反应条件
1: 100 percent / H2 / Lindlar catalyst / methanol / 20 °C 2: MnO2; 4 Angstroem molecular sieves / CH2Cl2 / Heating 3: NaCNBH3; AcOH / methanol / 0 °C 4: 83 percent / KHMDS / tetrahydrofuran; toluene / 6 h / -30 °C 5: 93 percent / TPAP; 4-Angstroem molecular sieves; NMO / acetonitrile 6: aq. NaClO2; NaH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 0 °C 7: NaBH4 / methanol / 20 °C 8: 96 percent / K2OsO2(OH)4; aq. citric acid; NMO / 2-methyl-propan-2-ol / 20 °C 9: 100 percent / tetrahydrofuran / Heating 10: n-Bu3SnH; AIBN / toluene / Heating 11: 90 percent / dimethyldioxirane / acetone / 18 h / 0 - 3 °C 12: 35 percent / Dess-Martin periodinane / CH2Cl2 / 20 °C 13: 95 percent / aq. NaClO2; NaH2PO4; HOSO2NH2 / 2-methyl-propan-2-ol / 20 °C 14: 74 percent / NaOMe / methanol / 20 °C 15: 45 percent / bis(2-oxo-3-oxazolidinyl)phosphinic chloride; Et3N / CH2Cl2 / 20 °C View Scheme
参考文献
Hayes, Christopher J.; Sherlock, Alexandra E.; Selby, Matthew D.
Organic and Biomolecular Chemistry, 2006 , vol. 4, # 2 p. 193 - 195