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Oligosaccharide synthesis with trichloroacetimidates disaccharides

For the synthesis of HA oligosaccharides, model glycosylations were carried out in solution and on PEG support. A glucosamine acceptor coupled with hydrojyl-terminated PEG monomethyl ether 11 was efficiently glycosylated with trichloroacetimidate donor 10 afford an orthogonally protected disaccharide 12 which can be used for the synthesis of HA sequences, see Scheme 3. [Pg.221]


See other pages where Oligosaccharide synthesis with trichloroacetimidates disaccharides is mentioned: [Pg.438]    [Pg.226]    [Pg.1264]    [Pg.1267]    [Pg.1269]    [Pg.601]    [Pg.226]    [Pg.224]    [Pg.120]    [Pg.221]    [Pg.514]    [Pg.516]    [Pg.521]    [Pg.224]    [Pg.98]    [Pg.247]    [Pg.60]    [Pg.618]    [Pg.496]    [Pg.510]    [Pg.209]    [Pg.32]    [Pg.236]    [Pg.392]    [Pg.518]    [Pg.193]    [Pg.20]    [Pg.55]   
See also in sourсe #XX -- [ Pg.298 , Pg.301 , Pg.302 , Pg.303 , Pg.304 ]




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Disaccharides

Oligosaccharide synthesis disaccharides

Oligosaccharide synthesis with trichloroacetimidates

Oligosaccharides disaccharides

Trichloroacetimidate

Trichloroacetimidates

Trichloroacetimidates, synthesis

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