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The oxazole-triamide rearrangement. Application to peptide synthesis
Authors:H.H. Wasserman  T.-J. Lu
Affiliation:Department of Chemistry, Yale University, New Haven, Connecticut 06511 USA
Abstract:The carboxyl group of a N-acylated amino acid may be protected by conversion to an oxazole derivative which, on photoxygenation, regenerates the carboxyl group in activated (triamide) form for peptide synthesis.
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