Enzymatic glycosylation of o-glycopeptid
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Michael Schultz; Horst Kunz
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Article
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1992
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Elsevier Science
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French
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O-Glycosylation of serine derivatives carried out with N-urethane protected glucosamine yields O-glycopeptides which are regio-and stereoselectively galactosylated with the aid of ~-1,4-galactosyltranaferase (EC 2.4.1.22 ). Chemical syntheses of glycopeptides require a complex methodology of multi-