
Carbohydrate Research p. 341 - 349 (1997)
Update date:2022-08-05
Topics:
Kappes, Thomas
Waldmann, Herbert
The development of the tetrabenzylglucosyloxycarbonyl (BGloc)- protecting group as an enzymatically removable urethane protecting function for peptide synthesis is described. BGloc-protected amino acids are readily synthesized by conversion of amino acid allyl esters into the respective isocyanates, subsequent treatment with 2,3,4,6-tetrabenzylglucose and C- terminal allyl ester cleavage. From BGloc masked dipeptide esters, which are accessible by standard methods of peptide chemistry, the N-terminal urethane is selectively cleaved off in high yield via removal of the benzyl ethers by hydrogenation followed by hydrolysis of the urethane by means of α- and β- glucosidase under very mild reaction conditions.
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