抄録
Alkylation of 2-phenylsulfinylethanol resulted syndiastereomer as the major products, although the ratio of syn/anti isomers varied depending on the alkyl groups. By application of this procedure to the chiral sulfoxides, optically active epoxides have been obtained in good yields.
| 本文言語 | English |
|---|---|
| ページ（範囲） | 2895-2898 |
| ページ数 | 4 |
| ジャーナル | Tetrahedron Letters |
| 巻 | 31 |
| 号 | 20 |
| DOI | |
| 出版ステータス | Published - 1990 |
ASJC Scopus subject areas
- 生化学
- 創薬
- 有機化学