Dedicated with best personal wishes to Prof. Dr. W. Fleischhucker on the occasion of his 65th birthday (16.1X.96) Khusimone (l), one of the main odor-donating compounds of vetiver oil is subject of the following study on structure/odor relationship. The omittance of the ethano bridge of the tricycli
Synthesis and Odor of Chiral Partial Structures of Khusimone. Part 3. Short communication
โ Scribed by Helmut Spreitzer; Andrea Pichler; Wolfgang Holzer; Claudia Schlager
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- German
- Weight
- 333 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
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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
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