Srikrishna, A and Babu, Ramesh R and Ravikumar, PC (2007) A Regioselective Total Synthesis of the Fungal Sesquiterpene $(\pm)$-Lagopodin A. In: Synlett (4). pp. 655-657.
Full text not available from this repository. (Request a copy)Abstract
A highly regiocontrolled total synthesis of fungal sesquiterpene lagopodin A, employing a combination of Claisen rearrangement-intramolecular diazoketone cyclopropanation and a highly regioselective cyclopropane ring cleavage, is described.
| Item Type: | Journal Article |
|---|---|
| Publication: | Synlett |
| Publisher: | Thieme Medical Publishers, Inc. |
| Additional Information: | Copyright of this article belongs to Thieme Medical Publishers, Inc. |
| Keywords: | natural products;total synthesis;rearrangement;ring closure;ring cleavage |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 03 Jun 2008 |
| Last Modified: | 27 Aug 2008 13:25 |
| URI: | http://eprints.iisc.ac.in/id/eprint/14151 |
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