The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate

dc.creator	Mihailović, Milhailo Lj.
dc.creator	Stojiljković, A.
dc.creator	Andrejević, Vladimir
dc.date.accessioned	2021-05-20T11:32:28Z
dc.date.available	2021-05-20T11:32:28Z
dc.date.issued	1965
dc.identifier.issn	0040-4039
dc.identifier.issn	1873-3581
dc.identifier.uri	https://cer.ihtm.bg.ac.rs/handle/123456789/4655
dc.description.abstract	The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).	sr
dc.language.iso	en	sr
dc.publisher	Elsevier	sr
dc.rights	restrictedAccess	sr
dc.source	Tetrahedron Letters	sr
dc.subject	unbranched primary alkyl	sr
dc.subject	arylalkyl amines	sr
dc.subject	lead tetraacetate	sr
dc.subject	oxidation	sr
dc.title	The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate	sr
dc.type	article	sr
dc.rights.license	ARR	sr
dcterms.abstract	Стојиљковић, A.; Aндрејевић, Владимир; Михаиловић, Михаило Љ.;
dc.citation.volume	6
dc.citation.issue	8
dc.citation.spage	461
dc.citation.epage	464
dc.identifier.doi	10.1016/S0040-4039(00)89979-7
dc.identifier.scopus	2-s2.0-50549200778
dc.type.version	publishedVersion	sr