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Design of linker 1. Cleavage by hydrogenolysis from a solid support reveals a conjugation site for the synthesis of glycoconjugates or glycan arrays and simultaneously removes permanent benzyl protecting groups. The linker can be coupled to amino- and chloro-functionalized resins. By placement of insert 2 on amino resins, an additional Zemplén cleavage site for fast LC–MS analysis is introduced.
