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11-脱氧甘草次酸的制备
引用本文:谢松梅,崔慧斐,臧恒昌.11-脱氧甘草次酸的制备[J].中国生化药物杂志,2007,28(2):118-119.
作者姓名:谢松梅  崔慧斐  臧恒昌
作者单位:山东大学,药学院,生化与生物技术药物研究所,山东,济南,250012
摘    要:目的制备11-脱氧甘草次酸。方法采用改进的克莱门森反应还原甘草次酸的11位羰基。结果制备了11-脱氧甘草次酸,并通过IR、NMR等手段对其结构进行了鉴定。结论改进的克莱门森还原法制备11-脱氧甘草次酸收率较高,对环境友好,而且简便。

关 键 词:甘草次酸  脱氧甘草次酸  克莱门森还原
文章编号:1005-1678(2007)02-0118-02
收稿时间:2006-11-20
修稿时间:2006年11月20

The preparation of deoxy-glycyrrhetinic acid
XIE Song-mei,CUI Hui-fei,ZANG Heng-chang.The preparation of deoxy-glycyrrhetinic acid[J].Chinese Journal of Biochemical Pharmaceutics,2007,28(2):118-119.
Authors:XIE Song-mei  CUI Hui-fei  ZANG Heng-chang
Institution:Institute of Biochemical and Biological Drug, School of Pharmaceutical Science, Shandong University, Jinan 250012, China
Abstract:Purpose To prepare 11-deoxy-glycyrrhetinic acid.MethodsReduction of the 11-caxbonyl group of glycyrrhetinic acid was done through modified Clemmensen reaction.Results11-deoxy-glycyrrhetinic acid was prepared and its structure was characterized by IR and NMR.ConclusionModified Clemmensen reduction was successfully used to prepare 11-deoxy-glycyrrhetinic acid with high yield.The preparing procedure was simple and friendly for environment.
Keywords:glycyrrhetinic acid  deoxy-glycyrrhetinic acid  Clemmensen reduction
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