Efficient and chemoselective alkyl bromoacetate-Zn mediated transesterification method
dc.contributor.buuauthor | Coşkun, Necdet | |
dc.contributor.buuauthor | Er, Mustafa | |
dc.contributor.department | Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü. | tr_TR |
dc.contributor.orcid | 0000-0003-3879-0813 | tr_TR |
dc.contributor.researcherid | AAK-4577-2020 | tr_TR |
dc.contributor.researcherid | B-1200-2012 | tr_TR |
dc.contributor.scopusid | 7004177880 | tr_TR |
dc.contributor.scopusid | 36099880000 | tr_TR |
dc.date.accessioned | 2023-03-23T10:11:28Z | |
dc.date.available | 2023-03-23T10:11:28Z | |
dc.date.issued | 2003-05-05 | |
dc.description.abstract | Alkyl bromoacetates were shown to be versatile transesterification reagents. Isoxazoles underwent chemoselective transesterification when treated with alkyl bromoacetate-Zn in THF at reflux. A suggested mechanism of the new reaction was discussed. | en_US |
dc.identifier.citation | Coşkun, N. ve Er, M. (2003). “Efficient and chemoselective alkyl bromoacetate-Zn mediated transesterification method”. Tetrahedron, 59(19), 3481-3485. | en_US |
dc.identifier.endpage | 3485 | tr_TR |
dc.identifier.issn | 0040-4020 | |
dc.identifier.issue | 19 | tr_TR |
dc.identifier.scopus | 2-s2.0-0037420837 | tr_TR |
dc.identifier.startpage | 3481 | tr_TR |
dc.identifier.uri | https://doi.org/10.1016/S0040-4020(03)00472-1 | |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0040402003004721 | |
dc.identifier.uri | http://hdl.handle.net/11452/31716 | |
dc.identifier.volume | 59 | tr_TR |
dc.identifier.wos | 000182704100012 | |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.wos | IC | en_US |
dc.indexed.wos | CCRE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.journal | Tetrahedron | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Chemoselective transesterification | en_US |
dc.subject | Reformatsky reagent | en_US |
dc.subject | Imidazoline 3-oxides | en_US |
dc.subject | Diastereoselective addition | en_US |
dc.subject | Regio | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Cyclization | en_US |
dc.subject.emtree | Electron transport | en_US |
dc.subject.emtree | High performance liquid chromatography | en_US |
dc.subject.emtree | Nuclear overhauser effect | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Proton nuclear magnetic resonance | en_US |
dc.subject.emtree | Stereochemistry | en_US |
dc.subject.emtree | Transesterification | en_US |
dc.subject.emtree | Bromoacetic acid | en_US |
dc.subject.emtree | Ester derivative | en_US |
dc.subject.emtree | Isoxazole derivative | en_US |
dc.subject.emtree | Tetrahydrofuran | en_US |
dc.subject.emtree | Zinc | en_US |
dc.subject.scopus | Nitrones; Direct; Hydroxylamines | en_US |
dc.subject.wos | Chemistry, organic | en_US |
dc.title | Efficient and chemoselective alkyl bromoacetate-Zn mediated transesterification method | en_US |
dc.type | Article | |
dc.wos.quartile | Q2 | en_US |
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