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dc.contributor.authorFuruya, Takeru
dc.contributor.authorStrom, Alexandra E.
dc.contributor.authorRitter, Tobias
dc.date.accessioned2012-02-10T21:07:52Z
dc.date.issued2009
dc.identifier.citationFuruya, Takeru, Alexandra E. Strom, and Tobias Ritter. 2009. Silver-mediated fluorination of functionalized aryl stannanes. Journal of the American Chemical Society 131(5): 1662-1663.en_US
dc.identifier.issn0002-7863en_US
dc.identifier.issn1520-5126en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:8156524
dc.description.abstractWe report a regiospecific silver-mediated fluorination of aryl stannanes. The presented reaction can afford complex fluoroarenes from readily available phenols in three steps. The operational simplicity and the broad substrate scope of the fluorination should render this reaction a useful tool for the synthesis of milligram to gram quantities of functionalized aryl fluorides. Silver-mediated oxidative transformations of aryl nucleophiles that proceed via bimetallic redox processes are a new avenue to develop carbon−heteroatom bond formations.en_US
dc.description.sponsorshipChemistry and Chemical Biologyen_US
dc.language.isoen_USen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofdoi:10.1021/ja8086664en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pubmed/19191693en_US
dash.licenseOAP
dc.subjectbenzene derivativesen_US
dc.subjectchemical synthesisen_US
dc.subjectchemistryen_US
dc.subjectfluorinated hydrocarbonsen_US
dc.subjectphenolsen_US
dc.subjectsilveren_US
dc.subjecttin compoundsen_US
dc.titleSilver-Mediated Fluorination of Functionalized Aryl Stannanesen_US
dc.typeJournal Articleen_US
dc.description.versionAuthor's Originalen_US
dc.relation.journalJournal of the American Chemical Societyen_US
dash.depositing.authorRitter, Tobias
dc.date.available2012-02-10T21:07:52Z
dc.identifier.doi10.1021/ja8086664*
dash.contributor.affiliatedRitter, Tobias


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