摘要
Four 6-phenyl- and 8-phenyltetrahydroisoquinolines were prepared by structural modifications of boldine nucleus. These involved four major reaction steps, including solvolysis of 2-hydroxyaporphine, ozonolysis of the C-9, 10 double bond of phenanthrene nucleus leading to the key intermediate, and final Pictet-Spengler cyclization to respective target products.
原文 | 英語 |
---|---|
頁(從 - 到) | 1573-1588 |
頁數 | 16 |
期刊 | Heterocycles |
卷 | 60 |
發行號 | 7 |
DOIs | |
出版狀態 | 已發佈 - 7月 1 2003 |
對外發佈 | 是 |
ASJC Scopus subject areas
- 分析化學
- 藥理
- 有機化學