抄録
Multi-substituted dihydrofurans were obtained from a palladium-catalysed coupling reaction between 2,3-alkadienols and ketones bearing an electron-withdrawing group at the α-position. Methanol as a solvent was essential for the initial dehydrative substitution to suppress the competitive hydroalkylation of the diene moiety. The substitution would be followed by intramolecular hydroalkoxylation under the same catalysis.
| 本文言語 | English |
|---|---|
| ページ（範囲） | 5102-5105 |
| ページ数 | 4 |
| ジャーナル | Chemical Communications |
| 巻 | 54 |
| 号 | 40 |
| DOI | |
| 出版ステータス | Published - 2018 1 1 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry