Abstract
A synthesis of cyanolide A, a diolide natural product, has been achieved using a diastereoselective Barbier reaction, early-stage glycosylation, and intramolecular oxa-Michael addition to form the THP ring.
| Original language | English |
|---|---|
| Article number | SS-2014-T0094-OP |
| Pages (from-to) | 1731-1738 |
| Number of pages | 8 |
| Journal | Synthesis |
| Volume | 46 |
| Issue number | 13 |
| DOIs | |
| Publication status | Published - Jul 2014 |
| Externally published | Yes |
ASJC Scopus Subject Areas
- Catalysis
- Organic Chemistry
Keywords
- Barbier reaction
- cyclisation
- glycosylation
- Michael addition
- natural products