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dc.contributor.authorMazzotti, Anthony Renato
dc.contributor.authorCampbell, Michael Glenn
dc.contributor.authorTang, Pingping
dc.contributor.authorMurphy, Jennifer Ann
dc.contributor.authorRitter, Tobias
dc.date.accessioned2014-06-17T16:17:37Z
dc.date.issued2013
dc.identifier.citationMazzotti, Anthony R., Michael G. Campbell, Pingping Tang, Jennifer M. Murphy, and Tobias Ritter. 2013. Palladium(III)-Catalyzed Fluorination of Arylboronic Acid Derivatives. Journal of the American Chemical Society 135, no. 38: 14012–14015.en_US
dc.identifier.issn0002-7863en_US
dc.identifier.issn1520-5126en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:12330896
dc.description.abstractA practical, palladium-catalyzed synthesis of aryl fluorides from arylboronic acid derivatives is presented. The reaction is operationally simple and amenable to multigram-scale synthesis. Evaluation of the reaction mechanism suggests a single-electron-transfer pathway, involving a Pd(III) intermediate that has been isolated and characterized.en_US
dc.description.sponsorshipChemistry and Chemical Biologyen_US
dc.language.isoen_USen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofdoi:10.1021/ja405919zen_US
dash.licenseOAP
dc.titlePalladium(III)-Catalyzed Fluorination of Arylboronic Acid Derivativesen_US
dc.typeJournal Articleen_US
dc.description.versionAccepted Manuscripten_US
dc.relation.journalJournal of the American Chemical Societyen_US
dash.depositing.authorRitter, Tobias
dc.date.available2014-06-17T16:17:37Z
dash.affiliation.otherDepartment of Psychiatry, Harvard Medical Schoolen_US
dc.identifier.doi10.1021/ja405919z*
workflow.legacycommentsFAR 2014en_US
dash.contributor.affiliatedMurphy, Jennifer
dash.contributor.affiliatedCampbell, Michael Glenn
dash.contributor.affiliatedTang, Pingping
dash.contributor.affiliatedMazzotti, Anthony Renato
dash.contributor.affiliatedRitter, Tobias
dc.identifier.orcid0000-0002-3590-3416


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