反应条件
1: 86 percent / BF3*OEt2; thiophenol / CH2Cl2 / 0.25 h / 0 °C 2: 99 percent / 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
Fujishima, Toshie; Konno, Katsuhiro; Nakagawa, Kimie; Kurobe, Mayuko; Okano, Toshio; Takayama, Hiroaki
Bioorganic and Medicinal Chemistry, 2000 , vol. 8, # 1 p. 123 - 134
