
Journal of Carbohydrate Chemistry p. 383 - 398 (1996)
Update date:2022-09-26
Topics:
Dekany, Gyula
Wright, Karen
Ward, Peter
Toth, Istvan
Sialyl Lewis X (SLex) analogs 2a and 2b were synthesised, where the N-acetyl-D-glucose and the D-galactose units of SLex 1 were replaced with an alkyl and a heteroalkyl spacer. Sulphate ester 6i was also synthesised from alcohol 6b and chlorosulphonic acid. A novel promoter, silver mercaptoethanesulphonate, was used to synthesise α-sialosides 2c, 7b and 7c.
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