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Synthesis and Odor of Chiral Partial Structures of Khusimone. Part 2

✍ 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

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✦ Synopsis


Abstract

Khusimone (1), one of the main odor‐donating compounds of vetiver oil, is subject of the following study on structure/odor relationship. Ring opening of the carbonyl‐functionalized 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.


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