“…Consequently, the absolute configuration of compound 27 was established as 3R, 9R, 9aR, 14S, 16S, and named dehydrocroomine B. By comparing 1D NMR data, dehydrostenine A (3) (Dong et al, 2017), dehydrostenine B (4) (Dong et al, 2017), neotuberostemonol (5) (Jiang et al, 2002), tuberostemonine D (6) (Pilli and Ferreira de Oliveira, 2000), tuberostemonine O (7) (Kil et al, 2014), 15α-didehydrotuberostemonine (8) (Lin and Fu, 1999), 9α-bisdehydrotuberostemonine (9) (Lin et al, 2008), isodidehydrotuberostemonine (10) (Lin et al, 2008), 15βdidehydrotuberostemonine (11) (Yue et al, 2014), didehydrotuberostemonine A (12) (Hu et al, 2009), tuberostemoline ( 14) (Lin et al, 2008), stemonatuberone C (15) (Yue et al, 2014), bisdehydrostemoninine (18) (Lin et al, 2006), stichoneurine E (19) (Park et al, 2013), tuberostemoamide (20) (Hou et al, 2019), stemona-lactam S (21) (Dong et al, 2017), stemona-Lactam O (22) (Jiang et al, 2002), stemoninine A (23) (Wang et al, 2008), tuberostemospiroline (25) (Hu et al, 2019), dehydrocroomine (28) (Lin et al, 2008), and sessilistemonamine C (29) (Wang et al, 2007) were proved to be known compounds.…”