| dc.contributor.author | Furuya, Takeru | |
| dc.contributor.author | Kaiser, Hanns Martin | |
| dc.contributor.author | Ritter, Tobias | |
| 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 | |
| dc.identifier.doi | 10.1002/anie.200802164 | * |
| dash.contributor.affiliated | Ritter, Tobias | |
