Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5229534 | Tetrahedron | 2005 | 6 Pages |
Abstract
Various 2-oxazolidinones were galvanostatically electrooxidized in the presence of various fluoride salts. It was found that a fluorine atom was introduced to the α-position of the nitrogen atom of N-acyl- and N-alkoxycarbonyl-2-oxazolidinones to provide the corresponding α-fluorinated products in moderate to good yields. In the case of N-phenoxycarbonyl derivative, fluorination took place on the phenyl group selectively.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yi Cao, Katsutoshi Suzuki, Toshiki Tajima, Toshio Fuchigami,