ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

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.

[img] PDF
sdarticle.pdf
Restricted to Registered users only

Download (152Kb) | Request a copy

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
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.ernet.in/id/eprint/13799

Actions (login required)

View Item View Item