Literature DB >> 14505883

A simple one-pot method for the synthesis of partially protected mono- and disaccharide building blocks using an orthoesterification-benzylation-orthoester rearrangement approach.

Balaram Mukhopadhyay1, Robert A Field.   

Abstract

A simple one-pot method is reported for making partially protected glycosyl acceptors from O-methyl or S-alkyl/aryl glycosides of D-glucose, D-galactose, D-arabinose, L-rhamnose, L-fucose and lactose via orthoester formation, benzylation and selective hydrolysis.

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Year:  2003        PMID: 14505883     DOI: 10.1016/s0008-6215(03)00349-5

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


  2 in total

1.  Streamlined Iterative Assembly of Thio-Oligosaccharides by Aqueous S-Glycosylation of Diverse Deoxythio Sugars.

Authors:  Peng Wen; Peijing Jia; Qiuhua Fan; Bethany J McCarty; Weiping Tang
Journal:  ChemSusChem       Date:  2022-01-10       Impact factor: 9.140

2.  Chemical synthesis of the pentasaccharide repeating unit of the O-specific polysaccharide from Escherichia coli O132 in the form of its 2-aminoethyl glycoside.

Authors:  Debasish Pal; Balaram Mukhopadhyay
Journal:  Beilstein J Org Chem       Date:  2019-10-28       Impact factor: 2.883

  2 in total

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