Palladium-Mediated Fluorination of Arylboronic Acids

DSpace/Manakin Repository

Palladium-Mediated Fluorination of Arylboronic Acids

Citable link to this page


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:
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
Citable link to this page:
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search