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
Link To Document :
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