“…The 13 C‐NMR and DEPT spectra displayed a total of 26 C‐atom resonances, of which 11 O‐bearing C‐atoms ( δ (C) 99.5 ( d ), 75.6 ( d ), 78.5 ( d ), 72.0 ( d ), 76.8 ( d ), 68.5 ( t ), 111.2 ( d ), 78.6 ( d ), 81.0 ( s ), 75.6 ( t ), and 66.2 ( t )), together with two anomeric H‐atoms ( δ (H) 4.55 ( d , J = 7.8) and 4.86 ( d , J = 2.4)) in the 1 H‐NMR spectrum, suggested the same sugar moiety presence as compound 1 . The NMR data of aglucone moiety of 2 coincided with that of monnieriside G, which indicated that 2 has the same aglucone moiety as monnieriside G . HMBCs ( Figure ) from H‐3 to C(2, 4, 10, 2a), H‐8 to C(6, 7, 9, 10), H‐2′ to C(4′a, 4′b), H‐3′ to C(5, 6, 7, 4′), H‐4′a to C(2′, 4′b), and H‐4′b to C(2′, 4′a) confirmed the skeleton of visamminol.…”