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- W3083501596 abstract "A convergent synthesis for erythropoietin (EPO) 1‐28 N‐glycopeptide hydrazides was developed. In this approach, EPO 1‐28 peptides were synthesized on the solid phase and converted to C‐terminal hydrazides after cleavage from the resin. After selective deprotection of the Asp24 side chain, the desired glycosylamine was coupled by pseudoproline‐assisted Lansbury aspartylation. Although the initial yields of the EPO 1‐28 glycopeptides were satisfactory, they could be markedly improved by increasing the purity of the peptide using a reversed‐phase high‐performance liquid chromatography (RP‐HPLC) purification of the protected peptide." @default.
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- W3083501596 date "2020-09-03" @default.
- W3083501596 modified "2023-10-05" @default.
- W3083501596 title "Strategies for the highly efficient synthesis of erythropoietin N‐glycopeptide hydrazides" @default.
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- W3083501596 doi "https://doi.org/10.1002/psc.3283" @default.
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