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A facile silyl linker strategy for the solid-phase synthesis of protected glycopeptide: Synthesis of an N-terminal fragment of IL-2 (1-10)

, : A facile silyl linker strategy for the solid-phase synthesis of protected glycopeptide: Synthesis of an N-terminal fragment of IL-2 (1-10). Tetrahedron 56(34): 6235-6243

An N-terminal glycodecapeptide fragment of interleukin 2 (1) was synthesized by solid-phase method utilizing a new silyl linker. The O-silylated Fmoc-Thr-OAll was attached to the commercial HMP-resin and peptide chain elongation was performed by Fmoc protocol to produce a protected heptapeptide (3-10), which was cleaved from the resin by fluoridolysis and used as the amino component for further condensation on the solid support. On the other hand, 6-hydroxyl group of an Fmoc-Thr(GalNAc)-OAll derivative was silylated with the linker and attached to the resin. Deallylation, block condensation with the heptapeptide (3-10), and elongation at N-terminal with two amino acids were performed on the resin. Fluoride ion-mediated cleavage released the N- and C-protected glycopeptide from the solid support in good efficiency. Fully deprotected glycopeptide was also synthesized through on-resin deallylation and acidic cleavage of the silyl ether linkage.


DOI: 10.1016/s0040-4020(00)00588-3

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