Literature DB >> 9691445

Synthesis of terminal disaccharide elements corresponding to the Ogawa and Inaba antigenic determinant from Vibrio cholerae O1.

A Arencibia-Mohar1, A Ariosa-Alvarez, O Madrazo-Alonso, E González Abreu, L García-Imia, G Sierra-González, V Verez-Bencomo.   

Abstract

Vibrio cholerae O1 LPS terminal mono- and disaccharide elements were synthesized by reduction of the azido group in several 4-amino-4,6-dideoxy-D-mannose mono- and disaccharide derivatives, followed by coupling with 2, 4-di-O-acetyl-3-deoxy-L-glycero-tetronic acid in the presence of 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline. This compound represents a useful model in order to elucidate the size of the epitopes which define Ogawa and Inaba serotypes from Vibrio cholerae O1.

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Year:  1998        PMID: 9691445     DOI: 10.1016/s0008-6215(97)10052-0

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


  3 in total

1.  Enhanced stereoselectivity of alpha-mannosylation under thermodynamic control using trichloroacetimidates.

Authors:  Shu-jie Hou; Pavol Kovác
Journal:  Carbohydr Res       Date:  2010-03-21       Impact factor: 2.104

2.  Synthesis of the conjugation ready, downstream disaccharide fragment of the O-PS of Vibrio cholerae O:139.

Authors:  Shujie Hou; Pavol Kováč
Journal:  Carbohydr Res       Date:  2011-02-25       Impact factor: 2.104

3.  Towards the Complete Synthetic O-Antigen of Vibrio cholerae O1, Serotype Inaba: Improved Synthesis of the Conjugation-ready Upstream Terminal Hexasaccharide Determinant.

Authors:  Mana Mohan Mukherjee; Peng Xu; Edwin D Stevens; Pavol Kováč
Journal:  RSC Adv       Date:  2019-11-08       Impact factor: 4.036

  3 in total

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