Srikrishna, A. ; Khan, I. A. ; Ramesh Babu, R. ; Sajjanshetty, A. (2007) The first total synthesis of (±)-laurokamurene B Tetrahedron, 63 (51). pp. 12616-12620. ISSN 0040-4020
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2007.10.021
Abstract
The first total synthesis of the rearranged aromatic sesquiterpene (±)-laurokamurene B, isolated from the Chinese red alga Laurencia okamurai Yamada, has been accomplished, confirming the structure of the natural product. A combination of Ireland-Claisen rearrangement and ring-closing metathesis was employed as key reactions.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Laurenes; Cuparenes; Laurokamurenes A and B; Ring-closing Metathesis; Ireland-Claisen Rearrangement |
| ID Code: | 48759 |
| Deposited On: | 15 Jul 2011 11:50 |
| Last Modified: | 15 Jul 2011 11:50 |
Repository Staff Only: item control page
