反应条件
1: CH2Cl2 / 0 deg C, 15 min; RT, 2 h 2: hydrogen / Raney Ni / methanol / 2 h / sonication 3: Et3N / CH2Cl2 / 0.5 h 4: 74 percent / 4-(1-dimethylamino)pyridine / acetonitrile / 2.5 h / Ambient temperature 5: 91 percent / NaBH4, CaCl2 / ethanol; tetrahydrofuran / -20 deg C, 15 min; RT, 45 min 6: 1) (COCl)2, DMSO, 2) Et3N / 1) CH2Cl2, -60 deg C, 15 min, 2) CH2Cl2, -60 deg C, 30 min 7: 1) potassium hexamethyldisilazide, 18-crown-6 / 1) THF, toluene, 1 h, -78 deg C, 2) THF, toluene, -78 deg C, 2 h 8: 71 percent / OsO4, Me3NO*2H2O / acetone; H2O / 2 h / Ambient temperature; sonication 9: 90 percent / NaOAc, hydrogen / Pd/C / methanol / Rt, 1 h; 35 deg C, 2 h 10: 97 percent / Dowex 50W400 / 4 h / Ambient temperature 11: 1) BH3*Me2S, 2) EtOH / 1) THF, 14 h, RT, 2) 2 h, reflux 12: 1) HCl, 2) Dowex 1X8-200 / 1) reflux, 30 min View Scheme
参考文献
Ferreira, Franck; Greck, Christine; Genet, Jean Pierre
Bulletin de la Societe Chimique de France, 1997 , vol. 134, # 6 p. 615 - 622