H-1 and C-13 NMR shifts for aldopyranose and aldofuranose monosaccharides: Conformational analysis and solvent dependence
UNSPECIFIED (1996) H-1 and C-13 NMR shifts for aldopyranose and aldofuranose monosaccharides: Conformational analysis and solvent dependence. MAGNETIC RESONANCE IN CHEMISTRY, 34 (10). pp. 755-760. ISSN 0749-1581Full text not available from this repository.
Ring H-1 and C-13 NMR chemical shifts for 14 aldopyranoses were measured in D2O and dimethyl-d(6) sulphoxide; those for eight aldofuranose monosaccharides were measured in dimethyl-d, sulphoxide. The effects of solvent are small. Shifts can be predicted with reasonable accuracy using algorithms having a minimum number of steric parameters, varying from one for aldofuranose C-13 shifts to eight for aldopyranose C-13 shifts.
|Item Type:||Journal Article|
|Subjects:||Q Science > QD Chemistry
Q Science > QC Physics
|Journal or Publication Title:||MAGNETIC RESONANCE IN CHEMISTRY|
|Publisher:||JOHN WILEY & SONS LTD|
|Number of Pages:||6|
|Page Range:||pp. 755-760|
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