反应条件
1: 204 mg / Et3N; DMAP / benzene / 0.5 h / 20 °C 2: 93 percent / PPTS / ethanol / 10 h / 50 °C 3: 79 percent / TPAP; 4 Angstroem molecular sieves; NMO / CH2Cl2 / 0.5 h / 20 °C 4: 19 percent / SmI2; HMPA; O2 / tetrahydrofuran / 1 h / -78 °C 5: Dess-Martin periodinane / CH2Cl2 / 0.5 h / 20 °C 6: 8.50 mg / NaBH4; CeCl3*7H2O / methanol / 0.08 h / 0 °C 7: 75 percent / 2,6-lutidine / CH2Cl2 / 1 h / 0 °C 8: 90 percent / DDQ; H2O / CH2Cl2 / 0.25 h / 0 °C 9: Dess-Martin periodinane / CH2Cl2 / 0.5 h / 20 °C 10: NaClO2; NaH2PO4*2H2O; 2-methyl-2-butene / 2-methyl-propan-2-ol; H2O / 0.5 h / 20 °C 11: 5.20 mg / HF*pyridine; pyridine / tetrahydrofuran / 48 h / 20 °C View Scheme
参考文献
Nagamitsu, Tohru; Takano, Daisuke; Fukuda, Takeo; Otoguro, Kazuhiko; Kuwajima, Isao; Harigaya, Yoshihiro; Omura, Satoshi
Organic Letters, 2004 , vol. 6, # 11 p. 1865 - 1867