Zobrazeno 1 - 10
of 13
pro vyhledávání: '"L. G. Saakyan"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:323-328
A study was carried out on the enamine rearrangement of iodoalkylates of the ethyl ester of 4,6-dimethyl-2-pyrimidinylacetic acid to give ethyl esters of 2-alkylamino-4,6-dimethylnicotinic acid, which proceeds upon the action of various amines. The r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99b12dcab56533a656ab57d8dfba2675
https://doi.org/10.1023/a:1017559100450
https://doi.org/10.1023/a:1017559100450
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:698-702
Condensation of 2-benzyl-4-hydrazino-6-methylpyrimidine with ethyl acetoacetate and its alkyl derivatives as well as with acetyl acetone, methyl methacrylate, and crotonaldehyde have given the corresponding 2-benzyl-4-methyl-6-(pyrazol-1-yl)pyrimidin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aeeefcf73ba358bf2be6a5125a1c5a1
https://doi.org/10.1007/bf02291802
https://doi.org/10.1007/bf02291802
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72705108fbda278c4e20f8cff86652d4
https://doi.org/10.1002/chin.199111209
https://doi.org/10.1002/chin.199111209
Publikováno v:
ChemInform. 24
The Dimroth rearrangement of 7-benzyl-5-methyl-1,2,4-triazolo[4,3-c]pyrimidine to 7-benzyl-5-methyl-1,2,4-triazolo[2,3-c]pyrimidine was realized by the action of sodium ethoxide and other nucleophilic agents. The rearrangement was investigated by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c929f5106036fd61d91f19d5760e6fb
https://doi.org/10.1002/chin.199338098
https://doi.org/10.1002/chin.199338098
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95d0a07c8743f79f4f11c6075ffb4464
https://doi.org/10.1002/chin.199801175
https://doi.org/10.1002/chin.199801175
Autor:
L. G. Saakyan, G. G. Danagulyan
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::365beb30e29e5af838df0226a9cd677e
https://doi.org/10.1002/chin.200032116
https://doi.org/10.1002/chin.200032116
Publikováno v:
ChemInform. 33
A study was carried out on the enamine rearrangement of iodoalkylates of the ethyl ester of 4,6-dimethyl-2-pyrimidinylacetic acid to give ethyl esters of 2-alkylamino-4,6-dimethylnicotinic acid, which proceeds upon the action of various amines. The r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::373dd5fc7f6f1e9b9c8f725ded6764be
https://doi.org/10.1002/chin.200202155
https://doi.org/10.1002/chin.200202155
Autor:
M. G. Zalinyan, G. A. Bulakhov, G. A. Panosyan, G. G. Danagulyan, P. B. Terent'ev, L. G. Saakyan
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:1332-1334
Refluxing 4-allyl-7-benzyl-5-methyl-1,2,4-triazolo[4,3-c]pyrimidine in an alcohol solution of sodium ethylate causes a Dimroth rearrangement together with a prototropic isomerization of the allyl fragment to give 7-benzyl-5-methyl-4-propenyl-1,2,4-tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b3ddace831f1185b68af87d157f2458
https://doi.org/10.1007/bf00532035
https://doi.org/10.1007/bf00532035
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:186-188
The Dimroth rearrangement of 7-benzyl-5-methyl-1,2,4-triazolo[4,3-c]pyrimidine to 7-benzyl-5-methyl-1,2,4-triazolo[2,3-c]pyrimidine was realized by the action of sodium ethoxide and other nucleophilic agents. The rearrangement was investigated by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9679f4978c72dde2445fd5e89917319c
https://doi.org/10.1007/bf00473941
https://doi.org/10.1007/bf00473941
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f4f1e275b2b87bc8455300bed1abc28
https://doi.org/10.1002/chin.200037051
https://doi.org/10.1002/chin.200037051