Yayın: A new regioselective synthesis and ambient light photochemistry of quinazolin-1-oxides
| dc.contributor.buuauthor | Coşkun, Necdet | |
| dc.contributor.buuauthor | Çetin, Meliha | |
| dc.contributor.department | Fen Edebiyat Fakültesi | |
| dc.contributor.department | Kimya Bölümü | |
| dc.contributor.scopusid | 7004177880 | |
| dc.contributor.scopusid | 7101935493 | |
| dc.date.accessioned | 2022-09-16T06:24:35Z | |
| dc.date.available | 2022-09-16T06:24:35Z | |
| dc.date.issued | 2007-02-01 | |
| dc.description.abstract | Quinazolin-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. | |
| dc.identifier.citation | Coşkun, N. ve Çetin, M. (2007). "A new regioselective synthesis and ambient light photochemistry of quinazolin-1-oxides". Tetrahedron, 63(14), 2966-2972. | |
| dc.identifier.doi | 10.1016/j.tet.2007.02.004 | |
| dc.identifier.endpage | 2972 | |
| dc.identifier.issn | 0040-4020 | |
| dc.identifier.issue | 14 | |
| dc.identifier.scopus | 2-s2.0-33847323427 | |
| dc.identifier.startpage | 2966 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tet.2007.02.004 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040402007001822 | |
| dc.identifier.uri | http://hdl.handle.net/11452/28770 | |
| dc.identifier.volume | 63 | |
| dc.identifier.wos | 000248356100003 | |
| dc.indexed.wos | SCIE | |
| dc.language.iso | en | |
| dc.publisher | Pergamon-Elsevier Science | |
| dc.relation.journal | Tetrahedron | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Ambient light photochemistry | |
| dc.subject | Ring chan tautomerism | |
| dc.subject | Acridone alkaloids | |
| dc.subject | N-oxides | |
| dc.subject | Quinazolines | |
| dc.subject | Quinoline | |
| dc.subject | 1,4-benzodiazepines | |
| dc.subject | Inhibitors | |
| dc.subject | Rearrangement | |
| dc.subject | Quinazolin-1-ol | |
| dc.subject | Photochemical deoxygenation | |
| dc.subject | Quinazolin-1-oxide | |
| dc.subject | Quinazolin-3-oxide | |
| dc.subject | Quinazolin-4(3H)-one | |
| dc.subject | Solvent effect | |
| dc.subject | Solvent isotope effect | |
| dc.subject.emtree | Light | |
| dc.subject.emtree | Hydrogen peroxide | |
| dc.subject.emtree | Oxide | |
| dc.subject.emtree | Quinazoline derivative | |
| dc.subject.emtree | Solvent | |
| dc.subject.emtree | Tungsten derivative | |
| dc.subject.emtree | Article | |
| dc.subject.emtree | Carbon nuclear magnetic resonance | |
| dc.subject.emtree | Cyclization | |
| dc.subject.emtree | Photochemistry | |
| dc.subject.emtree | Proton nuclear magnetic resonance | |
| dc.subject.emtree | Priority journal | |
| dc.subject.emtree | Quantum yield | |
| dc.subject.emtree | Reaction analysis | |
| dc.subject.emtree | Stereochemistry | |
| dc.subject.emtree | Synthesis | |
| dc.subject.emtree | Oxidation | |
| dc.subject.scopus | Uracil Derivatives; Biocomposites; Captions | |
| dc.subject.wos | Chemistry, organic | |
| dc.title | A new regioselective synthesis and ambient light photochemistry of quinazolin-1-oxides | |
| dc.type | Article | |
| dc.wos.quartile | Q1 | |
| dspace.entity.type | Publication | |
| local.contributor.department | Fen Edebiyat Fakültesi/Kimya Bölümü | |
| local.indexed.at | Scopus | |
| local.indexed.at | WOS |
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