Journal of the American Chemical Society, Vol.131, No.12, 4214-4214, 2009
Concise Enantioselective Synthesis of ent-Malbrancheamide B
A concise enantioselective synthesis of the fungal metabolite ent-malbrancheamide B was accomplished through the union of a C-prenylated proline derivative and a substituted indole pyruvic acid SEM enol ether, followed by a cationic double cyclization as the key step.