1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/28770
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dc.date.accessioned2022-09-16T06:24:35Z-
dc.date.available2022-09-16T06:24:35Z-
dc.date.issued2007-02-01-
dc.identifier.citationCoşkun, N. ve Çetin, M. (2007). "A new regioselective synthesis and ambient light photochemistry of quinazolin-1-oxides". Tetrahedron, 63(14), 2966-2972.en_US
dc.identifier.issn0040-4020-
dc.identifier.urihttps://doi.org/10.1016/j.tet.2007.02.004-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040402007001822-
dc.identifier.urihttp://hdl.handle.net/11452/28770-
dc.description.abstractQuinazolin-1-oxides were prepared by the oxidation of tetrahydroquinazolines with H2O2-tungstate and their ambient light photochemistry was investigated. Substituent effects on their photochemical cyclization and the reactions of the products 1aH- [1,2]oxazireno[2,3-a]quinazolines under photochemical and thermal conditions are reported. The cyclization of quinazolin-1-oxides and the reactions of 1aH-[1,2]oxazireno[2,3-a]quinazolines show pronounced solvent isotope and solvent effects.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmbient light photochemistryen_US
dc.subjectRing chan tautomerismen_US
dc.subjectAcridone alkaloidsen_US
dc.subjectN-oxidesen_US
dc.subjectQuinazolinesen_US
dc.subjectQuinolineen_US
dc.subject1,4-benzodiazepinesen_US
dc.subjectInhibitorsen_US
dc.subjectRearrangementen_US
dc.subjectQuinazolin-1-olen_US
dc.subjectPhotochemical deoxygenationen_US
dc.subjectQuinazolin-1-oxideen_US
dc.subjectQuinazolin-3-oxideen_US
dc.subjectQuinazolin-4(3H)-oneen_US
dc.subjectSolvent effecten_US
dc.subjectSolvent isotope effecten_US
dc.titleA new regioselective synthesis and ambient light photochemistry of quinazolin-1-oxidesen_US
dc.typeArticleen_US
dc.identifier.wos000248356100003tr_TR
dc.identifier.scopus2-s2.0-33847323427tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage2966tr_TR
dc.identifier.endpage2972tr_TR
dc.identifier.volume63tr_TR
dc.identifier.issue14tr_TR
dc.relation.journalTetrahedronen_US
dc.contributor.buuauthorCoşkun, Necdet-
dc.contributor.buuauthorÇetin, Meliha-
dc.subject.wosChemistry, organicen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ1en_US
dc.contributor.scopusid7004177880tr_TR
dc.contributor.scopusid7101935493tr_TR
dc.subject.scopusUracil Derivatives; Biocomposites; Captionsen_US
dc.subject.emtreeLighten_US
dc.subject.emtreeHydrogen peroxideen_US
dc.subject.emtreeOxideen_US
dc.subject.emtreeQuinazoline derivativeen_US
dc.subject.emtreeSolventen_US
dc.subject.emtreeTungsten derivativeen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCarbon nuclear magnetic resonanceen_US
dc.subject.emtreeCyclizationen_US
dc.subject.emtreePhotochemistryen_US
dc.subject.emtreeProton nuclear magnetic resonanceen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeQuantum yielden_US
dc.subject.emtreeReaction analysisen_US
dc.subject.emtreeStereochemistryen_US
dc.subject.emtreeSynthesisen_US
dc.subject.emtreeOxidationen_US
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