| Literature DB >> 9691445 |
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.Entities:
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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