Sixteen new thymol derivatives have been isolated from Eupatorium fortunei
and their structures determined based on spectroscopic data. They were clas
sified into three groups (i-iii) depending on the oxidation levels: (i) one
oxygen function at the 9-position, (ii) two oxygen functions at the 8- and
9-positions, and (iii) three oxygen functions at the 8-, 9-, and 10-positi
ons. The hydroxyl groups are acylated with tigloyl, angeloyl, acetyl, isobu
tyryl, 3-methyl-2-butenoyl, or 2-methylbutyryl moieties. The compounds havi
ng chiral centers showed no specific rotation and exist as racemic mixtures
.