“…57 (dd, J = 10.4, 5.3 Hz, H-1a, 1H), 4.40 (dd, J = 10.4, 3.1 Hz, H-1b, 1H), 5.08 (m, H-2, 1H), 4.32 (dd, J = 4.7, 3.2 Hz, H-3, 1H), 4.25(td, J = 5.5, 4.7, Hz, 1H) and 4.56 (t, J = 6.5 Hz, H-2′, 1H), whereas the carbons shifts of the respective centres were appeared at δ C 61.4, 52.0, 75.5, 72.4 and 72.7, respectively, which were in complete agreement with those of sphingolipids with a 2S,3S,4R,2R′ configuration(Muralidhar et al 2005;Kang et al 2007;Riaz et al 2007;Dongfack et al 2012). The optical rotations of 1 ([α] D = +41.0) and its methanolysis products ([α] D = 8.1 and +18.9) which were comparable with those of sphingolipids with a 2S,3S,4R,2′R configurations(Muralidhar et al 2005;Kang et al 2007;Dongfack et al 2012).…”