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2000
Volume 5, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Glycosidation reactions of 5-thioxylopyranosides were examined. The reaction of a 1,5-dithioxyloside derivative with N-iodosuccinimide and trifluoromethanesulfonate gave ring-opened products, but no glycosylated products. On the other hand, a 5-thioxylopyranosyl trichloroacetimidate derivative was found to react with aliphatic alcohols and a sugar alcohol to give a 5-thio analog of biologically important β(1,4)xylopyranoside structures.

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/content/journals/loc/10.2174/157017808785740390
2008-09-01
2025-09-06
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/content/journals/loc/10.2174/157017808785740390
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  • Article Type:
    Research Article
Keyword(s): 5-thioxylopyranose; glycosidation; glycosyl donor; thioglycoside; Thiosugar
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