Publication: Palladium-Mediated Fluorination of Arylboronic Acids
Open/View Files
Date
2008
Published Version
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley
The Harvard community has made this article openly available. Please share how this access benefits you.
Citation
Furuya, Takeru, Hanns Martin Kaiser, and Tobias Ritter. 2008. Palladium-mediated fluorination of arylboronic acids. Angewandte Chemie International Edition 47(32): 5993-5996.
Research Data
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.
Description
Other Available Sources
Keywords
boronic acids, fluorination, palladium, synthetic methods, tomography
Terms of Use
This article is made available under the terms and conditions applicable to Open Access Policy Articles (OAP), as set forth at Terms of Service