Aryliminodimagnesium Reagents. V. The Reaction with Bifunctional Nitroarenes
作者:Masao Okubo、Hiroyuki Aratani、Takayuki Gond\={o}、K\={o}ji Koga
DOI:10.1246/bcsj.56.788
日期:1983.3
yield of the bis(azoxy) and azoxy azo products was obtained in the same reaction with m-dinitrobenzene, which is less electron-accepting than the p-isomer. In the reaction of bis(p-nitrophenyl)methane, bis(p-nitrophenyl) sulfide and ether with five molar amounts of the reagent, ca. 70% combined yields of bis(azoxy), azoxy azo, and bis(azo) products were obtained. On the treatment of the nitrobenzaldehydes