Palladium-Mediated Fluorination of Arylboronic Acids

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Palladium-Mediated Fluorination of Arylboronic Acids

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Title: Palladium-Mediated Fluorination of Arylboronic Acids
Author: Ritter, Tobias; Furuya, Takeru; Kaiser, Hanns Martin

Note: Order does not necessarily reflect citation order of authors.

Citation: Furuya, Takeru, Hanns Martin Kaiser, and Tobias Ritter. 2008. Palladium-mediated fluorination of arylboronic acids. Angewandte Chemie International Edition 47(32): 5993-5996.
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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.
Published Version: doi:10.1002/anie.200802164
Terms of Use: This article is made available under the terms and conditions applicable to Open Access Policy Articles, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#OAP
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8301598

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  • FAS Scholarly Articles [7501]
    Peer reviewed scholarly articles from the Faculty of Arts and Sciences of Harvard University
 
 

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