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- W2067391302 abstract "To study the influence of carbohydrate variation on the properties of a peptide or a protein, it has become important to have access to several different glycoforms. This can be achieved by separating a mixture of glycoforms into components or by using different biological sources that produce different glycoforms. Furthermore, enzymatic glycosylation or deglycosylation can convert one glycoform to another. However, the most generally applicable approach for obtaining defined glycoprotein fragments is chemical synthesis. Technically, this can be carried out either in solution or, preferably for larger fragments, on a solid phase. The 9-fluorenylmethoxycarbonyl (Fmoc) modification of the original Merrifield scheme for solid-phase peptide synthesis is well suited for this purpose. The literature (1988 and onward) describes numerous successful syntheses of glycopeptides using this technique. This chapter reviews work published until mid-1993 on the synthesis of O-glycopeptides, with special emphasis on solid-phase syntheses." @default.
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- W2067391302 date "1986-01-01" @default.
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- W2067391302 title "Conformation-dependent O-glycosylation of threonine-containing dipeptides" @default.
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- W2067391302 doi "https://doi.org/10.1016/0008-6215(86)85036-4" @default.
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