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Merck
  • Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-gluco- and galactopyranoside.

Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-gluco- and galactopyranoside.

Carbohydrate research (2007-07-07)
Hong-Ming Chen, Stephen G Withers
摘要

The syntheses of 4-nitrophenyl beta-glycosides of the 3-thio and 4-thio analogues of the two principal 2-acetamido-2-deoxy-hexoses found in living systems, GlcNAc and GalNAc, are described. While synthesis of the 4-thio analogues could be achieved via nucleophilic displacements of sulfonate derivatives with thioacetate, problems with neighbouring group acetamido participation necessitated the use of sulfamidate intermediates for the 3-thio analogues. These 3- and 4-thio analogues are employed in the chemo-enzymatic synthesis of thio-oligosaccharide analogues of structures present in glycosaminoglycans, glycoproteins and glycolipids.

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Sigma-Aldrich
4-硝基苯基 N-乙酰基-β-D-氨基葡萄糖, ≥99% (TLC)
Sigma-Aldrich
4-硝基苯基-N-乙酰-β-D-半乳糖胺, ≥98%
Sigma-Aldrich
4-硝基苯基N-乙酰基-α-D-氨基葡萄糖, ≥98%
Sigma-Aldrich
4-Nitrophenyl N-acetyl-α-D-galactosaminide, substrate for N-acetyl-α-D-galactosaminidase