反应条件
1.1: 92 percent / thionyl chloride / CCl4 / 4 h / Heating 2.1: copper(I) cyanide / tetrahydrofuran; hexane / 0.25 h / 20 °C 2.2: 90 percent / boron trifluoride diethyl etherate / tetrahydrofuran; hexane / 0.5 h / -78 °C 3.1: 16 percent / potassium trimethylsilanoate / tetrahydrofuran / 25 h / 20 °C 4.1: sodium hydrogen carbonate; bromine / methanol; CCl4; H2O / 0.01 h / 20 °C 4.2: 63 percent / di-tert-butyl peroxyoxalate; diphenyl diselenide; tributyltin hydride / toluene / 2.5 h / 0 °C 5.1: 87 percent / 1,3-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / dimethylformamide / 1.33 h / 20 °C 6.1: hydrogen / Pd/C / tetrahydrofuran / 3 h / 20 °C 7.1: 6.5 mg / diethyl ether / 0.33 h / 20 °C View Scheme
参考文献
Bodkin, Jennifer A.; Humphries, Edward J.; McLeod, Malcolm D.
Australian Journal of Chemistry, 2003 , vol. 56, # 8 p. 795 - 803