ad3443a90732de456b27cc761869
https://doi.org/10.1007/s10593-019-02529-y
https://doi.org/10.1007/s10593-019-02529-y
Autor:
Oleg P. Demidov, Diana Yu. Pobedinskaya, Gulminat А. Amangasieva, Anastasia A. Borovleva, Ivan V. Borovlev, Elena K. Avakyan
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:623-631
Direct SNH amidation of 5-, 6-, 7-, and 8-nitroquinolines in anhydrous DMSO was used to obtain the respective aroylamino derivatives of nitro- and nitrosoquinolines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ac00450bbe8a4943d5c2817cf06e892
https://doi.org/10.1007/s10593-019-02508-3
https://doi.org/10.1007/s10593-019-02508-3
Autor:
Elena K. Avakyan, Ivan V. Borovlev, Diana Yu. Pobedinskaya, Anastasia A. Borovleva, Oleg P. Demidov, Gulminat A. Amangasieva
Publikováno v:
Synthesis. 50:3520-3530
Arylamination of 3-nitropyridine via the nucleophilic substitution of hydrogen leads to a mixture of 2-arylamino-5-nitropyridines and novel 2-arylamino-5-nitrosopyridines, with the latter as the major product. The proposed mechanism includes the form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16a38f1fda886394efb1790f8a99ca8e
https://doi.org/10.1055/s-0037-1610173
https://doi.org/10.1055/s-0037-1610173
Autor:
Ivan V. Borovlev, Elena K. Avakyan, Gulminat A. Amangasieva, Anastasia A. Borovleva, Oleg P. Demidov
Publikováno v:
Russian Journal of Organic Chemistry. 54:867-872
3-Nitropyridine reacted with nitrogen-centered carboxylic acid amide anions in anhydrous DMSO in the presence of K3Fe(CN)6 via oxidative nucleophilic substitution of hydrogen to give previously unknown N-(5-nitropyridin-2-yl) carboxamides. The reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea21338a56b522e2b377ce5d8a6a7c2b
https://doi.org/10.1134/s1070428018060076
https://doi.org/10.1134/s1070428018060076