4.8 Article

Lewis Acid Induced Anomerization of Se-Glycosides. Application to Synthesis of α-Se-GalCer

Journal

ORGANIC LETTERS
Volume 18, Issue 3, Pages 552-555

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b03591

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Funding

  1. Irish Research Council
  2. NUI Galway (College of Science PhD scholarship)
  3. Science Foundation Ireland (SFI) [12/IA/1398]
  4. European Regional Development Fund [14/SP/2710]
  5. Science Foundation Ireland (SFI) [14/SP/2710] Funding Source: Science Foundation Ireland (SFI)

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The TiCl4 induced anomerization of selenium glycosides of galacturonic acid derivatives is reported. The reaction was successful for galacturonic acid when various alkyl, alkenyl, alkynyl, saccharide, steroid, and lipid groups were attached to the anomeric Se atom. An increased amount of TiCl4 and/or higher temperature were needed to ensure completion of the reaction in some cases. Yields were higher for reactions carried out at higher dilution. The reaction was applied to the synthesis of Se-based mimics of the potent immunostimulant alpha-GalCer (KRN7000).

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