Abstract
An efficient synthesis of 3-substituted crotonaldehydes via alkyne-enol ether cross-metathesis in the presence of CuSO4 and in aqueous medium was developed. Crotonaldehydes were obtained in good yields from terminal aryl-alkynes as well as from terminal alkyl-alkynes. All of the reactions were carried out under microwave irradiation and were completed in a few minutes. Water was used as the cosolvent, making this approach safer, economic, and desiderable from an enviromental point of view.
| Original language | English |
|---|---|
| Pages (from-to) | 3172-3174 |
| Journal | The Journal of Organic Chemistry |
| Volume | 74 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 2009 |
Keywords
- quaternary ammonium group
- ring-closing metathesis
- Baylis-Hillman reaction
- olefin metathesis
- enyne metathesis
- catalyst-bearing
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