Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 19, Pages 1908-1909Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b104137c
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The protease-catalyzed synthesis of amino acid ester-carbohydrate conjugates as glycopeptide analogues has been achieved in a highly regioselective and carbohydrate-specific manner using amino acid vinyl ester acyl donors and minimally or completely unprotected carbohydrate acyl acceptors, which together probed active sites of proteases to reveal yield efficiencies that are modulated by the carbohydrate C-2 substituent, and that may be exploited to allow selective one-pot syntheses.
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