Abstract
The tautomeric structures of hipposudoric and norhipposudoric acids were investigated using a computational method. The results indicated that the most appropriate canonical structures for these compounds were different; hipposudoric acid possessed an enol form at the C9-carboxy group, while norhipposudoric acid had an enol form at the C5-oxo group.
Original language | English |
---|---|
Pages (from-to) | 1738-1740 |
Number of pages | 3 |
Journal | Chemistry Letters |
Volume | 44 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2015 |
ASJC Scopus subject areas
- Chemistry(all)