Zobrazeno 1 - 10 of 10 pro vyhledávání: '"G. S. Gimranova"'
1
Synthesis and molecular structure of 2,3,4,5-tetrahydro-1H-3-benzazepine derivatives and dimethyl 4-cyano-2,3,6,7-tetrahydro-1H-3-benzazonine-5,6-dicarboxylate
Autor: Anatoly T. Soldatenkov, Victor N. Khrustalev, J. A. Mamyrbekova-Bekro, K. B. Polyanskii, A. V. Malkova, S. A. Soldatova, G. S. Gimranova, N. M. Kolyadina
Publikováno v: Chemistry of Heterocyclic Compounds. 48:1332-1339
A study was carried out on the direction of 1,2,3,4-tetrahydroisoquinolinium quaternary salt rearrangements by the action of base with or without dimethyl acetylenedicarboxylate. These quaternary salts containing a methylene group at the nitrogen ato
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::545436cb53f68a34af6a09936dccf65c
https://doi.org/10.1007/s10593-012-1141-9
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2
Rearrangements of N-ethoxycarbonylmethyl-1,2,3,4-tetrahydroquinolinium halogenalkylates effected by sodium hydride. Synthesis of 2,3,4,5-tetrahydro-1H-3-benzazepines
Autor: K. B. Polyanskii, S. A. Soldatova, G. S. Gimranova, Anatoly T. Soldatenkov
Publikováno v: Russian Journal of Organic Chemistry. 44:750-754
Quaternary salts obtained from N-alkyl-1,2,3,4-tetrahydroisoquinolines and ethyl haloacetates or diethyl bromomalonate under the action of sodium hydride in boiling 1,4-dioxane were converted into N-alkyl-N-ethoxycarbonyl-2,3,4,5-tetrahydro-1H-3-benz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::edc83b74ad9fba1f2642c8f7eac64996
https://doi.org/10.1134/s1070428008050205
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3
Synthesis of pyrrolidines and tetrahydro-1H-azepines from 4-aryl-1-benzoyl(ethoxycarbonyl)methyl-1-methyl-1,2,3,6-tetrahydropyridinium halides
Autor: S. V. Akbulatov, G. S. Gimranova, Zh. A. Mamyrbekova, K. B. Polyanskii, Anatoly T. Soldatenkov, S. A. Soldatova
Publikováno v: Chemistry of Heterocyclic Compounds. 43:1420-1425
4-Aryl-1,2,3,6-tetrahydropyridinium quaternary salts which have a benzoylmethyl or ethoxycarbonylmethyl group on atom N-1 generate N-ylides when heated in the presence of NaH and they can rearrange in situ with contraction or expansion of the six-mem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::47b6af73777f34c03474a01dadc9e384
https://doi.org/10.1007/s10593-007-0219-2
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7
ChemInform Abstract: Rearrangements of N-Ethoxycarbonylmethyl-1,2,3,4-tetrahydroquinolinium Halogenalkylates Effected by Sodium Hydride. Synthesis of 2,3,4,5-Tetrahydro-1H-3-benzazepines
Autor: K. B. Polyanskii, G. S. Gimranova, Anatoly T. Soldatenkov, S. A. Soldatova
Publikováno v: ChemInform. 40
Quaternary salts obtained from N-alkyl-1,2,3,4-tetrahydroisoquinolines and ethyl haloacetates or diethyl bromomalonate under the action of sodium hydride in boiling 1,4-dioxane were converted into N-alkyl-N-ethoxycarbonyl-2,3,4,5-tetrahydro-1H-3-benz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2477260288ca661df475ee57139a3482
https://doi.org/10.1002/chin.200902174
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8
ChemInform Abstract: Synthesis of Pyrrolidines and Tetrahydro-1H-azepines from 4-Aryl-1-benzoyl (ethoxycarbonyl)methyl-1-methyl-1,2,3,6-tetrahydropyridinium Halides
Autor: S. V. Akbulatov, Anatoly T. Soldatenkov, Zh. A. Mamyrbekova, G. S. Gimranova, K. B. Polyanskii, S. A. Soldatova
Publikováno v: ChemInform. 39
4-Aryl-1,2,3,6-tetrahydropyridinium quaternary salts which have a benzoylmethyl or ethoxycarbonylmethyl group on atom N-1 generate N-ylides when heated in the presence of NaH and they can rearrange in situ with contraction or expansion of the six-mem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d706c9e2748a2a96a173cc7bd4565e4c
https://doi.org/10.1002/chin.200834175
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