Efficient synthesis of N-protected amino/peptide Weinreb amides from T3P and DBU
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文摘
The reaction of N¦Á-protected amino/peptide acid with N,O-dimethylhydroxylamine hydrochloride in the presence of T3P and DBU to obtain enantiomerically pure N¦Á-protected amino/peptidyl Weinreb amides in high yields has been described. Fmoc-Ala-Weinreb amide 2a is obtained as single crystal, and its structure was determined through X-ray crystallography.

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