
Abstract The 1 H and 13 C NMR spectral analysis of the glucoside renifolin, isolated from Pyrola renifolia , demonstrated the so far unknown binding site of the glucose moiety to be at C-8 and hence its structure as 8-β- D -glucosyloxy-2,7-dimethyl-1,4-dihydronaphthalen-5-ol. The earlier reported structure for the glucoside pirolatin, isolated from Pyrola japonica , was also reconfirmed by the 13 C NMR spectral analysis.
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