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Solvent effect on the conformation of the hydroxymethyl group established by molecular dynamics simulations of methyl-β-D-glucoside in water

✍ Scribed by L. M. J. Kroon-Batenburg; J. Kroon


Publisher
Wiley (John Wiley & Sons)
Year
1990
Tongue
English
Weight
470 KB
Volume
29
Category
Article
ISSN
0006-3525

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✦ Synopsis


Molecular dynamics simulations of methyl-P-D-glucoside in water are performed. Although the tg conformation of the hydroxymethylgroup is found to be the lowest in energy for the isolated molecule, it appears to be unstable in water. The well-known absence of a significant amount of the tg conformation in polar solvents can therefore be explained as a solvent effect.