Abstract
Benzyloxycarbonyl peptide p-nitrophenyl
esters have been prepared by the mixed carbonic anhydride method using amino
acid or peptide p-nitrophenyl esters as amino components. Removal of the
N-protecting group produces higher peptide active esters, which can then be
used either in a further peptide coupling reaction with a benzyloxycarbonyl
amino acid, or polymerized to form sequential polypeptides. The advantages and
limitations of the procedure are discussed.
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