Synthesis of Notoamide J: A Potentially Pivotal Intermediate in the Biosynthesis of Several Prenylated Indole Alkaloids.

TLDR: In this paper, an efficient total synthesis of notoamide J, a new prenylated indole alkaloid and potential biosynthetic precursor, is described, starting from l-proline and a substituted tryptophan derivative, also employing an oxidation and pinacol rearrangement for the formation of the oxindole in the final step.

Abstract: An efficient total synthesis of notoamide J, a new prenylated indole alkaloid and potential biosynthetic precursor, is described herein. Starting from l-proline and a substituted tryptophan derivative, this synthesis also employs an oxidation and pinacol rearrangement for the formation of the oxindole in the final step.