Abstract
The Mitsunobu reaction of optically active 1,2-O-benzylideneconduritol E with p-nitrobenzoic acid is found to occur with retention at the C-3 center and with inversion at the C-4 center which leads to a new route to optically active conduritol F.
| Original language | English |
|---|---|
| Pages (from-to) | 257-259 |
| Number of pages | 3 |
| Journal | Synlett |
| Volume | 1995 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - Mar 1 1995 |
| Externally published | Yes |
Keywords
- asymmetric dioxylation
- conduritol E
- conduritol F
- enantiocontrolled synthesis
- Mitsunobu reaction
ASJC Scopus subject areas
- Organic Chemistry