Abstract
A new strategy for the synthesis of the core skeleton of the benzophenanthridine alkaloid corynoline has been developed which is based on an intramolecular [4+2]-cycloaddition of an amino substituted isobenzofuran derivative.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 62-76 |
| Number of pages | 15 |
| Journal | Arkivoc |
| Volume | 2003 |
| Issue number | 14 |
| State | Published - 2003 |
| Externally published | Yes |
Keywords
- 1-amino substituted isobenzofuran
- Cycloaddition
- Diels-Alder
- Intramolecular
ASJC Scopus subject areas
- Organic Chemistry