1195901-22-4Relevant articles and documents
Oxidative amination of heteroaromatic zinc reagents mediated by PhI(OAc)2
Kienle, Marcel,Dunst, Cora,Knochel, Paul
, p. 5158 - 5161 (2009)
The oxidative amination of functionalized heterocycles has been achieved by using readily available heterocyclic zinc reagents and lithium amides. PhI(OAc)2 proved to be a suitable reagent for this oxidative amination
Preparation of heterocyclic amines via a copper(i)-mediated oxidative cross-coupling of organozinc reagents with lithium amides
Dunst, Cora,Kienle, Marcel,Knochel, Paul
experimental part, p. 2313 - 2318 (2010/08/21)
Functionalized heteroaromatic amines are readily prepared by the oxidative coupling of polyfunctional zinc amidocuprates using PhI(OAc)2 as oxidant. Various sensitive heterocyclic organometallics undergo this oxidative cross-coupling reaction furnishing aminated heteroaromatics. A high functional group tolerance and relative insensibility to steric hindrance characterize this general amination reaction. A practical procedure for the preparation of protected primary and secondary as well as tertiary heteroaryl amines is described. Georg Thieme Verlag Stuttgart - New York.