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Irritating ¦Ä 4.77 (H-7), ¦Ä 4.11 (H-8) showed NOE correlations in the difference Nuclear Overhauser Effect (dNOE) spectrum, which indicated that 1 possessed an erythro relative configuration.
The relative structure was further confirmed by NOESY correlations between H-8/H-2, 7, 6, and H-9(¦Ä 4.40)/H-2, 6. Enzymatic hydrolysis of 1 with cellulase gave the aglycone 1a.
The erythro configuration was also confirmed by the J7, 8-value (3.8 Hz) of 1a
The absolute structure of 1 was determined to be (7S, 8R) based on the negative cotton effects of 1 and 1a in its CD spectrum . The results above identified the structure of 1 as (7S,8R) guaiacylglycerol-8-O-4¡ä-sinapyl ether 9¡ä-O-¦Â-D-glucopyranoside.

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