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Synthesis of enantiopure aminonaphthol derivatives under conventional/ultrasonic technique and their ring-closure reaction

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dc.contributor.authorPelit, Emel
dc.contributor.authorTurgut, Zuhal
dc.date.accessioned2026-06-27T13:48:20Z
dc.date.issued2016
dc.description.abstractNew optically active aminoalkylnaphthols were obtained by condensation of 2-naphthol, substituted aromatic and heteroaromatic aldehydes and (R)-(+)-1-phenylethylamine or (S)-(-)-1-phenylethylamine under conventional methods and ultrasonic irradiation. The enantiopure aminoalkylnaphthol derivatives were converted in ring-closure reaction with formaldehyde to the corresponding naphthoxazine derivatives. (C) 2014 King Saud University. Production and hosting by Elsevier B.V. All rights reserved.en
dc.description.sponsorshipYildiz Technical University Foundation [26-01-02-02]
dc.description.urihttps://doi.org/10.1016/j.arabjc.2014.02.017
dc.identifier.doi10.1016/j.arabjc.2014.02.017
dc.identifier.eissn1878-5379
dc.identifier.endpage429
dc.identifier.issn1878-5352
dc.identifier.issue3
dc.identifier.startpage421
dc.identifier.urihttps://hdl.handle.net/20.500.14981/54990
dc.identifier.volume9
dc.identifier.wos000375599500013
dc.language.isoeng
dc.publisherELSEVIER SCIENCE BV
dc.relation.ispartofARABIAN JOURNAL OF CHEMISTRY
dc.rightsopenAccess
dc.subjectMannich reaction
dc.subjectUltrasonic irradiation
dc.subjectAminoalkylnaphthol compound
dc.subjectOne pot reaction
dc.subjectCATALYTIC ENANTIOSELECTIVE ADDITION
dc.subjectRICH AROMATIC-COMPOUNDS
dc.subjectONE-POT SYNTHESIS
dc.subjectULTRASOUND IRRADIATION
dc.subjectBETTI BASE
dc.subjectSTEREOSELECTIVE SYNTHESIS
dc.subjectARYL ALDEHYDES
dc.subjectDIETHYLZINC
dc.subjectAMINOALKYLATION
dc.subjectDIALKYLZINCS
dc.subjectChemistry
dc.titleSynthesis of enantiopure aminonaphthol derivatives under conventional/ultrasonic technique and their ring-closure reaction
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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