Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Glycopeptide Synthesis

Abstract
The selective C-terminal deprotection of acid- and base-labile multifunctional O-glycopeptide heptyl (Hep) esters is achieved under mild conditions (pH 7; 37 °C) by enzymatic hydrolysis with a lipase from Mucor javanicus.

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