The oxazole-triamide rearrangement. Application to peptide synthesis |
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Authors: | H.H. Wasserman T.-J. Lu |
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Affiliation: | Department of Chemistry, Yale University, New Haven, Connecticut 06511 USA |
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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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