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3,6,7-O-三乙氧羰甲基芒果苷的制备
引用本文:苏春丽,廖洪利. 3,6,7-O-三乙氧羰甲基芒果苷的制备[J]. 化学与生物工程, 2011, 0(9): 52-53. DOI: 10.3969/j.issn.1672-5425.2011.09.014
作者姓名:苏春丽  廖洪利
作者单位:1. 成都市食品药品检测中心,四川成都,610041
2. 成都医学院药学院,四川成都,610083
摘    要:以芒果苷和氯乙酸乙酯为原料,以N,N-二甲基甲酰胺为溶剂、碳酸钾为脱酸剂,制备了3,6,7-O-三乙氧羰甲基芒果苷,收率45.6%,其结构经核磁共振氢谱确证.

关 键 词:芒果苷  3,6,7-O-三乙氧羰甲基芒果苷  衍生物  制备

Preparation of 3,6,7-O-Tri-ethoxy-carbonyl-methyl-mangiferin
SU Chun-li,LIAO Hong-li. Preparation of 3,6,7-O-Tri-ethoxy-carbonyl-methyl-mangiferin[J]. Chemistry & Bioengineering, 2011, 0(9): 52-53. DOI: 10.3969/j.issn.1672-5425.2011.09.014
Authors:SU Chun-li  LIAO Hong-li
Affiliation:SU Chun-li1,LIAO Hong-li2(1.Food and Drug Inspection and Testing Center of Chengdu,Chengdu 610041,China,2.School of Pharmacy,Chengdu Medical College,Chengdu 610083,China)
Abstract:Using mangiferin and ethyl chloroacetate as raw material,N,N-dimethylformamide as solvent and potassium carbonate as depickling agent,3,6,7-O-tri-ethoxy-carbonyl-methyl-mangiferin was synthesized with a yield of 45.6%.And its structure was confirmed by 1HNMR.
Keywords:mangiferin  3  6  7-O-tri-ethoxy-carbonyl-methyl-mangiferin  derivative  preparation  
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