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Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction

Srikrishna, Adusumilli and Pardeshi, Vijendra H and Satyanarayana, Gedu (2010) Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction. In: Tetrahedron: Asymmetry, 21 (6). pp. 746-750.

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Official URL: http://dx.doi.org/10.1016/j.tetasy.2010.04.003

Abstract

Enantioselective formal total syntheses of the marine trisnorsesquiterpenes clavukerin A and isoclavukerin A, starting from (R)-limonene employing an RCM reaction as the key step, are described.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to Elsevier Science.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 12 Jul 2010 11:08
Last Modified: 19 Sep 2010 06:11
URI: http://eprints.iisc.ernet.in/id/eprint/29186

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