Zobrazeno 1 - 10
of 58
pro vyhledávání: '"M. Yu. Gavrilov"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:981-984
2-Methyl-4-oxo-1-phenyl-1,4-dihydropyrido[2,3-d]pyrimidine was acylated by succinic and trifluoroacetic anhydrides and also underwent the Claisen reaction with diethyl oxalate and ethyl oxanilate to give acyl derivatives at the methyl group, which, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91dd8a74af47b97f8735e2eeae27e707
https://doi.org/10.1007/bf02256985
https://doi.org/10.1007/bf02256985
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:1199-1202
In reaction with acylating agents, 2-aryl-2-methyl-7,8-dihydro-6H-pyrimido[4,5-b]pyrindin-4-ones are acylated at the methyl group and also enter into reaction with diethyl oxalate. 1-Aryl-2-phenacyl-7,8-dihydro-6H-pyrimido[4,5-b]pyrindin-4-ones under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa9f17c5c9bad9323add044c05ce79c9
https://doi.org/10.1007/bf02290870
https://doi.org/10.1007/bf02290870
Autor:
M. Yu. Gavrilov, T. A. Smirnova
Publikováno v:
Chemistry of Heterocyclic Compounds. 32:319-322
Esters of 3-cyano-2-oxo-5, 6-tri (tetra)-methylene-1, 2-dihydroisonicotinic and 2-amino-3-ethoxycarbonyl-5, 6-tri (tetra)methyleneisorticotinic acids have been obtained by the reaction of 2-oxocyclopentyl(hexyl)glyoxylic acid esters with malonic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cdb391e35d3c9daeed86b569ea15380
https://doi.org/10.1007/bf01169251
https://doi.org/10.1007/bf01169251
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3336da33f58b5a0c3007d9b54ad8c6ec
https://doi.org/10.1002/chin.199116172
https://doi.org/10.1002/chin.199116172
Publikováno v:
ChemInform. 24
Acetylation of 2-arylamino-5-carbethoxy-6-methylnicotinonitriles gave N-acetyl-2-arylamino-5-carbethoxy-6-methylnicotinonitriles, which, under the influence of hydrogen chloride, are cyclized to 1-aryl-1,4-dihydro-6-carbethoxy-2,7-dimethyl-4-oxopyrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::056f8840831013fae65e22ea1c2bb819
https://doi.org/10.1002/chin.199341194
https://doi.org/10.1002/chin.199341194
Publikováno v:
ChemInform. 24
Cyclization of 2-(N-acetyl-N-arylamino)nicotinonitriles in the presence of dry HCl gave 1-aryl-2-methyl-4-oxo-1,4-dihydropyrido[2,3-d]pyrimidines. It was shown that they are acylated by acetic anhydride, aroyl chlorides, and phenyl isocyanate at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecef7e103ef0ea230b6e98cfef391929
https://doi.org/10.1002/chin.199314205
https://doi.org/10.1002/chin.199314205
Autor:
A. V. Zakharov, L. M. Demina, G. N. Novoselova, M. Yu. Gavrilov, N. A. Gornova, M. E. Kon'shin
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b4bab5f785ec86de52e84f895acc8e2
https://doi.org/10.1002/chin.199429212
https://doi.org/10.1002/chin.199429212
Autor:
M. E. Kon'shin, M. Yu. Gavrilov
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f3c3a65100d37e064e499a240894a86
https://doi.org/10.1002/chin.199404173
https://doi.org/10.1002/chin.199404173
Autor:
L. P. Drovosekova, V. A. Khaldeeva, V. E. Kolla, M. Yu. Gavrilov, L. G. Mardanova, M. E. Kon'shin
Publikováno v:
ChemInform. 26
2-Alkoxy-5,6,7,8-tetrahydroquinoline-3-earboxamldes (I-VI). To a solution of sodium alc0holate prepared from 0.03 mole of sodium in 25 ml of the corresponding alcohol was added 4.2 g (0.02 mole) of 2-chloro-5,6,7,8-tetrahydroquinoline-3carboxytic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4027fbd4d08bb91ee94923d0ee7917a4
https://doi.org/10.1002/chin.199518154
https://doi.org/10.1002/chin.199518154
Autor:
M. E. Kon'shin, M. Yu. Gavrilov
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6c886d0617aebc900b6003b5b192100
https://doi.org/10.1002/chin.199551200
https://doi.org/10.1002/chin.199551200