“…1 H NMR (400 MHz, CD 3 OD) δ H 7.25 (d, J = 8.5 Hz, 2H, 6'), 6.97 (d, J = 8.4 Hz, 2H, 6''), Compound 4 (Smith et al 2006) 1 H NMR (600 MHz, CD 3 OD) δ H 7.72 (d, J = 16.1 Hz, 1H, H-8), 6.16 (d, J = 16.1 Hz, 1H, H-7), 5.92 (s,1H, H-4), 5.79 (s, 1H, H-10), 2.55 (d, J = 16.9 Hz, 1H, Ha-2), 2.19 (d, J = 16.9 Hz, 1H, Hb-2), 2.01 (d, J = 0.7 Hz, 3H, H-15), 1.95 (d, J = 1.2 Hz, 3H, H-14), 1.07 (s, 1H, H-13), 1.04 (s, 1H, H-12); 13 C NMR (150 MHz, CD 3 OD) δ C 201.1 (s, C-3), 171.7 (s, C-11), 166.9 (s, C-5), 147.7 (s, C-9), 136.4 (d, C-7),129.8 (d, C-8), 127.4 (d, C-4), 122.6 (d, C-10), 80.6 (s, C-6), 50.7 (t, C-2), 42.9 (s, C-1), 24.7 (q, C-12), 23.6 (q, C-13), 21.0 (q, C-15), 19.7 (q, C-14).Compound 5(Das et al 2007)1 H NMR (600 MHz, CD 3 OD) δ H 2.33 (t, J = 7.2 Hz, 4H, H-2, 7),1.66 (m, 4H, H-3, 6), 1.42 (m, 4H, H-4, 5); 13 C NMR (150 MHz, CD 3 OD) δ C 177.9 (s, -COOH, C-1, 8), 35.1 (t, C-2, 7), 29.9(t, C-3, 6), 26.0 (t, C-4, 5).Compound 6…”