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Semi-synthesis of neomangiferin from mangiferin
Authors:Xiong Wei  Danlin LiangMaoheng Ning  Qing WangXiangbao Meng  Zhongjun Li
Institution:State Key Laboratory of Natural and Biomimetic Drugs, Department of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing 100191, PR China
Abstract:Neomangiferin, a natural xanthone derivative bearing both O- and C-glucosides, was isolated from the leaves of Gentiana asclepiadea L. and has shown potential anti-diabetic activity. We describe herein the first semi-synthesis of neomangiferin from the natural C-glucoside mangiferin and glucose. The developed synthesis presents a facile protection strategy using Jurd’s method to distinguish the different phenolic hydroxyl groups. Following this strategy, the regioselective protection of 1,3,6-hydroxyl groups was accomplished and neomangiferin was prepared by glycosylation under the phase-transfer catalysis conditions.
Keywords:BTFBHTNGXSQEKE-KWXBTRJJSA-N  HNBYSLDQKIYNDN-VKNHHUHESA-N  CYAYKKUWALRRPA-UTAXJDLNSA-N  IHWQGRGLJMECHT-HGVZNJKASA-N  DGJKTEBHPGDNOK-PMMLLPECSA-N  CJEMJPGFQXNNEO-KMRLEEFYSA-N  AQFHBAOFLOLGPJ-INLJIPAOSA-N  VWNTXRHPSCQVAW-ADZDYRCLSA-N  VUWOVGXVRYBSGI-IRXABLMPSA-N  AEDDIBAIWPIIBD-ZJKJAXBQSA-N  GXYJLDXKJZDPSL-YVGQFNALSA-N  HEKNWRCUYPGKJZ-FSAHDPKXSA-N  YBPPWAMUOFRGMV-DHWGNVQLSA-N  PFYJVEAVCZXGHE-MIMHQUMTSA-N  FHCDCNLOUFWLNM-BSTCDMFOSA-N  AZVAZSMZIYXGFE-RPZFEVNFSA-N
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