Abstract
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) |
|---|---|
| Pages (from-to) | 2119-2122 |
| Number of pages | 4 |
| Journal | Journal of the Chemical Society C: Organic Chemistry |
| DOIs | |
| State | Published - 1971 |
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