An Fmoc-protected L-threonine building block carrying a Manα1-2Manα disaccharide, designed for solid-phase peptide synthesis (SPPS) of glycopeptides. The Nα-Fmoc group is removed under standard base conditions (piperidine) during chain elongation, while the free α-carboxylic acid is available for coupling to the growing resin-bound peptide. The sugar hydroxyl groups are protected as acetate esters (peracetate), which keep the glycan inert during synthesis and are removed under mild base (e.g., sodium methoxide / hydrazine) after assembly. The installed glycan is the O-mannose disaccharide Manα1-2Man, an extension of protein O-mannosylation, used to build O-mannosyl glycopeptides relevant to α-dystroglycan biology.