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