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-1,5,5-trimethylcyclohex-2-enyl)acetaldehyde.gif)
[(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, 18871897 (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
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c
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[(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, 18871897 (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
|
|