Angelmarin (1), a novel anti-cancer agent, was efficiently synthesized through a highly enantioselective epoxidation and a copper cyanide-mediated esterification of the hindered alcohol as the key steps in 53% overall yield.
Angelmarin(1),一种新型抗癌剂,通过高度对映选择性的环氧化反应和
铜氰化物介导的受阻醇酯化反应,作为关键步骤以53%的总产率高效合成。