Zobrazeno 1 - 10
of 10
pro vyhledávání: '"N. G. Balasanyan"'
Autor:
N. G. Balasanyan, A. A. Safaryan, G. G. Danagulyan, A. A. Karapetyan, M. G. Zalinyan, N. Sh. Mailyan
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:838-842
By reactions of substituted chloropyrimidines with the sodium salt of 2,2-dimethyltetrahydro-4-pyranone oxime, pyrimidinyloximes of 2,2-dimethyltetrahydro-4-pyranone have been obtained. On the basis of x-ray diffraction studies of the O-(2,4-dimethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbc955deadc7845b7ca984ed4cc68876
https://doi.org/10.1007/bf02253036
https://doi.org/10.1007/bf02253036
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:831-837
By the interaction of substituted chloropyrimidines with the sodium salts of oximes of aliphatic and alicyclic ketoximes, series of O-(4,6-dimethyl-2-pyrimidinyl)- and O-(2,4-dimethyl-6-pyrimidyl)ketoximes have been obtained. Through reactions of 2-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af13739ee65bdd11e6c22ebca0ac52e2
https://doi.org/10.1007/bf02253035
https://doi.org/10.1007/bf02253035
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:1328-1331
(2-Oxo-1-pyrrolidinyl)pyrimidines have been synthesized by thermal cyclization of certain N-(pyrimidinyl)-γ-aminobutyric acids. Reaction of 2-methyl-4-chloro-6-(2-oxo-1-pyrrolidinyl)pyrimidine with the sodium salts of acetone or acetophenone oximes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc793ec59759affee28827f61a9f567e
https://doi.org/10.1007/bf00532034
https://doi.org/10.1007/bf00532034
Autor:
N. G. Balasanyan, M. G. Zalinyan, A. A. Safaryan, G. G. Danagulyan, A. A. Karapetyan, N. Sh. Mailyan
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16efba86d3abb58f1945753c5c3b341d
https://doi.org/10.1002/chin.199802152
https://doi.org/10.1002/chin.199802152
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::009a8576640abfd4ee834f321842e3e8
https://doi.org/10.1002/chin.199803164
https://doi.org/10.1002/chin.199803164
Autor:
L. V. Korobchenko, E. A. Abgaryan, M. G. Zalinyan, N. G. Balasanyan, G. G. Danagulyan, E. I. Boreko, É. R. Kalashyan, I. K. Zubovich, N. P. Mishaeva, G. V. Vladyko
Publikováno v:
Pharmaceutical Chemistry Journal. 26:610-613
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eba3958409237efbf6de64ca92e80d10
https://doi.org/10.1007/bf00777143
https://doi.org/10.1007/bf00777143
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaa78cc82319f64ed21ad122e32d1310
https://doi.org/10.1002/chin.199029183
https://doi.org/10.1002/chin.199029183
Publikováno v:
Chemistry of Heterocyclic Compounds. 25:1369-1373
Chloropyrimidines react readily with the sodium salts of alkyl aryl ketoximes to give acetophenone O-(2,4-dimethylpyrimidin-6-yl)- and O-(4,6-dimethylpyrimidin-2-yl)oximes, the oximino-groups in which readily undergo nucleophilic substitution.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::365b2d1c8c1ebee065bcdff13434c030
https://doi.org/10.1007/bf00473866
https://doi.org/10.1007/bf00473866
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a302016c66547e67dec61aa2339a008c
https://doi.org/10.1002/chin.198843230
https://doi.org/10.1002/chin.198843230
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:468-468
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7519ebc885892f7746c606a4af67db8e
https://doi.org/10.1007/bf00478872
https://doi.org/10.1007/bf00478872