Copper/iron co-catalyzed alkoxycarbonylation of unactivated alkyl bromides

dc.bibliographicCitation.firstPage39eng
dc.bibliographicCitation.issue1eng
dc.bibliographicCitation.journalTitleCommunications Chemistryeng
dc.bibliographicCitation.lastPage213eng
dc.bibliographicCitation.volume1eng
dc.contributor.authorLi, Y.
dc.contributor.authorWu, X.-F.
dc.date.accessioned2020-07-13T11:01:16Z
dc.date.available2020-07-13T11:01:16Z
dc.date.issued2018
dc.description.abstractCarbonylative transformations of alkyl bromides have been explored less than those of aryl halides, in part because of the high barrier to activation of aryl bromides. Additionally, alkyl-metal reagents formed in situ can tend to undergo β-hydride elimination. Here we describe a copper/iron co-catalyzed alkoxycarbonylation of unactivated alkyl bromides. In the presence of catalytic quantities of iron and copper catalysts, primary, secondary, and tertiary alkyl bromides are carbonylatively transformed into the corresponding aliphatic esters in good yields. A potential reaction mechanism is proposed based on control experiments.eng
dc.description.fondsLeibniz_Fonds
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/3510
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/4881
dc.language.isoengeng
dc.publisherLondon : Springer Natureeng
dc.relation.doihttps://doi.org/10.1038/s42004-018-0039-6
dc.relation.issn2399-3669
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.otherCarbonylative transformationseng
dc.subject.otheralkyl bromideseng
dc.subject.otheralkoxycarbonylationeng
dc.titleCopper/iron co-catalyzed alkoxycarbonylation of unactivated alkyl bromideseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Li et al 2018, Copper.pdf
Size:
665.49 KB
Format:
Adobe Portable Document Format
Description:
Collections