Yayın: Selective oxidative deoximation with anhydrous Ce(IV) sulfate
| dc.contributor.author | Asutay, Oktay | |
| dc.contributor.author | Hamarat, Nilüfer | |
| dc.contributor.author | Uludağ, Nesimi | |
| dc.contributor.buuauthor | Coşkun, Necdet | |
| dc.contributor.department | Fen Edebiyat Fakültesi | |
| dc.contributor.department | Kimya Bölümü | |
| dc.contributor.researcherid | B-1200-2012 | |
| dc.contributor.scopusid | 7004177880 | |
| dc.date.accessioned | 2023-10-30T08:15:44Z | |
| dc.date.available | 2023-10-30T08:15:44Z | |
| dc.date.issued | 2015-06-17 | |
| dc.description.abstract | Anhydrous Ce(SO4)(2) in chloroform selectively converts oximes into the parent carbonyl compounds in good yields. Hammett correlations helped to indicate a plausible mechanism for the above reaction. The formation of 1-(dinitromethyl)benzene was assumed to be a product of isonitroso hydrogen reaction with arylaldoximes. | |
| dc.description.sponsorship | Namık Kemal Üniversitesi (NKUBAP.00.M6.AR.12.01) | |
| dc.identifier.citation | Asutay, O. vd. (2015). "Selective oxidative deoximation with anhydrous Ce(IV) sulfate". Tetrahedron Letters, 56(25), 3902-3904. | |
| dc.identifier.doi | 10.1016/j.tetlet.2015.04.111 | |
| dc.identifier.endpage | 3904 | |
| dc.identifier.issn | 0040-4039 | |
| dc.identifier.issue | 25 | |
| dc.identifier.scopus | 2-s2.0-84930181671 | |
| dc.identifier.startpage | 3902 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tetlet.2015.04.111 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040403915007686 | |
| dc.identifier.uri | http://hdl.handle.net/11452/34661 | |
| dc.identifier.volume | 56 | |
| dc.identifier.wos | 000356549600013 | |
| dc.indexed.wos | SCIE | |
| dc.indexed.wos | CCRE | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.relation.bap | NKUBAP.00.M6.AR.12.01 | |
| dc.relation.collaboration | Yurt içi | |
| dc.relation.journal | Tetrahedron Letters | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Chemistry | |
| dc.subject | Oxidation | |
| dc.subject | Oximes | |
| dc.subject | Reaction mechanism | |
| dc.subject | Hammett correlation | |
| dc.subject | Isonitroso hydrogen | |
| dc.subject | Parent carbonyl-compounds | |
| dc.subject | One-pot synthesis | |
| dc.subject | Preparative conversion | |
| dc.subject | Efficient | |
| dc.subject | Regeneration | |
| dc.subject | Derivatives | |
| dc.subject | Nitrate | |
| dc.subject.emtree | 1 (dinitromethyl)benzene | |
| dc.subject.emtree | Benzene | |
| dc.subject.emtree | Carbonyl derivative | |
| dc.subject.emtree | Cerium | |
| dc.subject.emtree | Chlorinated hydrocarbon | |
| dc.subject.emtree | Chloroform | |
| dc.subject.emtree | Hydrogen | |
| dc.subject.emtree | Nitrile oxide | |
| dc.subject.emtree | Oxime | |
| dc.subject.emtree | Sulfate | |
| dc.subject.emtree | Unclassified drug | |
| dc.subject.emtree | Article | |
| dc.subject.emtree | Chemical reaction | |
| dc.subject.emtree | Oxidative deoximation | |
| dc.subject.emtree | Room temperature | |
| dc.subject.scopus | Oximes; Carbonyl derivative; Ketone | |
| dc.subject.wos | Chemistry, organic | |
| dc.title | Selective oxidative deoximation with anhydrous Ce(IV) sulfate | |
| dc.type | Article | |
| dc.wos.quartile | Q2 | |
| dspace.entity.type | Publication | |
| local.contributor.department | Fen Edebiyat Fakültesi/Kimya Bölümü | |
| local.indexed.at | Scopus | |
| local.indexed.at | WOS |
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