Synthetic Hydrogen-Bonding Receptors for Biologically Essential Monosaccharides

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Author(s)

Abstract

Novel macrocyclic saccharide receptors that possess terpyridine skeletons as a hydrogen-bonding site are presented. On modification of the hydrogen-bonding sites and the macrocyclic bridges, the receptors showed selective bindings for ribofuranosides, deoxyribofuranosides, and glucopyranosides, respectively. The binding affinities of the receptors were very high, so that native monosaccharides were solubilized into non-polar solvents in the presence of the receptors. The hydrogen-bonding interactions and the binding modes between them were characterized by <SUP>1</SUP>H NMR spectroscopy.

Journal

  • Journal of Synthetic Organic Chemistry, Japan

    Journal of Synthetic Organic Chemistry, Japan 58(11), 1077-1083, 2000-11-01

    The Society of Synthetic Organic Chemistry, Japan

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Codes

  • NII Article ID (NAID)
    10008822231
  • NII NACSIS-CAT ID (NCID)
    AN0024521X
  • Text Lang
    ENG
  • Article Type
    REV
  • ISSN
    00379980
  • NDL Article ID
    5549715
  • NDL Source Classification
    ZP11(科学技術--化学・化学工業--有機化学・有機化学工業)
  • NDL Call No.
    Z17-256
  • Data Source
    CJP  NDL  J-STAGE 
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