反应条件
1: tetrahydrofuran / 2 h / Ambient temperature
2: 2 M aq. NaN3 / tetrahydrofuran; H2O / 2 h / Ambient temperature
3: toluene / 0.5 h / Heating
4: toluene / 2 h / 60 °C
5: 100 percent / hydrogen / 10percent Pd-C / ethanol / 2 h
6: acetonitrile / 1 h
7: NaBH3CN / acetonitrile / 12 h / 50 °C
8: 85 percent / molecular sieves 3 Angstroem / ethanol / 72 h / Heating
9: hydrogen, 60percent HClO4 / Pd-black / acetic acid / 20 h / Ambient temperature
10: 5 M KOH / methanol / 3 h / Ambient temperature
11: DCC / tetrahydrofuran
12: BH3*SMe2 / tetrahydrofuran / 3 h / Ambient temperature
13: CAN / acetonitrile; H2O / 0.08 h / Ambient temperature
14: 74 percent / Na2CO3 / ethanol / 3 h / Ambient temperature
15: 24 percent / LiClO4 / acetonitrile / 1 h / electrolysis
View Scheme
参考文献
Nishiyama, Shigeru; Cheng, Ji-Fei; Tao, Xue Liang; Yamamura, Shosuke
Tetrahedron Letters, 1991 , vol. 32, # 33 p. 4151 - 4154