反应条件
1: 77 percent / diisobutylaluminium hydride / CH2Cl2; hexane / 0.5 h / -20 °C
2: 60 percent / triphenylphosphine, imidazole, diisopropylamine, iodine / diethyl ether; acetonitrile / 3 h / Ambient temperature
3: 70 percent / azoisobutyronitrile, tributyltin hydride / aq. ethanol / 12 h / Ambient temperature
4: 70 percent / tetrabutylammonium fluoride / tetrahydrofuran / 2 h / Ambient temperature
5: 97 percent / pyridinium chlorochromate, sodium acetate, Celite / CH2Cl2 / 1.5 h / Ambient temperature
6: 71 percent / tetrahydrofuran; diethyl ether / 1.8 h / -78 - 0 °C
7: 95 percent / sodium acetate, pyridinium chlorochromate / CH2Cl2 / 2 h / Ambient temperature
8: 1.) sodium hydride / 1.) THF, RT, 1 h 2.) RT, overnight
9: 80 percent / 80percent aq CH3COOH / Ambient temperature
10: 77 percent / 1N aq NaHCO3, 1N aq KOH / ethanol; tetrahydrofuran / 4.5 h / 0 °C
View Scheme
参考文献
Barrish, Joel C.; Lee, Hsi Lin; Mitt, Toomas; Pizzolato, Giacomo; Baggiolini, Enrico G; Uskokovic, Milan R
Journal of Organic Chemistry, 1988 , vol. 53, # 18 p. 4282 - 4295