Structural Characterization of an Enantiomerically Pure Amino Acid Imidazolide and Direct Formation of the β-Lactam Nucleus from an α-Amino Acid

Decomposition of a diazo β-ketoamide derived from N-trityl serine imidazolide and N-protected acetanilides provides, instead of the expected
3-acyloxindole product, an enantiomerically pure (EP) β-lactam. The amino acid stereocenter is incorporated, the second chiral center is
induced, and trityl protection of the β-lactam ring is realized for the first time. The desired 3-acyloxindole is obtained from oxindole and
Tr-Ser(OBn)-imidazole, the X-ray of which provides the first structural determination of an EP amino acid imidazolide.