反应条件
1: triethylamine / dichloromethane / 0 - 20 °C / |Inert atmosphere
2: palladium diacetate; sodium carbonate; dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine / N,N-dimethyl-formamide; water / 100 °C
3: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane; water / 3 h / 0 - 20 °C
4: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 20 °C / |Inert atmosphere
5: water; hydrogenchloride / dichloromethane; methanol / 0 - 20 °C
6: triethylamine / dichloromethane / |Inert atmosphere; |Reflux
7: sodium carbonate; tetrakis(triphenylphosphine) palladium(0) / water; ethanol; toluene / 100 °C
8: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane; water / 3 h / 0 - 20 °C
9: pyridine / chloroform / |Inert atmosphere; |Reflux
10: trifluoroacetic acid / dichloromethane / 2 h / 0 °C / |Inert atmosphere; |Reflux
11: tris-(dibenzylideneacetone)dipalladium(0); (S)-i-Pr-PHOX / dichloromethane / 20 °C / |Inert atmosphere
12: Grubb's 2nd generation catalyst / 40 °C / |Inert atmosphere
13: triethyl phosphite / 170 °C / |Inert atmosphere
14: water; sodium hydroxide / tetrahydrofuran; methanol / 1 h / |Reflux
15: copper; quinoline / 3 h / 190 °C / |Inert atmosphere
16: sodium; naphthalene / ethylene glycol dimethyl ether / 0.25 h / -78 °C / |Inert atmosphere
View Scheme
参考文献
Suetsugu, Satoshi; Nishiguchi, Hiromi; Tsukano, Chihiro; Takemoto, Yoshiji
Organic Letters, 2014 , vol. 16, # 3 p. 996 - 999