反应条件
1.1: 4.50 g / 2,6-lutidine / CH2Cl2 / -20 - 20 °C
2.1: 90 percent / acetic acid / tetrahydrofuran; H2O / 12 h / 20 °C
3.1: 85 percent / NaBH4 / methanol / 0.5 h / 0 °C
4.1: ozone / CH2Cl2 / 0.5 h / -78 °C
4.2: 76 percent / NaBH4 / CH2Cl2; methanol
5.1: 100 percent / NaIO4 / H2O; tetrahydrofuran / 1.25 h / 0 - 20 °C
6.1: 83 percent / pyridinium chlorochromate; molecular sieves 4 Angstroem / CH2Cl2 / 2 h / 20 °C
7.1: 38 percent / BF3*Et2O / CH2Cl2 / 25 h / 0 - 20 °C
8.1: 99 percent / 2,6-lutidine / CH2Cl2 / -20 - 20 °C
9.1: HMPA; t-BuLi / tetrahydrofuran; hexane / 1.5 h / -50 - -43 °C
9.2: 87 percent / tetrahydrofuran; hexane / 1 h / -78 - -50 °C
10.1: pyridine; 4-(dimethylamino)pyridine / 20 °C
11.1: DDQ / CH2Cl2; H2O; toluene / 1 h / 20 °C
12.1: 24.7 mg / CaCO3 / methanol / 7 h / 20 °C
13.1: 2,4,6-trichlorobenzoyl chloride; triethylamine / toluene / 5 h / 20 °C
13.2: 84 percent / 4-(dimethylamino)pyridine / toluene / 0.5 h / 20 °C
14.1: pyridinium poly(hydrogen fluoride) / tetrahydrofuran / 12 h / 20 °C
15.1: 8.0 mg / mercury(II) perchlorate trihydrate; calcium carbonate / acetonitrile; H2O / 0.05 h / 20 °C
View Scheme
参考文献
Kurono, Masakuni; Isobe, Minoru
Tetrahedron, 2003 , vol. 59, # 48 p. 9609 - 9617