抄録
Treatment of S-alkyl thioesters with a reagent prepared from RCHBr2, Zn, TiCl4, and TMEDA in THF at 25°C gives Z-alkenyl sulfides selectively in good to excellent yields. Using the alkylidenation method, ketene dithioacetals and enamines are produced from 1,3-dithian-2-one and amides, respectively.
本文言語 | English |
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ページ(範囲) | 211-214 |
ページ数 | 4 |
ジャーナル | Tetrahedron Letters |
巻 | 30 |
号 | 2 |
DOI | |
出版ステータス | Published - 1989 |
外部発表 | はい |
ASJC Scopus subject areas
- 生化学
- 創薬
- 有機化学