Abstract
A cationic cobalt catalyst efficiently promoted the reaction of N-alkoxycarbonyloxyanilines at 30 °C, affording the corresponding ortho-aminophenols in good to high yields. As reported previously, our mechanistic studies including oxygen-18 labelling experiments indicate that the rearrangement of the alkoxycarbonyloxy group proceeds in [1,3]-manner. In this article, we discuss the overall picture of the cobalt-catalysed [1,3]-rearrangement reaction including details of the reaction conditions and substrate scope.
Original language | English |
---|---|
Pages (from-to) | 1972-1979 |
Number of pages | 8 |
Journal | Beilstein Journal of Organic Chemistry |
Volume | 14 |
DOIs | |
Publication status | Published - 2018 Jul 31 |
Keywords
- Anilines
- Cobalt catalyst
- Concerted reaction
- N–O bond
- Rearrangement