引用本文:
柳利, 陈祖兴, 王世敏, 杨桂春. 合成抗病毒母体三羟基核苷的新方法[J]. 应用化学,
1999, 16(1): 83-85.
Citation: Liu Li, Chen Zuxing, Wang Shimin, Yang Guichun. Syntheses of Antiviral Precursors:Trihydroxy Nucleosides[J]. Chinese Journal of Applied Chemistry, 1999, 16(1): 83-85.
Citation: Liu Li, Chen Zuxing, Wang Shimin, Yang Guichun. Syntheses of Antiviral Precursors:Trihydroxy Nucleosides[J]. Chinese Journal of Applied Chemistry, 1999, 16(1): 83-85.
合成抗病毒母体三羟基核苷的新方法
English
Syntheses of Antiviral Precursors:Trihydroxy Nucleosides
Abstract:
Title compounds were obtained by treating nucleosides with two antagonistic polymeric reagents, P-IO4- and P-BH4- in one-pot process.The method has the advantages of simple operation, mild reaction condition and unnecessary isolation of the intermediates with high yield.
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Key words:
- trihydroxy nucleoside
- / polymeric reagent
- / synthesis
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