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作 者:JIN XiaoLing YANG RuTing SHANG YaJing DAI Fang QIAN YiPing CHENG LiXia ZHOU Bo LIU ZhongLi
机构地区:[1]State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China
出 处:《Chinese Science Bulletin》2010年第25期2885-2890,共6页
基 金:supported by the National Natural Science Foundation of China (20972063 and 20621091);the 111 Project;Program for New Century Excellent Talents in University (NCET-06-0906)
摘 要:4-Hydroxycinnamic acid derivatives,including ferulic acid (FA) (1),sinapic acid (SA) (2) and caffeic acid (CA) (3),are widely distributed in the plant kingdom,and undergo oxidative cross-coupling leading to the corresponding dehydrodimers,trimers and even higher oligomers in plants. In order to evaluate the antioxidative ability of these 4-hydroxycinnamic acid derivatives and their oligomers,we synthesized 8-8'-bis-lactone-dimers (8-8'-DiFA (4),8-8'-DiSA (5) and 8-8'-DiCA (6)),as well as a new trimer (7),by the reaction of the corresponding monomers (1-3) with Ag2O in methanol,and assayed their free radical-scavenging activity by the reaction with 2,2-diphenyl-1-picrylhydrazyl radical (DPPH·). It was found that CA (3) and 8-8'-DiCA (6) bearing o-dihydroxyl groups exhibited significantly higher radical-scavenging activity than those bearing no such groups,and oxidative coupling of CA (3) resulted in remarkable enhancement in the activity.4-Hydroxycinnamic acid derivatives, including ferulic acid (FA) (1), sinapic acid (SA) (2) and caffeic acid (CA) (3), are widely distributed in the plant kingdom, and undergo oxidative cross-coupling leading to the corresponding dehydrodimers, trimers and even higher oligomers in plants. In order to evaluate the antioxidative ability of these 4-hydroxycinnamic acid derivatives and their oligomers, we synthesized 8-8'-bis-lactone-dimers (8-8'-DiFA (4), 8-8'-DiSA (5) and 8-8'-DiCA (6)), as well as a new trimer (7), by the reaction of the corresponding monomers (1-3) with Ag20 in methanol, and assayed their free radical-scavenging activ- ity by the reaction with 2,2-diphenyl-l-picrylhydrazyl radical (DPPH-). It was found that CA (3) and 8-8'-DiCA (6) bearing o-dihydroxyl groups exhibited significantly higher radical-scavenging activity than those bearing no such groups, and oxidative coupling of CA (3) resulted in remarkable enhancement in the activity.
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