反应条件
1: 85 percent / LiAlH4 / diethyl ether / 1 h / 0 - 22 °C
2: 1.) TsCl, DMAP, Et3N, 2.) TsOH, NaOCH3 / 1.) CH2Cl2, 22 deg C, 4 h, 2.) MeOH, 22 deg C, 16 h
3: Et3N, DMAP / CH2Cl2
4: NaH / tetrahydrofuran / 12 h
5: O3, pyridine / CH2Cl2
7: 76 percent / PDC, 3 Angstroem molecular sieves / CH2Cl2
8: 1.) CeI3 / 1.) THF, from -100 deg C to 0 deg C, 30 min, 2.) THF
9: 75 percent / CBr4, BaCO3, Ph3P / CH2Cl2 / 0.75 h
10: 82 percent / n-Bu3SnH, AIBN / toluene / 1 h / 65 °C
11: 98 percent / PPTs / methanol / 14 h / 22 °C
12: MnO2 / tetrahydrofuran / 5 h
13: NaCN / acetic acid / 16 h
View Scheme
参考文献
Williams; Moore; Yamada
Journal of Organic Chemistry, 1986 , vol. 51, # 20 p. 3916 - 3918