Browse by author
Lookup NU author(s): Dr Michael Carroll,
Dr Graham Smith
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The addition of radical scavengers to the fluoridation of diaryliodonium salts was demonstrated to improve significantly both the reproducibility of the process and the material yield of the desired fluoroarene products. It was also established that the selectivity of the process was not influenced by the presence of the radical scavengers. TEMPO and galvinoxyl were found to be the most suitable radical scavengers in the fluoridation process allowing the methodology to be used routinely for the first time. © 2006.
Author(s): Carroll MA, Nairne J, Smith G, Widdowson DA
Publication type: Article
Publication status: Published
Journal: Journal of Fluorine Chemistry
ISSN (print): 0022-1139
ISSN (electronic): 1873-3328
Publisher: Elsevier SA
Altmetrics provided by Altmetric