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Approach to the synthesis of (+)-Ifforestine. Model studies directed at the tetracyclic framework

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
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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.

Publication Type: Journal Article
Publisher: Elsevier
Copyright: 2003 Japan Institute of Heterocyclic Chemistry
URI: http://researchrepository.murdoch.edu.au/id/eprint/16842
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