Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers

dc.creator	Mihailović, Milhailo Lj.
dc.creator	Čeković, Živorad M.
dc.creator	Jeremić, Dragoslav
dc.date.accessioned	2021-05-17T11:29:49Z
dc.date.available	2021-05-17T11:29:49Z
dc.date.issued	1965
dc.identifier.issn	0040-4020
dc.identifier.issn	1464-5416
dc.identifier.uri	https://cer.ihtm.bg.ac.rs/handle/123456789/4628
dc.description.abstract	The lead tetraacetate oxidation of saturated aliphatic alcohols, with structures which do not permit 1,5-cyclization, gave tetrahydropyran derivatives in yields not exceeding 16%. The formation of a small amount of the rearranged ether, 2-ethyl-2-methyltetrahydrofuran, from 4,4-dimethyl-1-pentanol indicates that the cyclization reaction proceeds via an intermediate with carbonium ion character.	sr
dc.language.iso	en	sr
dc.publisher	Elsevier	sr
dc.relation	The Research Fund of SR Serbia, Yugoslavia	sr
dc.rights	restrictedAccess	sr
dc.source	Tetrahedron	sr
dc.subject	lead tetraacetate	sr
dc.subject	oxidation	sr
dc.subject	six-membered cyclic ethers	sr
dc.subject	saturated aliphatic alcohols	sr
dc.title	Lead tetraacetate oxidation of saturated aliphatic alcohols-IV. The formation of six-membered cyclic ethers	sr
dc.type	article	sr
dc.rights.license	ARR	sr
dcterms.abstract	Јеремић, Драгослав; Михаиловíћ, Милхаило Љ.; Чековић, Живорад М.;
dc.citation.volume	21
dc.citation.issue	10
dc.citation.spage	2813
dc.citation.epage	2821
dc.identifier.doi	10.1016/S0040-4020(01)98366-8
dc.identifier.scopus	2-s2.0-0141825638
dc.type.version	publishedVersion	sr