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Synthesis of 2,4-Disubstituted-3,4-Dihydro-2H-Naphth[2,1-e][1,3]Oxazines

dc.contributor.authorTurgut, Zuhal
dc.contributor.authorPelit, Emel
dc.contributor.authorTurhan, Kadir
dc.contributor.institutionauthorTURGUT, Zühal
dc.date.accessioned2026-06-27T13:07:34Z
dc.date.issued2009
dc.description.abstract2,4-Disubstituted-3,4-dihydro-2H-naphth[2,1-e][1,3]oxazines were prepared through the ring-closure reactions of the starting aminonaphthols with substituted aromatic and hetaryl aldehydes.en
dc.description.urihttps://doi.org/10.1007/978-1-4020-6955-0_39
dc.identifier.doi10.1007/978-1-4020-6955-0_39
dc.identifier.endpage346
dc.identifier.isbn978-1-4020-6954-3
dc.identifier.startpage343
dc.identifier.urihttps://hdl.handle.net/20.500.14981/50082
dc.identifier.wos000262502000039
dc.language.isoeng
dc.publisherSPRINGER
dc.relation.conference9th Eurasia Conference on Chemical Sciences
dc.relation.ispartofInnovations in Chemical Biology
dc.subjectAminonaphthol
dc.subjectbiological activity
dc.subjectnaphth-1,3-oxazines
dc.subjectring-closure reactions
dc.subjectRING-CHAIN TAUTOMERISM
dc.subjectN-ALKYLATION
dc.subjectBiochemistry & Molecular Biology
dc.subjectChemistry
dc.titleSynthesis of 2,4-Disubstituted-3,4-Dihydro-2H-Naphth[2,1-e][1,3]Oxazines
dc.typeProceedings Paper
dspace.entity.typePublication
local.import.sourceWOS

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