反应条件
1: 74 percent / iPr2NEt / methanol; acetonitrile 2: LDA / -120 °C 3: pyridine / CH2Cl2 / 0 °C 4: p-TSA, acetone / 6 h / Ambient temperature 5: 1.) BBN, 2.) Cs2CO3, AsPh3, Pd(dppf)2Cl2, H2O / 1.) THF, 25 deg C, 2 h, 2.) THF, DMF, 2 h 6: HCl / methanol / 3.5 h / 25 °C 7: 81 percent / <RuCl2((R)-BINAP)>2<NEt3>, H2, HCl / methanol / 14 h / 25 °C / 62057.8 Torr 8: 2,6-lutidine / CH2Cl2 / -78 - 20 °C 9: HCl / tetrahydrofuran; methanol / 0 °C 10: 1.) Et3N, 2,4,6-trichlorobenzoyl chloride, 2.) DMAP / 1.) THF, RT, 15 min, 2.) THF, toluene, 0.5 h 11: 82 percent / SmI2, NiI2 / tetrahydrofuran / 2 h / -78 °C 12: 91 percent / HF*pyridine / tetrahydrofuran / 5 h / 0 °C View Scheme
参考文献
Journal of the American Chemical Society, , vol. 121, # 30 p. 7050 - 7062
