Abstract
A strategy for the functionalization of lactones to afford cyclic ethers has been developed. The present synthesis involves palladium(0)-catalyzed carbonylation of lactone-derived enol phosphates and stereoselective hydroboration.
| Original language | English |
|---|---|
| Pages (from-to) | 838-840 |
| Number of pages | 3 |
| Journal | Synlett |
| Issue number | 6 |
| Publication status | Published - 2000 Jul 10 |
| Externally published | Yes |
Keywords
- Carbonylations
- Cyclic ether
- Enol phosphate
- Lactones
- Palladium
ASJC Scopus subject areas
- Organic Chemistry
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Cite this
Sasaki, M., Honda, S., Noguchi, T., Takakura, H., & Tachibana, K. (2000). Palladium-catalyzed carbonyaltion of lactone-derived enol phosphates: Stereoselective construction of functionalized cyclic ethers from lactones. Synlett, (6), 838-840.