Influence of Substituent Groups on Nuclear Reactivity in Formations of Substituted Biphenyls through Reactions of Aromatic Diazo and Cognate Compounds with Aromatic Liquids. I. The Nitro Group
The reaction of N-nitrosoacetanilide or benzenediazo hydroxide with bromobenzene gives all three isomerides of bromobiphenyls, the yields decreasing in the order ortho > meta > para. All the nuclear positions of bromobenzene are more reactive than benzene towards attack by the phenyl radicals.
304. The replacement of the diazonium by the nitro-group. Part IV. Decompositions involving neutral solutions of diazonium salts, with facile preparations of o- and p-dinitrobenzene
作者:Herbert H. Hodgson、Fred Heyworth、Edward R. Ward
DOI:10.1039/jr9480001512
日期:——
The Mechanism of the Oxynitration of Benzene<sup>1,2</sup>
作者:F. H. Westheimer、Edward Segel、Richard Schramm
DOI:10.1021/ja01196a011
日期:1947.4
Reduction of Diazonium Salts to Hydrocarbons with Alkaline Formaldehyde
作者:Ray Q. Brewster、John A. Poje
DOI:10.1021/ja01878a044
日期:1939.9
Makarowa; Nesmejanow, Zhurnal Obshchei Khimii, 1939, vol. 9, p. 771,773,776