摘要
以大黄素为起始原料经过Williamson醚合成,乙酰基保护,氧化,脱乙酰保护合成5个新型的6-烷氧基大黄酸4a～4e.对比研究了微波反应和常规反应对中间体3-烷氧基大黄素合成产率的影响.比较了在合成关键中间产物3a～3e时不同氧化体系对反应产率的影响,找到了最佳的氧化条件.所有目标化合物的结构都通过IR,1HNMR,MS和HRMS进行了表征.对目标化合物4a～4e进行了抑菌活性测试,结果表明随着取代烷氧基链的增长,抑菌活性呈规律性变化.
Five new 6-alkoxy rheins have been designed and synthesized through Williamson reaction,acetyl protection,oxidation reaction and deprotection. The effects of microwave and conventional method on the yield of 3-alkyl emodin derivatives were compared. The effects of different oxidants in the synthesis of 3a～3e were studied and the best oxidation conditions were found. All the structures have been confirmed by IR,1H NMR,MS and HRMS techniques. The minimal inhibitory concentration （MIC） assay indicated that antibacterial activity changes regularly,as the alkyl chain growth.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2010年第9期1335-1341,共7页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.20673084)
西南大学青年教师基金(No.swu208040)资助项目
关键词
大黄素
6-烷氧基大黄酸
微波
氧化
抑菌
emodin
6-alkoxy rhein
microwave
oxidation
antibacterial activity
