抄録
The title sugar analogues (13) were synthesized by starting with known methyl (E)-5,6-dideoxy-2,3-O-isopropylidene-6-nitro-α-d-lyxo-hex-5-enofuranoside (5a) in six steps through the key intermediate, methyl 5-deoxy-5-dimethoxy-phosphinyl-2,3-O-isopropylidene-α-d-mannofuranoside 8a). The products (13) were converted into the corresponding penta-O-acetyl-5-methoxyphosphinyl derivatives (14), whose structures and conformations (mostly 4C1) were established by spectroscopy.
| 本文言語 | English |
|---|---|
| ページ（範囲） | 2557-2564 |
| ページ数 | 8 |
| ジャーナル | Heterocycles |
| 巻 | 36 |
| 号 | 11 |
| DOI | |
| 出版ステータス | Published - 11月 1 1993 |
ASJC Scopus subject areas
- 分析化学
- 薬理学
- 有機化学