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作 者:王晋 郭冬冬 张永坡[1] 殷丛丛 赵晋忠[1] WANG Jin;GUO Dong-dong;ZHANG Yong-po;YIN Cong-cong;ZHAO Jin-zhong(Department of Basic courses,Shanxi Agricultural University,Taigu 030801,China)
出 处:《化学研究与应用》2024年第11期2583-2589,共7页Chemical Research and Application
基 金:国家自然科学基金项目(82274363)资助。
摘 要:以2,4,6-三羟基苯乙酮一水合物和对羟基苯甲醛为起始原料,经C-异戊烯基化反应、羟基保护、羟醛缩合、环合,脱保护合成了具有抗炎效果的天然产物山豆根酮A10和EuchrenoneA1,总收率分别为15.9%和12.8%。实验表明,山豆根酮A10具有一定的抗氧化活性。The efficient synthesis of two naturally occurring prenylated flavonoids,euchrenone A10 and euchrenone Al were obtained from p-hydroxybenzaldehyde and 2,4,6-trihydroxyacetophenone monohydrate through a series of steps including C-prenylation,hydroxyl group protection,aldol condensation,cyclization,and deprotection,with overall yields of 15.9%and 12.8%,respectively.Furthermore,their antioxidant activities were evaluated,revealing that euchrenone A10 exhibited superior antioxidant properties.
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