反应条件
1.1: 4.0 g / LiAlH4 / diethyl ether / 3 h / 0 °C
2.1: Cl2(PCy3)2Ru=CHPh / CH2Cl2 / 16 h / Heating
3.1: 60 percent / 4 Angstroem molecular sieves; NMO; TPAP / CH2Cl2 / 2 h / 20 °C
4.1: 75 percent / tetrahydrofuran / 1 h / -78 °C
5.1: 18-crown-6; KH / tetrahydrofuran / 3 h / 20 °C
5.2: 70 percent / n-BuLi / tetrahydrofuran; hexane / 3 h / -78 °C
6.1: 91 percent / PBu3 / benzene / 1 h
7.1: 98 percent / ammonium molybdate tetrahydrate; aq. H2O2 / ethanol / 0.5 h / -10 °C
8.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
8.2: 31 mg / tetrahydrofuran; hexane / 2 h / -78 °C
9.1: Na2HPO4; sodium amalgam / methanol / 3 h / -30 °C
9.2: 9 mg / HF*pyridine / tetrahydrofuran / 16 h / 20 °C
10.1: 95 percent / aq. LiOH / tetrahydrofuran / 3.5 h / 20 °C
View Scheme
参考文献
Berberich, Stephen M.; Cherney, Robert J.; Colucci, John; Courillon, Christine; Geraci, Leo S.; Kirkland, Thomas A.; Marx, Matthew A.; Schneider, Matthias F.; Martin, Stephen F.
Tetrahedron, 2003 , vol. 59, # 35 p. 6819 - 6832
