Abstract
The endiyne derivative, dynemicin, is postulated to undergo bioreductive cis ring opening of a benzylic epoxide and activate the endiyne unit for Bergman rearrangement to an arene-1,4-diyl.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1521-1522 |
| Number of pages | 2 |
| Journal | Tetrahedron Letters |
| Volume | 31 |
| Issue number | 11 |
| DOIs | |
| State | Published - 1990 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry