Abstract
Hydroperoxides, olefins, and arenediazonium salts selectively combine to give azo compounds via an iron(II)-mediated three-component reaction. Starting with a fragmentation liberating acetic acid, the hydroperoxides act as radical source and the diazonium ions as nitrogen-centered radical scavengers. © 2010 Elsevier Ltd. All rights reserved.
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Blank, O., Raschke, N., & Heinrich, M. R. (2010). Hydroperoxides and aryl diazonium salts as reagents for the functionalization of non-activated olefins. Tetrahedron Letters, 51(13), 1758–1760. https://doi.org/10.1016/j.tetlet.2010.01.098
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