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Chemistry of Heterocyclic Compounds

, Volume 17, Issue 11, pp 1120–1125 | Cite as

Synthesis and properties of 1-(5-halo-1-uracilyl)-β-D-glucofuranuronic acids

  • M. K. Kilevitsa
  • Yu. A. Maurin'sh
  • R. A. Paégle
  • É. É. Liepin'sh
  • A. A. Zidermane
  • M. Yu. Lidak
Article
  • 28 Downloads

Abstract

1-(5-Halo-1-uracilyl)-2, 5-di-O-acetyl-β-D-glucofuranurono-6,3-lactones were obtained by condensation of 2,4-bis(trimethylsilyl)-5-halouracils with 1,2,5-tri-O-acetyl-β-D-glucofuranurono;-6, 3-lactone. The chemical transformations of these compounds were studied. The structure of the glucuronides was proved by the IR, UV, circular dichroism, and NMR spectra.

Keywords

Organic Chemistry Circular Dichroism Trimethylsilyl Chemical Transformation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Publishing Corporation 1982

Authors and Affiliations

  • M. K. Kilevitsa
    • 1
  • Yu. A. Maurin'sh
    • 1
  • R. A. Paégle
    • 1
  • É. É. Liepin'sh
    • 1
  • A. A. Zidermane
    • 1
  • M. Yu. Lidak
    • 1
  1. 1.Institute of Organic SynthesisAcademy of Sciences of the Latvian SSRRiga

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