Approach to the synthesis of (+)-Ifforestine. Model studies directed at the tetracyclic framework
Tools
Tools
Tools
Roos, G.H.P. and Dastlik, K.A. (2003) Approach to the synthesis of (+)-Ifforestine. Model studies directed at the tetracyclic framework. Heterocycles, 60 (9). pp. 2023-2044.
Link to Published Version: http://dx.doi.org/10.3987/COM-03-9810
*Subscription may be required
*Subscription may be required
Abstract
In order to design an effective asymmetric synthesis of (+)-ifforestine, model approaches to the construction of the tetracyclic ring system have been investigated. These studies have identified two key synthons, a functionalized isatoic anhydride and a pipecolic acid derivative, as suitable AB- and D-ring portions for creation of the crucial diazopinedione C-ring.
| Item Type: | Journal Article |
|---|---|
| Publisher: | Elsevier |
| Copyright: | 2003 Japan Institute of Heterocyclic Chemistry |
| URI: | http://researchrepository.murdoch.edu.au/id/eprint/16842 |
 |
Item Control Page |
