Concise total synthesis of the marine natural product ageladine A.

Autor: Shengule SR; Department of Chemistry & Biomolecular Sciences, Macquarie University, Sydney, NSW 2109, Australia., Karuso P
Jazyk: angličtina
Zdroj: Organic letters [Org Lett] 2006 Aug 31; Vol. 8 (18), pp. 4083-4.
DOI: 10.1021/ol061584y
Abstrakt: 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.
Databáze: MEDLINE