Synthesis of methyl 2- O-β- d-xylopyranosyl- d-galactopyran-uronate, a pseudoaldobiouronic ester

The title compound has been synthesised by a route in which the key step was the condensation of methyl (benzyl 3,4- O-isopropylidene-β- d-galactopyranosid)-uronate with 2,3,4-tri- O-acetyl-α- d-xylopyranosyl bromide, followed by removal of the protecting groups.

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Bibliographic Details
Published in:Carbohydrate research 1979, Vol.73 (1), p.67-74
Main Authors: Boen Tjan, Sing, Poll, Dick J., Doornbos, Tamme
Format: Article
Language:English
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Summary:The title compound has been synthesised by a route in which the key step was the condensation of methyl (benzyl 3,4- O-isopropylidene-β- d-galactopyranosid)-uronate with 2,3,4-tri- O-acetyl-α- d-xylopyranosyl bromide, followed by removal of the protecting groups.
ISSN:0008-6215
1873-426X
DOI:10.1016/S0008-6215(00)85475-0