Formal Total Synthesis of (±)-Strictamine Based on a Gold-Catalyzed Cyclization

Abstract

A gold-catalyzed cyclization of 1-propargyl-1,2,3,4-tetrahydro-β-carboline led to formation the D-ring of strictamine. Functional group modifications of the resulting tetracyclic indolenine led to the formal total synthesis of (±)-strictamine.