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DEOXYSCHIZANDRIN 10,isolated from Schizandra chinensis baill,exhibits anti-hepatitisvirus activity.Recently considerable interest in the synthesis of 10 has arisen from its bioactiv-ities.In this note a new highly efficient route to synthesize(±)-deoxyschizandrin is re-ported.Our synthetic strategy(outlined in scheme 1)started from gallic acid 1 in 10 stepswith the overall yield of 12%,and employed I_2/NaOEt oxidative coupling reaction as a key