高等学校化学研究 ›› 2013, Vol. 29 ›› Issue (4): 695-698.doi: 10.1007/s40242-013-2519-7
Synthesis of Novel Flavanone Derivatives and Their Anti Staphylococcus aureus Evaluation
XU Qing-hui1, LI Ji-zhen1, HE Jiang-hua1, ZHAO Xin1, HUO Qi-sheng2
- 1. Department of Organic Chemistry, College of Chemistry, Jilin University, Changchun 130021, P. R. China;
2. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China
Synthesis of Novel Flavanone Derivatives and Their Anti Staphylococcus aureus Evaluation
XU Qing-hui1, LI Ji-zhen1, HE Jiang-hua1, ZHAO Xin1, HUO Qi-sheng2
- 1. Department of Organic Chemistry, College of Chemistry, Jilin University, Changchun 130021, P. R. China;
2. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China
摘要：
The authors synthesized two novel flavanones bearing iso-pentenyl side chain and evaluated their anti Staphylococcus aureus(S. aureus) activity. The target compounds 7a[2-5'-(1",2"-dimethylallyl)-2'-methoxy-4',5,7-tetrahydroxyflavanone] and 7b[2-5'-(1",2"-dimethylallyl)-3'-methoxy-4',5,7-tetrahydroxyflavanone] were synthesized respectively through total four steps starting from 2,4,6-trihydroxy acetophenone(3) and the corresponding iso-pentenyl substituted benzaldehyde(1), in which the 1,2-dimethyl-2-propenyl group had been introduced previously via abnormal Claisen rearrangement. The bioactivities of the two flavanones against S. aureus strains ATCC 25923, 29213, and MRSA 252 were evaluated, showing the same minimum inhibitory concentration(MIC) value of 16 μg/mL.