反应条件
1: BF3*OEt2; thiophenol / CH2Cl2 / 0.25 h / 0 °C 2: 2,6-lutidine / CH2Cl2 / 0.5 h / 0 °C 3: PPh3; triethylamine / Pd2(dba)3*CHCl3 / toluene / 2 h / 120 °C 4: camphorsulfonic acid / methanol / 12 h / 20 °C View Scheme
参考文献
Konno, Katsuhiro; Maki, Shojiro; Fujishima, Toshie; Zhaopeng, Liu; Miura, Daishiro; Chokki, Manabu; Takayama, Hiroaki
Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 2 p. 151 - 156
