Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The protease-catalyzed synthesis of amino acid est-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 substitutent, and that may be exploited to allow selective one-pot syntheses.

Type

Journal article

Journal

Chem Commun (Camb)

Publication Date

07/10/2001

Pages

1908 - 1909

Keywords

Acylation, Amino Acids, Binding Sites, Carbohydrates, Catalysis, Endopeptidases, Esterification, Glycopeptides, Kinetics, Oxidation-Reduction, Peptide Biosynthesis, Stereoisomerism