抜粋
Anodic fluorination of 2-cyano-1-methylpyrrole 1 using Et3N·5HF in an undivided cell provided 5,5-difluoro-1-methyl-3-pyrrolin-2-one (5a). The Diels-Alder reaction of 5a with various dienes was successfully carried out to provide gem-difluorinated heterocyclic compounds in excellent yields.
| 元の言語 | English |
|---|---|
| ページ（範囲） | 2597-2600 |
| ページ数 | 4 |
| ジャーナル | Synthesis |
| 発行部数 | 17 |
| DOI | |
| 出版物ステータス | Published - 2002 1 1 |
| 外部発表 | Yes |
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
フィンガープリント A facile synthesis of gem-difluorinated heterocyclic compounds using anodic fluorination of 2-cyano-1-methylpyrrole as a key step' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。
これを引用
Tajima, T., & Fuchigami, T. (2002). A facile synthesis of gem-difluorinated heterocyclic compounds using anodic fluorination of 2-cyano-1-methylpyrrole as a key step. Synthesis, (17), 2597-2600. https://doi.org/10.1055/s-2002-35621