Concise total synthesis of the marine natural product ageladine A

Sudhir R. Shengule, Peter Karuso

Research output: Contribution to journalArticleResearchpeer-review

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.

LanguageEnglish
Pages4083-4084
Number of pages2
JournalOrganic Letters
Volume8
Issue number18
DOIs
Publication statusPublished - 31 Aug 2006

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Biological Products
Condensation
condensation
synthesis
products
2-aminohistamine
Ageladine A

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Shengule, Sudhir R. ; Karuso, Peter. / Concise total synthesis of the marine natural product ageladine A. In: Organic Letters. 2006 ; Vol. 8, No. 18. pp. 4083-4084.
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Concise total synthesis of the marine natural product ageladine A. / Shengule, Sudhir R.; Karuso, Peter.

In: Organic Letters, Vol. 8, No. 18, 31.08.2006, p. 4083-4084.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

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AU - Shengule, Sudhir R.

AU - Karuso, Peter

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