Literature DB >> 16472788

A highly concise preparation of O-deacetylated arylthioglycosides of N-acetyl-D-glucosamine from 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-D-glucopyranosyl chloride and aryl thiols or disulfides.

Keith A Stubbs1, Matthew S Macauley, David J Vocadlo.   

Abstract

An expedient and mild route to a range of aryl 2-acetamido-2-deoxy-1-thio-beta-D-glucopyranosides has been devised from 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-alpha-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.

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Year:  2006        PMID: 16472788     DOI: 10.1016/j.carres.2005.12.009

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


  1 in total

Review 1.  Insight on Mercapto-Coumarins: Synthesis and Reactivity.

Authors:  Eslam Reda El-Sawy; Ahmed Bakr Abdelwahab; Gilbert Kirsch
Journal:  Molecules       Date:  2022-03-26       Impact factor: 4.411

  1 in total

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