摘要

The natural variability in the enantiomeric distribution of biologically active chiral terpenoids in Solidago canadensis L. essential oil from Kumaon was evaluated by enantioselective capillary GC, capillary GC, and GC-MS. Germacrene D, a sesquiterpene hydrocarbon, was noticed as the major compound, contributing 56.7%, 75.5% and 69.7% to the samples, while other constituents with variable compositions were limonene (0.2 to 12.5%), bornyl acetate (2.1 to 2.9%), delta-elemene (2.4 to 3.2), beta-elemene (1.3 to 1.8%), and elemol (1.4 to 2.6%). The enantiomeric excess has been determined for germacrene D with (+)-enantiomer (> 41.8% to > 47%) dominating over the (-)-enantiomer in all the samples. Furthermore, there has been above 95% enantiomeric excess for (R)-(+)-limonene (> 95.1% to > 99%), whereas moderate to low excess for (1R)-(+)-alpha-pinene (> 47.9%), and (1S)-(-)-beta-pinene (> 30.3%) was established. Notably, only (-)-bornyl acetate was found as a single enantiomer with > 99% enantiomeric excess. However, for all the identified chiral terpenoids, the enantiomeric distribution varied within only a narrow range in all the samples.