“…In the IR spectrum, absorption bands of hydroxyl (3530 cm À1 ) and ester carbonyl (1782 and 1736 cm À1 ) were observed. The 1 H and 13 C NMR data (Table 1) showed resonances typical of an eudesmane sesquiterpene skeleton similar to 1a,8a-dihydroxy-5aH,10a-eudesma-3,11(13)-dien-6-olide (10) (Triana et al, 2013) H-20), an oxygenated methine resonance at d H 5.08 (1H, q, J = 6.2, H-18), two additional acetyl groups at C-18 and C-1 (d C 169.2, 20.7 and 170.1, 20.9) and an additional tertiary carbon at d C 76.2 (C-17).…”