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. Author manuscript; available in PMC: 2017 Jun 8.
Published in final edited form as: Can J Chem. 2016 Feb 9;94(11):927–935. doi: 10.1139/cjc-2015-0606

Table 2.

Experimental observables for residue A of the ΔUA containing disaccharides 3–5.

3 4 5



Residue A NMR Theoretical NMR Theoretical NMR Theoretical
3J coupling (Hz)a
H1–H2 3.4 2.7 3.0 2.7 3.7 2.9
H2–H3 2.5 2.5 2.5 2.8 2.8
H3–H4 4.7 5.0 4.7 5.0 4.4 4.8
Population (1H2:2H1) 70:30 80:20 76:24 80:20 67:33 76:24
NOEs (Å)
H1A–H3B 3.5 2.7 3.3 2.4 2.9
H1A–H5B 3.5 3.1 3.6 3.3
a

J couplings for H1–H2, H2–H3, and H3–H4 in the 1H2 ring form are 1.7, 1.2, and 5.8 Hz, respectively, and for the 2H1 form are 6.7, 7.8, and 1.6 Hz, respectively. The J values were independent of the anomeric configuration (α or β) at the reducing terminus.