Srikrishna, A and Lakshmi, BV (2005) Formal total synthesis of (+/-)-herbertene-1,13-diol and (+/-)-alpha-herbertenol via Ireland ester Claisen rearrangement and RCM reaction sequence. In: Synlett (7). pp. 1173-1175.
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Official URL: http://www.thieme-connect.de/DOI/DOI?10.1055/s-200...
Abstract
A combination of Ireland ester Claisen rearrangement and ring-closing metathesis (RCM) reactions has been employed for efficient formal total syntheses of herbertene-1,13-diol and α-herbertenol, sesquiterpenes containing two vicinal quaternary carbon atoms on a cyclopentane ring.
Item Type: | Journal Article |
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Publication: | Synlett |
Publisher: | Thieme Medical Publishers |
Additional Information: | Copyright of this article belongs to Thieme Medical Publishers. |
Keywords: | (±)-herbertene-1;13-diol;(±)-α-herbertenol;Ireland ester Claisen rearrangement. |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 22 Jul 2009 07:56 |
Last Modified: | 22 Jul 2009 07:56 |
URI: | http://eprints.iisc.ac.in/id/eprint/17082 |
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