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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Abstract

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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