反应条件
1.1: 30 percent aq. hydrogen peroxide; phenylselenic acid / CH2Cl2 / 48 h / 20 °C
1.2: KOH / methanol / 0.5 h / 20 °C
2.1: KOH / dimethylsulfoxide / 3 h / 20 °C
3.1: 100 percent / hydrogen / 20 percent Pd(OH)2/C / methanol / 18 h / 20 °C
4.1: 98 percent / pyridine / diethyl ether / 4 h / 20 °C
5.1: AlCl3 / CH2Cl2 / 3 h / 20 °C
5.2: 94 percent / aq. HCl / methanol / 0.5 h / Heating
6.1: 60 percent / Huenig base / CH2Cl2 / 24 h / 20 °C
7.1: 77 percent / aq. K2CO3; n-Bu3NHSO4 / benzene / 20 h / 20 °C
8.1: NaH / dimethylsulfoxide / 3 h / 20 °C
8.2: aq. oxalic acid / 0 °C
8.3: AcOH; conc. HCl / 1.5 h
9.1: (COCl)2; DIPEA; DMSO / CH2Cl2 / 0.5 h / -78 - 20 °C
10.1: HMPA / tetrahydrofuran / 16 h / -85 - 20 °C
View Scheme
参考文献
Domon; Uguen
Tetrahedron Letters, 2000 , vol. 41, # 29 p. 5501 - 5505