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Reconciling solvent effects on rotamer populations in carbohydrates — A joint MD and NMR analysis()
The rotational preferences of the hydroxymethyl group in pyranosides is known to depend on the local environment, whether in solid, solution, or gas phase. By combining molecular dynamics (MD) simulations with NMR spectroscopy the rotational preferences for the ω angle in methyl 2,3-di-O-methyl-α-D-...
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| I publikationen: | Can J Chem |
|---|---|
| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2006
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4276422/ https://ncbi.nlm.nih.gov/pubmed/25544777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1139/v06-036 |
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