Приказ основних података о документу
The reaction of lead tetra-acetate with some acyclic hydroxy-ethers
dc.creator | Mihailović, Milhailo Lj. | |
dc.creator | Miloradović, M. | |
dc.date.accessioned | 2021-06-07T14:33:04Z | |
dc.date.available | 2021-06-07T14:33:04Z | |
dc.date.issued | 1966 | |
dc.identifier.issn | 0040-4020 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4685 | |
dc.description.abstract | By means of lead tetra-acetate in refluxing benzene open-chain 1,2-, 1,3-, 1,4- and 1,5-hydroxy-ethers are mainly converted to the corresponding five-membered or six-membered cylic products. Thus, 2-alkoxy-1-ethanols afford 2-substituted 1,3-dioxolanes in 50-53% yield and 4-ethoxy-1-butanol gives 2-ethoxytetrahydrofuran in 52% yield; 3-alkoxy-1-propanols are oxidized to the corresponding 2-substituted 1,3-dioxans in 26-40% yield and 5-ethoxy-1-pentanol cyclizes to 2-ethoxytetrahydropyran in 46% yield. 2-Phenoxyethanol undergoes ring closure to 1,4-benzodioxan in 15% yield. | sr |
dc.language.iso | en | sr |
dc.publisher | Elsevier | sr |
dc.relation | The Serbian Republic Research Fund | sr |
dc.relation | The Yugoslav Federal Research Fund | sr |
dc.rights | restrictedAccess | sr |
dc.source | Tetrahedron | sr |
dc.subject | acyclic hydroxy-ethers | sr |
dc.subject | lead tetra-acetate | sr |
dc.subject | synthesis | sr |
dc.subject | ring closure | sr |
dc.subject | cyclisation | sr |
dc.title | The reaction of lead tetra-acetate with some acyclic hydroxy-ethers | sr |
dc.type | article | sr |
dc.rights.license | ARR | sr |
dcterms.abstract | Михаиловíћ, Милхаило Љ.; Милорадовић, М.; | |
dc.citation.volume | 22 | |
dc.citation.issue | 2 | |
dc.citation.spage | 723 | |
dc.citation.epage | 738 | |
dc.identifier.doi | 10.1016/0040-4020(66)80043-1 | |
dc.identifier.scopus | 2-s2.0-0042455524 | |
dc.type.version | publishedVersion | sr |