反应条件
1.1: 51 percent / ammonium formate; tributylphosphine / Pd(OAc)2 / benzene / 24 h / 50 °C 2.1: 26 percent / Ti(O-i-Pr)4; i-PrMgCl / diethyl ether / 1 h / -50 °C 3.1: 59 percent / I2 / CH2Cl2 / 12 h / 20 °C 4.1: 100 percent / Et3N; DMAP / CH2Cl2 / 6 h / 20 °C 5.1: 9-BBN / tetrahydrofuran / 0.83 h / 28 °C / microwave irradiation 5.2: 50 percent / K3PO4*3H2O; H2O / PdCl2(dppf) / tetrahydrofuran; dimethylformamide / 5 h / 60 °C 6.1: 84 percent / aq. NaOH / methanol / 36 h / 50 °C 7.1: Et3N; 2,4,6-trichlorobenzoyl chloride / tetrahydrofuran / 0.33 h / 20 °C 7.2: 88 percent / DMAP / toluene; tetrahydrofuran / 1 h 8.1: 99 percent / HF*pyridine / tetrahydrofuran 9.1: 49 percent / 3,3-dimethyldioxirane / CH2Cl2 / -35 °C View Scheme
参考文献
Sawada, Daisuke; Shibasaki, Masakatsu
Angewandte Chemie - International Edition, 2000 , vol. 39, # 1 p. 209 - 213