Srikrishna, A. ; Beeraiaha, B. ; Gowri, V. (2009) Enantiospecific approach to the tricyclic core structure of tricycloillicinone, ialibinones, and takaneones via ring-closing metathesis reaction Tetrahedron, 65 (13). pp. 2649-2654. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2009.01.096
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: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Tricyclo[5.3.1.01,5]undecane; (S)-Campholenaldehyde; Enantiospecific Synthesis; RCM Reaction; Diquinanes; Illicinones |
| ID Code: | 48788 |
| Deposited On: | 15 Jul 2011 11:52 |
| Last Modified: | 15 Jul 2011 11:52 |
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