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Sulfamate-Tethered Aza-Wacker Strategy for a Kasugamine Synthon.

Gour Hari MandalShyam Sathyamoorthi
Published in: The Journal of organic chemistry (2023)
We present our preparation of a kasugamine synthon, which proceeds in 14 steps from a literature epoxide. We expect that this kasugamine derivative can be used for the total syntheses of kasugamycin, minosaminomycin, and analogue antibiotics. A key step in the synthesis is our laboratory's sulfamate-tethered aza-Wacker cyclization.
Keyphrases
  • systematic review
  • molecularly imprinted
  • water soluble
  • high resolution