(lS,4S)-trans-dihydrocarvone - caraway = (2S,5S)-5-isopropenyl-2-methylcyclohexanone Ref: G. F. Russell & J. I. Hills, Odor Differences between Enantiomeric Isomers, Science, Vol. 172, 1043-1044 (1971);

(1R,4R)-trans-dihydrocarvone - Spearmint = (2R,5R)-5-isopropenyl-2-methylcyclohexanone Ref: G. F. Russell & J. I. Hills, Odor Differences between Enantiomeric Isomers, Science, Vol. 172, 1043-1044 (1971)

(1R,4S)-cis-dihydrocarvone - Odor - akin to musty and woody), but panelists had no difficulty distinguishing between the enantiomeric pairs. = (2R,5S)-5-isopropenyl-2-methylcyclohexanone Ref: G. F. Russell & J. I. Hills, Odor Differences between Enantiomeric Isomers, Science, Vol. 172, 1043-1044 (1971);

(1S,4R)-cis-dihydrocarvone - Odor - akin to musty and woody), but panelists had no difficulty distinguishing between the enantiomeric pairs. = (2S,5R)-5-isopropenyl-2-methylcyclohexanone Ref: G. F. Russell & J. I. Hills, Odor Differences between Enantiomeric Isomers, Science, Vol. 172, 1043-1044 (1971)

Ionones, Irones, Damascones & Structurally Related Odorants

Acyclics (Alcohols, Esters, Acids, Aldehydes)

Lactones

Sesquiterpenoid Related Odorants