Abstract
The deacylation of glucose, galactose and mannose pentaacetates, galactose and mannose penta(3-bromo)benzoates, as well as the dealkylation of 2,3,4,6-tetra-O-acetyl and 2,3,4,6-tetra-O-(3-bromo)benzoyl methyl α-D-glucopyranosides have been studied. In addition, a computational study on the deacylation of β-D-glucose pentaacetate has been carried out with density functional theory (B3LYP/6-31G*). The anomeric effect during deacetylation and dealkylation has been clearly demonstrated in both experimental and computational results.
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Wang, Z. D., Mo, Y., Chiou, C. L., & Liu, M. (2010). A Simple preparation of 2,3,4,6-tetra-O-acyl-gluco-, galactoand mannopyranoses and relevant theoretical study. Molecules, 15(1), 374–384. https://doi.org/10.3390/molecules15010374
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