Srikrishna, A and Beeraiah, B and Gowri, VS (2009) Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction. In: Tetrahedron, 65 (13). pp. 2649-2654.
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Abstract
Enantiospecific synthesis of the tricyclic core structure present in the biologically active natural products tricycloillicinone, ialibinones, and takaneones, starting from the readily available campholenaldehyde employing a transannular RCM reaction as the key step, has been accomplished.
| Item Type: | Journal Article |
|---|---|
| Publication: | Tetrahedron |
| Publisher: | Elsevier Science |
| Additional Information: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Tricyclo[5.3.1.0]1(+)S]undecane;(S)-Campholenaldehyde; Enantiospecific synthesis; RCM reaction;Diquinanes;Illicinones. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 01 May 2009 03:23 |
| Last Modified: | 19 Sep 2010 05:29 |
| URI: | http://eprints.iisc.ac.in/id/eprint/19667 |
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