Enantioselective total synthesis and assignment of the absolute configuration of (+)-laurokamurene B

Srikrishna, Adusumilli and Beeraiah, Baire and Babu, Ramesh R (2008) Enantioselective total synthesis and assignment of the absolute configuration of (+)-laurokamurene B. In: Tetrahedron: Asymmetry, 19 (5). pp. 624-627.

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Abstract

The first enantioselective total synthesis of the rearranged aromatic sesquiterpene (+)-laurokamurene B, isolated from the Chinese red algae Laurencia okamurai Yamada, has been accomplished starting from (S)-campholenaldehyde, establishing the absolute configuration of laurokamurenes.

Item Type:	Journal Article
Publication:	Tetrahedron: Asymmetry
Publisher:	Elsevier
Additional Information:	Copyright of this article belongs to Elsevier.
Department/Centre:	Division of Chemical Sciences > Organic Chemistry
Date Deposited:	02 May 2008
Last Modified:	19 Sep 2010 04:44
URI:	http://eprints.iisc.ac.in/id/eprint/13799

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