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dc.contributor.authorTang, Pingping
dc.contributor.authorWang, Weike
dc.contributor.authorRitter, Tobias
dc.date.accessioned2012-02-17T23:38:05Z
dc.date.issued2011
dc.identifier.citationTang, Pingping, Weike Wang, and Tobias Ritter. 2011. Deoxyfluorination of phenols. Journal of the American Chemical Society 133(30): 11482–11484.en_US
dc.identifier.issn0002-7863en_US
dc.identifier.issn1520-5126en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:8191172
dc.description.abstractAn operationally simple ipso fluorination of phenols with a new deoxyfluorination reagent is presented.en_US
dc.description.sponsorshipChemistry and Chemical Biologyen_US
dc.language.isoen_USen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofdoi:10.1021/ja2048072en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pubmed/21736304en_US
dash.licenseOAP
dc.subjectx-ray crystallographyen_US
dc.subjectchemistryen_US
dc.subjectfluorinated hydrocarbonsen_US
dc.subjectchemical synthesisen_US
dc.subjectmolecular modelsen_US
dc.subjectmolecular structureen_US
dc.subjectstereoisomerismen_US
dc.subjectphenolsen_US
dc.titleDeoxyfluorination of Phenolsen_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.available2012-02-17T23:38:05Z
dc.identifier.doi10.1021/ja2048072*
dash.contributor.affiliatedTang, Pingping
dash.contributor.affiliatedRitter, Tobias


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