[α]D −21.5 (c 1.66, CHCl3). 1H NMR (300 MHz, CDCl3): δ 6.88 (m, 1H, Libraries olefinic), 5.70 (d, 1H, J = 6.7 Hz, olefinic), 4.10 (q, 2H, J = 6.7 Hz, –OCH2), 3.76 (q, 1H, J = 6.0 Hz, –CH), 2.20 (m, 2H, allylic –CH2), 1.50 (m, 2H, –CH2), 1.24 (m, 3H, –CH3), 1.08 (d, 3H, J = 6.0 Hz, –CH3), 0.84 (s,

9H, 3× –CH3), 0.01 (s, 6H, 2× –CH3); 13C NMR (75 MHz, CDCl3): δ 149.6, 120.9, 67.7, 51.5, 37.8, 28.4, 25.3, 25.2, 23.9, −4.4, −4.3; IR (neat): 3457, 2949, 1722, 1656, 1440, 1277, 1196, 1045, 844 cm−1. To a stirred solution of ester 12 (6.7 g, 24.63 mmol) in dry CH2Cl2 (30 mL) at −78 °C, DIBAL-H (35 mL, 49.26 mmol, 20 mol% in toluene) was added and stirred at the same temperature for 2 h. The reaction mixture was quenched with few drops of MeOH and aq. sodium potassium tartrate (5 mL) and

filtered Venetoclax concentration through celite. It was dried (Na2SO4), evaporated to give 13 (4.7 g, 77%) as a colorless liquid. [α]D −30.6 (c 1.07, CHCl3); 1H NMR (300 MHz, CDCl3): δ 5.78 (m, 1H, olefinic), 5.03 (q, 1H, J = 17.3, 42.3 Hz, olefinic), Enzalutamide order 4.0 (m, 1H, –CH), 3.82 (m, 2H, –CH2), 2.2 (d, 1H, J = 6.7 Hz, –CH2), 1.46 (m, 2H, –CH2), 1.07 (d, 3H, J = 6.0 Hz, –CH2), 0.83 (s, 9H, 3× –CH3), 0.01 (s, 6H, 2× –CH3); 13C NMR (75 MHz, CDCl3): δ 133.4, 128.9, 68.3, 63.8, 38.8, 28.5, 25.7, 23.1, 17.9, −4.9, −4.2; IR: 3363, 2926, 2856, 1496, 1443 cm−1. To a cooled (−20 °C) suspension of activated powdered 4 Å MS (1.5 g) in CH2Cl2 (20 mL), (−)-DIPT (0.57 g, 2.45 mmol) in dry CH2Cl2 (2 mL)) Ti(OiPr)4 (0.36 mL, 1.22 mmol) and cumene hydroperoxide (4.4 M, 3.8 mL, 24.59 mmol) were added sequentially and stirred for 20 min. A solution of alcohol 13 (3.0 g, 12.29 mmol) in CH2Cl2 (10 mL) was added at −20 °C. The resulting mixture was stirred at the same temperature for 3 h. The reaction mixture was quenched with 10% NaOH sat. NaCl solution (30 mL) and stirred at room temperature for 4 h. It was filtered

through celite, dried (Na2SO4) and evaporated to give 14 (2.4 g, 75%) as a colorless liquid. [α]D +20.5 (c 0.31, CHCl3); 1H NMR (300 MHz, CDCl3): below δ 3.80 (m, 2H, –CH2), 3.56 (m, 1H, –CH), 2.85 (d, 2H, J = 14.3 Hz, 2× –CH), 1.84 (t, 1H, J = 6.7 Hz, –OH), 1.64–1.41 (m, 4H, 2× –CH2), 1.07 (d, 3H, J = 6.0 Hz, –CH3), 0.83 (s, 9H, 3× –CH3), 0.01 (s, 6H, 2× –CH3); 13C NMR (75 MHz, CDCl3): δ 68.1, 61.6, 58.