229345-02-2

Upstream product

• 182485-44-5 N-(4-Phenylacetoxybenzyloxycarbonyl)-L-serine(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl) 

Downstream Products

• 287178-81-8 N-(4-Phenylacetoxybenzyloxycarbonyl)-L-seryl(O-2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-L-seryl(O-tert-butyl)-L-seryl(O-tert-butyl)-glycine tert-butyl ester 

Relevant academic research and scientific papers

Enzymatic protecting group techniques for glyco- And phosphopeptide chemistry: Synthesis of a glycophosphopeptide from human serum response factor

The covalent modification of proteins by phosphorylation and by glycosylation with GlcNAc residues are important regulatory processes which mediate biological signal transduction. For the study of such biological phenomena in molecular detail characterist

Chemoenzymatic synthesis of a characteristic glycophosphopeptide from the transactivation domain of the serum response factor

Glycopeptides, phosphopeptides, and glycophosphopeptides can be synthesized efficiently by a strategy based on a combination of suitable enzyme-labile protecting groups. Thus, probes for biological studies can be accessed. An example is the glycosylated a