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See reference [7]
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Schmidt's group first disclosed the idea of conformational change of the sialyl acceptor to enhance the reactivity of the C8-hydroxy group. They exploited the 1,7-lactonated sialyl acceptor for 8-O-sialylation but obtained mainly β-disialoside. See reference [7].
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Furuhata's group first reported the 8-O-sulfonylation of neuraminic acid. They also confirmed that no migration or cleavage of the sulfonyl group at the C8-hydroxy group had occurred during the full deacylation and saponification process: M. Tanaka, T. Kai, X.-L. Sun, H. Takayanagi, K. Furuhata, Chem. Pharm. Bull. 1995, 43, 2095-2098.
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