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The structure of α-vetivone (isonootkatone)

✍ Scribed by James A. Marshall; Niels H. Andersen

Publisher
Elsevier Science
Year
1967
Tongue
French
Weight
241 KB
Volume
8
Category
Article
ISSN
0040-4039

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✦ Synopsis

The naturally occurring sesquiterpenes 8-vetivone and a -vetivone have long been regarded as isomeric hydroaaulenones &and 2)1*2 which differ only in the stereochemistry of their respective C-6 methyl substituents. Whereas detailed studies of 6-vetivone have been reported, 43 a-vetivone has received little attention and, in fact, has never been chemically

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Synthesis and odor of chiral partial str
Synthesis and odor of chiral partial structures of β-vetivone. I.
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Several, stereoisomeric, monocyclic analogs of (-)-␤-vetivone (1), one of the main constituents of vetiver oil, were studied to determine whether the olfactory properties of (-)-␤-vetivone (1) could be reproduced from these structurally simpler, synthetically accessible compounds. The effects of dia

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Several stereoisomeric, monocyclic analogs of (-)-␤-vetivone (1), one of the main constituents of vetiver oil, were studied to examine if the olfactory properties of (-)-␤-vetivone (1) could be reproduced from these structurally simpler, synthetically accessible compounds. The effects of diastereome