Title of article :
A highly concise preparation of O-deacetylated arylthioglycosides of N-acetyl-d-glucosamine from 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-d-glucopyranosyl chloride and aryl thiols or disulfides
Author/Authors :
Keith A. Stubbs، نويسنده , , Matthew S. Macauley، نويسنده , , David J. Vocadlo، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2006
Pages :
6
From page :
1764
To page :
1769
Abstract :
An expedient and mild route to a range of aryl 2-acetamido-2-deoxy-1-thio-β-d-glucopyranosides has been devised from 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-d-glucopyranosyl chloride and arylthiols or aryl disulfides using phase transfer catalysis conditions. This simple procedure compresses up to three synthetic steps into a one-pot reaction, obviating the need for tedious workups and chromatography and directly furnishes crystalline materials in good yields. The procedure is compatible with a range of thiols and disulfides and may be amenable for preparing a wide range of thioglycosides with various glycons and aglycons.
Keywords :
Disulfides , Arylthiols , One-pot synthesis , Enzyme substrate , Enzyme inhibitor , Thioglycoside , Phase transfer reaction
Journal title :
Carbohydrate Research
Serial Year :
2006
Journal title :
Carbohydrate Research
Record number :
965799
Link To Document :
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