316. A rearrangement of o-aminodiphenyl ethers. Part III. 2-Acylamidodiphenyl ethers
作者:Kenneth C. Roberts、Charles G. M. de Worms
DOI:10.1039/jr9350001309
日期:——
Schoepff, Chemische Berichte, 1889, vol. 22, p. 900
作者:Schoepff
DOI:——
日期:——
Reverdin; Crepieux, Chemische Berichte, 1903, vol. 36, p. 3267
作者:Reverdin、Crepieux
DOI:——
日期:——
The smiles rearrangement
作者:J. Skarżewski、Z. Skrowaczewska
DOI:10.1016/0040-4020(76)80075-0
日期:1976.1
The products of the reaction between various β-(N-acylamino)ethoxides and β-(amino)ethoxides with 2,4-dinitrofluorobenzene resulted from an intramolecular nucleophilic aromatic substitution (the Smiles reaction) combined with acyl group migration from nitrogen to oxygen. Stepwise and concerted mechanisms were considered, and evidence for the stepwise mechanism was provided by the synthesis of an intermediate