They are commonly used as glycosyl donors in glycosylation reactions to build complex carbohydrate structures. The trifluoroacetimidate group enhances the reactivity, making it easier to form glycosidic bonds.
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p-Methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside
phenyl 2-O-(o-nitrobenzyl)-3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranoside
5,6-O-isopropylidene-D-mannono-1,4-lactone
(2R,3S,6S)-2-(hydroxymethyl)-6-phenyl-3,6-dihydro-2H-pyran-3-ol
4-methoxybenzyl 2,3-O-isopropylidene-4-O-<3,4,6-tri-O-benzoyl-2-(benzoyloxyimino)-2-deoxy-β-D-arabino-hexopyranosyl>-α-L-rhamnopyranoside
