Issue 7, 1998
From the journal:

Chemical Communications

A unique and highly facile method for synthesising disulfide linked neoglycoconjugates: a new approach for remodelling of peptides and proteins

Wallace M. Macindoe,   Anita H. van Oijen  and  Geert-Jan Boons  

Abstract

An asymmetric disulfide linkage, formed by conjugation of a 5-nitropyridine-2-sulfenyl activated thioglycoside and a protein or pre-assembled peptide sequence, represents a good structural mimic of natural asparagine glycosylation.

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Article information

DOI
https://doi.org/10.1039/A708701B
Article type
Paper

Chem. Commun., 1998, 847-848

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A unique and highly facile method for synthesising disulfide linked neoglycoconjugates: a new approach for remodelling of peptides and proteins

W. M. Macindoe, A. H. van Oijen and G. Boons, Chem. Commun., 1998, 847 DOI: 10.1039/A708701B

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