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dc.contributor.author	Ritter, Tobias
dc.contributor.author	Furuya, Takeru
dc.contributor.author	Kaiser, Hanns Martin
dc.date.accessioned	2012-03-01T19:08:25Z
dc.date.issued	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.identifier.uri	http://nrs.harvard.edu/urn-3:HUL.InstRepos:8301598
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
dash.depositing.author	Ritter, Tobias
dc.date.available	2012-03-01T19:08:25Z

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  Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University

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