From the Total Synthesis of Semi–Viriditoxin, Semi–Viriditoxic Acid and Dimeric Naphthopyranones to their Biological Activities in Burkitt B Cell Lymphoma

Abstract

AbstractDimeric naphthopyranones are known to be biologically active, however, for the corresponding monomeric naphthopyranones this information is still elusive. Here the first enantioselective total synthesis of semi‐viriditoxic acid as well as the synthesis of semi–viriditoxin and derivatives is reported. The key intermediate in the synthesis of naphthopyranones is an α,β‐unsaturated δ‐lactone, which we synthesized in two different ways (Ghosez–cyclization and Grubbs ring–closing metathesis), while the domino–Michael–Dieckmann reaction of the α,β‐unsaturated δ‐lactone with an orsellinic acid derivative is the key reaction. A structure‐activity relationship study was performed measuring the cytotoxicity in Burkitt B lymphoma cells (Ramos). The dimeric structure was found to be crucial for biological activity: Only the dimeric naphthopyranones showed cytotoxic and apoptotic activity, whereas the monomers did not display any activity at all.