反应条件
1.1: dimethyldioxirane / methanol; acetone / 2 h / 0 °C 2.1: 652 mg / CSA / acetone / 0 - 20 °C 3.1: 94 percent / sodium cyanoborohydride; TFA / tetrahydrofuran / 0.5 h / 0 °C 4.1: 92 percent / imidazole / dimethylformamide / 2 h / 20 °C 5.1: 85 percent / guanidinium nitrate; NaOMe / methanol; CH2Cl2 / 2.5 h / 40 °C 6.1: 91 percent / K2CO3 / acetonitrile / 1 h / Heating 7.1: 82 percent / Red-Al / tetrahydrofuran; toluene / 0 °C 8.1: 73 percent / BF3*OEt2 / CH2Cl2 / 0 °C 9.1: 92 percent / pyridine; DMAP / 20 °C 10.1: 100 percent / aq. HF / acetonitrile / 3 h / 20 °C 11.1: 92 percent / Dess-Martin periodinane / CH2Cl2 / 0.67 h / 20 °C 12.1: 84 percent / H2 / Pd/C / tetrahydrofuran / 18 h / 20 °C / 760.05 Torr 13.1: 89 percent / i-Pr2NEt / CH2Cl2 / 3 h / Heating 14.1: 99 percent / K2CO3 / methanol / 0.5 h / 20 °C 15.1: 94 percent / WSCD*HCl; DMAP / CH2Cl2 / 0.17 h / 20 °C 16.1: 98 percent / hydrazine / acetonitrile / 1.33 h / 20 °C 17.1: TFA / 2,2,2-trifluoro-ethanol / 3 h / 20 °C 18.1: 18.0 mg / pyridine; DMAP / 0.5 h / 20 °C 19.1: 92 percent / Zn; AcOH / diethyl ether / 2.5 h / 20 °C 20.1: 96 percent / AcOH; sodium cyanoborohydride / methanol / 1 h / 20 °C 21.1: 89 percent / Pd(PPh3)2Cl2; AcOH; n-Bu3SnH / CH2Cl2 / 0.33 h / 20 °C 22.1: 4-formyl-1-methylpyridinium benzenesulfonate / dimethylformamide; CH2Cl2 / 0.25 h / 20 °C 22.2: DBU / dimethylformamide; CH2Cl2 / 0.42 h / 20 °C 22.3: 54 percent / aq. citric acid / CH2Cl2; dimethylformamide / 0.67 h / 20 °C 23.1: 96 percent / sodium acetate / ethanol / 5.5 h / 20 °C 24.1: 93 percent / silver nitrate / acetonitrile; H2O / 17 h / 20 °C View Scheme
参考文献
Journal of the American Chemical Society, , vol. 124, # 23 p. 6552 - 6554