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Synthesis of new 1,3-disubstituted-2,3-dihydro-1H-naphth-[1,2e][1,3]oxazines

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dc.contributor.authorTurgut, Zuhal
dc.contributor.authorPelit, Emel
dc.contributor.authorKoycu, Adem
dc.date.accessioned2026-06-27T13:01:59Z
dc.date.issued2007
dc.description.abstract1,3-Disubstituted-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazines were prepared through the ring-closure reactions of the aminobenzylnaphthols with substituted aryl- and heteroarylaldehydes.en
dc.description.urihttps://doi.org/10.3390/12030345
dc.identifier.doi10.3390/12030345
dc.identifier.endpage352
dc.identifier.issn1420-3049
dc.identifier.issue3
dc.identifier.pubmed17851393
dc.identifier.startpage345
dc.identifier.urihttps://hdl.handle.net/20.500.14981/49258
dc.identifier.volume12
dc.identifier.wos000245437400008
dc.language.isoeng
dc.publisherMOLECULAR DIVERSITY PRESERVATION INTERNATIONAL
dc.relation.ispartofMOLECULES
dc.rightsopenAccess
dc.subjectbiological activity
dc.subjectring-closure reactions
dc.subjectnaphth-1,3-oxazines
dc.subjectamino-benzylnaphthols
dc.subjectRING-CHAIN TAUTOMERISM
dc.subjectN-ALKYLATION
dc.subjectBiochemistry & Molecular Biology
dc.subjectChemistry
dc.titleSynthesis of new 1,3-disubstituted-2,3-dihydro-1H-naphth-[1,2e][1,3]oxazines
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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