A convenient and rapid approach for the syntheses of (-)-kaerophyllin (1),(-)-hinokinin (2) and (±)-isohinokinin (3) was described. The key steps were involved in condensation of aromatic aldehyde and alkylation ...A convenient and rapid approach for the syntheses of (-)-kaerophyllin (1),(-)-hinokinin (2) and (±)-isohinokinin (3) was described. The key steps were involved in condensation of aromatic aldehyde and alkylation of the resulting ester to give the complete skeleton of dibenzylbutyrolactone-lignan. Hydrolysis,followed by resolution with quinine,reduction and when appropriate,oxidation gave the title compound. The asymmetric total synthesis of the kaerophyllin (1) was reported for the first time.展开更多
文摘A convenient and rapid approach for the syntheses of (-)-kaerophyllin (1),(-)-hinokinin (2) and (±)-isohinokinin (3) was described. The key steps were involved in condensation of aromatic aldehyde and alkylation of the resulting ester to give the complete skeleton of dibenzylbutyrolactone-lignan. Hydrolysis,followed by resolution with quinine,reduction and when appropriate,oxidation gave the title compound. The asymmetric total synthesis of the kaerophyllin (1) was reported for the first time.
