ChemInform Abstract: Synthesis and Odor of Chiral Partial Structures of Khusimone. Part 3.
โ Scribed by H. SPREITZER; A. PICHLER; W. HOLZER; C. SCHLAGER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 26 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Synthesis and Odor of Chiral Partial Structures of Khusimone. Part 3. -Khusimone (I) is one of the main odor-donating compounds of vetiver oil. For structure-odor relationship studies the bicyclic partial structure (II) missing the methano bridge is considered. Unexpectedly, (II) cannot be obtained since epimerization favors (III). Compound (III) exhibits an intense woody and camphoraceous odor, but lacks the typical vetiver odor. -(SPREITZER, H.;
๐ SIMILAR VOLUMES
Several stereoisomeric, monocyclic analogs of (-)-โค-vetivone (1), one of the main constituents of vetiver oil, were studied to examine if the olfactory properties of (-)-โค-vetivone (1) could be reproduced from these structurally simpler, synthetically accessible compounds. The effects of diastereome
Several, stereoisomeric, monocyclic analogs of (-)-โค-vetivone (1), one of the main constituents of vetiver oil, were studied to determine whether the olfactory properties of (-)-โค-vetivone (1) could be reproduced from these structurally simpler, synthetically accessible compounds. The effects of dia