Abstract
Bis(trifluoromethyl) substituted hetero-1,3-dienes can be transformed into partially fluorinated five-membered heterocycles by a new reductive cyclization protocol. Certain members of the new class of heterocycles represent versatile building blocks. α-Trifluoromethyl a-amino acids, trifluoromethyl substituted butenolides and a-trifluoromethyl-y-keto acids are readily available via 5-fluoro-4-trifluoromethyloxazoles and 2-fluoro-3-trifluoromethylfurans, respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 569-592 |
| Number of pages | 24 |
| Journal | Heterocycles |
| Volume | 69 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Dec 2006 |
| Externally published | Yes |
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