Article ID Journal Published Year Pages File Type
1315230 Journal of Fluorine Chemistry 2007 6 Pages PDF
Abstract

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.

Graphical abstractThe addition of a radical scavenger (e.g. TEMPO) significantly improves both the reproducibility and the material yield in the formation of fluoroarenes by the fluoridation of diaryliodonium salts. Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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