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dc.contributor.authorSladojevich, Filippo
dc.contributor.authorArlow, Sophie I.
dc.contributor.authorTang, Pingping
dc.contributor.authorRitter, Tobias
dc.date.accessioned2017-10-16T19:14:11Z
dc.date.issued2013
dc.identifier.citationSladojevich, Filippo, Sophie I. Arlow, Pingping Tang, and Tobias Ritter. 2013. Late-Stage Deoxyfluorination of Alcohols with PhenoFluor. Journal of the American Chemical Society 135, no. 7: 2470–2473.en_US
dc.identifier.issn0002-7863en_US
dc.identifier.issn1520-5126en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:34222825
dc.description.abstractAn operationally simple protocol for the selective deoxyfluorination of structurally complex alcohols is presented. Several fluorinated derivatives of natural products and pharmaceuticals have been prepared to showcase the potential of the method for late-stage diversification and its functional group compatibility. A series of simple guidelines for predicting the selectivity in substrates with multiple alcohols is given.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/ja3125405en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596866/en_US
dc.relation.hasversionhttp://rittergroup.org/pdf/2013-2470j.pdfen_US
dash.licenseMETA_ONLY
dc.titleLate-Stage Deoxyfluorination of Alcohols with PhenoFluoren_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalJournal of the American Chemical Societyen_US
dash.depositing.authorRitter, Tobias
dash.embargo.until10000-01-01
dc.identifier.doi10.1021/ja3125405*
workflow.legacycommentsFAR 2014 meta.darken_US
dash.contributor.affiliatedSladojevich, Filippo
dash.contributor.affiliatedTang, Pingping
dash.contributor.affiliatedRitter, Tobias


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