Concise total synthesis of the marine natural product ageladine A
RIS ID
49631
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. ?? 2006 American Chemical Society.
Publication Details
Shengule, S. R. & Karuso, P. (2006). Concise total synthesis of the marine natural product ageladine A. Organic Letters, 8 (18), 4083-4084.