反应条件
1: 83 percent / PdCl2(PPh3)2, LiCl / dimethylformamide / 2 h / 80 °C 2: (PhSeO)2O / CH2Cl2 / 0.25 h / 23 °C 3: Bu4NF / tetrahydrofuran / 0.17 h / 23 °C 4: 91 percent / 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, DMAP / CH2Cl2 / 0.5 h / 23 °C 5: 0.5 h / -40 °C 6: 1.) i-Pr2NEt, 2.) tert-butyl alcohol, N-tert-butyl-N',N',N'',N''-tetramethylguanidine / 1.) 0 deg C, 30 min, 2.) 23 deg C 7: 23 °C 8: 84 percent / PdCl2(PPh3)2, Bu3SnH, HOAc / CH2Cl2 / 0.08 h / 23 °C 9: 70 percent / <N-methylpyridinium-4-carboxaldehyde>iodide, 1,8-diazabicyclo<6.4.0>undec-7-ene, DMF / CH2Cl2 / 0.67 h / 23 °C 10: 82 percent / silica gel / ethanol / 23 °C 11: aq. CF3COOH / tetrahydrofuran / 9 h / 23 °C 12: aq. AgNO3 / acetonitrile / 11 h / 23 °C View Scheme
参考文献
Corey; Gin, David Y.; Kania, Robert S.
Journal of the American Chemical Society, 1996 , vol. 118, # 38 p. 9202 - 9203