Prikaz osnovnih podataka o dokumentu
Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide
dc.creator | Jevtić, Ivana I. | |
dc.creator | Došen-Mićović, Ljiljana I. | |
dc.creator | Ivanović, Evica | |
dc.creator | Ivanović, Milovan D. | |
dc.date.accessioned | 2020-12-17T21:36:09Z | |
dc.date.available | 2020-12-17T21:36:09Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 0039-7881 | |
dc.identifier.uri | http://aspace.agrif.bg.ac.rs/handle/123456789/4055 | |
dc.description.abstract | An 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.publisher | Georg Thieme Verlag Kg, Stuttgart | |
dc.relation | info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172032/RS// | |
dc.rights | restrictedAccess | |
dc.source | Synthesis-Stuttgart | |
dc.subject | Hofmann rearrangement | en |
dc.subject | amides | en |
dc.subject | stereoselectivity | en |
dc.subject | cyclization | en |
dc.subject | heterocycles | en |
dc.title | Hofmann Rearrangement of Carboxamides Mediated by N-Bromoacetamide | en |
dc.type | article | |
dc.rights.license | ARR | |
dc.citation.epage | 1560 | |
dc.citation.issue | 10 | |
dc.citation.other | 48(10): 1550-1560 | |
dc.citation.rank | M22 | |
dc.citation.spage | 1550 | |
dc.citation.volume | 48 | |
dc.identifier.doi | 10.1055/s-0035-1561405 | |
dc.identifier.scopus | 2-s2.0-84961231076 | |
dc.identifier.wos | 000375877100012 | |
dc.type.version | publishedVersion |