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SYNTHESIS OF 1,3-DISUBSTITUED-2,3-DIHYDRO-1H-NAFT[1,3] OXAZINE COMPOUNDS

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dc.contributor.authorOzturkcan, S. Arda
dc.contributor.authorTurgut, Zuhal
dc.date.accessioned2026-06-27T13:06:33Z
dc.date.issued2009
dc.description.abstractIn this study, Betti's classical procedur[1], a Mannich-type aminoalkylation reaction of 2-naphtol with furan2-, furan-3-, thiphene-3-, pyridine-4-and naptalene-2-carbaldehydes was applied in the presence of ammonia. 1,3-disubstituted-2,3-dihydro-1H-naphtoxazines were synthesized The structures of the obtained new compounds have been clarified by spectroscopic methods (FTIR, H-1 NMR, C-13 NMR and MS) and confirmed with elemental analysis results.en
dc.identifier.eissn1304-7191
dc.identifier.endpage176
dc.identifier.issn1304-7205
dc.identifier.issue3
dc.identifier.startpage171
dc.identifier.urihttps://hdl.handle.net/20.500.14981/49840
dc.identifier.volume27
dc.identifier.wos000219488100002
dc.language.isoeng
dc.publisherYILDIZ TECHNICAL UNIV
dc.relation.ispartofSIGMA JOURNAL OF ENGINEERING AND NATURAL SCIENCES-SIGMA MUHENDISLIK VE FEN BILIMLERI DERGISI
dc.subjectHeterocyclic compounds
dc.subject1,3-Oxazine compounds
dc.subjectring closure
dc.subjectEngineering
dc.titleSYNTHESIS OF 1,3-DISUBSTITUED-2,3-DIHYDRO-1H-NAFT[1,3] OXAZINE COMPOUNDS
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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