Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1389414 | Carbohydrate Research | 2006 | 4 Pages |
Abstract
Benzyl β-d-galactofuranoside was efficiently obtained from 1,2,3,5,6-penta-O-benzoyl-α,β-d-galactofuranose, via benzyl 2,3,5,6-tetra-O-benzoyl-β-d-galactofuranoside. Conditions for the O-debenzylation were investigated in order to evaluate the synthetic application of the benzyl group as an anomeric protector of a galactofuranose moiety in synthetic strategies involving galactofuranose.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Karina Mariño, Luciana Baldoni, Carla Marino,