反应条件
1.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / 1.5 h / -78 - 0 °C / |Inert atmosphere
1.2: 0.25 h / -78 °C / |Inert atmosphere
2.1: 2,6-dimethylpyridine / tetrahydrofuran / 0.5 h / -50 °C / |Inert atmosphere
3.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 1 h / -78 - -40 °C / |Inert atmosphere
3.2: 0 - 22 °C / |Inert atmosphere
4.1: sodium dihydrogen phosphate monohydrate; 2-methyl-but-2-ene; sodium chlorite / water; tert-butyl alcohol / 3 h / 22 °C / |Inert atmosphere
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 4-(N,N-dimethlyamino)pyridine / dichloromethane / 16 h / 22 °C / |Inert atmosphere
6.1: C52H67Cl2NOW / benzene; toluene / 2.5 h / 22 °C / 1 Torr / |Inert atmosphere; |Glovebox
7.1: pyridine hydrogenfluoride / tetrahydrofuran / 36 h / 22 °C / |Inert atmosphere
View Scheme
参考文献
Wang, Chenbo; Yu, Miao; Kyle, Andrew F.; Jakubec, Pavol; Dixon, Darren J.; Schrock, Richard R.; Hoveyda, Amir H.
Chemistry - A European Journal, 2013 , vol. 19, # 8 p. 2726 - 2740