| Literature DB >> 17193200 |
Hiroyuki Sakauchi1, Hiromasa Kiyota, Shin-ya Takigawa, Takayuki Oritani, Shigefumi Kuwahara.
Abstract
Both enantiomers of lavandulol (1), an important constituent of lavender oil, were prepared by enzymatic optical resolution, and the odor quality of the single antipodes were evaluated. The fragrance of the nature-identical (R)-enantiomer ('weak floral, herbal odor with slightly lemon-like, fresh citrus fruity nuance') was superior to those of both the unnatural (S)-enantiomer ('very weak odor') and the racemate ('weak floral, herbal odor').Entities:
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Year: 2005 PMID: 17193200 DOI: 10.1002/cbdv.200590088
Source DB: PubMed Journal: Chem Biodivers ISSN: 1612-1872 Impact factor: 2.408