“…[3]. The1 H-NMR spectra of the side chain revealed the presence of the three secondary methyl groups [δ H 1.11 (H 3 -21), δ C 24.1 (C-21), δ H 0.88 (H 3 -26), δ C 22.9 (C-26), δ H 0.89 (H 3 -27) and δ C 22.8 (C-27)] and a double bond [δ H 5.79 (H-22), δ C 138.1 (C-22), δ H 5.34 (H-23) and δ C 128.8 (C-23)] (Table 1). The ROESY correlations of H 3 -18/H-20 and H-21; H 3 -21/H β -12, H-22 and H-16 and the chemical shifts of H 3 -21 (δ H 1.11) allowed to determine the 20R-configuration [4].…”