c

[(1S)-1,5,5-trimethylcyclohex-2-en-1-yl]acetaldehyde - Odor description: The racemate, (R)-, and (S)-enantiomers were very similar, camphoric with less or more marked methanolic notes Ref: K. Wiñska and C. Wawrzeñczyk, Synthesis of Chiral Odoriferous Oxy-derivatives of 1,5,5-Trimethylcyclohexene, Polish J. Chem., 81, 1887–1897 (2007) as reviewd in Elisabetta Brenna, Claudio Fuganti, Francesco G. Gatti, and Stefano Serra, Biocatalytic Methods for the Synthesis of Enantioenriched Odor Active Compounds, Chem. Rev., Article ASAP, DOI: 10.1021/cr100289r, Publication Date (Web): May 20, 2011

c

[(1R)-1,5,5-trimethylcyclohex-2-en-1-yl]acetaldehyde - Odor description: The racemate, (R)-, and (S)-enantiomers were very similar, camphoric with less or more marked methanolic notes Ref: K. Wiñska and C. Wawrzeñczyk, Synthesis of Chiral Odoriferous Oxy-derivatives of 1,5,5-Trimethylcyclohexene, Polish J. Chem., 81, 1887–1897 (2007) as reviewd in Elisabetta Brenna, Claudio Fuganti, Francesco G. Gatti, and Stefano Serra, Biocatalytic Methods for the Synthesis of Enantioenriched Odor Active Compounds, Chem. Rev., Article ASAP, DOI: 10.1021/cr100289r, Publication Date (Web): May 20, 2011

Ionones, Irones, Damascones & Structurally Related Odorants

Acyclics (Alcohols, Esters, Acids, Aldehydes)

Lactones

Sesquiterpenoid Related Odorants