Zobrazeno 1 - 10
of 15
pro vyhledávání: '"I. A. Fedyunyaeva"'
Publikováno v:
Dyes and Pigments. 64:125-134
We investigate the reactions of mono-substituted squaraines with CH-acidic nucleophiles, heterocyclic methylene bases and thionating reagents. The reactions of mono-substituted squaraines with malononitrile, cyano- and nitroacetic esters, barbituric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89a363c343436a6958266c1ea9137331
https://doi.org/10.1016/j.dyepig.2004.05.003
https://doi.org/10.1016/j.dyepig.2004.05.003
Autor:
I. G. Ermolenko, Alexander V. Mazepa, O. S. Galkina, N. A. Popova, Leonid D. Patsenker, I. A. Fedyunyaeva, B. M. Krasovitskii, O. N. Lyubenko
Publikováno v:
Chemistry of Heterocyclic Compounds. 39:525-533
It has been shown that dimethylamino-substituted 2,5-diaryloxazoles and 2,5-diaryl-1,3,4-oxadiazoles undergo heterocyclization under Vilsmeier-Haack conditions with the participation of the dimethylamino group to form quinazolinium salts. The oxazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f500f6ee1c1af11ef7d5dfda2280225c
https://doi.org/10.1023/a:1024777700217
https://doi.org/10.1023/a:1024777700217
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:707-711
A comparison of the PMR spectra of 5-phenyl-2-methyl derivatives of oxazole, 1,3,4-oxadiazole, and 1, 3, 4-triazole with the spectrum of toluene leads to the conclusion that the electron-acceptor character of the heterocycles drops off in the order o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21fce2a5f2ad03f03b47530f4b029a2d
https://doi.org/10.1007/bf02291804
https://doi.org/10.1007/bf02291804
Publikováno v:
Chemistry of Heterocyclic Compounds. 32:285-289
Condensation of 4-(3, 5-diphenylpyrazol-1-yl)benzoyl chloride with hydrochlorides of ω-aminomethyl aryl ketones or aroyl hydrazines and subsequent cyclization of the condensation products in phosphorus oxychloride gave new effective luminophors. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdb93efe9a165610595ffa2fbf3fa1f7
https://doi.org/10.1007/bf01169244
https://doi.org/10.1007/bf01169244
Autor:
I. A. Fedyunyaeva, V. M. Shershukov
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:204-207
Condensation of 4-chlorosulfonyl- and 4-fluorosulfonyl-benzoyl chlorides with p-dimethylamino-α-aminoacetophenone followed by cyclodehydration of the resulting amides leads to the formation of 4-(5-dimethylaminophenyl-2-oxazolyl)benzenesulfonyl hali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f7f04fd6ee769a8c6eefe4cd362f2d3
https://doi.org/10.1007/bf00531666
https://doi.org/10.1007/bf00531666
Autor:
V. M. Shershukov, I. A. Fedyunyaeva
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::527ca173ec1b1f5312ead1313116bd21
https://doi.org/10.1002/chin.199405161
https://doi.org/10.1002/chin.199405161
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f75f88af73b2e4f9373e5b22ff547504
https://doi.org/10.1002/chin.199643092
https://doi.org/10.1002/chin.199643092
Publikováno v:
ChemInform. 29
A comparison of the PMR spectra of 5-phenyl-2-methyl derivatives of oxazole, 1,3,4-oxadiazole, and 1, 3, 4-triazole with the spectrum of toluene leads to the conclusion that the electron-acceptor character of the heterocycles drops off in the order o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61e1d9a479f92f8926d45f78e8774264
https://doi.org/10.1002/chin.199801021
https://doi.org/10.1002/chin.199801021
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48879fb496d34bb5fc89492e64e5bbea
https://doi.org/10.1002/chin.200130052
https://doi.org/10.1002/chin.200130052
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:623-625
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36d466fa62c7fb95551e1e09fa57dde4
https://doi.org/10.1007/bf02290862
https://doi.org/10.1007/bf02290862