Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
71176 | Journal of Molecular Catalysis B: Enzymatic | 2007 | 6 Pages |
Abstract
The deacylation under hydrolytic conditions of methyl 2,3,5-tri-O-acetyl-α-d-ribofuranoside, methyl 2,3,5-tri-O-acetyl-β-d-ribofuranoside, methyl 2,3,5-tri-O-acetyl-α,β-d-arabinofuranosides and alkyl 2,3,5-tri-O-acetyl-α,β-xylofuranosides have been studied using banana whole tissue as biocatalyst. Reaction regioselectivity strongly depends on substrate structure. Hydrolysis of methyl 2,3,5-tri-O-acetyl-α-d-ribofuranoside afforded methyl 2,3-di-O-acetyl-α-d-ribofuranoside in quantitative yield.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Marisa Taverna-Porro, Luis E. Iglesias, Javier M. Montserrat, Adolfo M. Iribarren,