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Concise total synthesis of the marine natural product ageladine A

Sudhir R Shengule1, Peter Karuso

  • 1Department of Chemistry & Biomolecular Sciences, Macquarie University, Sydney, NSW 2109, Australia.

Organic Letters
|August 25, 2006
PubMed

Abstract:

A total synthesis of ageladine A has been achieved by exploiting a Pictet-Spengler-type condensation between 2-aminohistamine and 4,5-dibromo-2-formylpyrrole as the key step.

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