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 |
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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 |