抄録
A new method for ynolate synthesis via the cleavage of ester dianions has been developed. The key intermediates, ester dianions, generated from α-bromocarboxylic acid ester enolates via lithium-halogen exchange turned out to be so labile that they were cleaved rapidly to give ynolates.
| 本文言語 | 英語 |
|---|---|
| ページ（範囲） | 4433-4436 |
| ページ数 | 4 |
| ジャーナル | Tetrahedron Letters |
| 巻 | 38 |
| 号 | 25 |
| DOI | |
| 出版ステータス | 出版済み - 6 23 1997 |
| 外部発表 | はい |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry