| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224288 | Tetrahedron | 2008 | 7 Pages |
Abstract
A stereoselective total synthesis of the tricyclic sesquiterpene (â)-seychellene, starting from (R)-carvone via (R)-3-methylcarvone has been accomplished, employing a combination of intermolecular Michael addition-intramolecular Michael addition sequence, a stereoselective hydrogenation, and an intramolecular alkylation reaction.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Srikrishna, G. Ravi,