抄録
(+)-Altholactone 1 and (+)-7-epi-altholactone 3 were constructed from D-gulonolactone whereas their respective enantiomers (-)-altholactone 2 and (-)-7-epi- altholactone 4 were synthesised from D-mannose, involving stereocontrolled reduction of the lactols 21 and 12 as a key step.
本文言語 | English |
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ページ(範囲) | 8685-8698 |
ページ数 | 14 |
ジャーナル | Tetrahedron |
巻 | 50 |
号 | 29 |
DOI | |
出版ステータス | Published - 1994 |
ASJC Scopus subject areas
- 生化学
- 創薬
- 有機化学