抜粋
Palladium complex of 2-(phosphinoaryl)pyridine 1b, which is an effective catalyst for asymmetric allylic alkylation (denoted as AAA) of acyclic alkenyl carboxylate, was also found to be a highly effective catalyst for AAA of cyclic alkenyl carboxylate: high enantioselectivities of 87% ee and 94% ee were achieved in the reactions of 2-cyclohexenyl and 2-cycloheptenyl pivalates, respectively.
| 元の言語 | 英語 |
|---|---|
| ページ（範囲） | 284-286 |
| ページ数 | 3 |
| ジャーナル | Synlett |
| 発行部数 | 2 |
| DOI | |
| 出版物ステータス | 出版済み - 2001 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry
フィンガープリント 2-(Phosphinoaryl)pyridine ligand (2): Asymmetric allylic alkylation of 2-cycloalkenyl carboxylate' 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
Ito, K., Kashiwagi, R., Hayashi, S., Uchida, T., & Katsuki, T. (2001). 2-(Phosphinoaryl)pyridine ligand (2): Asymmetric allylic alkylation of 2-cycloalkenyl carboxylate. Synlett, (2), 284-286. https://doi.org/10.1055/s-2001-10794