Приказ основних података о документу

dc.creatorJevtić, Ivana I.
dc.creatorDošen-Mićović, Ljiljana I.
dc.creatorIvanović, Evica
dc.creatorIvanović, Milovan D.
dc.date.accessioned2020-12-17T21:36:09Z
dc.date.available2020-12-17T21:36:09Z
dc.date.issued2016
dc.identifier.issn0039-7881
dc.identifier.urihttp://aspace.agrif.bg.ac.rs/handle/123456789/4055
dc.description.abstractAn efficient, one-pot procedure for the Hofmann rearrangement of aromatic and aliphatic amides has been developed. Methyl and benzyl carbamates are produced with N-bromoacetamide in the presence of lithium hydroxide or lithium methoxide, in high yields. -Phenylamino amides gave five-membered cyclic ureas stereospecifically. Side products of aryl or benzyl bromination were minimized. This procedure offers an easy access to various protected amines or diamines, which represent important synthetic precursors.en
dc.publisherGeorg Thieme Verlag Kg, Stuttgart
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172032/RS//
dc.rightsrestrictedAccess
dc.sourceSynthesis-Stuttgart
dc.subjectHofmann rearrangementen
dc.subjectamidesen
dc.subjectstereoselectivityen
dc.subjectcyclizationen
dc.subjectheterocyclesen
dc.titleHofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamideen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage1560
dc.citation.issue10
dc.citation.other48(10): 1550-1560
dc.citation.rankM22
dc.citation.spage1550
dc.citation.volume48
dc.identifier.doi10.1055/s-0035-1561405
dc.identifier.scopus2-s2.0-84961231076
dc.identifier.wos000375877100012
dc.type.versionpublishedVersion


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Приказ основних података о документу