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  • Synthèse du 2-amino-3-O-(L
  • Add time:08/14/2019         Source:sciencedirect.com

    2-Amino-3-O-(L-1-carboxyethyl)-2-deoxy-D-glucose (isomuramic acid), an isomer of muramic acid, and its N-acetyl derivative have been synthesized from benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α- and β-D-glucopyranoside by condensation with D-2-chloropropionic acid, followed by removal of the protective groups. N-Acetylisomuramic acid can be differentiated from its D-1-carboxyethyl isomer (N-acetylmuramic acid) by chromatography and by the circular dichroism spectrum of the internal ester of the methyl α-D-glycopyranosides.

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    Prev:Synthesis of 1-C-linked diphosphate analogues of UDP-N-Ac-glucosamine and UDP-N-Ac-muramic acid
    Next: Total synthesis of uridine diphosphate-N-acetylmuramoyl-l)

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