Synthesis of isogranulatimide analogues possessing a pyrrole moiety instead of an imidazole heterocycle
โ Scribed by Bernadette Hugon; Bruno Pfeiffer; Pierre Renard; Michelle Prudhomme
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 224 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
An efficient four step synthesis from commercial indoles of isogranulatimide analogues is reported. In the new compounds, the imidazole moiety is replaced by a pyrrole unit, the indole part is substituted or not in 5-position and the nitrogen of the imide moiety bears or not a methyl substituent.
๐ SIMILAR VOLUMES
The synthesis of a new family of isogranulatimides analogues is described in which a 7-azaindole replaces the indole moiety. The key step is the photocyclization of the aza didemnimide intermediates which leads to two isomeric analogues of isogranulatimides A and B. A derivative bearing a carbohydra
A synthesis in a few steps of a new family of granulatimide analogues was performed. In the new compounds, the aromatic framework of granulatimide is modified by replacement of the imidazole unit by a maleimide moiety. The synthesis of a water-soluble analogue is also presented.