| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1411784 | Journal of Molecular Structure | 2007 | 6 Pages |
Abstract
The structure of some glucosamine Schiff bases has been studied by means of ab initio RHF and DFT calculation and CP/MAS 13C and 15N NMR measurements. The anomeric and tautomeric equilibria in a DMSO solution have been studied by 1H, 13C and 15N NMR spectroscopy. The anomeric composition of d-2-glucosamine Schiff bases in the solid state and in DMSO solution has been shown to depends on the tautomeric form of Schiff bases and electronic properties of substituents on the aromatic ring.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
B. Kołodziej, E. Grech, W. Schilf, B. Kamieński, M. Makowski, Z. Rozwadowski, T. Dziembowska,