Srikrishna, A and Pardeshi, Vijendra H (2010) Enantiospecific total synthesis of aciphyllene. In: Tetrahedron, 66 (41). pp. 8160-8168.
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Official URL: http://dx.doi.org/10.1016/j.tet.2010.08.045
Abstract
Enantiospecific total synthesis of the sesquiterpene aciphyllene and its three epimers have been described starting from the readily available monoterpene (R)-limonene employing an intramolecular type II carbonyl ene reaction as the key step. (C) 2010 Elsevier Ltd. All rights reserved.
Item Type: | Journal Article |
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Publication: | Tetrahedron |
Publisher: | Elsevier Science |
Additional Information: | Copyright of this article belongs to Elsevier Science. |
Keywords: | Sesquiterpenes; Aciphyllenes; Limonene; Intramolecular type II carbonyl ene reaction; Enantiospecific synthesis. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 26 Oct 2010 07:24 |
Last Modified: | 26 Oct 2010 07:24 |
URI: | http://eprints.iisc.ac.in/id/eprint/33401 |
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