Synthetic Studies toward the Mannopeptimycins: Synthesis of Orthogonally Protected beta-Hydroxyenduracididines

摘要

The asymmetric synthesis of the nonproteinogenic amino acids (2S,35,4'S)-beta-hydroxyenduracididine 3 and (2R,3S,4'S)-beta-hydroxyenduracididine 4 in orthogonally protected form in 15 total steps from Garner's aldehyde is reported. The former and N-glycosylated form of the latter are found in the glycopeptide antibiotic mannopeptimycin.