• Title of article

    Thiosugars II. A novel approach to thiodisaccharides The synthesis of 3-deoxy-4-thiocellobiose from levoglucosenone

  • Author/Authors

    Zbigniew J. Witczak، نويسنده , , Renu Chhabra، نويسنده , , Hong Chen، نويسنده , , Xiang-Qun Xie، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 1997
  • Pages
    9
  • From page
    167
  • To page
    175
  • Abstract
    An expeditious methodology for the synthesis of β-(1 → 4)-3-deoxythiodisaccharides (3-deoxythiocellobiose) has been developed. The methodology is based on the stereoselective Michael addition of 2,3,4,6-tetra-O-acetyl-1-thio-β-d-glucose to levoglucosenone, followed by stereoselective reduction at C-2 with l-Selectride® and DIBAH, followed by acetolysis to the target thiodisaccharide derivative.
  • Keywords
    6-Anhydro-3 , Levoglucosenone , 4-dideoxy-?-d-glycero-hex-3-enopyranos-2-ulose , Michael additions , 3-Deoxythiocellobiose , 1 , Thiosugars
  • Journal title
    Carbohydrate Research
  • Serial Year
    1997
  • Journal title
    Carbohydrate Research
  • Record number

    961813