Concise total synthesis of the marine natural product ageladine A

Sudhir R. Shengule, Peter Karuso*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    46 Citations (Scopus)

    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.

    Original languageEnglish
    Pages (from-to)4083-4084
    Number of pages2
    JournalOrganic Letters
    Volume8
    Issue number18
    DOIs
    Publication statusPublished - 31 Aug 2006

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