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PubMed:3197039 JSONTXT 34 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-143 Sentence denotes The determination of the structure of blood group oligosaccharides from fully assigned 1H-n.m.r. spectra for solutions in non-aqueous solvents.
T1 0-143 Sentence denotes The determination of the structure of blood group oligosaccharides from fully assigned 1H-n.m.r. spectra for solutions in non-aqueous solvents.
TextSentencer_T2 144-393 Sentence denotes The fully assigned 1H-n.m.r. spectra of a blood group A tetrasaccharide and of a blood group H hexasaccharide in dimethyl sulfoxide and in pyridine by use of two-dimensional COSY and homonuclear Hartmann-Hann coherence transfer methods are reported.
T2 144-393 Sentence denotes The fully assigned 1H-n.m.r. spectra of a blood group A tetrasaccharide and of a blood group H hexasaccharide in dimethyl sulfoxide and in pyridine by use of two-dimensional COSY and homonuclear Hartmann-Hann coherence transfer methods are reported.
TextSentencer_T3 394-491 Sentence denotes The 1H-n.m.r. spectra of both of these compounds in deuterium oxide had been previously assigned.
T3 394-491 Sentence denotes The 1H-n.m.r. spectra of both of these compounds in deuterium oxide had been previously assigned.
TextSentencer_T4 492-812 Sentence denotes Since the relative proton chemical shifts in the three solvents are quite different, resonances which overlap or are strongly coupled for one solvent may be well resolved for another, thus providing an extension of the method of complete proton assignments for determination of the structure of complex oligosaccharides.
T4 492-812 Sentence denotes Since the relative proton chemical shifts in the three solvents are quite different, resonances which overlap or are strongly coupled for one solvent may be well resolved for another, thus providing an extension of the method of complete proton assignments for determination of the structure of complex oligosaccharides.
TextSentencer_T5 813-1204 Sentence denotes Although the rotational correlation times (tau c) of these oligosaccharides are similar to the reciprocal of the spectrometer frequency, either negative or positive n.O.e. values were measurable for both oligosaccharides in all three solvents in one-dimensional difference spectroscopy by taking advantage of the dependence of tau c on the solvent viscosity and, thus, on sample temperature.
T5 813-1204 Sentence denotes Although the rotational correlation times (tau c) of these oligosaccharides are similar to the reciprocal of the spectrometer frequency, either negative or positive n.O.e. values were measurable for both oligosaccharides in all three solvents in one-dimensional difference spectroscopy by taking advantage of the dependence of tau c on the solvent viscosity and, thus, on sample temperature.
TextSentencer_T6 1205-1505 Sentence denotes Whereas n.O.e. depend strongly on temperature and solvent viscosity, the ratios of the effects between protons on the same pyranoside ring and those on different rings were observed to be similar, suggesting that the oligosaccharide conformations are not strongly dependent on solvent or temperature.
T6 1205-1505 Sentence denotes Whereas n.O.e. depend strongly on temperature and solvent viscosity, the ratios of the effects between protons on the same pyranoside ring and those on different rings were observed to be similar, suggesting that the oligosaccharide conformations are not strongly dependent on solvent or temperature.