Abstract
A general synthesis of γ-trifluoromethyl α,β-unsaturated γ-butyrolactones is described. The fluoride-catalyzed nucleophilic addition of a trifluoromethyl (CF3) group generated from (trifluoromethyl)trimethylsilane (CF3SiMe3, Ruppert-Prakash reagent) to a masked maleic anhydride 1 (cyclopentadiene-maleic anhydride adduct) provides the corresponding adducts 2 with high stereoselectivity. The γ-trifluoromethyl α,β-unsaturated γ-butyrolactones 4 were obtained after treatment of the adducts 2 with Grignard reagents, followed by flash-vacuum pyrolysis.
| Original language | English |
|---|---|
| Pages (from-to) | 6650-6658 |
| Number of pages | 9 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 11 |
| Issue number | 38 |
| DOIs | |
| Publication status | Published - 14 Oct 2013 |
| Externally published | Yes |
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