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The first total synthesis of (±)-laurokamurene B

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
Publication: Tetrahedron
Publisher: Elsevier
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
URI: http://eprints.iisc.ac.in/id/eprint/14297

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