抄録
The alkylation of ethyl (S)- and (R)-4,5-epoxy-2-pentenoates (11) and (12), chiral terminal γ,δ-epoxy acrylates prepared from D-mannitol, by trialkylaluminum in the presence of water occurs rcgioselectively at the γ position, i.e., at the internal position, to yield a sole product respectively with net inversion of configuration. The method provides useful chiral synthons for natural product synthesis.
本文言語 | 英語 |
---|---|
ページ(範囲) | 3419-3422 |
ページ数 | 4 |
ジャーナル | Tetrahedron Letters |
巻 | 38 |
号 | 19 |
DOI | |
出版ステータス | 出版済み - 1997/05/12 |
ASJC Scopus 主題領域
- 生化学
- 創薬
- 有機化学