CONDENSATION OF ETHYL ACETOACETATE WITH NAPHTHALENE-DIOLS - THE SYNTHESIS OF SOME NOVEL COUMARINS AND CHROMONES .1.

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dc.contributor.authorOYMAN, U
dc.contributor.authorGUNAYDIN, K
dc.date.accessioned2024-06-12T11:23:37Z
dc.date.available2024-06-12T11:23:37Z
dc.date.issued1994
dc.departmentTrakya Üniversitesien_US
dc.description.abstractIn Simonis reaction with ethyl acetoacetate naphthalene-2,6-diol gives 8-hydroxy-3-methyl-1 H-naphtho[2,1-b]pyran-l-one and naphthalene-2,7-diol gives the related 9-hydroxy isomer. In Pechman reactions, the former diet yields a coumarin, 8-hydroxy-1-methyl-3H-naphtho[2,1-b]-pyran-3-one, with the corresponding orientation, but the latter diol gives a coumarin, 8-hydroxy-4-methyl-2H-naphtho[2,3-b]-pyran-2-one, with an unusual linear annelation pattern.en_US
dc.identifier.endpage764en_US
dc.identifier.issn0037-9646
dc.identifier.issue12en_US
dc.identifier.startpage763en_US
dc.identifier.urihttps://hdl.handle.net/20.500.14551/26547
dc.identifier.volume103en_US
dc.identifier.wosWOS:A1994QC98500007en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherSoc Chimique Belgiqueen_US
dc.relation.ispartofBulletin Des Societes Chimiques Belgesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject[No Keywords]en_US
dc.titleCONDENSATION OF ETHYL ACETOACETATE WITH NAPHTHALENE-DIOLS - THE SYNTHESIS OF SOME NOVEL COUMARINS AND CHROMONES .1.en_US
dc.typeArticleen_US

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