Abstract
We developed a mild, rapid process employing AgF and thioamides to produce α,α-difluoromethylene amines efficiently. This method exhibited remarkable tolerance toward various functional groups present in N-sulfonylthioamides, thereby broadening the scope of difluoromethylene sulfonamides through a straightforward approach. Additionally, we applied this approach to synthesize various perfluoroalkyl amines, establishing practical synthetic routes for exploring these compounds in pharmaceutical chemistry and materials science.
| Original language | English |
|---|---|
| Pages (from-to) | 14341-14347 |
| Number of pages | 7 |
| Journal | Journal of Organic Chemistry |
| Volume | 89 |
| Issue number | 19 |
| DOIs | |
| State | Published - 4 Oct 2024 |
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