Concise total synthesis of the marine natural product ageladine A

Sudhir R. Shengule; Peter Karuso

doi:10.1021/ol061584y

Concise total synthesis of the marine natural product ageladine A

Sudhir R. Shengule, Peter Karuso^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

48 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 language	English
Pages (from-to)	4083-4084
Number of pages	2
Journal	Organic Letters
Volume	8
Issue number	18
DOIs	https://doi.org/10.1021/ol061584y
Publication status	Published - 31 Aug 2006

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title = "Concise total synthesis of the marine natural product ageladine A",

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.",

author = "Shengule, {Sudhir R.} and Peter Karuso",

year = "2006",

month = aug,

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doi = "10.1021/ol061584y",

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AU - Shengule, Sudhir R.

AU - Karuso, Peter

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N2 - 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.

AB - 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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JO - Organic Letters

JF - Organic Letters

IS - 18

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Concise total synthesis of the marine natural product ageladine A

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