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Thomsen-Friedenreich antigen

Because O-glycosylation can also be accomplished with active esters (e.g., penta-fluorophenyl esters) [11] of Fmoc serine and threonine, the Fmoc technique provides a general method for the synthesis of glycopeptides. Thomsen-Friedenreich antigen glycopeptides and neoglycoproteins have been obtained by this method in preparative amounts [12], In combination with acid-labile polymeric benzyl ester anchors, this Fmoc technique was applied to solid-phase syntheses of glycopeptides [11,13,14]. [Pg.266]

L. Kroger, A. Scudlo, and J. Thiem, Subsequent enzymatic galactosylation and sialylation towards sialylated Thomsen-Friedenreich antigen components, Adv. Synth. Catal., 348 (2006) 1217—1227. [Pg.365]

See other pages where Thomsen-Friedenreich antigen is mentioned: [Pg.167]    [Pg.550]    [Pg.547]    [Pg.241]    [Pg.176]    [Pg.218]    [Pg.57]    [Pg.249]    [Pg.375]    [Pg.317]    [Pg.530]    [Pg.97]    [Pg.321]    [Pg.270]    [Pg.277]    [Pg.176]    [Pg.177]    [Pg.676]    [Pg.31]    [Pg.77]   
See also in sourсe #XX -- [ Pg.266 ]

See also in sourсe #XX -- [ Pg.1390 , Pg.1816 , Pg.2068 ]

See also in sourсe #XX -- [ Pg.422 ]



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