Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5221228 | Tetrahedron | 2010 | 9 Pages |
Abstract
A one pot [Cu]-promoted SNAr reaction of electron-deficient halobenzenes with sodium azide and the reduction of the intermediate aryl azides under the same Cu(II)–ascorbate redox conditions leading to anilines has been documented. Control experiments revealed that both ascorbate and proline play important role in the reaction path way. Further, the use of this catalytic Cu(II)–ascorbate redox system has been explored for the synthesis of arylthioethers.
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