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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.identifier.issn1070-4280
dc.identifier.issn1608-3393
dc.identifier.urihttps://dx.doi.org/10.1134/S107042800606011X
dc.identifier.urihttps://hdl.handle.net/11480/5515
dc.descriptionWOS: 000239375600011en_US
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.en_US
dc.language.isoengen_US
dc.publisherMAIK NAUKA/INTERPERIODICA/SPRINGERen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[0-Belirlenecek]en_US
dc.titleElectrophilic substitution reactions of indole alkaloids with alpha,beta-unsaturated carbonyl compounds in the presence of K10 montmorilloniteen_US
dc.typearticleen_US
dc.relation.journalRUSSIAN JOURNAL OF ORGANIC CHEMISTRYen_US
dc.departmentNiğde ÖHÜen_US
dc.identifier.volume42en_US
dc.identifier.issue6en_US
dc.identifier.startpage879en_US
dc.identifier.endpage882en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthor[0-Belirlenecek]
dc.identifier.doi10.1134/S107042800606011X


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