| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1315157 | Journal of Fluorine Chemistry | 2006 | 6 Pages |
Abstract
A new preparation method of 1,1,2,2-tetrafluoro-2-(trifluoroethenyloxy)-ethanesulfonyl fluoride (8) has been developed utilizing the unique performance of the imidazole protective group. Namely, the electrodonating character of the imidazole protective group on the sulfonyl group enables the formation of the novel intermediate monomer, which can be easily converted to 8 by the reaction with HF.
Graphical abstractA new preparation method of 1,1,2,2-tetrafluoro-2-(trifluoroethenyloxy)-ethanesulfonyl fluoride has been developed utilizing the unique performance of the imidazole protective group. Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Nobuyuki Uematsu, Nobuto Hoshi, Masanori Ikeda,