Abstract
An efficient method to synthesize (Z)-keto-enyne and its epoxide, possible key intermediates in the total synthesis of maduropeptin chromophore, has been developed through a BuLi-mediated reductive opening of α-bromoepoxide.
| Original language | English |
|---|---|
| Pages (from-to) | 1494-1496 |
| Number of pages | 3 |
| Journal | Synlett |
| Issue number | 10 |
| Publication status | Published - 2000 |
Keywords
- Enynes
- Epoxides
- Halides
- Ring opening
- Stereoselective synthesis
ASJC Scopus subject areas
- Organic Chemistry