Synthesis and Odor of Chiral Partial Structures of Khusimone. Part 2
β Scribed by Helmut Spreitzer; Andrea Pichler; Wolfgang Holzer; Manocher Shahabi
- Book ID
- 102861477
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- German
- Weight
- 517 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Khusimone (1), one of the main odorβdonating compounds of vetiver oil, is subject of the following study on structure/odor relationship. Ring opening of the carbonylβfunctionalized bridge of the tricyclic khusimone leads to the bicyclic structures 2a/b. The enantioselective approach to these degraded structures is described, and the olfactory consequences are studied. Starting point of the synthesis is an enantiomerically pure enone ester which is easily obtainable from camphorsulfonic acid.
π SIMILAR VOLUMES
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. -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 (-)-β€-vetivone (1), one of the main constituents of vetiver oil, were studied to examine if the olfactory properties of (-)-β€-vetivone (1) could be reproduced from these structurally simpler, synthetically accessible compounds. The effects of diastereome