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Enantiospecific synthesis of the tricyclic core structure of lippifolianes

Srikrishna, Adusumilli and Babu, Ramesh R and Beeraiah, Baire (2010) Enantiospecific synthesis of the tricyclic core structure of lippifolianes. In: Tetrahedron: Asymmetry, 21 (6). pp. 719-724.

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Official URL: http://dx.doi.org/10.1016/j.tetasy.2010.04.001

Abstract

An enantiospecific synthesis of the [6.6.3]-tricyclic carbon framework, 2,6,6,9-tetra-methyltricyclo[5.4.0.02,4]undecane, present in the sesquiterpenes lippifolianes and the diterpenes cyclosclareol, metasequoic acids and parguerols, starting from the readily available monoterpene (R)-carvone, is described.

Item Type: Journal Article
Publication: Tetrahedron: Asymmetry
Publisher: Elsevier Science
Additional Information: Copyright of this article belongs to Elsevier Science.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 13 Jul 2010 05:56
Last Modified: 19 Sep 2010 06:11
URI: http://eprints.iisc.ac.in/id/eprint/29185

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