NMR Characterization of Flavanone Naringenin 7-O-Glycoside Diastereomer

NMR Characterization of Flavanone Naringenin 7-O-Glycoside Diastereomer

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To discriminate R and S flavanone glycoside using NMR, the mixture of R and S naringenin 7-O-glycoside was first isolated from Gleditsia sinensis.1H and 13C NMR data of the mixture were recorded with 1H NMR, 13C NMR, 1H-1H COSY, School Accessories 1H-13C HSQC and 1H-13C HMBC in DMSO-d6 solution.The two diastereomers were then separated with chiral chromatographic isolation, with their absolute configurations determined by circular dichroism.To avoid the disturbance of protons from glucose residues to dihydroflavonoid, 1H NMR spectra were acquired for pure R and S naringenin 7-O-glycoside and their mixture in CD3CN.The two diastereomers showed the largest proton chemical shift differences at the end group of glucose residue (H-1") ORG ROSE SOAP BAR with a chemical shift difference of 9.

4 Hz.The OH-5 proton showed a chemical shift difference of 5.8 Hz.The chemical shift of the three protons on ring C were all influenced by configuration.