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Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1
dc.creator | Mićović, Vukić M. | |
dc.creator | Mamuzić, R. I. | |
dc.creator | Jeremić, Dragoslav | |
dc.creator | Mihailović, Milhailo Lj. | |
dc.date.accessioned | 2021-05-17T11:28:24Z | |
dc.date.available | 2021-05-17T11:28:24Z | |
dc.date.issued | 1964 | |
dc.identifier.issn | 0040-4020 | |
dc.identifier.issn | 1464-5416 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/4627 | |
dc.description.abstract | When oxidized with lead tetraacetate 1-heptanol and 1-octanol undergo cyclization to give as major products the corresponding 2-alkyltetrahydrofurans, accompanied by a small amount of the isomeric tetrahydropyran derivatives. Secondary aliphatic alcohols, under similar conditions, are converted to a mixture of cis and trans 2,5-dialkyltetrahydrofurans. | sr |
dc.language.iso | en | sr |
dc.publisher | Elsevier | sr |
dc.rights | restrictedAccess | sr |
dc.source | Tetrahedron | sr |
dc.subject | lead tetraacetate | sr |
dc.subject | oxidation | sr |
dc.subject | saturated aliphatic alcohols | sr |
dc.subject | tetrahydropyran | sr |
dc.title | Reactions with lead tetraacetate-I. Oxidation of saturated aliphatic alcohols part 1 | sr |
dc.type | article | sr |
dc.rights.license | ARR | sr |
dcterms.abstract | Мамузић, Р. И.; Мићовић, Вукић М.; Јеремић, Драгослав; Михаиловíћ, Милхаило Љ.; | |
dc.citation.volume | 20 | |
dc.citation.issue | 10 | |
dc.citation.spage | 2279 | |
dc.citation.epage | 2287 | |
dc.identifier.doi | 10.1016/S0040-4020(01)97615-X | |
dc.identifier.scopus | 2-s2.0-0000187709 | |
dc.type.version | publishedVersion | sr |