Direct sialic acid 4-OAc substitution by nitrogen, sulfur and carbon nucleophiles with retention of stereochemistry

  • Bozzola T
  • Nilsson U
  • Ellervik U
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Abstract

A direct one-step nucleophilic substitution of the 4-OAc of acetyl protected Neu5Ac is presented.A direct one-step nucleophilic substitution of the 4-OAc of acetyl protected Neu5Ac is presented. Previously published methods for direct substitution of the 4-OAc are limited to cyclic secondary amines. Here we present conditions that allow for a much wider range of nitrogen nucleophiles as well as thiols and cyanide, to be used. The present investigation significantly broadens the scope of 4-aminations and allows for the introduction of a wide variety of different nucleophiles.

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Bozzola, T., Nilsson, U. J., & Ellervik, U. (2022). Direct sialic acid 4-OAc substitution by nitrogen, sulfur and carbon nucleophiles with retention of stereochemistry. RSC Advances, 12(19), 11992–11995. https://doi.org/10.1039/d2ra01576e

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