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5 To a stirred solution of epoxy alcohol 1 (20 mg, 0.172 mmol) and ketene acetal 5 (79 mg, 0.344 mmol) in CH2Cl2 (0.6 mL) were added 2,6-lutidine (70 µL, 0.603 mmol) and TBSOTf (79 µL, 0.344 mmol) at -78 °C. The reaction mixture was warmed to r.t. and stirred for 1 h. Then it was poured into a mixture of MTBE (5 mL) and buffer pH 5.5 (3 mL). The organic layer was separated and the aqueous phase was extracted with MTBE (3 × 5 mL). The combined organic layer was washed with 20% aq NaHSO3 solution (3 × 5 mL), H2O (3 × 5 mL), buffer pH 7 (3 × 5 mL) and brine (3 × 5 mL), dried and concentrated. The resulting residue was subjected to chromatography on silica gel. Elution with hexane-EtOAc (10:1) furnished the product 8 (Felkin product, 4,5-syn:anti = 3:1) as a colorless oil (55.2 mg, 0.120 mmol, 70%).
Main Product (syn-8): 1H NMR (400 MHz, CDCl3): δ = 7.04 (dd, J = 15.6, 7.8 Hz, 1 H), 5.76 (dd, J = 15.6, 1.3 Hz, 1 H), 3.73 (s, 3 H), 3.70 (dd, J = 13.1, 5.3 Hz, 1 H), 3.57 (dt, J = 13.3, 5.9 Hz, 1 H), 2.61 (m, 1 H), 1.69 (ddq, J = 13.3, 5.3, 1.1 Hz, 1 H), 1.53-1.51 (m, 2 H), 1.05 (d, J = 6.8 Hz, 3 H), 0.91 (s, 9 H), 0.89 (s, 9 H), 0.85-0.79 (m, 6 H), 0.07 (s, 6 H), 0.05 (s, 6 H). 13C NMR (100 MHz, CDCl3): δ = 167.6, 153.8, 120.2, 75.9, 74.8, 51.8, 41.3, 40.1, 27.4, 26.67, 26.62, 26.41, 26.39, 18.9, 18.6, 14.2, 11.2, 9.6, -3.1, -3.1, -3.5, -3.8. HRMS: m/z calcd for C20H41O4Si2 [8 - t-butyl]: 401.2543; found: 401.2542.