Concise total synthesis of the marine natural product ageladine A

Sudhir R. Shengule, Peter Karuso*

*Corresponding author for this work

Research output: Contribution to journalArticle

43 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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