Journal article
Approach to the synthesis of (+)-Ifforestine. Model studies directed at the tetracyclic framework
Heterocycles, Vol.60(9), pp.2023-2044
2003
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.
Details
- Title
- Approach to the synthesis of (+)-Ifforestine. Model studies directed at the tetracyclic framework
- Authors/Creators
- G.H.P. Roos (Author/Creator)K.A. Dastlik (Author/Creator)
- Publication Details
- Heterocycles, Vol.60(9), pp.2023-2044
- Publisher
- Elsevier
- Identifiers
- 991005542021207891
- Copyright
- 2003 Japan Institute of Heterocyclic Chemistry
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
Metrics
62 Record Views