Abstract
The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by x-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.
| Original language | English |
|---|---|
| Pages (from-to) | 1266-1271 |
| Number of pages | 6 |
| Journal | Chemistry of Heterocyclic Compounds |
| Volume | 33 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 1997 |
| Externally published | Yes |