“…); 1 H NMR (500 MHz,1H), 1.25 (s, 3H), 0.91 -0.81 (m, 1H); 13 C NMR (125 MHz, CDCl 3 ) δ 31.84, 29.61, 29.57, 29.28, 22.61, 14.04 (Jatoi et al, 2007). 7), C 10 H 22 O, Colourless liquid, Yields 63 mg; IR (υ max , cm -1 ): 3324 (O-H), 2917, 2849 (C-H); 1 H NMR (500 MHz,J = 6.7 Hz,1H),1.56 (dt,J = 8.3,6.6 Hz,1H), 1.29 (s, 3H), 1.28 (d, J = 5.0 Hz, 1H), 1.25 (s, 12H), 0.88 (t, J = 7.0 Hz, 1H); 13 C NMR (125 MHz,CDCl3) δ 63.33,33.02,32.14,29.91,29.82,29.65,29.58,25.95,22.91,14.34; HR-ESI-MS (+ve mode): 158.0958 [M] + (de Brito-Filho et al 2017). 8), C 20 H 40 O, Colourless oil, Yields 4 mg; IR (υ max , cm -1 ): 3400 (O-H), 2918, 2849 (C-H), 1631 (C=C); 1 H NMR (500 MHz, Chloroform-d) δ 3.64 (t, J = 6.6 Hz, 1H), 1.62 (s, 0H), 1.55 (dq, J = 14.5, 7.3, 6.9 Hz, 1H), 1.32 (s, 10H), 1.31 -1.27 (m, 2H), 1.25 (d, J = 9.4 Hz, 2H), 1.25 (s, 12H), 0.92 -0.81 (m, 3H); 13 C NMR (125 MHz, CDCl 3 ) δ 140.37, 123.06, 63.13, 39.88, 37.44, 37.37, 37.30, 36.67, 35.04, 32.81, 32.70, 29.45, 25.14, 24.81, 24.48, 22.71, 22.64, 19.76, 19.73 (Itoh et al 2018).…”