“…In the 1 H-NMR spectrum, the presence of a para-substituted benzene ring was shown by proton signals 6.81 (1H, d, J ¼ 8:6 Hz) and 7.61 (1H, d, J ¼ 8:6 Hz), in addition to a meta-substituted benzene ring due to two doublets at 6.07 (1H, d, J ¼ 2:0 Hz) and 6.30 (1H, d, J ¼ 2:0 Hz). The HMBC and COSY spectra allowed complete assignment and identification of the aglycone as 4, 2 0 , 4 0 , 6 0 -tetrahydroxybenzophenone (iriflophenone) (18,19). The usual acidhydrolysis of compound 2 gave iriflophenone.…”