“…The NMR data of 2 closely resembled those of salpratlactone C, a known 11-nor-abietane diterpenoid bearing a benzopyran-2,5-dione isolated from Salvia prattii, 18 suggesting that these two diterpenoids share the same carbon skeleton. The main differences were the presence of an oxygenated methine (δ H 4.91, d, J = 10.2 Hz, H-6; δ C 67.4, C-6) and a methine (δ H 1.81, d, J = 10.2 Hz, H-5; δ C 53.3, C-5) in 2, instead of an endocyclic Δ 5 (6) double bond (δ H 6.41, s, H-6; δ C 171.3, C-5; 113.6, C-6) in salpratlactone C. Thus, wulfenioidin E (2) is a hydrated derivative of salpratlactone C, confirmed by the HMBC correlations from H-6 to C-5 and C-7, as well as by 1 H− 1 H COSY correlations of H-5/H-6 (Figure 1). The relative configuration in compound 2 was established based on scalar coupling constants (Table 2) and ROESY data analysis.…”