lipid-a has been researched along with trifluoromethanesulfonic-acid* in 1 studies
1 other study(ies) available for lipid-a and trifluoromethanesulfonic-acid
Article | Year |
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Zinc triflate-promoted glycosidation: synthesis of lipid A disaccharide intermediates.
Zinc triflate was found to be superior to the heavy metal salts as a promoter in the Koenigs-Knorr type glycosidation reaction in the synthesis of lipid A disaccharide intermediates. It readily promoted the reaction of a complex glycosyl bromide with a reducing sugar moiety and gave the disaccharide with beta-selectivity in good yield. This method would be suitable for the bulk preparation of lipid A disaccharide intermediates. Topics: Carbohydrate Sequence; Chromatography, Thin Layer; Disaccharides; Glycosylation; Lipid A; Magnetic Resonance Spectroscopy; Mass Spectrometry; Mesylates; Molecular Sequence Data; Spectrophotometry, Infrared; Zinc | 1992 |