Electrophilic substitution reactions of indole alkaloids with alpha,beta-unsaturated carbonyl compounds in the presence of K10 montmorillonite

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dc.contributor.authorSarioez, O.
dc.contributor.authorAbdullah, M. I.
dc.date.accessioned2019-08-01T13:38:39Z
dc.date.available2019-08-01T13:38:39Z
dc.date.issued2006
dc.departmentNiğde ÖHÜ
dc.description.abstractReactions of indole, 1-methylindole, and 3-methylindole with dimethyl acetylenedicarboxylate in the presence of K10 montmorillonite as a catalyst led to the formation of the corresponding dimethyl 2,2-bis(indolyl)butanedioates. The reaction of 2-methylindole with dimethyl acetylenedicarboxylate gave dimethyl 2-(2-methyl-1H-indol-3-yl)maleate and dimethyl 2-methyl-1H-1-benzoazepine-3,,4-dicarboxylate. Dimethyl 1,5-dimethyl-1H-1-benzoazepine-3,4-dicarboxylate was obtained by treatment of 1,3-dimethylindole with dimethyl acetylenedicarboxylate using K 10 clay as a catalyst.
dc.identifier.doi10.1134/S107042800606011X
dc.identifier.endpage882
dc.identifier.issn1070-4280
dc.identifier.issn1608-3393
dc.identifier.issue6
dc.identifier.scopus2-s2.0-33745879171
dc.identifier.scopusqualityQ4
dc.identifier.startpage879
dc.identifier.urihttps://dx.doi.org/10.1134/S107042800606011X
dc.identifier.urihttps://hdl.handle.net/11480/5515
dc.identifier.volume42
dc.identifier.wosWOS:000239375600011
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthor[0-Belirlenecek]
dc.language.isoen
dc.publisherMAIK NAUKA/INTERPERIODICA/SPRINGER
dc.relation.ispartofRUSSIAN JOURNAL OF ORGANIC CHEMISTRY
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleElectrophilic substitution reactions of indole alkaloids with alpha,beta-unsaturated carbonyl compounds in the presence of K10 montmorillonite
dc.typeArticle

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