Zobrazeno 1 - 8
of 8
pro vyhledávání: '"V. V. Esenbaeva"'
Publikováno v:
Russian Journal of General Chemistry. 89:1927-1930
The reactions of 2-, 3-, 4-aminopyridines or 4-aminoquinoline with hydrolytically stable tropylium salts (perchlorate or tetrafluoroborate) have afforded N-(1′-cyclohepta-2′,4′,6′-trienyl)-2-aminopyridine, N-(1′-cyclohepta-2′,4′,6′-tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e02e6d40264902673cb5f7fd76ccb18
https://doi.org/10.1134/s1070363219090305
https://doi.org/10.1134/s1070363219090305
Publikováno v:
Russian Journal of General Chemistry. 88:2691-2694
The reactions of tropylium salts with 2,5-diamino-1,3,4-thiadiazol, 3,5-diamino-1,2,4-thiadiazol, and 2,6-diaminopyridine have given novel products of substitution of hydrogen atoms of two amino groups in thiadiazols and of hydrogen atoms at С3 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cd9057dacd460d3876e12774d54bc23
https://doi.org/10.1134/s1070363218120368
https://doi.org/10.1134/s1070363218120368
Autor:
L. P. Yunnikova, V. V. Esenbaeva
Publikováno v:
Russian Journal of Organic Chemistry. 54:1018-1022
Tropylium, xanthylium, and tritylium salts characterized by different stabilities differently reacted with biologically active amines. The reactions of tropylium perchlorate and tetrafluoroborate with 4-(cyclohepta-2,4,6-trien-1-yl)aniline was accomp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9c491536250cc55e1ca7d9ec1f3827e
https://doi.org/10.1134/s1070428018070084
https://doi.org/10.1134/s1070428018070084
Autor:
L. P. Yunnikova, V. V. Esenbaeva
Publikováno v:
Russian Journal of Organic Chemistry. 55:1982-1984
Nicotinic, isonicotinic, and furan-2-carboxylic acid hydrazides reacted with 2 equiv of tropylium perchlorate or tetrafluoroborate to give the corresponding N′N′-di(cyclohepta-2,4,6-trein-1-yl) derivatives as a result of electrophilic substitutio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20d7f175cd96912c8b4dc4e2b670bcb2
https://doi.org/10.1134/s1070428019120315
https://doi.org/10.1134/s1070428019120315
Publikováno v:
Russian Journal of Organic Chemistry. 55:1985-1987
Reactions of thioxanthylium tetrafluoroborate with pharmacophoric heterocyclic amines, pyrimidin-2-amine, 4,6-dimethylpyrimidin-2-amine, 2-aminopyrimidine-4,6-diol, and 1,3,4-thiadiazole-2,5-diamine, gave stable products of electrophilic substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f24eaf495f15b3438c723142b52c4cf
https://doi.org/10.1134/s1070428019120327
https://doi.org/10.1134/s1070428019120327
Autor:
V. V. Esenbaeva, L. P. Yunnikova
Publikováno v:
Russian Journal of General Chemistry. 88:829-831
By the reaction of urea, thiourea, sulfanilamide or sulfadimethoxine with tropylium tetrafluoroborate new products of substitution of hydrogen atom by the tropylium motif at the amide nitrogen atom or at the amino group of the benzene ring have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b2fc6f246825e173a2827208e387560
https://doi.org/10.1134/s107036321804031x
https://doi.org/10.1134/s107036321804031x
Autor:
L. P. Yunnikova, V. V. Esenbaeva
Publikováno v:
Russian Journal of General Chemistry. 86:1769-1771
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8955790570a9f8f763d8324ae1131066
https://doi.org/10.1134/s1070363216070392
https://doi.org/10.1134/s1070363216070392
Autor:
L. P. Yunnikova, V. V. Esenbaeva
Publikováno v:
Russian Journal of Organic Chemistry. 50:1697-1698
In this case the reaction of [4+2]-cycloaddition occurred where the Schiff base acted not like a dienophile [4] but like a diene, and the 1,2diphenylcyclopropene was the ene component of the reaction. The formation of compound III proceeds presumably
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ea6258e6a4fe1cbf9362102b75da435
https://doi.org/10.1134/s1070428014110281
https://doi.org/10.1134/s1070428014110281