c

(1S,5R)-(+)-Myrtenal diethyl acetal - Probability levels of significant differentiation between the enantiomer pairs - >25.0% with 37 untrained panelists; >90.0% with 29 expert panelists; overall >98.0% (all 66 panelists). No comments on the odor of the enantiomers was provided in Theimer's paper. = (1S,5R)-2-(diethoxymethyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene Ref: E.T. Theimer and Mina R. McDaniel, Odor and optical activity, J. Soc. Cosmet. Chem. 22, 5-26 (1971)

c

(1R,5S)-(+)-Myrtenal diethyl acetal - Probability levels of significant differentiation between the enantiomer pairs - >25.0% with 37 untrained panelists; >90.0% with 29 expert panelists; overall >98.0% (all 66 panelists). No comments on the odor of the enantiomers was provided in Theimer's paper. = (1R,5S)-2-(diethoxymethyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene Ref: E.T. Theimer and Mina R. McDaniel, Odor and optical activity, J. Soc. Cosmet. Chem. 22, 5-26 (1971)

Ionones, Irones, Damascones & Structurally Related Odorants

Acyclics (Alcohols, Esters, Acids, Aldehydes)

Lactones

Sesquiterpenoid Related Odorants