Palladium-Mediated Fluorination of Arylboronic Acids

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Palladium-Mediated Fluorination of Arylboronic Acids

Show simple item record Ritter, Tobias Furuya, Takeru Kaiser, Hanns Martin 2012-03-01T19:08:25Z 2008
dc.identifier.citation Furuya, Takeru, Hanns Martin Kaiser, and Tobias Ritter. 2008. Palladium-mediated fluorination of arylboronic acids. Angewandte Chemie International Edition 47(32): 5993-5996. en_US
dc.identifier.issn 1433-7851 en_US
dc.description.abstract Saving the best for last: Novel palladium complexes allow mild, two-step fluorination of aryl boronic acids (see scheme). The reaction is regiospecific, functional-group tolerant, has a broad substrate scope, and is ideally suited for the introduction of fluorine substituents at a late stage for aryl fluoride synthesis. en_US
dc.description.sponsorship Chemistry and Chemical Biology en_US
dc.language.iso en_US en_US
dc.publisher Wiley en_US
dc.relation.isversionof doi:10.1002/anie.200802164 en_US
dash.license OAP
dc.subject boronic acids en_US
dc.subject fluorination en_US
dc.subject palladium en_US
dc.subject synthetic methods en_US
dc.subject tomography en_US
dc.title Palladium-Mediated Fluorination of Arylboronic Acids en_US
dc.type Journal Article en_US
dc.description.version Accepted Manuscript en_US
dc.relation.journal Angewandte Chemie International Edition en_US Ritter, Tobias 2012-03-01T19:08:25Z

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