“…In the 1 H‐NMR spectrum ( Table ), the most representative signals were three singlet methyls at δ (H) 1.11, 1.98, 2.09, an acetoxy methyl at δ (H) 2.29 ( s ), and an olefinic proton at δ (H) 5.76 ( s ). The 13 C‐NMR indicated 17 carbon resonances which included an α , β ‐unsaturated ketone moiety ( δ (C) 159.0, 126.9, and 191.2), an α , β ‐unsaturated‐ γ ‐lactone moiety ( δ (C) 145.2, 122.6, and 170.4), and one oxygenated sp 2 carbon signal at δ (C) 149.0 . These NMR data indicated that 1 was an eudesmanolide .…”