Issue 19, 2022

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

Abstract

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
10 Mar 2022
Accepted
13 Apr 2022
First published
19 Apr 2022
This article is Open Access
Creative Commons BY license

RSC Adv., 2022,12, 11992-11995

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

T. Bozzola, U. J. Nilsson and U. Ellervik, RSC Adv., 2022, 12, 11992 DOI: 10.1039/D2RA01576E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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