A robust iron catalyst for the selective hydrogenation of substituted (iso)quinolones

dc.bibliographicCitation.firstPage8134
dc.bibliographicCitation.issue42
dc.bibliographicCitation.journalTitleChemical Scienceeng
dc.bibliographicCitation.lastPage8141
dc.bibliographicCitation.volume9
dc.contributor.authorSahoo, Basudev
dc.contributor.authorKreyenschulte, Carsten
dc.contributor.authorAgostini, Giovanni
dc.contributor.authorLund, Henrik
dc.contributor.authorBachmann, Stephan
dc.contributor.authorScalone, Michelangelo
dc.contributor.authorJunge, Kathrin
dc.contributor.authorBeller, Matthias
dc.date.accessioned2023-04-27T11:59:28Z
dc.date.available2023-04-27T11:59:28Z
dc.date.issued2018
dc.description.abstractBy applying N-doped carbon modified iron-based catalysts, the controlled hydrogenation of N-heteroarenes, especially (iso)quinolones, is achieved. Crucial for activity is the catalyst preparation by pyrolysis of a carbon-impregnated composite, obtained from iron(ii) acetate and N-aryliminopyridines. As demonstrated by TEM, XRD, XPS and Raman spectroscopy, the synthesized material is composed of Fe(0), Fe3C and FeNx in a N-doped carbon matrix. The decent catalytic activity of this robust and easily recyclable Fe-material allowed for the selective hydrogenation of various (iso)quinoline derivatives, even in the presence of reducible functional groups, such as nitriles, halogens, esters and amides. For a proof-of-concept, this nanostructured catalyst was implemented in the multistep synthesis of natural products and pharmaceutical lead compounds as well as modification of photoluminescent materials. As such this methodology constitutes the first heterogeneous iron-catalyzed hydrogenation of substituted (iso)quinolones with synthetic importance.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12094
dc.identifier.urihttp://dx.doi.org/10.34657/11128
dc.language.isoeng
dc.publisherCambridge : RSC
dc.relation.doihttps://doi.org/10.1039/c8sc02744g
dc.relation.essn2041-6539
dc.relation.issn2041-6520
dc.rights.licenseCC BY-NC 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0
dc.subject.ddc540
dc.subject.otherAmideseng
dc.subject.otherCarboneng
dc.subject.otherCatalyst activityeng
dc.subject.otherDoping (additives)eng
dc.subject.otherHydrogenationeng
dc.subject.otherLead compoundseng
dc.subject.otherNanocatalystseng
dc.subject.otherCatalyst preparationeng
dc.subject.otherImpregnated compositeseng
dc.subject.otherIron-based catalysteng
dc.subject.otherNano-structured catalysteng
dc.subject.otherPhotoluminescent materialseng
dc.subject.otherQuinoline derivativeeng
dc.subject.otherSelective hydrogenationeng
dc.subject.otherSynthesized materialseng
dc.subject.otherIron compoundseng
dc.titleA robust iron catalyst for the selective hydrogenation of substituted (iso)quinoloneseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorLIKAT
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
c8sc02744g.pdf
Size:
2.78 MB
Format:
Adobe Portable Document Format
Description:
Collections