Literature DB >> 21044780

Syntheses of p-nitrophenyl 3- and 4-thio-β-D-glycopyranosides.

Hong-Ming Chen1, Stephen G Withers.   

Abstract

Thioglycosides have proved to be useful, enzymatically stable analogs of glycosides for structural and mechanistic studies and their synthesis is considerably simplified through the use of thioglycoligases. As part of an investigation into the use of thioglycosides as potential pharmacological chaperones, and as components of glycoproteins and glycolipids, the syntheses of p-nitrophenyl 3-thio-β-D-galactopyranoside, phenyl 1,4-dithio-β-D-glucopyranoside, p-nitrophenyl 4-thio-β-D-mannopyranoside and p-nitrophenyl 2-acetamido-2-deoxy-4-thio-β-D-mannopyranoside are described.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21044780     DOI: 10.1016/j.carres.2010.10.001

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  2 in total

1.  Binuclear copper(II) complexes discriminating epimeric glycosides and α- and β-glycosidic bonds in aqueous solution.

Authors:  Susanne Striegler; Qiu-Hua Fan; Nigam P Rath
Journal:  J Catal       Date:  2016-06       Impact factor: 7.920

Review 2.  Enzymatic synthesis of glycosides: from natural O- and N-glycosides to rare C- and S-glycosides.

Authors:  Jihen Ati; Pierre Lafite; Richard Daniellou
Journal:  Beilstein J Org Chem       Date:  2017-09-05       Impact factor: 2.883

  2 in total

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