期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 66, 期 3, 页码 991-996出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo005758f
关键词
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A critically important strategy for synthetic chemistry is the development of domino processes: those capable of concatenating multiple transformations into a single step. Such transformations not only provide an increase in synthetic efficiency, but also imply the development of a significant degree of mechanistic understanding. We report herein a new domino reaction, in which a chromium-manganese redox couple is employed both to catalytically reduce an o-hydroxy nitroarene and to oxidatively cyclize a subsequently formed imine. We find that the reaction is most effective for starting o-hydroxy nitroarenes with a strongly electron-withdrawing group at the para position.
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