Srikrishna, A and Khan, IA and Babu, Ramesh R and Sajjanshetty, A (2007) The first total synthesis of (±)-laurokamurene B. In: Tetrahedron, 63 (51). pp. 12616-12620.
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The first total synthesis of the rearranged aromatic sesquiterpene (\pm)-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:||Journal Article|
|Additional Information:||Copyright of this article belongs to Elsevier.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||13 Jun 2008|
|Last Modified:||19 Sep 2010 04:45|
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