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.
Full text not available from this repository. (Request a copy)
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 |
|---|---|
| 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 |
Actions (login required)
 |
View Item |
