N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.
|Original language||English (US)|
|Number of pages||4|
|Journal||Journal of the Chemical Society C: Organic Chemistry|
|State||Published - Jan 1 1971|