抄録
The stereoselective total synthesis of the title compound starting from D-glucose is described. The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reaction to build the phenanthridone skeleton.
本文言語 | English |
---|---|
ページ(範囲) | 4525-4528 |
ページ数 | 4 |
ジャーナル | Tetrahedron Letters |
巻 | 32 |
号 | 35 |
DOI | |
出版ステータス | Published - 1991 |
ASJC Scopus subject areas
- 生化学
- 創薬
- 有機化学