Abstract
The consecutive stereoselective introduction of carbon nucleophiles at the 4- and 1-positions of a suitable pseudoglycal is shown to be an efficient route to the chiral 1,4-disubstituted tetrahydropyran (2), an early zincophorin synthon.
| Original language | English |
|---|---|
| Pages (from-to) | 1473-1488 |
| Number of pages | 16 |
| Journal | Synthetic Communications |
| Volume | 25 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 1 May 1995 |
ASJC Scopus subject areas
- Organic Chemistry