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dc.creatorAndrejević Vladimir
dc.creatorBjelaković, Mira
dc.creatorMihailović, Milan M.
dc.creatorMihailović, Mihailo Lj.
dc.date.accessioned2021-02-02T06:45:45Z
dc.date.available2021-02-02T06:45:45Z
dc.date.issued1985
dc.identifier.issn0018-019X
dc.identifier.issn1522-2675
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4185
dc.description.abstractUnsubstituted medium‐ring 1,2‐epoxycycloalkanes and certain vic‐epoxyalkanes are reduced to the corresponding alcohols very slowly when LiAlH4 alone is used as reducing agent. However, the combination of LiAlH4 and AlCl3, in a 2:1 molar ratio (with respect to 1 mol‐equiv. of epoxide) used in refluxing Et2O, greatly enhances these reductions, rendering them of interest for practical purposes.
dc.publisherWileyde
dc.rightsrestrictedAccess
dc.sourceHelvetica Chimica Actade
dc.subject1,2‐epoxycycloalkanes
dc.subjectReduction
dc.subjectalcohols
dc.subjectLiAlH4
dc.subjectAlCl3
dc.titleThe Reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloridede
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractМихаиловић, Михаило Љ.; Михаиловић, Милан М.; Бјелаковић, Мира; Aндрејевић Владимир;
dc.citation.volume68
dc.citation.issue7
dc.citation.spage2030
dc.citation.epage2032
dc.identifier.doi10.1002/hlca.19850680727
dc.identifier.scopus2-s2.0-84987472492
dc.type.versionpublishedVersion


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