Abstract
Synthesis of both enantiomers of methyl 4,5-didehydrojasmonate (1, Δ4,5-MJA; >99.8% ee), a constituent of jasmin absolute, established the absolute configuration of the natural product, and their odor quality was evaluated. The fragrance of the natural (3S,7R)-enantiomer (a fresh natural, sweet floral fruity odor, reminiscent of Jasmin and Ylang Ylang flower, more intensive and tenacious) was superior to that of the unnatural (3R,7S)-enantiomer (a floral green odor with slight metallic green aspect, less intensive than the natural form) and the racemate (green-floral note, having weak and less volume than methyl jasmonate). Odor difference between natural and unnatural enantiomers of methyl jasmonate (2) is also reported.
| Original language | English |
|---|---|
| Pages (from-to) | 654-659 |
| Number of pages | 6 |
| Journal | Chemistry and Biodiversity |
| Volume | 3 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 2006 |
| Externally published | Yes |
ASJC Scopus subject areas
- Bioengineering
- Biochemistry
- General Chemistry
- Molecular Medicine
- Molecular Biology
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