反应条件
1.1: 80 percent / (+/-)-camphorsulfonic acid / methanol / 20 °C 2.1: 74 percent / silver(I) oxide / CH2Cl2 / 50 °C 3.1: 97 percent / lithium bis(trimethylsilyl)amide / tetrahydrofuran / -20 - -10 °C 4.1: 80 percent / tert-butyllithium / tetrahydrofuran / -96 - -78 °C 5.1: 83 percent / Zn(BH4)2 / diethyl ether / 2 h / -20 °C 6.1: 93 percent / imidazole / dimethylformamide / 50 °C 7.1: 81 percent / tert-butyllithium; hexamethylphosphoramide / tetrahydrofuran / -78 - -40 °C 8.1: 83 percent / (bis(trifluoroacetoxy)iodo)benzene / tetrahydrofuran; H2O; methanol / 20 °C 9.1: 99 percent / 1,3-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH2Cl2 / 24 h / -5 °C 10.1: 90 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / CH2Cl2 / 20 °C / pH 7 11.1: 99 percent / (COCl)2; dimethyl sulfoxide; triethylamine / CH2Cl2 12.1: 82 percent / CrCl2 / tetrahydrofuran / 0 - 20 °C 13.1: N-methylpyrrolidinone; [Pd{P(2-furyl)3}2Cl2]; hexamethyltin / 20 °C 13.2: [Pd{P(2-furyl)3}2Cl2]; N-methylpyrrolidinone / 20 °C 14.1: 81 percent / LiAlH(OtBu)3 / tetrahydrofuran / -10 °C 15.1: 81 percent / 4-pyrrolidinopyridine / CH2Cl2 16.1: 89 percent / lithium hydroxide / H2O; tetrahydrofuran / 0 °C 17.1: 88 percent / 2,6-lutidine / CH2Cl2 / -20 - 20 °C 18.1: 66 percent / 2,6-lutidine / CH2Cl2 / -20 °C 19.1: 88 percent / 1,3-dicyclohexylcarbodiimide; 4-(dimethylamino)pyridine / CH2Cl2 / 0 - 20 °C 20.1: 81 percent / potassium carbonate / dimethylformamide / 20 °C 21.1: 78 percent / lithium bis(trimethylsilyl)amide / tetrahydrofuran / -78 - -20 °C 22.1: 80 percent / dimedone / [Pd(PPh3)4] / tetrahydrofuran / 20 °C 23.1: PhI(OAc)2 / acetonitrile; H2O / 0 °C 24.1: 2,9-dimethyl-1,10-phenanthroline; pyridine / CH2Cl2 / 20 °C 25.1: 61 percent / pyridine*HF / tetrahydrofuran / 50 °C View Scheme
参考文献
Maddess, Matthew L.; Tackett, Miles N.; Watanabe, Hidenori; Brennan, Paul E.; Spilling, Christopher D.; Scott, James S.; Osborn, David P.; Ley, Steven V.
Angewandte Chemie - International Edition, 2007 , vol. 46, # 4 p. 591 - 597