“…7 Hz, H-6a), 4.07 (dd, 1H, H-4), 4.00 (dd, 1H, H-6b), 2.76 (d, 1H, 3-OH), 1.50 (s, 3H, 1,2-CH 3 ′), 1.45 (s, 3H, 5,6-CH 3 ′), 1.37 (s, 3H, 5,6-CH 3 ″), and 1.32 (s, 3H, 1,2-CH 3 ″) ppm. 13 C NMR (125.76 MHz, CDCl 3 , 23 °C): δ = 111.9 (1,2-q C), 109.8 (5,6-q C), 105.4 (C-1), 85.2 (C-2), 81.2 (C-4), 75.2 (C-3), 73.5 (C-5), 67.7 (C-6), 26.9 (1,2-CH 3 ′ and 5,6- 3.82 (dd, 1H, J 6a,5 = 2.3, J 6a,6b = −11.9 Hz, H-6a), 3.64 (dd, 1H, J 6b,5 = 5. 7 Hz, H-6b), 3.36 (dd, 1H, J 4,3 = 8.7 Hz, J 4,5 = 9.8 Hz, H-4), 3.24 (ddd, 1H, H-5), 3.18 (dd, 1H, J 3,2 = 9.0 Hz, H-3), 3.17 (dd, 1H, H-2), and 3.05−1.42 (br m, 10H, carborane−BH) ppm.…”