Palladium-Mediated Fluorination of Arylboronic Acids
| 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. |
| Full Text & Related Files: |
Angew. Chem. Int. 2008, 47, 5993.pdf (1.213Mb; PDF) 
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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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