“…Complete the assignment of the remaining resonances of the aglycone in the 13 C NMR spectrum of 1 was achieved by analysis of the HSQC and HMBC data , which confirmed the presence of isorhamnetin (3,5,7,4 0 -tetrahydroxy-3 0 -methoxyflavone). A full list of the corresponding assignments is given in Table 1 (Chabani et al, 2013;Fang et al, 2013;Prescott et al, 2013). The COSY and 1 H NMR spectra of 1 showed also four aromatic protons at d H 6.71 (2H, d, J = 8.6 Hz), 7.18 (2H, d, J = 8.6 Hz) and two olefinic protons at d H 6.05 (d, J = 15.9 Hz) and 7.39 (d, J = 15.9 Hz).…”