Abstract
Trifluoropyruvamides in their hydrated form readily react with diazo esters affording new trifluoromethyl epoxides. Activating the pyruvamide with trifluoroacetic anhydride leads to a complete change in selectivity with the formation of a new diazo compound.
| Original language | English |
|---|---|
| Pages (from-to) | 797-798 |
| Number of pages | 2 |
| Journal | Synlett |
| Volume | 1997 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 1 Jan 1997 |
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