Abstract
A novel route to C-amides of the antiviral drug Foscarnet via the PFA diester 4 is described. The reaction with amines is facilitated by in situ intramolecular cyclization to form a more reactive intermediate.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1325-1326 |
| Number of pages | 2 |
| Journal | Synlett |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 1998 |
| Externally published | Yes |
ASJC Scopus subject areas
- Organic Chemistry